Yasuhiro Honda, MD
Clinical Professor, Medicine - Cardiovascular Medicine
Academic Appointments
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Clinical Professor, Medicine - Cardiovascular Medicine
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Member, Cardiovascular Institute
Administrative Appointments
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Director, Stanford Cardiovascular Core Analysis Laboratory (2016 - Present)
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Co-Director, Stanford Cardiovascular Core Analysis Laboratory (2005 - 2015)
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Assistant Director, Stanford Cardiovascular Core Analysis Laboratory (1999 - 2004)
Boards, Advisory Committees, Professional Organizations
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International Editorial Board, Cardiovascular Intervention and Therapeutics (2010 - Present)
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FAHA, American Heart Association (2008 - Present)
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FACC, American College of Cardiology (2005 - Present)
Professional Education
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Postdoctoral Fellowship, Stanford University, CA (1998)
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Fellowship, Kobe General Hospital, Japan (1995)
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Residency, Kobe General Hospital, Japan (1992)
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Medical Education (MD), Kyoto University, Japan (1990)
Community and International Work
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International Working Group on Intracoronary OCT Standardization and Validation
Topic
Optical Coherence Tomography
Location
International
Ongoing Project
Yes
Opportunities for Student Involvement
No
Clinical Trials
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ABSORB III Randomized Controlled Trial (RCT)
Not Recruiting
The ABSORB III RCT is a prospective randomized, single-blind, multi-center trial. It is the pivotal trial to support the US pre-market approval (PMA) of Absorb™ Bioresorbable Vascular Scaffold (BVS). The ABSORB III includes additional two trials i.e. ABSORB III PK (pharmacokinetics) sub-study and ABSORB IV RCT trial which are maintained under one protocol because both trial designs are related, ABSORB IV is the continuation of ABSORB III and the data from ABSORB III and ABSORB IV will be pooled to support the ABSORB IV primary endpoint. Both the trials will evaluate the safety and effectiveness of Absorb BVS.
Stanford is currently not accepting patients for this trial.
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AVJ-301 Clinical Trial: A Clinical Evaluation of AVJ-301 (Absorb™ BVS) in Japanese Population
Not Recruiting
Prospective, Randomized (2:1), active control, single-blind, non-inferiority, multicenter, Japanese Clinical Trial to evaluate the safety and effectiveness of Absorb™ BVS (AVJ-301) in the treatment of subjects with ischemic heart disease caused by de novo native coronary artery lesions in Japanese population by comparing to approved metallic drug eluting stent.
Stanford is currently not accepting patients for this trial.
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FAST Feasibility Study
Not Recruiting
A prospective multi-center, single arm feasibility study to assess the safety and performance of the Boston Scientific Fully Absorbable Scaffold.
Stanford is currently not accepting patients for this trial.
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TARGET BP I Clinical Trial
Not Recruiting
The TARGET BP I Trial is a randomized, blinded, multi-center, international, sham-procedure controlled trial, comparing renal denervation performed with the Peregrine System Kit in the treatment group to the sham control group (without renal denervation - no alcohol infusion). Subjects will be randomized in a 1:1 fashion to treatment versus sham control via central randomization.
Stanford is currently not accepting patients for this trial.
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The TARGET BP OFF-MED Trial
Not Recruiting
To obtain an assessment of the efficacy and safety of renal denervation by alcohol-mediated neurolysis using the Peregrine Kit in hypertensive subjects in the absence of antihypertensive medications.
Stanford is currently not accepting patients for this trial.
Graduate and Fellowship Programs
All Publications
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Prognostic value of intravascular ultrasound early after heart transplantation.
European heart journal
2023
View details for DOI 10.1093/eurheartj/ehad648
View details for PubMedID 37850514
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Intracoronary Imaging and Its Use in Interventional Cardiology.
Interventional cardiology clinics
2023; 12 (2): xv-xvi
View details for DOI 10.1016/j.iccl.2023.01.002
View details for PubMedID 36922071
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Invasive Coronary Physiology in Heart Transplant Recipients: State-of-the-Art Review.
Journal of the Society for Cardiovascular Angiography & Interventions
2023; 2 (3): 100627
Abstract
Cardiac allograft vasculopathy is a leading cause of allograft failure and death among heart transplant recipients. Routine coronary angiography and intravascular ultrasound in the early posttransplant period are widely accepted as the current standard-of-care diagnostic modalities. However, many studies have now demonstrated that invasive coronary physiological assessment provides complementary long-term prognostic data and helps identify patients who are at risk of accelerated cardiac allograft vasculopathy and acute rejection.
View details for DOI 10.1016/j.jscai.2023.100627
View details for PubMedID 39130712
View details for PubMedCentralID PMC11307478
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IMPACT OF MYOCARDIAL BRIDGING ON LONG TERM OUTCOMES AFTER HEART TRANSPLANTATION: AN INTRAVASCULAR ULTRASOUND OBSERVATION FROM AN INTERNATIONAL MULTICENTER HEART TRANSPLANT REGISTRY
ELSEVIER SCIENCE INC. 2023: 1390
View details for Web of Science ID 000990866101402
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Impact of myocardial bridging on coronary artery plaque formation and long-term mortality after heart transplantation.
International journal of cardiology
2023
Abstract
OBJECTIVES: This study aimed to explore the impact of myocardial bridging (MB) on early development of cardiac allograft vasculopathy and long-term graft survival after heart transplantation.BACKGROUND: MB has been reported to be associated with acceleration of proximal plaque development and endothelial dysfunction in native coronary atherosclerosis. However, its clinical significance in heart transplantation remains unclear.METHODS: In 103 heart-transplant recipients, serial (baseline and 1-year post-transplant) volumetric intravascular ultrasound (IVUS) analyses were performed in the first 50 mm of the left anterior descending (LAD) artery. Standard IVUS indices were evaluated in 3 equally divided LAD segments (proximal, middle, and distal segments). MB was defined by IVUS as an echolucent muscular band lying on top of the artery. The primary endpoint was death or re-transplantation, assessed for up to 12.2 years (median follow-up: 4.7 years).RESULTS: IVUS identified MB in 62% of the study population. At baseline, MB patients had smaller intimal volume in the distal LAD than non-MB patients (p = 0.002). During the first year, vessel volume decreased diffusely irrespective of the presence of MB. Intimal growth diffusely distributed in non-MB patients, whereas MB patients demonstrated significantly augmented intimal formation in the proximal LAD. Kaplan-Meier analysis revealed significantly lower event-free survival in patients with versus without MB (log-rank p = 0.02). In multivariate analysis, the presence of MB was independently associated with late adverse events [hazard ratio 5.1 (1.6-22.2)].CONCLUSION: MB appears to relate to accelerated proximal intimal growth and reduced long-term survival in heart-transplant recipients.
View details for DOI 10.1016/j.ijcard.2023.03.014
View details for PubMedID 36893856
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Heterogeneous vascular response after implantation of bare nitinol self-expanding stents in the swine femoropopliteal artery.
Cardiovascular intervention and therapeutics
2022
Abstract
BACKGROUND: Mechanism of femoropopliteal in-stent restenosis has been underappreciated.AIM: The aim of this animal study was to elucidate vascular response after femoropopliteal bare nitinol self-expanding stents (SESs) implantation.METHODS: Misago, Smart Flex, or Innova stent was randomly implanted in 36 swine femoropopliteal arteries. At week 4, quantitative vessel analysis (QVA) was performed on 36 legs, of which 18 underwent histological evaluation after angiography. The remaining 18 legs underwent QVA and histological evaluation at week 13.RESULTS: Fibrin deposition was excessive at week 4. Internal elastic lamina (IEL) progressively enlarged over time, and vessel injury developed from mild level at week 4 to moderate level at week 13. Vessel inflammatory reaction was mild to moderate at week 4, and was moderate to severe at week 13. Increased fibrin deposition was an early-acting, IEL enlargement and increased vessel inflammation were long-acting, and increased vessel injury and giant cells infiltration were late-acting contributors to neointimal hyperplasia (NIH). Stent type altered time-dependent process of vessel injury, vessel inflammation, eosinophils and giant cells infiltration. Misago had less fibrin deposition and vessel enlargement, and less progressive vessel injury, vessel inflammation, and eosinophils and giant cells infiltration. Net lumen as assessed by percent diameter stenosis or minimum lumen diameter was preserved with Misago, but was not preserved with the other stents.CONCLUSIONS: In the context of bare nitinol SES platform with less progressive mechanical stress and inflammatory reaction, the advantage of less NIH outweighed the disadvantage of less vessel enlargement, leading to net lumen preservation.
View details for DOI 10.1007/s12928-022-00889-5
View details for PubMedID 36255689
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Invasive Coronary Imaging Assessment for Cardiac Allograft Vasculopathy: State-of-the-Art Review.
Journal of the Society for Cardiovascular Angiography & Interventions
2022; 1 (4): 100344
Abstract
Heart transplantation is the standard of care treatment for end-stage heart failure. Therapeutic advances including enhanced immunosuppression and aggressive infectious prophylaxis have led to increased life-expectancy following transplantation; however, cardiac allograft vasculopathy (CAV) remains a leading cause of morbidity and mortality. Although coronary angiography is the current guideline-recommended diagnostic modality for invasive CAV screening, it is limited in its ability to detect early and/or diffuse disease. Efforts to improve outcomes for heart transplant recipients with CAV have focused on developing diagnostic tools with greater sensitivity to capture early CAV in order to better understand the pathobiology and implement treatment to slow disease progression sooner after transplant. The contemporary invasive imaging armamentarium for CAV surveillance includes coronary angiography, intravascular ultrasound, and newer technologies including optical coherence tomography and near-infrared spectroscopy. The present review outlines the use of and data in support of these imaging platforms in the CAV arena and highlights the potential advantages and limitations of each of these modalities.
View details for DOI 10.1016/j.jscai.2022.100344
View details for PubMedID 39131933
View details for PubMedCentralID PMC11307976
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Multicenter Evaluation of Volumetric Intravascular Ultrasound Early After Heart Transplantation and Long-Term Prognosis
ELSEVIER SCIENCE INC. 2022: S315-S316
View details for Web of Science ID 000780119701018
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Colocalization of Coronary Plaque with Wall Shear Stress in Myocardial Bridge Patients.
Cardiovascular engineering and technology
2022
Abstract
PURPOSE: Patients with myocardial bridges (MBs) have a higher prevalence of atherosclerosis. Wall shear stress (WSS) has previously been correlated with plaque in coronary artery disease patients, but such correlations have not been investigated in symptomatic MB patients. The aim of this paper was to use a multi-scale computational fluid dynamics (CFD) framework to simulate hemodynamics in MB patient, and investigate the co-localization of WSS and plaque.METHODS: We identified N = 10 patients from a previously reported cohort of 50 symptomatic MB patients, all of whom had plaque in the proximal vessel. Dynamic 3D models were reconstructed from coronary computed tomography angiography (CCTA), intravascular ultrasound (IVUS) and catheter angiograms. CFD simulations were performed to compute WSS proximal to, within and distal to the MB. Plaque was quantified from IVUS images in 2 mm segments and registered to CFD model. Plaque area was compared to absolute and patient-normalized WSS.RESULTS: WSS was lower in the proximal segment compared to the bridge segment (6.1 ± 2.9 vs. 16.0 ± 7.1 dynes/cm2, p value < 0.01). Plaque area and plaque burden measured from IVUS peaked at 1-3 cm proximal to the MB entrance, coinciding with the first diagonal branch. Normalized WSS showed a statistically significant moderate correlation with plaque area (r = 0.41, p < 0.01).CONCLUSION: WSS may be obtained non-invasively in MB patients and provides a surrogate marker of plaque area. Using CFD, it may be possible to non-invasively assess the extent of plaque area, and identify patients who could benefit from frequent monitoring or medical management.
View details for DOI 10.1007/s13239-022-00616-4
View details for PubMedID 35296987
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Microcirculatory Resistance Predicts Allograft Rejection and Cardiac Events After Heart Transplantation.
Journal of the American College of Cardiology
2021; 78 (24): 2425-2435
Abstract
BACKGROUND: Single-center data suggest that the index of microcirculatory resistance (IMR) measured early after heart transplantation predicts subsequent acute rejection.OBJECTIVES: The goal of this study was to validate whether IMR measured early after transplantation can predict subsequent acute rejection and long-term outcome in a large multicenter cohort.METHODS: From 5 international cohorts, 237 patients who underwent IMR measurement early after transplantation were enrolled. The primary outcome was acute allograft rejection (AAR) within 1 year after transplantation. A key secondary outcome was major adverse cardiac events (MACE) (the composite of death, re-transplantation, myocardial infarction, stroke, graft dysfunction, and readmission) at 10 years.RESULTS: IMR was measured at a median of 7weeks (interquartile range: 3-10weeks) post-transplantation. At 1 year, the incidence of AAR was 14.4%. IMR was associated proportionally with the risk of AAR (per increase of 1-U IMR; adjusted hazard ratio [aHR]: 1.04; 95% confidence interval [CI]: 1.02-1.06; p < 0.001). The incidence of AAR in patients with an IMR≥18 was 23.8%, whereas the incidence of AAR in those with an IMR<18 was 6.3% (aHR: 3.93; 95%CI: 1.77-8.73; P=0.001). At 10 years, MACE occurred in 86 (36.3%) patients. IMR was significantly associated with the risk of MACE (per increase of 1-U IMR; aHR: 1.02; 95%CI: 1.01-1.04; P=0.005).CONCLUSIONS: IMR measured early after heart transplantation is associated with subsequent AAR at 1 year and clinical events at 10 years. Early IMR measurement after transplantation identifies patients at higher risk and may guide personalized posttransplantation management.
View details for DOI 10.1016/j.jacc.2021.10.009
View details for PubMedID 34886963
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Fractional Flow Reserve-Guided PCI as Compared with Coronary Bypass Surgery.
The New England journal of medicine
2021
Abstract
BACKGROUND: Patients with three-vessel coronary artery disease have been found to have better outcomes with coronary-artery bypass grafting (CABG) than with percutaneous coronary intervention (PCI), but studies in which PCI is guided by measurement of fractional flow reserve (FFR) have been lacking.METHODS: In this multicenter, international, noninferiority trial, patients with three-vessel coronary artery disease were randomly assigned to undergo CABG or FFR-guided PCI with current-generation zotarolimus-eluting stents. The primary end point was the occurrence within 1 year of a major adverse cardiac or cerebrovascular event, defined as death from any cause, myocardial infarction, stroke, or repeat revascularization. Noninferiority of FFR-guided PCI to CABG was prespecified as an upper boundary of less than 1.65 for the 95% confidence interval of the hazard ratio. Secondary end points included a composite of death, myocardial infarction, or stroke; safety was also assessed.RESULTS: A total of 1500 patients underwent randomization at 48 centers. Patients assigned to undergo PCI received a mean (±SD) of 3.7±1.9 stents, and those assigned to undergo CABG received 3.4±1.0 distal anastomoses. The 1-year incidence of the composite primary end point was 10.6% among patients randomly assigned to undergo FFR-guided PCI and 6.9% among those assigned to undergo CABG (hazard ratio, 1.5; 95% confidence interval [CI], 1.1 to 2.2), findings that were not consistent with noninferiority of FFR-guided PCI (P=0.35 for noninferiority). The incidence of death, myocardial infarction, or stroke was 7.3% in the FFR-guided PCI group and 5.2% in the CABG group (hazard ratio, 1.4; 95% CI, 0.9 to 2.1). The incidences of major bleeding, arrhythmia, and acute kidney injury were higher in the CABG group than in the FFR-guided PCI group.CONCLUSIONS: In patients with three-vessel coronary artery disease, FFR-guided PCI was not found to be noninferior to CABG with respect to the incidence of a composite of death, myocardial infarction, stroke, or repeat revascularization at 1 year. (Funded by Medtronic and Abbott Vascular; FAME 3 ClinicalTrials.gov number, NCT02100722.).
View details for DOI 10.1056/NEJMoa2112299
View details for PubMedID 34735046
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Intravascular Imaging to Guide PCI for Acute Myocardial Infarction: Shifting From "Whether" to "How".
JACC. Cardiovascular interventions
2021
View details for DOI 10.1016/j.jcin.2021.09.010
View details for PubMedID 34756538
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Prognostic value of comprehensive intracoronary physiology assessment early after heart transplantation.
European heart journal
2021
Abstract
AIMS: We evaluated the long-term prognostic value of invasively assessing coronary physiology after heart transplantation in a large multicentre registry.METHODS AND RESULTS: Comprehensive intracoronary physiology assessment measuring fractional flow reserve (FFR), the index of microcirculatory resistance (IMR), and coronary flow reserve (CFR) was performed in 254 patients at baseline (a median of 7.2weeks) and in 240 patients at 1year after transplantation (199 patients had both baseline and 1-year measurement). Patients were classified into those with normal physiology, reduced FFR (FFR≤0.80), and microvascular dysfunction (either IMR≥25 or CFR≤2.0 with FFR>0.80). The primary outcome was the composite of death or re-transplantation at 10years. At baseline, 5.5% had reduced FFR; 36.6% had microvascular dysfunction. Baseline reduced FFR [adjusted hazard ratio (aHR) 2.33, 95% confidence interval (CI) 0.88-6.15; P=0.088] and microvascular dysfunction (aHR 0.88, 95% CI 0.44-1.79; P=0.73) were not predictors of death and re-transplantation at 10years. At 1year, 5.0% had reduced FFR; 23.8% had microvascular dysfunction. One-year reduced FFR (aHR 2.98, 95% CI 1.13-7.87; P=0.028) and microvascular dysfunction (aHR 2.33, 95% CI 1.19-4.59; P=0.015) were associated with significantly increased risk of death or re-transplantation at 10years. Invasive measures of coronary physiology improved the prognostic performance of clinical variables (chi2 improvement: 7.41, P=0.006). However, intravascular ultrasound-derived changes in maximal intimal thickness were not predictive of outcomes.CONCLUSION: Abnormal coronary physiology 1year after heart transplantation was common and was a significant predictor of death or re-transplantation at 10years.
View details for DOI 10.1093/eurheartj/ehab568
View details for PubMedID 34665224
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Impact of Diastolic Vessel Restriction on Quality of Life in Symptomatic Myocardial Bridging Patients Treated With Surgical Unroofing: Preoperative Assessments With Intravascular Ultrasound and Coronary Computed Tomography Angiography.
Circulation. Cardiovascular interventions
2021; 14 (10): e011062
Abstract
[Figure: see text].
View details for DOI 10.1161/CIRCINTERVENTIONS.121.011062
View details for PubMedID 34665656
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Head-to-head comparison of quantitative measurements between intravascular imaging systems: An in vitro phantom study.
International journal of cardiology. Heart & vasculature
2021; 36: 100867
Abstract
Introduction: The present study aimed to compare the accuracy of quantitative measurements by contemporary intravascular imaging systems including optical frequency domain imaging (OFDI), frequency domain optical coherence tomography (FD-OCT), and 6 intravascular ultrasound (IVUS) systems.Methods: We imaged five cylindrical phantom models made from an acrylic resin with known lumen diameters (1.51, 2.03, 3.04, 4.04, and 5.04 mm, respectively) using OFDI (FastView and LUNAWAVE, Terumo), FD-OCT (Dragonfly JP and ILUMIEN OPTIS, Abbott Vascular), and 6 mechanically rotating IVUS systems including a system, two 40-MHz, one 45-MHz, two 60-Mhz and one broad-band frequency IVUS systems. The OFDI, FD-OCT, and IVUS images were obtained using automated motorized pullback in a tank filled with 37-degree Celsius saline and, in cases of OFDI and FD-OCT, contrast-saline mixture (1:1 ratio) and contrast under the system setting of the refractive index for the corresponding flush medium.Results: All the imaging systems showed good accuracy and excellent precision of lumen measurement with the relative differences between the measured diameter and actual phantom diameter being ranging from -2.9% to 8.0% and minimum standard deviations of the measured diameters (≤0.02 mm).Conclusion: The present study demonstrated that contemporary intravascular imaging systems including OFDI, FD-OCT, and IVUS provided clinically acceptable accuracy and excellent precision of quantitative lumen measurement in phantom models in vitro across a wide range of dimensions. Future research to confirm these findings in vivo are warranted.
View details for DOI 10.1016/j.ijcha.2021.100867
View details for PubMedID 34504947
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IMPACT OF DIASTOLIC VESSEL RESTRICTION ON CLINICAL SYMPTOMS IN PATIENTS WITH SYMPTOMATIC MYOCARDIAL BRIDGING
ELSEVIER SCIENCE INC. 2021: 165
View details for Web of Science ID 000647487500165
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Intravascular ultrasound predictors of long-term outcomes following ABSORB bioresorbable scaffold implantation: A pooled analysis of the ABSORB III and ABSORB Japan trials.
Journal of cardiology
2021
Abstract
BACKGROUND: The long-term prognostic impact of IVUS findings following Absorb BVS implantation remains uncertain. This study aimed to identify the IVUS predictors of long-term clinical outcomes following ABSORB bioresorbable vascular scaffold (BVS) implantation from the pooled IVUS substudy cohorts of the ABSORB III and Japan trials.METHODS: A total of 298 lesions in 286 patients were enrolled with 2:1 randomization to ABSORB BVS vs. cobalt-chromium everolimus-eluting stents. This sub-analysis included 168 lesions of 160 patients in the Absorb arm whose post-procedural quantitative IVUS were available. The primary endpoint of this analysis was device-oriented composite endpoint (DOCE) of target lesion failure, including cardiac death, target vessel-related myocardial infarction, or ischemia-driven target lesion revascularization. The median follow-up duration was 4.9 [3.1-5.0] years.RESULTS: During follow-up, DOCE occurred in 10.1% of lesions treated with Absorb BVS. Among several post-procedural IVUS indices associated with DOCE, non-uniform device expansion (defined as uniformity index=minimum / maximum device area) (hazard ratio 0.47 per 0.1 increase [95%CI 0.28 to 0.77]; p=0.003) and residual reference plaque burden (hazard ratio 4.01 per 10% increase [95%CI 1.50 to 10.77]; p=0.006) were identified as independent predictors of DOCE by Cox multivariable analysis.CONCLUSIONS: Nonuniform device expansion and substantial untreated residual plaque in reference segments were associated with long-term adverse events following BVS implantation. Baseline imaging to identify the appropriate device landing zone and procedural imaging to achieve uniform device expansion if possible (e.g. through post-dilatation) may improve clinical outcomes of BVS implantation.CLINICAL TRIAL REGISTRATION: URL: http://www.clinicaltrials.gov. Unique identifier: NCT01751906 (ABSORB III); NCT01844284 (ABSORB Japan).
View details for DOI 10.1016/j.jjcc.2021.03.005
View details for PubMedID 33893022
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Deep learning-based intravascular ultrasound segmentation for the assessment of coronary artery disease.
International journal of cardiology
2021
Abstract
BACKGROUND: Accurate segmentation of the coronary arteries with intravascular ultrasound (IVUS) is important to optimize coronary stent implantation. Recently, deep learning (DL) methods have been proposed to develop automatic IVUS segmentation. However, most of those have been limited to segmenting the lumen and vessel (i.e. lumen-intima and media-adventitia borders), not applied to segmenting stent dimension. Hence, this study aimed to develop a DL method for automatic IVUS segmentation of stent area in addition to lumen and vessel area.METHODS: This study included a total of 45,449 images from 1576 IVUS pullback runs. The datasets were randomly split into training, validation, and test datasets (0.7:0.15:0.15). After developing the DL-based system to segment IVUS images using the training and validation datasets, we evaluated the performance through the independent test dataset.RESULTS: The DL-based segmentation correlated well with the expert-analyzed segmentation with a mean intersection over union (± standard deviation) of 0.80 ± 0.20, correlation coefficient of 0.98 (95% confidence intervals: 0.98 to 0.98), 0.96 (0.95 to 0.96), and 0.96 (0.96 to 0.96) for lumen, vessel, and stent area, and the mean difference (± standard deviation) of 0.02 ± 0.57, -0.44 ± 1.56 and - 0.17 ± 0.74 mm2 for lumen, vessel and stent area, respectively.CONCLUSION: This automated DL-based IVUS segmentation of lumen, vessel and stent area showed an excellent agreement with manual segmentation by experts, supporting the feasibility of artificial intelligence-assisted IVUS assessment in patients undergoing coronary stent implantation.
View details for DOI 10.1016/j.ijcard.2021.03.020
View details for PubMedID 33741429
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Drug-eluting stent thrombosis: current and future perspectives.
Cardiovascular intervention and therapeutics
2021
Abstract
Over the past 40years, the safety and efficacy of percutaneous coronary intervention has dramatically improved by overcoming several challenges. The introduction of drug-eluting stent (DES) in particular was a major breakthrough in interventional cardiology. Compared to bare-metal stents, first-generation DES (G1-DES) has dramatically reduced the rates of in-stent restenosis and subsequent target lesion revascularization. However, major safety concerns surrounding stent thrombosis (ST) emerged with G1-DES in clinical practice as a result of the high incidences of death, myocardial infarction, and repeat revascularization associated with ST. To overcome these limitations, second-generation DES (G2-DES) has been developed with an improved stent platform with thinner strut and biocompatible durable or biodegradable polymers. Indeed, G2-DES, when compared with G1-DES, has improved clinical outcomes by reducing the risk of late thrombotic events while maintaining anti-restenotic efficacy, whereas ST still occurs, even with the use of G2-DES. This review gives an overview of pathophysiology, risk factors, and outcomes of ST after DES implantation. Additionally, we discuss the management and prevention of ST.
View details for DOI 10.1007/s12928-021-00754-x
View details for PubMedID 33439454
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Bioresorbable vascular scaffolds versus everolimus-eluting stents: a biomechanical analysis of the ABSORB III Imaging substudy
EUROINTERVENTION
2020; 16 (12): E989-+
Abstract
The Absorb bioresorbable vascular scaffold (BVS) has high rates of target lesion failure (TLF) at three years. Low wall shear stress (WSS) promotes several mechanisms related to device TLF. We investigated the impact of BVS compared to XIENCE V (XV) on coronary WSS after device deployment.In the prospective, randomised, controlled ABSORB III Imaging study (BVS [n=77] or XV [n=36]), computational fluid dynamics were performed on fused angiographic and intravascular ultrasound (IVUS) images of post-implanted vessels. Low WSS was defined as <1 Pa. There were no differences in demographics, clinical risks, angiographic reference vessel diameter or IVUS minimal lumen diameter between BVS and XV patients. A greater proportion of vessels treated with BVS compared to XV demonstrated low WSS across the whole device (BVS: 17/77 [22%] vs XV: 2/36 [6%], p<0.029). Compared to XV, BVS demonstrated lower median circumferential WSS (1.73 vs 2.21 Pa; p=0.036), outer curvature WSS (p=0.026), and inner curvature WSS (p=0.038). Similarly, BVS had lower proximal third WSS (p=0.024), middle third WSS (p=0.047) and distal third WSS (p=0.028) when compared to XV. In a univariable logistic regression analysis, patients who received BVS were 4.8 times more likely to demonstrate low WSS across the scaffold/stent when compared to XV patients. Importantly, in a multivariable linear regression model, hypertension (beta: 0.186, p=0.023), lower contrast frame count velocity (beta: -0.411, p<0.001), lower post-stent residual plaque burden (beta: -0.338, p<0.001), lower % underexpanded frames (beta: -0.170, p=0.033) and BVS deployment (beta: 0.251, p=0.002) remained independently associated with a greater percentage of stented coronary vessel areas exposed to low WSS.In this randomised controlled study, the Absorb BVS was 4.8 times more likely than the XV metallic stent to demonstrate low WSS. BVS implantation, lower blood velocity and lower residual post-stent plaque burden were independently associated with greater area of low WSS.
View details for DOI 10.4244/EIJ-D-19-01128
View details for Web of Science ID 000600744700008
View details for PubMedID 32091401
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Current status of hybrid intravascular ultrasound and optical coherence tomography catheter for coronary imaging and percutaneous coronary intervention.
Journal of cardiology
2020
Abstract
Both intravascular ultrasound (IVUS) and optical coherence tomography (OCT) play a crucial role in elucidating the pathophysiology of coronary artery disease (CAD) with the goal to improve patient outcomes of medical and/or interventional CAD management. However, no single intravascular imaging technique has been proven to provide complete and detailed evaluation of all CAD lesions due to some limitations. Although sequential use of multiple modalities may sometimes be performed, there may be issues related to risk, time, and cost. To overcome these problems, several hybrids involving dual-probe combined IVUS-OCT catheters have been developed. The aim of this review article is to demonstrate some limitations of stand-alone imaging devices for evaluation of CAD, summarize the advances in hybrid IVUS-OCT imaging devices, discuss the technical challenges, and present the potential value in the clinical setting, especially in patients receiving medical or interventional CAD management.
View details for DOI 10.1016/j.jjcc.2020.08.012
View details for PubMedID 33158714
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A First-in-Human Study of the Second-Generation, Thin-Strut, Everolimus- Eluting Bioresorbable Scaffold: Final IVUS and OCT Results From the FAST Clinical Trial
ELSEVIER SCIENCE INC. 2020: B117–B118
View details for Web of Science ID 000597114500257
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Intravascular Ultrasound Radiofrequency Signal Analysis for Simultaneous Assessment of Functional Significance and Structural Abnormality of Intermediate Coronary Artery Lesions
ELSEVIER SCIENCE INC. 2020: B123–B124
View details for Web of Science ID 000597114500272
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Invasive Assessment of Myocardial Bridging in Patients with Angina and No Obstructive Coronary Artery Disease.
EuroIntervention : journal of EuroPCR in collaboration with the Working Group on Interventional Cardiology of the European Society of Cardiology
2020
Abstract
AIMS: Angina and no obstructive CAD (ANOCA) is common. A potential cause of angina in this patient population is a myocardial bridge (MB). We studied the anatomical and hemodynamic characteristics of an MB in patients with angina and no obstructive CAD.METHODS AND RESULTS: Using intravascular ultrasound (IVUS), we identified 184 MBs in 154 patients. We evaluated MB length, arterial compression, and halo thickness. MB muscle index (MMI) was defined as MB length*halo thickness. Hemodynamic testing of the MB was performed using an intracoronary pressure/Doppler flow wire at rest and during dobutamine stress. We defined an abnormal diastolic fractional flow reserve (dFFR) as ≤0.76 during stress. The median MB length was 22.9 mm, arterial compression 30.9%, and halo thickness 0.5mm. The median MMI was 12.1. Endothelial and microvascular dysfunction were present in 85.4% and 22.1%, respectively. At peak dobutamine stress, 94.2% of patients had a dFFR≤0.76 within and/or distal to the MB. MMI was associated with an abnormal dFFR.CONCLUSIONS: In select patients with ANOCA who have an MB by IVUS, a majority have evidence of a hemodynamically significant dFFR during dobutamine stress, suggesting the MB as a cause of their angina. A comprehensive invasive assessment of such patients during coronary angiography provides important diagnostic information that can guide management.
View details for DOI 10.4244/EIJ-D-20-00779
View details for PubMedID 33074153
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Association between abdominal fat distribution and coronary plaque instability in patients with acute coronary syndrome.
Nutrition, metabolism, and cardiovascular diseases : NMCD
2020
Abstract
BACKGROUND AND AIMS: This study aimed to assess possible association of detailed abdominal fat profiles with coronary plaque characteristics in patients with acute coronary syndrome (ACS).METHODS AND RESULTS: In 60 patients with ACS, culprit arteries were evaluated at 1-mm intervals (length analyzed: 66±28mm) by grayscale and integrated backscatter intravascular ultrasound (IB-IVUS) before percutaneous coronary intervention. Standard IVUS indexes (as a volume index: volume/length), plaque components (as percent tissue volume) and fibrous cap thickness (FCT) were assessed by IB-IVUS. Plain abdominal computed tomography was performed to evaluate subcutaneous adipose tissue (SAT) area, visceral adipose tissue (VAT) area, and VAT/SAT ratio. While SAT area only correlated with vessel volume (r=0.27, p=0.04), VAT area correlated positively with vessel (r=0.30, p=0.02) and plaque (r=0.33, p=0.01) volumes and negatively with FCT (r=-0.26, p=0.049), but not with percent plaque volume and plaque tissue components. In contrast, higher VAT/SAT ratio significantly correlated with higher percent lipid (r=0.34, p=0.008) and lower percent fibrous (r=-0.34, p=0.007) volumes with a trend toward larger percent plaque volume (r=0.19, p=0.15), as well as thinner FCT (r=-0.53, p<0.0001). In the multiple regression analysis, higher VAT/SAT ratio was independently associated with higher percent lipid with lower percent fibrous volumes (p=0.03 for both) and thinner fibrous cap thickness (p=0.0001).CONCLUSION: Coronary plaque vulnerability, defined as increased lipid content with thinner fibrous cap thickness, appears to be more related to abnormal abdominal fat distribution, or so-called hidden obesity, compared with visceral or subcutaneous fat amount alone in patients with ACS.
View details for DOI 10.1016/j.numecd.2020.03.017
View details for PubMedID 32448720
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FEASIBILITY OF IVUS-DERIVED FFR AS A NOVEL TECHNIQUE TO ESTIMATE FUNCTIONAL SEVERITY OF CORONARY STENOSIS: SYSTEMATIC EVALUATION OF THE METHODS TO DETERMINE THE REFERENCE LUMEN AREA FOR AUTOMATED FFR CALCULATION
ELSEVIER SCIENCE INC. 2020: 1387
View details for Web of Science ID 000522979101373
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The Absorb Bioresorbable Vascular Scaffold Demonstrates Low Wall Shear Stress and High Eccentricity Index: Hemodynamic Insights From the ABSORB III Imaging Study
ELSEVIER SCIENCE INC. 2020: S42–S43
View details for Web of Science ID 000513916500109
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Long-term clinical outcomes with use of an angiotensin-converting enzyme inhibitor early after heart transplantation.
American heart journal
2020; 222: 30–37
Abstract
BACKGROUND: The safety and efficacy of angiotensin converting enzyme inhibition (ACEI) after heart transplantation (HT) is unknown. This study examined long-term clinical outcomes after ACEI in HT recipients.METHODS: The ACEI after HT study was a prospective, randomized trial that tested the efficacy of ACEI with ramipril after HT. In this study, long-term clinical outcomes were assessed in 91 patients randomized to either ramipril or placebo (median, 5.8 years). The primary endpoint was a composite of death, retransplantation, hospitalization for rejection or heart failure, and coronary revascularization.RESULTS: The primary endpoint occurred in 10 of 45 patients (22.2%) in the ramipril group and in 14 of 46 patients (30.4%) in the placebo group (Hazard ratio (HR), 0.68; 95% CI, 0.29-1.51; P = .34). When the analysis was restricted to comparing patients who remained on a renin-angiotensin system inhibitor beyond 1 year with those who did not, there was a trend to improved outcomes (HR, 0.54; 95% CI, 0.22-1.28, P = .16). There was no significant difference in creatinine, blood urea nitrogen, and potassium at 3 years after randomization. The cumulative incidence of the primary endpoint was significantly higher in patients in whom the index of microcirculatory resistance increased from baseline to 1 year compared with those in whom it did not (39.1 vs 17.4%, HR: 3.36; 95% CI, 1.07-12.7; P = .037).CONCLUSION: The use of ramipril after HT safely lowers blood pressure and is associated with favorable long-term clinical outcomes. Clinical Trial Registration-URL: https://www.clinicaltrials.gov. Unique identifier: NCT01078363.
View details for DOI 10.1016/j.ahj.2020.01.003
View details for PubMedID 32007823
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Randomized Comparison Between Everolimus-Eluting Bioresorbable Scaffold and Metallic Stent: Multimodality Imaging Through 3 Years.
JACC. Cardiovascular interventions
2020; 13 (1): 116–27
Abstract
The aim of this study was to investigate the vascular responses and fates of the scaffold after bioresorbable vascular scaffold (BVS) implantation using multimodality imaging.Serial comprehensive image assessments after BVS implantation in the context of a randomized trial have not yet been reported.In the ABSORB Japan trial, 400 patients were randomized to a BVS (n = 266) or a cobalt-chromium everolimus-eluting stent (n = 134). Through 3 years, patients underwent serial angiography and intravascular ultrasound or optical coherence tomography (OCT).Luminal dimension at 3 years was consistently smaller with the BVS than with the cobalt-chromium everolimus-eluting stent (mean angiographic minimal luminal diameter 2.04 ± 0.63 mm vs. 2.40 ± 0.56 mm, mean difference -0.37 mm [95% confidence interval: -0.50 to -0.24 mm]; p < 0.001), mainly because of smaller device area (6.13 ± 2.03 mm2 vs. 7.15 ± 2.16 mm2, mean difference -1.04 mm2 [95% confidence interval: -1.66 to -0.42 mm2]; p < 0.001), and larger neointimal area (2.10 ± 0.61 mm2 vs. 1.86 ± 0.64 mm2, mean difference 0.24 mm2 [95% confidence interval: 0.06 to 0.43 mm2]; p = 0.01) by OCT. BVS-treated vessels did not show previously reported favorable vessel responses, such as positive vessel remodeling, late luminal enlargement, and restoration of vasomotion, although the OCT-based healing score was on average zero (interquartile range: 0.00 to 0.00). At 3 years, intraluminal scaffold dismantling (ISD) was observed in 14% of BVS. On serial OCT, ISD was observed in 6 lesions at 2 years, where the struts had been fully apposed at post-procedure, while ISD was observed in 12 lesions at 3 years, where 8 lesions were free from ISD on 2-year OCT. In 5 cases of very late scaffold thrombosis, strut discontinuities were detected in all 4 cases with available OCT immediately before reintervention.In this multimodality serial imaging study, luminal dimension at 3 years was smaller with the BVS than with the cobalt-chromium everolimus-eluting stent. ISD, suspected to be one of the mechanisms of very late BVS thrombosis, was observed in a substantial proportion of cases at 3 years, which developed between post-procedure and 2 years and even beyond 2 years. (AVJ-301 Clinical Trial: A Clinical Evaluation of AVJ-301 [Absorb™ BVS] in Japanese Population [ABSORB JAPAN]; NCT01844284).
View details for DOI 10.1016/j.jcin.2019.09.047
View details for PubMedID 31918929
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Off-Pump Mini Thoracotomy Versus Sternotomy for Left Anterior Descending Myocardial Bridge Unroofing.
The Annals of thoracic surgery
2020
Abstract
Myocardial bridge (MB) of the left anterior descending (LAD) coronary artery occurs in approximately 25% of the population. For patients with a symptomatic, hemodynamically significant MB who fail medical therapy, MB unroofing represents the optimal surgical management. Here, we evaluated minimally invasive MB unroofing in selected patients compared with sternotomy.MB unroofing was performed in 141 adult patients via sternotomy on-pump (ST-on, n=40), sternotomy off-pump (ST-off, n=62), or mini thoracotomy off-pump (MT, n=39). Angina symptoms were assessed preoperatively and 6-months postoperatively using the Seattle Angina Questionnaire. Matching included all MT patients and 31 ST-off patients with similar MB characteristics, no previous cardiac surgery or coronary interventions, and no concomitant procedures.MT patients tended to have a shorter MB length than ST-on and ST-off patients (2.57 vs 2.93 vs 3.09 cm, p=0.166). ST-on patients had a longer hospital stay than ST-off and MT patients (5.0 vs 4.0 vs 3.0 days, p<0.001), and more blood transfusions (15.2% vs 0.0% vs 2.6%, p=0.002). After matching, MT patients had a shorter hospital stay than ST-off patients (3.0 vs 4.0 days, p=0.005). No deaths or major complications occurred in any group. In all groups, MB unroofing yielded significant symptomatic improvement regarding physical limitation, angina stability, angina frequency, treatment satisfaction, and quality of life.We report the largest experience of off-pump minimally invasive MB unroofing, which may be safely performed in carefully selected patients, yielding dramatic improvements in angina symptomatology at 6 months after surgery.
View details for DOI 10.1016/j.athoracsur.2020.11.023
View details for PubMedID 33333083
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Scaffold underexpansion and late lumen loss after bioresorbable scaffold implantation: Insights from ABSORB JAPAN trial.
International journal of cardiology. Heart & vasculature
2020; 31: 100623
Abstract
Device underexpansion is associated with late adverse outcomes after bioresorbable vascular scaffold (BVS) implantation. This study, representing official IVUS results of the ABSORB Japan trial, aimed to characterize IVUS findings, focusing specifically on acute device expansion, and to investigate its impact on late lumen loss (LLL) with Absorb-BVS compared with cobalt-chromium everolimus-eluting stents (CoCr-EES).ABSORB Japan enrolled 148 patients (2:1 randomization) in the IVUS cohort. Serial IVUS was prescheduled at post-procedure and 3 years. Acute device expansion was evaluated with respect to the degree and uniformity of the implanted device.Overall, Absorb-BVS showed smaller and more nonuniform device expansion at post-procedure, compared with CoCr-EES, which was particularly prominent in small-vessel lesions. In serial analysis, Absorb-BVS showed unique associations of smaller device expansion (r = 0.40, p = 0.001) and more nonuniformity (r = 0.29, p = 0.007) at post-procedure with greater LLL at 3 years, primarily attributable to greater negative remodeling (r = 0.39, p = 0.006). In contrast, acute device expansion showed no relation with subsequent lumen change in CoCr-EES. In Absorb-BVS, ischemic-driven target lesion or vessel revascularization (ID-TLR or ID-TVR) at 3 years occurred more frequently in small- versus large-vessel lesions (12.5% vs. 0%, p = 0.04 for ID-TLR and 15.6% vs. 2.3%, p = 0.08 for ID-TVR). Conversely, Absorb BVS had no target lesion nor vessel failure, even in small-vessel lesions, when adequate device expansion was achieved at post-procedure.Unlike CoCr-EES, underexpansion was associated with greater negative remodeling and LLL in Absorb-BVS. This may in part account for the poorer outcomes of Absorb-BVS than CoCr-EES when under-expanded.
View details for DOI 10.1016/j.ijcha.2020.100623
View details for PubMedID 32944608
View details for PubMedCentralID PMC7481138
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The ABSORB III and ABSORB Japan Trials: Final Intravascular Ultrasound Results
ELSEVIER SCIENCE INC. 2019: B172
View details for Web of Science ID 000487306300173
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Impact of Myocardial Bridging on Long-Term Outcomes After Heart Transplantation: Risk Stratification With IVUS-Determined Anatomical Properties
ELSEVIER SCIENCE INC. 2019: B342
View details for Web of Science ID 000487306300343
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Feasibility of IVUS-Derived FFR as a Novel Technique to Estimate Functional Severity of Coronary Stenosis
ELSEVIER SCIENCE INC. 2019: B325
View details for Web of Science ID 000487306300326
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Intravascular Ultrasound Predictors of Long-Term Outcomes Following ABSORB Bioresorbable Scaffold Implantation: A Pooled Analysis of the ABSORB III and ABSORB Japan Trials
ELSEVIER SCIENCE INC. 2019: B177
View details for Web of Science ID 000487306300178
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Early invasive assessment of the coronary microcirculation predicts subsequent acute rejection after heart transplantation
INTERNATIONAL JOURNAL OF CARDIOLOGY
2019; 290: 27–32
View details for DOI 10.1016/j.ijcard.2019.04.018
View details for Web of Science ID 000470826500005
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Current clinical use of intravascular ultrasound imaging to guide percutaneous coronary interventions.
Cardiovascular intervention and therapeutics
2019
Abstract
During the past three decades, since the invention of intravascular ultrasound (IVUS), it has become increasingly important as daily clinical applications. However, it evolved with no Japanese standards for the measurement of images, the index of percutaneous coronary intervention (PCI) procedures, and the reporting of results. Accordingly, the purpose of this review article is to provide an optimal and consistent approach to IVUS usage during PCI for clinicians and investigators.
View details for DOI 10.1007/s12928-019-00603-y
View details for PubMedID 31281937
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Comparison between instantaneous wave-free ratio versus morphometric assessments by intracoronary imaging
HEART AND VESSELS
2019; 34 (6): 926–35
View details for DOI 10.1007/s00380-018-1320-4
View details for Web of Science ID 000468750200006
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Early invasive assessment of the coronary microcirculation predicts subsequent acute rejection after heart transplantation.
International journal of cardiology
2019
Abstract
BACKGROUND: Acute allograft rejection (AAR) plays an important role in patient and graft survival; therefore, more emphasis should be placed on its prediction. This study aimed to investigate baseline clinical and diagnostic variables associated with subsequent AAR during the first year post-transplant, especially focusing on early physiologic and anatomic measures.METHODS: This study enrolled 88 heart transplant patients who underwent fractional flow reserve (FFR), coronary flow reserve (CFR), the index of microcirculatory resistance (IMR) and intravascular ultrasound (IVUS) in the left anterior descending artery at baseline (within 8 weeks post-transplant). Cardiac index (CI), pulmonary capillary wedge pressure (PCWP), mean pulmonary artery pressure (mPAP), right atrial pressure and left ventricular ejection fraction were also evaluated. AAR was defined as acute cellular rejection of grade ≥2R and/or pathological antibody-mediated rejection of grade ≥pAMR2.RESULTS: During the first year post-transplant, 25.0% of patients experienced AAR. Patients with AAR during the first year showed higher rates of recipient obesity, lower rates of recipient-donor sex mismatch and rATG and tacrolimus uses, higher PCWP, mPAP and IMR, and lower CFR at baseline, compared with those without. In the multivariate analysis, only baseline IMR ≥ 16.0 was independently associated with AAR during the first year, demonstrating high negative predictive value (96.7%).CONCLUSIONS: Invasively assessing microvascular resistance (baseline IMR ≥ 16.0) in the early post-transplant period was an independent determinant of subsequent acute allograft rejection during the first year post-transplant, suggesting that early assessment of IMR may enhance patient risk stratification and target medical therapies to improve patient outcome.
View details for PubMedID 30987835
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Cardiac function response to stenting in atherosclerotic renal artery disease with and without heart failure: results from the Carmel study
ESC HEART FAILURE
2019; 6 (2): 319–27
View details for DOI 10.1002/ehf2.12391
View details for Web of Science ID 000464451900010
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INTRAVASCULAR ULTRASOUND PREDICTORS OF 4-YEAR CLINICAL OUTCOMES FOLLOWING ABSORB BIORESORBABLE SCAFFOLD IMPLANTATION: INSIGHTS FROM THE ABSORB JAPAN TRIAL
ELSEVIER SCIENCE INC. 2019: 1305
View details for Web of Science ID 000460565901318
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PERIARTERIAL NEOVASCULARIZATION AND ATTENUATED-SIGNAL PLAQUE PREDICT LONG-TERM MORTALITY AFTER HEART TRANSPLANTATION: RISK STRATIFICATION WITH IVUS-DETERMINED CORONARY INFLAMMATORY FINDINGS
ELSEVIER SCIENCE INC. 2019: 1428
View details for Web of Science ID 000460565901440
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A FIRST-IN-HUMAN STUDY OF THE SECOND-GENERATION, THIN-STRUT, EVEROLIMUS-ELUTING BIORESORBABLE SCAFFOLD: 6-MONTH IVUS AND OCT RESULTS FROM THE FAST CLINICAL TRIAL
ELSEVIER SCIENCE INC. 2019: 1111
View details for Web of Science ID 000460565901124
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Association of Endothelin-1 With Accelerated Cardiac Allograft Vasculopathy and Late Mortality Following Heart Transplantation
JOURNAL OF CARDIAC FAILURE
2019; 25 (2): 97–104
View details for DOI 10.1016/j.cardfail.2018.12.001
View details for Web of Science ID 000460190800004
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Cardiac function response to stenting in atherosclerotic renal artery disease with and without heart failure: results from the Carmel study.
ESC heart failure
2019
Abstract
Consensus-derived guidelines recommend renal stenting for patients with atherosclerotic renal artery disease (ARAD) and heart failure (HF). The aim of this prospective multi-centre observational study was to verify our hypothesis that changes in E/e', an echocardiographic correlate of left ventricular (LV) filling pressure, following renal stenting may differ between ARAD patients with and without HF.This study enrolled de novo ARAD patients undergoing renal stenting at 14 institutions. The primary endpoint was the difference in E/e' change between ARAD patients with and without HF. Clinical and echocardiographic data were prospectively collected at baseline, the day following renal stenting, and 1 month and 6 months afterwards. ARAD patients with HF were defined as patients with New York Heart Association (NYHA) Class 2 and more, or a history of HF hospitalization. A total of 76 patients were included, and 39% were ARAD patients with HF. ARAD patients with HF had significantly lower estimated glomerular filtration rate (P = 0.028) and higher NYHA functional class (P < 0.001) and Minnesota Living with Heart Failure Questionnaire (MLHFQ) score (P = 0.001) than ARAD patients without HF. Also, ARAD patients with HF had significantly lower LV ejection fraction (P = 0.003) and e'-velocity (P = 0.003) and higher E/e' ratio (P = 0.001), left atrial volume index (LAVI) (P = 0.046), LV end-diastolic volume (LVEDV) (P = 0.001), LV end-systolic volume (LVESV) (P = 0.001), and LV mass index (P = 0.009) than ARAD patients without HF. All procedures were successful. In contrast to blood pressure and renal function, there was a significant interaction in E/e' (Pinteraction < 0.001) between time and HF, and ARAD patients with HF showed a significant (P < 0.001) decrease in E/e' albeit those without HF. By the same token, there was a significant interaction in NYHA class (Pinteraction < 0.001), MLHFQ score (Pinteraction = 0.018), E-velocity (Pinteraction = 0.002), LAVI (Pinteraction = 0.001), LVEDV (Pinteraction = 0.003), and LVESV (Pinteraction = 0.001) between time and HF with a significant improvement in all these variables in ARAD patients with HF (NYHA class, P = 0.001; MLHFQ score, P = 0.002; E-velocity, P = 0.005; LAVI, P = 0.001; LVEDV, P = 0.017; and LVESV, P = 0.011).Change in LV filling pressure after renal stenting differed between ARAD patients with and without HF, with a significant improvement in LV filling pressure in patients with HF-ARAD. These unique findings might support clinical cardiac benefits of renal artery stenting in ARAD patients with HF.
View details for PubMedID 30614643
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Intravascular ultrasound radiofrequency signal analysis of blood speckles: Physiological assessment of intermediate coronary artery stenosis.
Catheterization and cardiovascular interventions : official journal of the Society for Cardiac Angiography & Interventions
2019
Abstract
This study aimed to systematically investigate feasibility of radiofrequency intravascular ultrasound (RF-IVUS) analysis of blood signals for assessing functionally significant coronary stenosis.First, in-vivo human study was performed to evaluate 83 intermediate coronary lesions from 75 patients, using 40-MHz RF-IVUS, fractional flow reserve (FFR) and instantaneous wave-free ratio (iFR). Average blood integrated-backscatter (IB) values within lumen were measured at proximal and distal segments to the stenosis; ΔIB values between the two sites were calculated. Second, bench-test was performed to assess relationships of blood IB values to blood flow velocity and hematocrit using 40 and 60-MHz RF-IVUS.In in-vivo study, ΔIB values across the stenosis significantly correlated with both FFR (r = -.85, p < .0001) and iFR (r = -.65, p < .0001), which was confirmed in small minimum lumen area (MLA) lesions (MLA <2.0 mm2 ). Receiver operating characteristic curve analyses identified the best cut-off value as 10.06 of ΔIB values for predicting FFR ≤0.8 and iFR ≤0.89 (sensitivity 76.2 and 95.5%, specificity 100 and 82.0%, positive predictive value 100 and 65.6%, negative predictive value 80.4 and 98.0%, accuracy 92.9 and 92.8% for FFR and iFR). Bench-test study also identified that blood IB values exponentially changed as a function of blood flow velocity at any given hematocrit in both 40 and 60-MHz RF-IVUS.This study supports the potential utility of RF-IVUS analysis of blood signals to estimate functional ischemia, demonstrating relationships of blood ΔIB values to FFR and iFR, as well as relationships between blood IB values and flow velocity.
View details for DOI 10.1002/ccd.28612
View details for PubMedID 31778026
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Association of Endothelin-1 with Accelerated Cardiac Allograft Vasculopathy and Late Mortality Following Heart Transplantation.
Journal of cardiac failure
2018
Abstract
BACKGROUND: Endothelin-1 (ET-1) has been implicated in the development of post-heart transplantation (HT) cardiac allograft vasculopathy (CAV), but has not been well-studied in humans.METHODS AND RESULTS: In 90 HT patients, plasma ET-1 was measured within 8 weeks of HT (baseline) via a competitive enzyme-linked immunosorbent assay. 3D volumetric intravascular ultrasound of the left anterior descending artery was performed at baseline and at 1 year. Accelerated CAV (lumen volume loss) was defined using the 75th percentile as a cutoff. Patients were followed beyond the first year post-HT for late death or re-transplantation. A receiver operative characteristic curve demonstrated that a baseline ET-1 concentration of 1.75 pg/mL provided the best accuracy for diagnosis of accelerated CAV at 1 year [area under the curve=0.69 (0.57-0.82), p=0.007]. In multivariate logistic regression, a higher baseline ET-1 concentration was independently associated with accelerated CAV [odds ratio (OR)=2.13, 95% confidence interval (CI): 1.15-3.94; p=0.01]; this relationship persisted when ET-1 was dichotomized at 1.75 pg/mL (OR=4.88, 95% CI: 1.69-14.10; p=0.003). Eighteen deaths occurred during a median follow-up period of 3.99 (2.51-9.95) years. Treated as a continuous variable, baseline ET-1 was not associated with late mortality in multivariate Cox regression [hazard ratio (HR)=1.22, 95% CI: 0.72-2.05; p=0.44]. However, ET-1 >1.75 pg/mL conferred a significantly lower cumulative event-free survival on Kaplan-Meier analysis (p=0.047), and was independently associated with late mortality (HR=2.94, 95% CI: 1.12-7.72; p=0.02).CONCLUSIONS: Elevated ET-1 early after HT is an independent predictor of accelerated CAV and late mortality, suggesting that ET-1 has durable prognostic value in the HT arena.
View details for PubMedID 30543947
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Comparison between instantaneous wave-free ratio versus morphometric assessments by intracoronary imaging.
Heart and vessels
2018
Abstract
Anatomical measurements obtained by intracoronary imaging devices are reported to correlate significantly with fractional flow reserve (FFR). Instantaneous wave-free ratio (iFR) is a nonhyperemic index of stenosis severity with discordant reports regarding its accuracy in relation to FFR. There is no information on the correlation of iFR with measurements derived from intracoronary imaging devices. The purpose of this study was to assess the relationship among iFR, intravascular ultrasound (IVUS), and optical frequency domain imaging (OFDI) parameters. Eighty lesions in 72 patients who underwent elective angiography and had intermediate lesions were enrolled. All lesions were assessed by iFR, FFR, IVUS, and OFDI. iFR was ≤0.89 in 21 (26%) lesions and FFR was ≤0.80 in 41 (51%) lesions. iFR correlated significantly with both IVUS-derived minimum lumen area (MLA) (r=0.375, p=0.003) and OFDI-derived MLA (r=0.357, p=0.005). FFR also correlated significantly with both IVUS-derived MLA (r=0.472, p<0.001) and OFDI-derived MLA (r=0.445, p<0.001). Among the lesions with FFR ≤0.80, iFR>0.89 (mismatch) was observed in 20 lesions. There was no lesion with iFR ≤0.89 (reverse mismatch) among the lesions with FFR>0.80. The lesion location among three major coronary vessels was related with the discrepancy between iFR and FFR (p=0.007). In conclusion, iFR and FFR showed a significant correlation with IVUS and OFDI measurements. The discrepancy of iFR and FFR was associated with the lesion locations.
View details for PubMedID 30535756
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Impact of Myocardial Bridging on Long-Term Mortality After Heart Transplantation: Risk Stratification With Ivus-Determined Cardiac Allograft Vasculopathy
LIPPINCOTT WILLIAMS & WILKINS. 2018
View details for Web of Science ID 000528619403405
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Long-Term Vascular Response to Bioresorbable Scaffolds Versus Metallic Stents in Coronary Lesions with Myocardial Bridging: A Potential Benefit of Vascular Restoration Under Dynamic Compression Force
ELSEVIER SCIENCE INC. 2018: B128
View details for DOI 10.1016/j.jacc.2018.08.1452
View details for Web of Science ID 000455137100308
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Attenuated-Signal Plaque and Long-Term Vessel Response after Bioresorbable Scaffold Implantation: IVUS Insights from the ABSORB JAPAN Trial
ELSEVIER SCIENCE INC. 2018: B68
View details for DOI 10.1016/j.jacc.2018.08.1270
View details for Web of Science ID 000455137100159
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Bioresorbable Scaffold for Treatment of Coronary Artery Lesions Intravascular Ultrasound Results From the ABSORB Japan Trial
JACC-CARDIOVASCULAR INTERVENTIONS
2018; 11 (7): 648–61
Abstract
The aim of this study was to characterize post-procedural intravascular ultrasound (IVUS) findings in the ABSORB Japan trial, specifically stratified by the size of target coronary arteries.Despite overall noninferiority confirmed in recent randomized trials comparing bioresorbable vascular scaffolds (BVS) (Absorb BVS) and cobalt-chromium everolimus-eluting metallic stents (CoCr-EES), higher event rates of Absorb BVS have been reported with suboptimal deployment, especially in small coronary arteries.In the ABSORB Japan trial, 150 patients (2:1 randomization) were scheduled in the IVUS cohort. Small vessel was defined as mean reference lumen diameter <2.75 mm. Tapered-vessel lesions were defined as tapering index (proximal/distal reference lumen diameter) ≥1.2.Overall, IVUS revealed that the Absorb BVS arm had smaller device expansion than the CoCr-EES arm did, which was particularly prominent in small- and tapered-vessel lesions. Higher tapering index was also associated with higher rates of incomplete strut apposition in Absorb BVS, but not in CoCr-EES. With respect to procedural techniques, small-vessel lesions were treated more frequently with noncompliant balloons at post-dilatation but using significantly lower pressure in the Absorb BVS arm. In contrast, tapered-vessel lesions were post-dilated at equivalent pressure but with significantly smaller balloon catheters in the Absorb BVS arm, compared with the CoCr-EES arm.The significantly smaller device expansion especially in small vessels may account for the poorer outcomes of Absorb BVS in this lesion type. Appropriate optimization strategy, possibly different between polymeric and metallic devices, needs to be established for bioresorbable scaffold technology. (AVJ-301 Clinical Trial: A Clinical Evaluation of AVJ-301 Absorb™ BVS) in Japanese Population [ABSORB JAPAN]; NCT01844284).
View details for PubMedID 29622143
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BIORESORBABLE SCAFFOLD FOR TREATMENT OF CORONARY ARTERY LESIONS: FINAL INTRAVASCULAR ULTRASOUND RESULTS FROM THE ABSORB JAPAN TRIAL
ELSEVIER SCIENCE INC. 2018: 1020
View details for DOI 10.1016/S0735-1097(18)31561-4
View details for Web of Science ID 000429659702270
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Bioresorbable Scaffold for the Treatment of Calcified Coronary Lesions: IVUS Insights from the ABSORB Japan Trial
ELSEVIER SCIENCE INC. 2017: B19
View details for Web of Science ID 000413459200044
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Impact of Underexpansion on IVUS-Derived Wall Shear Stress Patterns with Bioresorbable Scaffolds and Metallic DES: Insights from the ABSORB III Imaging Substudy
ELSEVIER SCIENCE INC. 2017: B187
View details for Web of Science ID 000413459200453
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Association Between Scaffold Under-Expansion and Late Lumen Loss after Bioresorbable Scaffold Implantation: IVUS and Angiographic Insights from the ABSORB Japan Trial
ELSEVIER SCIENCE INC. 2017: B5
View details for Web of Science ID 000413459200012
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Differential Late Stent Enlargement and Vascular Response Following New-Generation Self-Expanding Stent Implantation in Tapered Peripheral Arteries: Insights from Serial Optical Coherence Tomography
ELSEVIER SCIENCE INC. 2017: B165–B166
View details for Web of Science ID 000413459200401
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Comparison of Bioresorbable Scaffold Measurements between Intravascular Ultrasound and Quantitative Coronary Angiography in the ABSORB Japan Trial
ELSEVIER SCIENCE INC. 2017: B57–B58
View details for Web of Science ID 000413459200131
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Influence of analysis interval size on optical coherence tomography assessments of stent therapy for superficial femoral artery lesions
OXFORD UNIV PRESS. 2017: 1087
View details for Web of Science ID 000440509304316
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Impact of attenuated-signal plaque observed by intravascular ultrasound on vessel response after drug-eluting stent implantation
ATHEROSCLEROSIS
2017; 259: 68-74
Abstract
The aim of this study was to investigate the impact of attenuated-signal plaque (ASP) observed by intravascular ultrasound (IVUS) on vessel response after drug-eluting stent implantation.Data were derived from the IVUS cohort of the J-DESsERT trial comparing paclitaxel- and sirolimus-eluting stents. Serial IVUS analysis (pre- and post-intervention, and 8-month follow-up) was performed in 136 non-AMI lesions. ASP was defined as hypoechoic plaque with ultrasound attenuation without calcification. Calcified plaque (CP) was defined as brightly echoreflective plaque with acoustic shadowing. ASP and CP scores were calculated by grading their measured angle as 0 to 4 for 0°, <90°, 90-180°, 180-270° and >270°, respectively. The entire stented segment was analyzed at 1-mm intervals.At pre-intervention, ASP was observed in 40.4% of lesions, and this group had greater % neointimal volume (%NIV) at follow-up than the no-ASP group (p = 0.011). ASP score at pre-intervention positively correlated with %NIV (p = 0.023). During the follow-up, ASP score significantly decreased (p < 0.001), and CP score significantly increased (p < 0.001), with a negative correlation between them (p < 0.001). A decrease in the ASP score was associated with less %NIV in PES (p = 0.031), but not in SES (p = 0.229).The greater extent of plaque with IVUS-signal attenuation at pre-intervention and its persistence during follow-up were associated with neointimal proliferation, possibly representing sustained inflammatory status, depending on the type of DES used.
View details for DOI 10.1016/j.atherosclerosis.2017.02.009
View details for Web of Science ID 000397736900011
View details for PubMedID 28327450
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PERI-STRUT LOW INTENSITY AREA PREDICTS NEOINTIMAL PROGRESSION ASSOCIATED WITH LATE ENLARGEMENT OF SELF-EXPANDING NITINOL STENTS IN SUPERFICIAL FEMORAL ARTERIES: AN OPTICAL COHERENCE TOMOGRAPHY STUDY
ELSEVIER SCIENCE INC. 2017: 999
View details for Web of Science ID 000397342301521
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Impact of Analysis Interval Size on the Quality of Optical Frequency Domain Imaging Assessments of Stent Implantation for Lesions of the Superficial Femoral Artery
CATHETERIZATION AND CARDIOVASCULAR INTERVENTIONS
2017; 89 (4): 735-745
Abstract
This study aimed to investigate the influence of analysis interval size on optical frequency domain imaging (OFDI) assessment of stent therapy for lesions of the superficial femoral artery (SFA).No consensus or validating data are available with respect to the methodology of intravascular imaging analysis for the peripheral arteries.OFDI was performed for 30 SFA lesions, during endovascular therapy and at the 6-month follow-up. Initially, lumen and stent borders were traced at 1-mm axial intervals. Volumes were calculated using a PC-based software, and the volume index (VI) was defined as the volume divided by the stent length. Two additional OFDI analyses were performed using 2-mm and 5-mm intervals, thereby reducing the number of cross-sectional image frames analyzed.The mean stent length was 89.7 ± 35.2 mm. The mean difference in baseline minimum lumen area (MLA) was 0.4 mm(2) between MLA values from the 1-mm and 2-mm interval analyses, and 2.2 mm(2) between MLA values from the 1-mm and 5-mm interval analyses. In volumetric analysis, there were excellent correlations and good agreements for stent, lumen, and neointimal VI measurements obtained on the basis of different analysis intervals.Using large intervals in OFDI analyses of SFA lesions resulted in few differences in measurement variability of volumetric parameters. However, planar analysis for MLA assessment can be susceptible to high variability when large intervals are applied. © 2016 Wiley Periodicals, Inc.
View details for DOI 10.1002/ccd.26673
View details for Web of Science ID 000397300300034
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Impact of stent diameter on vascular response after self-expanding paclitaxel-eluting stent implantation in the superficial femoral artery.
Journal of cardiology
2017
Abstract
The optimal sizing of self-expanding paclitaxel-eluting stents (PES) in the treatment for superficial femoral artery (SFA) lesions is unclear. This study sought to investigate the influence of PES diameter on stent patency in SFA lesions using optical frequency domain imaging (OFDI).A total of 20 de novo SFA lesions were randomized 1:1 to receive either self-expanding PES with a nominal diameter of 6mm or 8mm. Follow-up angiography and OFDI was scheduled six months after stent implantation, and volumetric OFDI analysis was performed to evaluate vascular response to the stents. Volume index (VI) was defined as the volume divided by the stent length. The primary end point was lumen VI at the 6-month follow-up. Secondary end point was minimum lumen diameter (MLD) by quantitative vascular angiography (QVA) at the follow-up.Stent length was 78.0±23.9mm in the 6-mm group and 70.0±23.6mm in the 8-mm group (p=0.46). Baseline QVA data were also similar between the two groups. MLD immediately after stent implantation was similar between the two groups (4.2±0.5mm in the 6-mm group and 3.9±0.5mm in the 8-mm group, p=NS). At the 6-month follow-up, MLD was greater in the 8-mm group compared to the 6-mm group (4.0±1.0mm vs. 3.2±0.4mm, p<0.05). Stent VI was larger in the 8-mm group (28.4±6.7mm(3)/mm vs. 22.2±1.2mm(3)/mm, p=0.01). Neointimal VI was similar between the two groups (5.8±2.9mm(3)/mm vs. 5.2±2.6mm(3)/mm, p=0.68). Lumen VI was greater in the 8-mm group (23.2±7.6mm(3)/mm vs. 17.3±2.6mm(3)/mm, p=0.04).Chronic stent enlargement resulted in greater lumen area after implantation of self-expanding PES with a large diameter at the mid-term follow-up. Stent diameter might be important for stent patency in procedure with PES for SFA lesions.
View details for DOI 10.1016/j.jjcc.2016.12.011
View details for PubMedID 28254383
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Coronary Endothelial Dysfunction and the Index of Microcirculatory Resistance as a Marker of Subsequent Development of Cardiac Allograft Vasculopathy.
Circulation
2017; 135 (11): 1093–95
View details for PubMedID 28289008
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Impact of Stent Size Selection on Acute and Long-Term Outcomes After Drug-Eluting Stent Implantation in De Novo Coronary Lesions.
Circulation. Cardiovascular interventions
2017; 10 (10)
Abstract
Although significant undersizing often results in incomplete stent apposition or underexpansion, the possible impact of oversized stent implantation on arterial wall injury has not been systematically investigated with drug-eluting stents. The aim of this study was to investigate the impact of stent oversizing on acute and long-term outcomes after drug-eluting stents implantation in de novo coronary lesions.Serial (baseline and 6-12 months) coronary angiography and intravascular ultrasound were performed in 2931 lesions treated with drug-eluting stents (355 sirolimus, 846 paclitaxel, 1387 zotarolimus, and 343 everolimus). The percentage of stent oversizing to angiographic reference vessel diameter (RVD) was calculated as (nominal stent diameter-RVD)/RVD×100 (%). Clinical outcomes, including target lesion revascularization and stent thrombosis, were followed for 1 year. Overall, smaller preintervention RVD was associated with higher percentage of stent oversizing (P<0.001). The significant oversizing group underwent less post-dilatation (P=0.002) but achieved greater stent expansion (P<0.001) and less incomplete stent apposition (P<0.001) without increase of edge dissection after procedure. When stratified by vessel size and stent oversizing, progressive decreases of restenosis (P=0.002) and target lesion revascularization rates (P=0.007) were found in favor of larger vessel size and oversized stents. Stent thrombosis was observed the most in small RVD with low percentage of stent oversizing group among the subgroups (P=0.040).The positive impact of stent oversizing was documented on procedural and clinical outcomes. In particular, small vessels treated with smaller stents were associated with greater adverse events, suggesting that aggressive selection of larger stents, with appropriate attention to edge effects, may optimize long-term outcomes, even in drug-eluting stents implantation.
View details for PubMedID 28951394
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Angiotensin-Converting Enzyme Inhibition Early After Heart Transplantation.
Journal of the American College of Cardiology
2017; 69 (23): 2832–41
Abstract
Cardiac allograft vasculopathy (CAV) remains a leading cause of mortality after heart transplantation (HT). Angiotensin-converting enzyme inhibitors (ACEIs) may retard the development of CAV but have not been well studied after HT.This study tested the safety and efficacy of the ACEI ramipril on the development of CAV early after HT.In this prospective, multicenter, randomized, double-blind, placebo-controlled trial, 96 HT recipients were randomized to undergo ramipril or placebo therapy. They underwent coronary angiography, endothelial function testing; measurements of fractional flow reserve (FFR) and coronary flow reserve (CFR) and the index of microcirculatory resistance (IMR); and intravascular ultrasonography (IVUS) of the left anterior descending coronary artery, within 8 weeks of HT. At 1 year, the invasive assessment was repeated. Circulating endothelial progenitor cells (EPCs) were quantified at baseline and 1 year.Plaque volumes at 1 year were similar between the ramipril and placebo groups (162.1 ± 70.5 mm(3) vs. 177.3 ± 94.3 mm(3), respectively; p = 0.73). Patients receiving ramipril had improvement in microvascular function as shown by a significant decrease in IMR (21.4 ± 14.7 to 14.4 ± 6.3; p = 0.001) and increase in CFR (3.8 ± 1.7 to 4.8 ± 1.5; p = 0.017), from baseline to 1 year. This did not occur with IMR (17.4 ± 8.4 to 21.5 ± 20.0; p = 0.72) or CFR (4.1 ± 1.8 to 4.1 ± 2.2; p = 0.60) in the placebo-treated patients. EPCs decreased significantly at 1 year in the placebo group but not in the ramipril group.Ramipril does not slow development of epicardial plaque volume but does stabilize levels of endothelial progenitor cells and improve microvascular function, which have been associated with improved long-term survival after HT. (Angiotensin Converting Enzyme [ACE] Inhibition and Cardiac Allograft Vasculopathy; NCT01078363).
View details for PubMedID 28595700
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Assessment of bioresorbable scaffold with a novel high-definition 60 MHz IVUS imaging system: Comparison with 40-MHz IVUS referenced to optical coherence tomography.
Catheterization and cardiovascular interventions : official journal of the Society for Cardiac Angiography & Interventions
2017
Abstract
In vivo assessment of bioresorbable scaffold (BRS) is of growing clinical interest. The novel 60MHz high-definition intravascular ultrasound (HD-IVUS) has been developed to overcome the limitations of conventional 40 MHz IVUS. This study aimed to evaluate the performance and limitations of 60 MHz HD-IVUS compared with 40 MHz IVUS with respect to polymeric-strut visualization, quantitative and qualitative analysis, and feasibility of high-speed pullback in the assessment of BRS.In a bench-test model, 361 struts were analyzed to evaluate the influence of ultrasound-beam angles and proximity of adjacent struts on IVUS visualization of BRS struts. Various settings were created by deforming the BRS and positioning the transducer offcenter. In an in vivo swine coronary model, scaffold and lumen areas, degree of visible external elastic membrane, incomplete strut apposition, and strut fracture were evaluated in 59 matched cross-sections obtained at conventional (0.5 mm/sec) and high speed (10 mm/sec) pullbacks. Both studies utilized optical coherence tomography (OCT) as reference. Overall, 60 MHz HD-IVUS demonstrated significantly improved visualization of polymeric struts compared with 40 MHz IVUS (well-visualized: 84.5% vs 62.3%, not visible: 4.4% vs 13.9%, respectively. P < 0.001), which was less affected by the beam angle and adjacent strut proximity. In the in vivo model, 60-MHz HD-IVUS showed better agreement of area measurements and strut abnormalities with OCT than 40 MHz IVUS. These findings were also confirmed on high-speed pullback images of 60 MHz HD-IVUS.As referenced to OCT, this study showed superiority of 60 MHz HD-IVUS over 40 MHz IVUS in the assessment of BRS with feasibility of high-speed pullback imaging.
View details for PubMedID 28707349
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Comparing the vascular response in implantation of self-expanding, bare metal nitinol stents or paclitaxel-eluting nitinol stents in superficial femoral artery lesions: a serial optical frequency domain imaging study
EUROINTERVENTION
2016; 12 (12): 1551-1558
Abstract
This study sought to investigate differences in vascular response between self-expanding bare metal nitinol stents (BMS) and paclitaxel-eluting nitinol stents (PES), in superficial femoral artery (SFA) disease, using optical frequency domain imaging (OFDI).Six months after stent implantation, follow-up quantitative vascular angiography (QVA) and OFDI assessment were scheduled to evaluate vascular response. Volume index (VI) was defined as volume divided by stent length. The primary endpoint was OFDI-derived late lumen area loss, defined as lumen VI post stent implantation minus lumen VI at follow-up. A total of 28 SFA lesions were analysed, with cases randomised to receive either BMS or PES implantation. QVA-derived diameter stenosis at six-month follow-up was lower in the PES group than in the BMS group (28.5% vs. 39.7%, p=0.04). After six months, BMS VI increased by 33.8% (20.7±3.7 to 27.7±3.5 mm3/mm), whilst PES exhibited an increase of 32.1% (19.0±2.3 to 25.1±4.7 mm3/mm). Neointimal VI was smaller (7.4±2.6 mm3/mm vs. 10.5±3.2 mm3/mm, p<0.01) and late lumen area loss was lower (2.9±1.3 mm3/mm vs. 5.6±2.8 mm3/mm, p<0.01) in the PES group.Serial volumetric OFDI analyses confirmed significantly smaller amounts of neointimal tissue and lower late lumen area loss following PES implantation for SFA lesions at short-term follow-up.
View details for Web of Science ID 000392688700020
View details for PubMedID 27998849
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Early Left Ventricular Dysfunction is Associated with Cardiac Allograft Vasculopathy and Late Mortality After Heart Transplantation
ELSEVIER SCIENCE INC. 2016: B331
View details for DOI 10.1016/j.jacc.2016.09.909
View details for Web of Science ID 000398590400337
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Bioresorbable Vascular Scaffold for the Treatment of Tapered Coronary Lesions
ELSEVIER SCIENCE INC. 2016: B165
View details for DOI 10.1016/j.jacc.2016.09.541
View details for Web of Science ID 000397332900398
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Comparison between Instantaneous Wave-Free Ratio and Fractional Flow Reserve versus Morphometric Assessments by Intracoronary Imaging Devices
ELSEVIER SCIENCE INC. 2016: B218
View details for DOI 10.1016/j.jacc.2016.09.676
View details for Web of Science ID 000398590400066
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Characteristics of Late-Acquired Incomplete Stent Apposition: A Comparison With First-Generation and Second-Generation Drug-Eluting Stents.
journal of invasive cardiology
2016; 28 (8): 323-329
Abstract
This study aim was to investigate the morphometric parameters of late-acquired incomplete stent apposition (ISA) following use of Cypher sirolimus-eluting stent (SES; Cordis), Taxus paclitaxel-eluting stent (PES; Boston Scientific), and Resolute zotarolimus-eluting stent (ZES; Medtronic).Characteristics of late-acquired ISA between first-generation and second-generation drug-eluting stents (DESs) have not been systematically examined.Late-acquired ISA was defined as separation of at least 1 stent strut from the vessel wall with evidence of blood speckle behind the strut, where poststent implantation intravascular ultrasound (IVUS) revealed complete apposition. A total of 30 late-acquired ISA cases (12 SES, 10 PES, 8 ZES) were included in this IVUS analysis. Corresponding cross-sections at post procedure were selected for comparison. Vessel, lumen, peristent tissue, and stent area were measured in the late-acquired ISA arc as referenced to stent center.Late-acquired ISA area was 2.4 ± 1.5 mm² in SES, 2.2 ± 2.7 mm² in PES, and 0.9 ± 0.6 mm² in ZES (P=.02 for SES vs ZES). Vessel area increased from post procedure to follow-up in SES (4.6 ± 1.7 mm² to 7.0 ± 2.5 mm²; P<.01) and PES (3.6 ± 1.7 mm² to 5.7 ± 3.8 mm²; P=.06), but not in ZES. Vessel expansion was the main mechanism in SES and PES groups; however, tissue regression and stent recoil, as well as vessel expansion, also contributed to late-acquired ISA in ZES. Per-patient analyses demonstrated that vessel expansion was the predominant mechanism of late-acquired ISA in 83% of SES, 60% in PES, and 50% of ZES cases.The magnitude and mechanism of late-acquired ISA appear to be different between first-generation and second-generation DESs, possibly due to varying vessel response to different stent component types.
View details for PubMedID 26689416
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Attenuated-Signal Plaque Progression Predicts Long-Term Mortality After Heart Transplantation: IVUS Assessment of Cardiac Allograft Vasculopathy.
Journal of the American College of Cardiology
2016; 68 (4): 382-392
Abstract
Although cardiac allograft vasculopathy (CAV) is typically characterized by diffuse coronary intimal thickening with pathological vessel remodeling, plaque instability may also play an important role in CAV. Previous studies of native coronary atherosclerosis have demonstrated associations between attenuated-signal plaque (ASP), plaque instability, and adverse clinical events.This study's aim was to characterize the association between ASP and long-term mortality post-heart transplantation.In 105 heart transplant recipients, serial (baseline and 1-year post-transplant) intravascular ultrasound was performed in the first 50 mm of the left anterior descending artery. The ASP score was calculated by grading the measured angle of attenuation from grades 0 to 4 (specifically, 0°, 1° to 90°, 91° to 180°, 181° to 270°, and >270°) at 1-mm intervals. The primary endpoint was all-cause death or retransplantation.At 1-year post-transplant, 10.5% of patients demonstrated ASP progression (newly developed or increased ASP). Patients with ASP progression had a higher incidence of acute cellular rejection during the first year (63.6% vs. 22.3%; p = 0.006) and tendency for greater intimal growth (percent intimal volume: 9.2 ± 9.3% vs. 4.4 ± 5.3%; p = 0.07) than those without. Over a median follow-up of 4.6 years, there was a significantly lower event-free survival rate in patients with ASP progression at 1-year post-transplant compared with those without. In contrast, maximum intimal thickness did not predict long-term mortality.ASP progression appears to reflect chronic inflammation related to acute cellular rejection and is an independent predictor of long-term mortality after heart transplantation. Serial assessments of plaque instability may enhance identification of high-risk patients who may benefit from closer follow-up and targeted medical therapies.
View details for DOI 10.1016/j.jacc.2016.05.028
View details for PubMedID 27443435
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Acute stent recoil and optimal balloon inflation strategy: an experimental study using real-time optical coherence tomography.
EuroIntervention
2016; 12 (2): e190-8
Abstract
Our aim was to evaluate stent expansion and acute recoil at deployment and post-dilatation, and the impact of post-dilatation strategies on final stent dimensions.Optical coherence tomography (OCT) was performed on eight bare metal platforms of drug-eluting stents (3.0 mm diameter, n=6 for each) during and after balloon inflation in a silicone mock vessel. After nominal-pressure deployment, a single long (30 sec) vs. multiple short (10 sec x3) post-dilatations were performed using a non-compliant balloon (3.25 mm, 20 atm). Stent areas during deployment with original delivery systems were smaller in stainless steel stents than in cobalt-chromium and platinum-chromium stents (p<0.001), whereas subsequent acute recoil was comparable among the three materials. At post-dilatation, acute recoil was greater in cobalt-chromium and platinum-chromium stents than in stainless steel stents (p<0.001), resulting in smaller final stent areas in cobalt-chromium and platinum-chromium stents than in stainless steel stents (p<0.001). In comparison between conventional and latest-generation cobalt-chromium stents, stent areas were not significantly different after both deployment and post-dilatation. With multiple short post-dilatations, acute recoil was significantly improved from first to third short inflation (p<0.001), achieving larger final area than a single long inflation, despite stent materials/designs (p<0.001).Real-time OCT revealed significant acute recoil in all stent types. Both stent materials/designs and post-dilatation strategies showed a significant impact on final stent expansion.
View details for DOI 10.4244/EIJV12I2A32
View details for PubMedID 27290678
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Association of periarterial neovascularization with progression of cardiac allograft vasculopathy and long-term clinical outcomes in heart transplant recipients
JOURNAL OF HEART AND LUNG TRANSPLANTATION
2016; 35 (6): 752-759
Abstract
This study investigated the relationship between periarterial neovascularization, development of cardiac allograft vasculopathy (CAV), and long-term clinical outcomes after heart transplantation. Proliferation of the vasa vasorum is associated with arterial inflammation. The contribution of angiogenesis to the development of CAV has been suggested.Serial (baseline and 1-year post-transplant) intravascular ultrasound was performed in 102 heart transplant recipients. Periarterial small vessels (PSV) were defined as echolucent luminal structures <1 mm in diameter, located ≤2 mm outside of the external elastic membrane. The signal void structures were excluded when they connected to the coronary lumen (considered as side branches) or could not be followed in ≥3 contiguous frames. The number of PSV was counted at 1-mm intervals throughout the first 50 mm of the left anterior descending artery, and the PSV score was calculated as the sum of cross-sectional values. Patients with a PSV score increase of ≥ 4 between baseline and 1-year post-transplant were classified as the "proliferative" group. Maximum intimal thickness was measured for the entire analysis segment.During the first year post-transplant, the proliferative group showed a greater increase in maximum intimal thickness (0.33 ± 0.36 mm vs 0.10 ± 0.28 mm, p < 0.001) and had a higher incidence of acute cellular rejection (50.0% vs 23.9%, p = 0.025) than the non-proliferative group. On Kaplan-Meier analysis, cardiac death-free survival rate over a median of 4.7 years was significantly lower in the proliferative group than in the non-proliferative group (hazard ratio, 3.10; p = 0.036).The increase in PSV, potentially representing an angioproliferative response around the coronary arteries, was associated with early CAV progression and reduced survival after heart transplantation.
View details for DOI 10.1016/j.healun.2016.02.002
View details for PubMedID 27068036
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Intravascular Ultrasound-Derived Stent Dimensions as Predictors of Angiographic Restenosis Following Nitinol Stent Implantation in the Superficial Femoral Artery
JOURNAL OF ENDOVASCULAR THERAPY
2016; 23 (3): 424-432
Abstract
To identify intravascular ultrasound (IVUS) measurements that can predict angiographic in-stent restenosis (ISR) following nitinol stent implantation in superficial femoral artery (SFA) lesions.A retrospective review was conducted of 97 patients (mean age 72.9±8.9 years; 63 men) who underwent IVUS examination during endovascular treatment of 112 de novo SFA lesions between July 2012 and December 2014. Self-expanding bare stents were implanted in 46 lesions and paclitaxel-eluting stents in 39 lesions. Six months after stenting, follow-up angiography was conducted to assess stent patency. The primary endpoint was angiographic ISR determined by quantitative vascular angiography analysis at the 6-month follow-up. Variables associated with restenosis were sought in multivariate analysis; the results are presented as the odds ratio (OR) and 95% confidence interval (CI).At follow-up, 27 (31.8%) angiographic ISR lesions were recorded. The lesions treated with uncoated stents were more prevalent in the ISR group compared with the no restenosis group (74.1% vs 44.8%, p=0.02). Lesion length was longer (154.4±79.5 vs 109.0±89.3 mm, p=0.03) and postprocedure minimum stent area (MSA) measured by IVUS was smaller (13.9±2.8 vs 16.3±1.6 mm(2), p<0.001) in the ISR group. Multivariate analysis revealed that bare stent use (OR 7.11, 95% CI 1.70 to 29.80, p<0.01) and longer lesion length (OR 1.08, 95% CI 1.01 to 1.16, p=0.04) were predictors of ISR, while increasing postprocedure MSA (OR 0.58, 95% CI 0.41 to 0.82, p<0.01) was associated with lower risk of ISR. Receiver operating characteristic analysis identified a MSA of 15.5 mm(2) as the optimal cutpoint below which the incidence of restenosis increased (area under the curve 0.769).Postprocedure MSA can predict ISR in SFA lesions, which suggests that adequate stent enlargement during angioplasty might be required for superior patency.
View details for DOI 10.1177/1526602816641669
View details for Web of Science ID 000376287000003
View details for PubMedID 27044270
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Invasive Assessment of Coronary Physiology Predicts Late Mortality After Heart Transplantation
CIRCULATION
2016; 133 (20): 1945-1950
Abstract
-The aim of this study is to determine the prognostic value of invasively assessing coronary physiology early after heart transplantation.-Seventy-four cardiac transplant recipients had fractional flow reserve (FFR), coronary flow reserve (CFR), the index of microcirculatory resistance (IMR) and intravascular ultrasound (IVUS) performed down the left anterior descending coronary artery soon after (baseline) and 1 year after heart transplantation. The primary endpoint was the cumulative survival free of death or retransplantation at a mean follow-up of 4.5±3.5 years. The cumulative event-free survival was significantly lower in patients with an FFR<0.90 at baseline (42 vs 79%, p=0.01) or an IMR≥20 measured one year after heart transplantation (39 vs. 69%, p=0.03). Patients in whom IMR decreased or did not change from baseline to 1 year had higher event-free survival compared to those patients with an increase in IMR (66 vs. 36%, p=0.03). FFR<0.90 at baseline (hazards ratio [HR] 0.13, 95% confidence interval [CI] 0.02-0.81, p=0.03), IMR ≥20 at 1 year (HR 3.93, 95% CI 1.08-14.27, p=0.04) and rejection during the first year (HR 6.00, 95% CI 1.56-23.09, p=0.009) were independent predictors of death/retransplantation, while IVUS parameters were not.-Invasive measures of coronary physiology (FFR and IMR) determined early after heart transplantation are significant predictors of late death or retransplantation.
View details for DOI 10.1161/CIRCULATIONAHA.115.018741
View details for PubMedID 27143679
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EARLY CORONARY ENDOTHELIAL DYSFUNCTION PREDICTS ACCELERATED PLAQUE PROGRESSION 1 YEAR AFTER CARDIAC TRANSPLANTATION: SERIAL VOLUMETRIC EVALUATION BY INTRAVASCULAR ULTRASOUND
ELSEVIER SCIENCE INC. 2016: 364
View details for DOI 10.1016/S0735-1097(16)30365-5
View details for Web of Science ID 000375188701208
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ASSESSMENT OF BIORESORBABLE SCAFFOLD STRUTS WITH A NOVEL HIGH-DEFINITION 60MHZ IVUS IMAGING SYSTEM: COMPARISON WITH 40MHZ IVUS AND OPTICAL COHERENCE TOMOGRAPHY
ELSEVIER SCIENCE INC. 2016: 255
View details for DOI 10.1016/S0735-1097(16)30256-X
View details for Web of Science ID 000375188701099
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BIORESORBABLE SCAFFOLD FOR THE TREATMENT OF LESIONS IN SMALL CORONARY ARTERIES: IVUS INSIGHTS FROM THE ABSORB JAPAN TRIAL
ELSEVIER SCIENCE INC. 2016: 368
View details for DOI 10.1016/S0735-1097(16)30369-2
View details for Web of Science ID 000375188701212
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IMPACT OF FINAL STENT DIMENSIONS ON ANGIOGRAPHIC RESTENOSIS FOLLOWING SELF-EXPANDING NITINOL STENT IMPLANTATION IN THE SUPERFICIAL FEMORAL ARTERY LESION
ELSEVIER SCIENCE INC. 2016: 313
View details for DOI 10.1016/S0735-1097(16)30314-X
View details for Web of Science ID 000375188701157
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IMPACT OF STENT DIAMETER ON STENT PATENCY AFTER SELF-EXPANDING PACLITAXEL-ELUTING STENT IMPLANTATION IN THE SUPERFICIAL FEMORAL ARTERY: AN INTERIM REPORT
ELSEVIER SCIENCE INC. 2016: 312
View details for DOI 10.1016/S0735-1097(16)30313-8
View details for Web of Science ID 000375188701156
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ENDOTHELIUM DEPENDENT AND INDEPENDENT VASODILATOR RESPONSES AFTER HEART TRANSPLANTATION: GEOGRAPHIC DISTRIBUTION AND ASSOCIATION WITH PROGRESSION OF CARDIAC ALLOGRAFT VASCULOPATHY
ELSEVIER SCIENCE INC. 2016: 254
View details for DOI 10.1016/S0735-1097(16)30255-8
View details for Web of Science ID 000375188701098
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FRACTIONAL FLOW RESERVE IN PATIENTS WITH ANGINA IN THE ABSENCE OF OBSTRUCTIVE CORONARY ARTERY DISEASE: IS THERE SUCH A THING AS NORMAL CORONARY ARTERIES?
ELSEVIER SCIENCE INC. 2016: 375
View details for DOI 10.1016/S0735-1097(16)30376-X
View details for Web of Science ID 000375188701219
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ANGIOTENSIN-CONVERTING ENZYME INHIBITION EARLY AFTER CARDIAC TRANSPLANTATION: A MULTI-CENTER, RANDOMIZED, DOUBLE-BLIND TRIAL COMPARING RAMIPRIL VERSUS PLACEBO
ELSEVIER SCIENCE INC. 2016: 1445
View details for DOI 10.1016/S0735-1097(16)31446-2
View details for Web of Science ID 000375188702291
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Quantitative precision of optical frequency domain imaging: direct comparison with frequency domain optical coherence tomography and intravascular ultrasound.
Cardiovascular intervention and therapeutics
2016; 31 (2): 79-88
Abstract
No systematic validation study is available with optical frequency domain imaging (OFDI), directly compared with frequency domain optical coherence tomography (FD-OCT) and intravascular ultrasound (IVUS). Controversy also remains about the impact of different stent contour tracing methods by OFDI/FD-OCT. In vitro: coronary phantom models (1.51-5.04 mm) were imaged with OFDI, FD-OCT, and IVUS, demonstrating excellent quantitative precision with a slight overestimation of mean lumen diameter (difference 0.01-0.02 mm). In vivo: corresponding 64 OFDI/IVUS images of stented coronary segments from 20 swines were analyzed. Minimum lumen area by OFDI was larger than IVUS at baseline (P < 0.001), whereas it was smaller than IVUS at follow-up. When stent was traced at leading edges of struts by OFDI, minimum stent area was similar between OFDI and IVUS (P = 0.60). When traced at the highest intensity points of struts by OFDI, it was significantly larger in OFDI than in IVUS (P < 0.001). Three modalities have clinically acceptable precision across the wide range of lumen diameters. In vivo measurements by OFDI and IVUS could slightly be discrepant depending on the parameters and time points. In stent assessment by OFDI, the 2 methods led to a small but systematic difference; therefore, consistency in methodology is advised for comparative studies.
View details for DOI 10.1007/s12928-015-0349-x
View details for PubMedID 26271203
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Functional Versus Anatomic Assessment of Myocardial Bridging by Intravascular Ultrasound: Impact of Arterial Compression on Proximal Atherosclerotic Plaque.
Journal of the American Heart Association
2016; 5 (4)
Abstract
The presence of a myocardial bridge (MB) has been shown to promote atherosclerotic plaque formation proximal to the MB, presumably because of hemodynamic disturbances provoked by retrograde blood flow toward this segment in cardiac systole. We aimed to determine the anatomic and functional properties of an MB related to the extent of atherosclerosis assessed by intravascular ultrasound.We enrolled 100 patients with angina but no significant obstructive coronary artery disease who had an intravascular ultrasound-detected MB in the left anterior descending artery (median age 54 years, 36% male). The MB was identified with intravascular ultrasound by the presence of an echolucent band (halo). Anatomically, the MB length was 22±13 mm, and halo thickness was 0.7±0.6 mm. Functionally, systolic arterial compression was 23±12%. The maximum plaque burden up to 20 mm proximal to the MB entrance was significantly greater than the maximum plaque burden within the MB segment. Among the intravascular ultrasound-defined MB properties, arterial compression was the sole MB parameter that demonstrated a significant positive correlation with maximum plaque burden up to 20 mm proximal to the MB entrance (r=0.254, P=0.011 overall; r=0.545, P<0.001 low coronary risk). In multivariate analysis, adjusting for clinical characteristics and coronary risk factors, arterial compression was independently associated with maximum plaque burden up to 20 mm proximal to the MB entrance.In patients with an MB in the left anterior descending artery, the percentage of arterial compression is related directly to the burden of atherosclerotic plaque located proximally to the MB, particularly in patients who otherwise have low coronary risk. This may prove helpful in identifying high-risk MB patients.
View details for DOI 10.1161/JAHA.114.001735
View details for PubMedID 27098967
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Relative dose and vascular response after drug-eluting stent implantation: A dosimetric 3D-intravascular ultrasound study
INTERNATIONAL JOURNAL OF CARDIOLOGY
2016; 204: 211-217
Abstract
In drug-eluting stents (DESs), the theoretical drug dose exposed to the vessel wall per stent surface area may vary due to the fixed loading dose and differences in the stent surface area once expanded in varying vessel sizes. The aim of this study was to evaluate the potential effects of different dose intensities, as estimated by 3D-IVUS dosimetry, on vascular response after DES implantation.Follow-up (6-9 months) 3D-IVUS was performed in 840 coronary lesions treated with a single DES of the following types: sirolimus (SES, n=148), paclitaxel (PES, n=162), Endeavor zotarolimus (E-ZES, n=233), Resolute zotarolimus (R-ZES, n=147), and everolimus (EES, n=150). Volume index (volume/length, mm(3)/mm) was obtained for vessel, lumen, plaque, stent, and neointima. In each lesion, exposed dose intensity was calculated as known loading dose divided by measured luminal surface area of the stented segment. Lesions were divided into tertiles based on the exposed dose intensity: high, medium, and low dose groups.The exposed dose intensity ranged 0.74-1.76 μg/mm(2) for SES, 0.41-1.18 μg/mm(2) for PES, 0.71-1.57 μg/mm(2) for E-ZES, 0.72-1.63 μg/mm(2) for R-ZES, and 0.40-0.99 μg/mm(2) for EES. All types of DES showed no significant difference in neointimal hyperplasia among the 3 groups, except that E-ZES showed significantly less neointimal hyperplasia in the high dose group.Detailed 3D-IVUS revealed significant lesion-to-lesion variability in dose intensity exposed to the vessel wall following DES implantation. However, the major types of DES appear to yield equally effective neointimal suppression, despite the varying dose intensity, except for E-ZES.
View details for DOI 10.1016/j.ijcard.2015.11.130
View details for Web of Science ID 000367008200059
View details for PubMedID 26681540
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Paradoxical Vessel Remodeling of the Proximal Segment of the Left Anterior Descending Artery Predicts Long-Term Mortality After Heart Transplantation.
JACC. Heart failure
2015; 3 (12): 942-952
Abstract
This study investigated the association between arterial remodeling and geographic distribution of cardiac allograft vasculopathy (CAV), and outcomes after heart transplantation.CAV is characterized by a combination of coronary intimal thickening and pathological vessel remodeling, which varies at different locations in coronary arteries.In 100 transplant recipients, serial volumetric intravascular ultrasonography (IVUS) was performed at baseline and 1 year post-transplantation in the first 50 mm of the left anterior descending artery (LAD). IVUS indices were evaluated in the entire segment and 3 equally divided LAD segments. Paradoxical vessel remodeling was defined as [Δvessel volume/Δintimal volume <0].After 1 year, death or re-transplantation occurred in 20 patients over a median follow-up period of 4.7 years. Paradoxical vessel remodeling was observed in 57%, 41%, 50%, and 40% for the entire vessel, proximal, middle, and distal LAD segments, respectively. Kaplan-Meier analysis revealed a significantly lower event-free rate of survival in patients with paradoxical vessel remodeling involving the proximal LAD segment, which was not present when involving the entire LAD or mid and distal LAD segments. In multivariate analysis, paradoxical vessel remodeling of the proximal LAD segment was independently associated with death or re-transplantation (hazard ratio [HR]: 11.18; 95% confidence interval [CI]: 2.39 to 83.23; p = 0.0015).Despite the diffuse nature of CAV, paradoxical vessel remodeling of the proximal LAD segment at 1 year was the primary determinant of long-term mortality or re-transplantation. Assessment of arterial remodeling combined with coronary intimal thickening may enhance identification of high-risk patients who may benefit from closer follow-up and targeted medical therapies.
View details for DOI 10.1016/j.jchf.2015.07.013
View details for PubMedID 26577615
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Physiologic Assessment of Intermediate Coronary Artery Stenosis by Intravascular Ultrasound Radiofrequency Signal Analysis of Blood Speckles: A Comparison with Fractional Flow Reserve and Instantaneous Wave-Free Ratio
ELSEVIER SCIENCE INC. 2015: B59–B60
View details for DOI 10.1016/j.jacc.2015.08.175
View details for Web of Science ID 000363329000127
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Factors Affecting Quantitative Stent Assessment by Optical Frequency Domain Imaging: In Vivo Direct Comparison with Intravascular Ultrasound
ELSEVIER SCIENCE INC. 2015: B134–B135
View details for DOI 10.1016/j.jacc.2015.08.352
View details for Web of Science ID 000363329000294
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Head-to-Head Comparison of Two Commercially Available Automated Detection Algorithms for Lumen Contour in Optical Coherence Tomography Analysis
ELSEVIER SCIENCE INC. 2015: B136
View details for DOI 10.1016/j.jacc.2015.08.356
View details for Web of Science ID 000363329000298
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Association between Increased Number of Septal Branches within the Myocardial Bridge and Abnormal Diastolic-Fractional Flow Reserve
ELSEVIER SCIENCE INC. 2015: B139–B140
View details for DOI 10.1016/j.jacc.2015.08.964
View details for Web of Science ID 000363329000305
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Variability in Quantitative Precision of Intravascular Imaging Modalities: Head-to-Head Comparison of Currently Available Coronary Imaging Systems
ELSEVIER SCIENCE INC. 2015: B142
View details for DOI 10.1016/j.jacc.2015.08.971
View details for Web of Science ID 000363329000311
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Assessment of Bioresorbable Scaffold With a Novel High-Definition 60MHz IVUS Imaging System: Comparison With Conventional 40MHz IVUS and Optical Coherence Tomography
ELSEVIER SCIENCE INC. 2015: B146–B147
View details for DOI 10.1016/j.jacc.2015.08.980
View details for Web of Science ID 000363329000320
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Impact of Stent Size Selection on Acute and Long-Term Outcomes after Drug-Eluting Stent Implantation in De Novo Coronary Lesions
ELSEVIER SCIENCE INC. 2015: B225
View details for DOI 10.1016/j.jacc.2015.08.1025
View details for Web of Science ID 000363329000498
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Effect of Sex Differences on Invasive Measures of Coronary Microvascular Dysfunction in Patients With Angina in the Absence of Obstructive Coronary Artery Disease
JACC-CARDIOVASCULAR INTERVENTIONS
2015; 8 (11): 1433-1441
Abstract
This study investigated sex differences in coronary flow reserve (CFR) and the index of microcirculatory resistance (IMR) in patients with angina in the absence of obstructive coronary artery disease.Coronary microvascular dysfunction is associated with worse long-term outcomes, especially in women. Coronary flow reserve (CFR) and the index of microcirculatory resistance (IMR) are 2 methods of assessing the coronary microcirculation.We prospectively enrolled 117 women and 40 men with angina in the absence of obstructive coronary artery disease. We performed CFR, IMR, fractional flow reserve, and quantitative coronary angiography in the left anterior descending artery. Coronary flow was assessed with a thermodilution method by obtaining mean transit time (Tmn) (an inverse correlate to absolute flow) at rest and hyperemia.All patients had minimal atherosclerosis by quantitative coronary angiography (% diameter stenosis: 23.2 ± 12.3%), and epicardial disease was milder in women (fractional flow reserve: 0.88 ± 0.04 vs. 0.87 ± 0.04; p = 0.04). IMR was similar between the sexes (20.7 ± 9.8 vs. 19.1 ± 8.0; p = 0.45), but CFR was lower in women (3.8 ± 1.6 vs. 4.8 ± 1.9; p = 0.004). This was primarily due to a shorter resting Tmn in women (p = 0.005), suggesting increased resting coronary flow, whereas hyperemic Tmn was identical (p = 0.79). In multivariable analysis, female sex was an independent predictor of lower CFR and shorter resting Tmn.Despite similar microvascular function in women and men by IMR, CFR is lower in women. This discrepancy appears to be due to differences in resting coronary flow between the sexes. The effect of sex differences should be considered in interpretation of physiological indexes using resting coronary flow.
View details for DOI 10.1016/j.jcin.2015.03.045
View details for Web of Science ID 000361757600013
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Effect of Sex Differences on Invasive Measures of Coronary Microvascular Dysfunction in Patients With Angina in the Absence of Obstructive Coronary Artery Disease.
JACC. Cardiovascular interventions
2015; 8 (11): 1433-41
Abstract
This study investigated sex differences in coronary flow reserve (CFR) and the index of microcirculatory resistance (IMR) in patients with angina in the absence of obstructive coronary artery disease.Coronary microvascular dysfunction is associated with worse long-term outcomes, especially in women. Coronary flow reserve (CFR) and the index of microcirculatory resistance (IMR) are 2 methods of assessing the coronary microcirculation.We prospectively enrolled 117 women and 40 men with angina in the absence of obstructive coronary artery disease. We performed CFR, IMR, fractional flow reserve, and quantitative coronary angiography in the left anterior descending artery. Coronary flow was assessed with a thermodilution method by obtaining mean transit time (Tmn) (an inverse correlate to absolute flow) at rest and hyperemia.All patients had minimal atherosclerosis by quantitative coronary angiography (% diameter stenosis: 23.2 ± 12.3%), and epicardial disease was milder in women (fractional flow reserve: 0.88 ± 0.04 vs. 0.87 ± 0.04; p = 0.04). IMR was similar between the sexes (20.7 ± 9.8 vs. 19.1 ± 8.0; p = 0.45), but CFR was lower in women (3.8 ± 1.6 vs. 4.8 ± 1.9; p = 0.004). This was primarily due to a shorter resting Tmn in women (p = 0.005), suggesting increased resting coronary flow, whereas hyperemic Tmn was identical (p = 0.79). In multivariable analysis, female sex was an independent predictor of lower CFR and shorter resting Tmn.Despite similar microvascular function in women and men by IMR, CFR is lower in women. This discrepancy appears to be due to differences in resting coronary flow between the sexes. The effect of sex differences should be considered in interpretation of physiological indexes using resting coronary flow.
View details for DOI 10.1016/j.jcin.2015.03.045
View details for PubMedID 26404195
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Association between blood glucose variability and coronary plaque instability in patients with acute coronary syndromes
CARDIOVASCULAR DIABETOLOGY
2015; 14
Abstract
Blood glucose variability is receiving considerable attention as a new risk factor for coronary artery disease. This study aimed to investigate the association between blood glucose variability and coronary plaque tissue characteristics.In 57 patients with acute coronary syndrome, integrated backscatter intravascular ultrasound (IB-IVUS) and gray-scale IVUS were performed before balloon dilatation or stent implantation in the culprit vessels. Standard IVUS indices were evaluated for volume index (volume/length), and plaque components were measured by IB-IVUS for percent tissue volume. In addition to conventional glucose indicators, blood glucose variability in a stable state was determined by calculating the mean amplitude of glycemic excursions (MAGE) using a continuous glucose monitoring system.Higher MAGE values were significantly correlated with larger percent plaque volumes (r = 0.32, p = 0.015), and increased lipid (r = 0.44, p = 0.0006) and decreased fibrous (r = -0.45, p = 0.0005) plaque components. In contrast, HbA1c or fasting plasma glucose values were not significantly correlated with plaque volumes and percent plaque components. Homeostasis model assessment of insulin resistance values were positively correlated with vessel (r = 0.35, p = 0.007) and plaque (r = 0.27, p = 0.046) volumes, but not with percent plaque components. In multiple regression analysis, higher MAGE values were independently associated with increased lipid (β = 0.80, p = 0.0035) and decreased fibrous (β = -0.79, p = 0.0034) contents in coronary plaques.Among all glucose indicators studied, only higher blood glucose variability was an independent determinant of increased lipid and decreased fibrous contents with larger plaque burden, suggesting blood glucose variability as one of the important factors related to coronary plaque vulnerability.
View details for DOI 10.1186/s12933-015-0275-3
View details for Web of Science ID 000359704400001
View details for PubMedCentralID PMC4546046
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PARADOXICAL ARTERIAL REMODELING OF THE PROXIMAL SEGMENT OF THE LEFT ANTERIOR DESCENDING ARTERY PREDICTS LONG-TERM MORTALITY AFTER HEART TRANSPLANTATION
ELSEVIER SCIENCE INC. 2015: A1740
View details for DOI 10.1016/S0735-1097(15)61740-5
View details for Web of Science ID 000375328802062
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INVASIVE CORONARY PHYSIOLOGY AT ONE YEAR PREDICTS LATE MORTALITY AFTER HEART TRANSPLANTATION
ELSEVIER SCIENCE INC. 2015: A1685
View details for DOI 10.1016/S0735-1097(15)61685-0
View details for Web of Science ID 000375328802007
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ASSOCIATION OF PERIARTERIAL NEOVASCULARIZATION WITH PROGRESSION OF CARDIAC ALLOGRAFT VASCULOPATHY AND LONG-TERM CLINICAL OUTCOMES IN HEART TRANSPLANT RECIPIENTS
ELSEVIER SCIENCE INC. 2015: A1710
View details for DOI 10.1016/S0735-1097(15)61710-7
View details for Web of Science ID 000375328802032
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IMPACT OF MYOCARDIAL BRIDGING ON CORONARY ARTERY PLAQUE FORMATION AND LONG-TERM MORTALITY AFTER HEART TRANSPLANTATION
ELSEVIER SCIENCE INC. 2015: A1741
View details for DOI 10.1016/S0735-1097(15)61741-7
View details for Web of Science ID 000375328802063
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A Y-shaped bifurcation-dedicated stent for the treatment of de novo coronary bifurcation lesions: an IVUS analysis from the BRANCH trial.
EuroIntervention
2015; 10 (11): e1-8
Abstract
Aims: The aim of this IVUS substudy was to assess the efficacy of the Y-shaped Medtronic bifurcation-dedicated stent (BDS) for the treatment of de novo coronary bifurcated lesions. Methods and results: In the BRANCH trial, post-procedure IVUS was performed in 45 patients. IVUS was available in both branches in 19 lesions and only the main branch (MB) in 26 lesions. IVUS analysis included four distinct locations: proximal MB, bifurcation site, distal MB, and side branch (SB). Lumen symmetry was calculated as minimum/maximum lumen diameters. The quantity of isolated stent struts across the SB ostium was used to assess inadequate strut apposition to the carina resulting in partial jailing of the SB orifice. A minimum stent area (MSA) <4 mm2 was found in 0% of proximal and distal MB, and in 15.4% of SB. In SB, MSA was located mainly at mid or distal segments (84.6%), rather than at the SB ostium. Eccentric stent expansion and edge dissection were seen primarily at proximal MB. Isolated struts were seen in only 20.9% of SB ostia with a minimum length of 0.7±0.4 mm. Conclusions: Implantation of BDS resulted in adequate stent dimensions and strut apposition at the carina and SB ostium. ClinicalTrials.gov Identifier: NCT0060732.
View details for DOI 10.4244/EIJY14M08_16
View details for PubMedID 25169593
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Association between blood glucose variability and coronary plaque instability in patients with acute coronary syndromes.
Cardiovascular diabetology
2015; 14: 111-?
Abstract
Blood glucose variability is receiving considerable attention as a new risk factor for coronary artery disease. This study aimed to investigate the association between blood glucose variability and coronary plaque tissue characteristics.In 57 patients with acute coronary syndrome, integrated backscatter intravascular ultrasound (IB-IVUS) and gray-scale IVUS were performed before balloon dilatation or stent implantation in the culprit vessels. Standard IVUS indices were evaluated for volume index (volume/length), and plaque components were measured by IB-IVUS for percent tissue volume. In addition to conventional glucose indicators, blood glucose variability in a stable state was determined by calculating the mean amplitude of glycemic excursions (MAGE) using a continuous glucose monitoring system.Higher MAGE values were significantly correlated with larger percent plaque volumes (r = 0.32, p = 0.015), and increased lipid (r = 0.44, p = 0.0006) and decreased fibrous (r = -0.45, p = 0.0005) plaque components. In contrast, HbA1c or fasting plasma glucose values were not significantly correlated with plaque volumes and percent plaque components. Homeostasis model assessment of insulin resistance values were positively correlated with vessel (r = 0.35, p = 0.007) and plaque (r = 0.27, p = 0.046) volumes, but not with percent plaque components. In multiple regression analysis, higher MAGE values were independently associated with increased lipid (β = 0.80, p = 0.0035) and decreased fibrous (β = -0.79, p = 0.0034) contents in coronary plaques.Among all glucose indicators studied, only higher blood glucose variability was an independent determinant of increased lipid and decreased fibrous contents with larger plaque burden, suggesting blood glucose variability as one of the important factors related to coronary plaque vulnerability.
View details for DOI 10.1186/s12933-015-0275-3
View details for PubMedID 26289581
View details for PubMedCentralID PMC4546046
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Baseline and 9 Months IVUS Analysis of the Bifurcation-Dedicated Biolimus A9-Eluting Axxess Stent System: The DIVERGE IVUS Substudy
CATHETERIZATION AND CARDIOVASCULAR INTERVENTIONS
2014; 84 (7): 1062-1070
Abstract
Percutaneous treatment of complex coronary bifurcation lesions remains challenging, even in the drug-eluting stent era. We sought to evaluate the baseline and 9 months intravascular ultrasound (IVUS) analysis of the Axxess™ stent, a self-expanding, Biolimus A9™-eluting, and dedicated bifurcation stent.We enrolled the first 76 patients from selected sites of the 302 patients large DIVERGE trial (a prospective, single-arm, multicenter trial evaluating the safety and efficacy of the Axxess stent). Both baseline and 9 months IVUS images were collected for serial two-dimensional (2D) and 3D analysis. A minimal amount and a low percentage of neointimal volume index were seen in the Axxess stent at 9 months (0.4 ± 0.6 mm(3) /mm and 4.3 ± 5.2%, respectively). Vessel, lumen, and stent volume indices increased significantly (respectively, 17.0 ± 3.6 to 18.9 ± 3.7 mm(3) /mm, P < 0.0001; 7.3 ± 2.0 to 9.2 ± 2.5 mm(3) /mm, P < 0.0001; and 7.4 ± 2.0 to 9.6 ± 2.6 mm(3) /mm, P < 0.0001). This resulted in minimum lumen area (MLA) enlargement (6.1 ± 1.9 to 7.2 ± 2.3 mm(2) , P < 0.0001), whereas peristent plaque area decreased (8.7 ± 2.5 to 8.5 ± 2.1 mm(3) /mm, P = 0.016). At 9 months, 16 (26%) incomplete stent apposition (ISA) persisted from baseline, while six resolved (9.7%). Only one (2%) ISA was late acquired. In the additional distal sirolimus-eluting stents, MLA decreased from 4.3 ± 1.1 to 4.1 ± 1.2 mm(2) (P = 0.04) at 9 months for the main branch, and from 3.4 ± 1.2 to 3.2 ± 1.2 mm(2) (P = 0.09) for the side branch.The dedicated bifurcation Axxess stent system demonstrates significant stent volume increase with minimal neointimal formation and a low incidence of late-acquired ISA at 9 months. © 2014 Wiley Periodicals, Inc.
View details for DOI 10.1002/ccd.25414
View details for Web of Science ID 000345514400009
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First-in-Man Study of the Low-Dose Paclitaxel Using the COBRA-P Drug-Eluting Coronary Stent System With a Novel Biodegradable Coating in De Novo Coronary Lesions: IVUS Results From the PLUS-ONE Trial
CATHETERIZATION AND CARDIOVASCULAR INTERVENTIONS
2014; 84 (7): 1101-1109
View details for DOI 10.1002/ccd.25351
View details for Web of Science ID 000345514400016
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Validation of High Speed Pullback of a Novel High-Definition Intravascular Ultrasound System
ELSEVIER SCIENCE INC. 2014: B102
View details for DOI 10.1016/j.jacc.2014.07.399
View details for Web of Science ID 000359649700347
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Transformation of Attenuated-Signal Plaque into Calcified Plaque After DES Implantation
ELSEVIER SCIENCE INC. 2014: B102
View details for DOI 10.1016/j.jacc.2014.07.397
View details for Web of Science ID 000359649700345
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Atherosclerotic Plaque Formation Relates to Myocardial Bridging in Left Anterior Descending Coronary Arteries
ELSEVIER SCIENCE INC. 2014: B104
View details for DOI 10.1016/j.jacc.2014.07.406
View details for Web of Science ID 000359649700354
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Precision of a Novel High-Definition 60MHz IVUS in Quantitative Measurement: Comparison with Conventional 40MHz IVUS and Optical Coherence Tomography
ELSEVIER SCIENCE INC. 2014: B105–B106
View details for DOI 10.1016/j.jacc.2014.07.410
View details for Web of Science ID 000359649700358
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Head-to-Head Comparison of Automated versus Manual Detection for Lumen Contour and Stent Struts in Optical Coherence Tomography Analysis
ELSEVIER SCIENCE INC. 2014: B116
View details for DOI 10.1016/j.jacc.2014.07.444
View details for Web of Science ID 000359649700391
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Impact of Coronary Artery Size on Physiologic Microcirculatory Indices: A Volumetric Intravascular Ultrasound Study with Coronary Flow Assessment
ELSEVIER SCIENCE INC. 2014: B91
View details for DOI 10.1016/j.jacc.2014.07.362
View details for Web of Science ID 000359649700312
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Attenuated-Signal Plaque and Cardiac Allograft Vasculopathy: A Serial Volumetric IVUS Study of Heart Transplant Recipients
ELSEVIER SCIENCE INC. 2014: B102
View details for DOI 10.1016/j.jacc.2014.07.398
View details for Web of Science ID 000359649700346
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Appropriate Intravascular Ultrasound Measurement Intervals for Assessment of Cardiac Allograft Vasculopathy after Heart Transplantation
ELSEVIER SCIENCE INC. 2014: B105
View details for DOI 10.1016/j.jacc.2014.07.407
View details for Web of Science ID 000359649700355
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VOLUMETRIC VERSUS PLANAR INTRAVASCULAR ULTRASOUND ANALYSIS TO ASSESS SEVERITY OF CARDIAC ALLOGRAFT VASCULOPATHY
ELSEVIER SCIENCE INC. 2014: A1765
View details for DOI 10.1016/S0735-1097(14)61768-X
View details for Web of Science ID 000359579102523
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ASSOCIATION BETWEEN ABDOMINAL FAT DISTRIBUTION AND CORONARY TISSUE CHARACTERISTICS IN PATIENTS WITH ACUTE CORONARY SYNDROMES
ELSEVIER SCIENCE INC. 2014: A1796
View details for DOI 10.1016/S0735-1097(14)61799-X
View details for Web of Science ID 000359579102554
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IMPACT OF VESSEL STRETCH AND PLAQUE REDUCTION ON NEOINTIMAL PROLIFERATION AFTER DRUG-ELUTING STENT IMPLANTATION: A POOLED VOLUMETRIC INTRAVASCULAR ULTRASOUND ANALYSIS
ELSEVIER SCIENCE INC. 2014: A1764
View details for DOI 10.1016/S0735-1097(14)61767-8
View details for Web of Science ID 000359579102522
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RELATIONSHIP BETWEEN BLOOD FLOW VELOCITY AND RADIOFREQUENCY SIGNAL ANALYSIS OF BLOOD SPECKLES: AN EXPERIMENTAL STUDY USING INTEGRATED BACKSCATTER IVUS
ELSEVIER SCIENCE INC. 2014: A1776
View details for DOI 10.1016/S0735-1097(14)61779-4
View details for Web of Science ID 000359579102534
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CORONARY PHYSIOLOGICAL INDICES IN PATIENTS WITH MYOCARDIAL BRIDGING
ELSEVIER SCIENCE INC. 2014: A1691
View details for DOI 10.1016/S0735-1097(14)61694-6
View details for Web of Science ID 000359579102449
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Intravascular Ultrasound Analysis of Small Vessel Lesions Treated with the Sparrow Coronary Stent System: Results of the CARE II Trial
CATHETERIZATION AND CARDIOVASCULAR INTERVENTIONS
2014; 83 (1): 19-24
Abstract
OBJECTIVES: The aim of this study was to evaluate the Sparrow sirolimus-eluting stent (Sparrow-SES) against the Sparrow bare-metal stent (Sparrow-BMS) and conventional balloon-expandable bare-metal stent (BMS: Driver/Micro-Driver(®) stent, Medtronic Vascular, Santa Rosa, CA). BACKGROUND: The Sparrow(®) stent (Biosensors International, Singapore) consists of a guide wire-based, self-expandable, ultra-thin nitinol stent. The performance of this device with sirolimus in a fully biodegradable polymer has not been determined. METHODS: A total of 74 patients were included in this intravascular ultrasound (IVUS) sub-study of the CARE II trial, which was a prospective, randomized, multicenter trial in the treatment of single de novo native coronary artery lesions in vessels ranging from 2.0 mm to 2.75 mm in diameter (Sparrow-SES: n = 31, Sparrow-BMS: n = 22, BMS: n = 21). RESULTS: Stent volume index (VI) was significantly increased 8-month later in Sparrow-SES and Sparrow-BMS, but not in BMS (4.0±1.0 to 4.6±1.0 mm(3) /mm, p<0.0001, 4.0±0.6 to 4.4±0.8 mm(3) /mm, p<0.05, and 5.2±1.0 to 5.1±0.9 mm(3) /mm, p=0.421, respectively). % neointimal obstruction in Sparrow-SES was significantly smaller than those in Sparrow-BMS and BMS at follow-up (17.6±9.4 vs. 36.2±13.8 and 39.9±11.1%, p<0.001). Sparrow-SES showed a mean 15% stent expansion and good suppression of neointimal proliferation, resulting in a significantly lower percentage of change in lumen VI during follow-up period (Sparrow-SES: -6.2±16.2%, Sparrow-BMS: -30.4±11.6%, BMS: -40.4±10.0%, p<0.001). CONCLUSIONS: The self-expanding Sparrow-SES demonstrated chronic stent expansion, good suppression of neointimal proliferation and resulted in a more preserved lumen in stented small vessels compared with the Sparrow-BMS and conventional balloon expandable BMS. © 2013 Wiley Periodicals, Inc.
View details for DOI 10.1002/ccd.24867
View details for Web of Science ID 000328631400007
View details for PubMedID 23413202
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Basic Concepts and Clinical Applications of Intravascular Imaging
Vascular Imaging of the Central Nervous System: Physical Principles, Clinical Applications, and Emerging Techniques
2014: 347–70
View details for Web of Science ID 000362331100022
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Contemporary infrapopliteal intervention for limb salvage and wound healing: harmonization of revascularization and wound management.
Circulation journal
2014; 78 (7): 1540-1549
Abstract
Infrapopliteal arterial disease is a significant cause of critical limb ischemia (CLI), whether single-segment or multisegment disease. The collaboration between the tremendous advancements in endovascular technology and the refinement of endovascular techniques has renewed the classic infrapopliteal interventions during the past decade. With this paradigm shift in the treatment of CLI, the role of a comprehensive approach of different disciplines for tissue loss is becoming greater. Given the increasing global burden of CLI, we review the cutting-edge diagnostic and endovascular approaches to infrapopliteal artery disease, and the importance of wound management in optimizing clinical outcomes.
View details for PubMedID 24964979
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Histological characteristics of myocardial bridge with an ultrasonic echolucent band. Comparison between intravascular ultrasound and histology.
Circulation journal
2014; 78 (2): 502-504
View details for PubMedID 24172077
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Safety and efficacy of low-dose paclitaxel utilizing the cobra-P drug-eluting stent system with a novel biodegradable coating in de novo coronary lesions: the PLUS-ONE first-in-man study.
Cardiovascular revascularization medicine : including molecular interventions
2014; 15 (1): 18-22
Abstract
The Cobra-P drug-eluting stent (DES) system consists of cobalt chromium alloy with bio-absorbable siloxane sol-gel matrix coating that elutes low dose paclitaxel within 6 months. The aim of this first-in-man trial was to evaluate the safety and performance of 2 doses of the Cobra-P DES.A total of 60 lesions (54 patients) were sequentially assigned to 2 different paclitaxel doses: group A (3.7 μg/18mm, n=30) or group B (8 μg/18mm, n=30). The primary endpoint was MACE at 4 months defined as cardiac death, myocardial infarction, and target lesion revascularization.Patient and lesion characteristics were matched between the 2 groups except for male sex. MACE at 4 months was 3.3% and 0% respectively (P=1.000) and at 1-year follow-up remained unchanged. In-stent late loss at 4 months was similar in both groups (0.36 ± 0.30mm and 0.34 ± 0.20mm P=.773).In this FIM study, implantation of the Cobra-P low dose paclitaxel-eluting stent with a bioabsorbable sol-gel coating was proven to be feasible and safe. Moderate neointimal proliferation was observed as well as an acceptable MACE rate up to 1 year.
View details for DOI 10.1016/j.carrev.2013.10.001
View details for PubMedID 24315045
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Relation Between Periarterial Neovascularization and Progression of Coronary Allograft Vasculopathy: A Serial IVUS Study of Cardiac Transplant Patients
LIPPINCOTT WILLIAMS & WILKINS. 2013
View details for Web of Science ID 000332162905312
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Effects of Metabolic Syndrome on Arterial Responses to Drug-Eluting Stents: Obesity Paradox and Sex-Associated Differences
LIPPINCOTT WILLIAMS & WILKINS. 2013
View details for Web of Science ID 000332162903500
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Impact of Stent Patency on Proximal and Distal Vessel Segments After Various Drug-Eluting Stent Implantation: Pooled Intravascular Ultrasound Analyses
LIPPINCOTT WILLIAMS & WILKINS. 2013
View details for Web of Science ID 000332162905282
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Impact of Myocardial Bridging on Coronary Endothelial Dysfunction and Atherosclerotic Plaque Formation
LIPPINCOTT WILLIAMS & WILKINS. 2013
View details for Web of Science ID 000332162906321
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Peri-stent contrast staining and very late stent thrombosis after sirolimus-eluting stent implantation: an observation from the RESTART (REgistry of Stent Thrombosis for review And Re-evaluaTion) angiographic substudy.
EuroIntervention
2013; 9 (7): 831-840
Abstract
Aims: The aim of the study was to clarify the angiographic characteristics of stent thrombosis (ST) in relation to sirolimus-eluting stents (SES). Methods and results: RESTART is a Japanese registry of SES-associated ST. As an angiographic substudy, coronary angiograms at baseline, at six to 12 months and at the time of ST were analysed. Angiograms of 313 patients (early ST [EST] 169 patients, late ST [LST] 59 patients, and very late ST [VLST] 85 patients) were investigated. Residual dissection post procedure was more frequently seen in the EST group. Stent fracture was more frequently seen in the VLST group than in the EST and LST groups (16.5%, 3.0%, and 3.4%, respectively; p<0.001). Peri-stent contrast staining (PSS), defined as contrast staining outside the stent contour extending to ≥20% of the stent diameter, was remarkably more prevalent in the VLST group than in the EST and LST groups (34.1%, 4.7%, and 6.8%, respectively; p<0.001). Conclusions: Abnormal angiographic findings such as PSS and stent fracture were found significantly more frequently in lesions with VLST than in lesions with EST and LST.
View details for DOI 10.4244/EIJV9I7A137
View details for PubMedID 23410581
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Assessments of Lipid Plaque and Thrombus With a Novel High-Definition 60-MHz IVUS Imaging System: Comparison with Conventional 40-MHz IVUS and Optical Coherence Tomography
ELSEVIER SCIENCE INC. 2013: B201–B202
View details for DOI 10.1016/j.jacc.2013.08.1410
View details for Web of Science ID 000329845600655
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Association between Glycemic Variability and Coronary Tissue Characteristics in Patients with Acute Coronary Syndromes
ELSEVIER SCIENCE INC. 2013: B195
View details for DOI 10.1016/j.jacc.2013.08.1391
View details for Web of Science ID 000329845600636
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Pre-interventional Plaque Composition Assessed by Virtual Histology Intravascular Ultrasound Predicts Plaque Shift after Stent Implantation
ELSEVIER SCIENCE INC. 2013: B171–B172
View details for DOI 10.1016/j.jacc.2013.08.1316
View details for Web of Science ID 000329845600564
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Acute Stent Expansion in the Latest-Generation Drug-Eluting Stent Platforms: An Experimental Study Using Optical Coherence Tomography
ELSEVIER SCIENCE INC. 2013: B180
View details for DOI 10.1016/j.jacc.2013.08.1341
View details for Web of Science ID 000329845600588
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Variability in quantitative and qualitative analysis of intravascular ultrasound and frequency domain optical coherence tomography
CATHETERIZATION AND CARDIOVASCULAR INTERVENTIONS
2013; 82 (3): E192-E199
Abstract
BACKGROUND: Frequency-domain optical coherence tomography (FD-OCT) is an intravascular imaging technique now available in the United States. However, the importance of level of training required for analysis using intravascular ultrasound (IVUS) and FD-OCT is unclear. The aim of this study was to evaluate inter- and intra-observer variability between expert and beginner analysts interpreting IVUS and FD-OCT images. METHODS AND RESULTS: Two independent expert analysts and two independent beginner analysts evaluated a total of 226 ± 2 stent cross-sections with IVUS and 232 ± 2 stent cross-sections with FD-OCT in 14 patients after stenting. Inter- and intra-observer variability for determining stent volume index (VI), as well as identifying incomplete stent apposition and dissection were assessed. The inter- and intra-observer variability of stent VI was minimal for both beginner and expert analysts regardless of imaging technology (random variability: 0.38 vs. 0.05 mm(3) /mm for IVUS, 0.26 vs. 0.08 mm(3) /mm for FD-OCT). Although qualitative IVUS analysis at the patient level revealed no significant difference between beginners and experts, this was not the case for FD-OCT. The number of overall qualitative findings noted by beginner and expert analysts were more variable (overestimated or underestimated) with FD-OCT. CONCLUSION: Despite varying levels of training, the increased resolution of FD-OCT compared to IVUS provides better detection and less variability in quantitative image analysis. On the contrary, this increased resolution not only increases the rate but also the variability of detection of qualitative image analysis, especially for beginner analysts. © 2013 Wiley Periodicals, Inc.
View details for DOI 10.1002/ccd.24871
View details for Web of Science ID 000323454100008
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FINAL IVUS RESULTS FROM THE DESOLVE-I FIRST-IN-HUMAN TRIAL: LONG-TERM ARTERIAL RESPONSE TO A NOVEL SIROLIMUS-ELUTING STENT WITH FULLY ABSORBABLE POLYMER AND CRYSTALLINE DRUG
62nd Annual Scientific Session of the American-College-of-Cardiology
ELSEVIER SCIENCE INC. 2013: E1666–E1666
View details for Web of Science ID 000316555201771
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ACCELERATED NEOINTIMAL HYPERPLASIA AFTER DES IMPLANTATION IN LESIONS WITH IVUS-SIGNAL ATTENUATION: A 3D-IVUS ANALYSIS FROM THE J-DESSERT TRIAL
62nd Annual Scientific Session of the American-College-of-Cardiology
ELSEVIER SCIENCE INC. 2013: E1790–E1790
View details for Web of Science ID 000316555201895
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IMPACT OF POST-DILATATION STRATEGIES AND STENT MATERIALS ON CHRONIC STENT AREA PRESERVATION: AN EXPERIMENTAL STUDY USING OPTICAL COHERENCE TOMOGRAPHY
62nd Annual Scientific Session of the American-College-of-Cardiology
ELSEVIER SCIENCE INC. 2013: E1657–E1657
View details for Web of Science ID 000316555201762
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PREDICTORS OF LATE TARGET LESION REVASCULARIZATION AFTER ENDEAVOR AND RESOLUTE ZOTAROLIMUS-ELUTING STENT IMPLANTATION: 3D-INTRAVASCULAR ULTRASOUND AND ANGIOGRAPHIC ANALYSES
62nd Annual Scientific Session of the American-College-of-Cardiology
ELSEVIER SCIENCE INC. 2013: E1777–E1777
View details for Web of Science ID 000316555201882
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PLAQUE ASSESSMENT WITH A NOVEL HIGH-DEFINITION 60-MHZ IVUS IMAGING SYSTEM: COMPARISON WITH CONVENTIONAL 40 MHZ IVUS AND OPTICAL COHERENCE TOMOGRAPHY
62nd Annual Scientific Session of the American-College-of-Cardiology
ELSEVIER SCIENCE INC. 2013: E1878–E1878
View details for Web of Science ID 000316555202082
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IMPACT OF MYOCARDIAL BRIDGING ON MAJOR ADVERSE CARDIAC EVENTS: VERY LONG-TERM CLINICAL OUTCOMES FOLLOWING FIRST- AND SECOND-GENERATION DRUG-ELUTING STENT IMPLANTATION
62nd Annual Scientific Session of the American-College-of-Cardiology
ELSEVIER SCIENCE INC. 2013: E1725–E1725
View details for Web of Science ID 000316555201830
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Duplex criteria for in-stent restenosis in the superficial femoral artery
CATHETERIZATION AND CARDIOVASCULAR INTERVENTIONS
2013; 81 (4): E199-E205
Abstract
To elucidate the optimal cutoff and accuracy of duplex ultrasonography (DUS) parameters for in-stent restenosis (ISR) after nitinol stenting in the superficial femoral artery (SFA).Few data are available regarding the performance of DUS for binary ISR based on quantitative vessel analysis (QVA) in the era of SFA nitinol stenting.This retrospective study included 74 in-stent stenoses of SFA who underwent DUS before follow-up angiography. DUS parameters, such as peak systolic velocity (PSV) and the peak systolic velocity ratio (PSVR), were compared with percent diameter stenosis (%DS) from a QVA basis.There was a statistically significant correlation (P < 0.001) between "%DS and PSV" and "%DS and PSVR," and the correlation with %DS proved to be stronger in PSVR (R = 0.720) than in PSV (R = 0.672). The best performing parameter for ISR (50% or greater stenosis) was revealed PSVR, as the areas under the receiver operator characteristics curves using PSVR and PSV were 0.908 and 0.832, respectively. A PSVR cut off value of 2.85 yielded the best predictive value with sensitivity of 88%, specificity of 84%, and accuracy of 86%. The positive predictive value was 85% and the negative predictive value was 88%.A PSVR of 2.85 is the optimal threshold for ISR after nitinol stenting in the SFA. Further large prospective studies are required for the validation and establishment of uniform criteria for DUS parameters.
View details for DOI 10.1002/ccd.24509
View details for Web of Science ID 000315416600004
View details for PubMedID 22639187
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Improved automated lumen contour detection by novel multifrequency processing algorithm with current intravascular ultrasound system
CATHETERIZATION AND CARDIOVASCULAR INTERVENTIONS
2013; 81 (3): E173-E177
Abstract
The aim of this study was to evaluate a new fully automated lumen border tracing system based on a novel multifrequency processing algorithm.We developed the multifrequency processing method to enhance arterial lumen detection by exploiting the differential scattering characteristics of blood and arterial tissue. The implementation of the method can be integrated into current intravascular ultrasound (IVUS) hardware.This study was performed in vivo with conventional 40-MHz IVUS catheters (Atlantis SR Pro™, Boston Scientific Corp, Natick, MA) in 43 clinical patients with coronary artery disease. A total of 522 frames were randomly selected, and lumen areas were measured after automatically tracing lumen borders with the new tracing system and a commercially available tracing system (TraceAssist™) referred to as the "conventional tracing system." The data assessed by the two automated systems were compared with the results of manual tracings by experienced IVUS analysts.New automated lumen measurements showed better agreement with manual lumen area tracings compared with those of the conventional tracing system (correlation coefficient: 0.819 vs. 0.509). When compared against manual tracings, the new algorithm also demonstrated improved systematic error (mean difference: 0.13 vs. -1.02 mm(2) ) and random variability (standard deviation of difference: 2.21 vs. 4.02 mm(2) ) compared with the conventional tracing system.This preliminary study showed that the novel fully automated tracing system based on the multifrequency processing algorithm can provide more accurate lumen border detection than current automated tracing systems and thus, offer a more reliable quantitative evaluation of lumen geometry.
View details for DOI 10.1002/ccd.23274
View details for Web of Science ID 000315339400004
View details for PubMedID 21805600
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Impact of Diabetes Mellitus on Vessel Response in the Drug-Eluting Stent Era Pooled Volumetric Intravascular Ultrasound Analyses
CIRCULATION-CARDIOVASCULAR INTERVENTIONS
2012; 5 (6): 763-771
Abstract
Exaggerated neointimal hyperplasia is considered as the primary mechanism for increased restenosis in patients with diabetes mellitus (DM) treated with bare-metal stent. However, the vessel response in DM and non-DM treated with different drug-eluting stents (DES) has not been systematically evaluated.We investigated 3D intravascular ultrasound (postprocedure and 6 to 9 months) in 971 patients (267 with DM and 704 without DM) treated with sirolimus- (n=104), paclitaxel- (n=303), zotarolimus- (n=391), or everolimus- (n=173) eluting stents. Volumetric data were standardized by length as volume index (VI). At postprocedure, lumen VI at the stented segment was significantly smaller in DM than in non-DM, whereas vessel VI was similar between the 2 groups. At follow-up, neointimal obstruction and maximum cross-sectional narrowing (neointimal area/stent area) were not significantly different between the 2 groups with no interaction for the DES type. Consequently, lumen VI was smaller in DM than in non-DM at follow-up. In the reference segments, residual plaque burden at postprocedure was significantly greater in DM than in non-DM, although change in lumen VI was similar between the 2 groups. The arterial responses at the reference segments also showed no interaction for the DES type.DM and non-DM lesions showed similar vessel response in both in-stent and reference segments regardless of the DES type. In the DES era, the follow-up lumen in DM patients seems to be determined primarily by the smaller lumen at postprocedure rather than exaggerated neointima within the stent or plaque proliferation at the reference segments.
View details for DOI 10.1161/CIRCINTERVENTIONS.111.962878
View details for Web of Science ID 000313576500014
View details for PubMedID 23149332
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Predictors of adverse clinical outcomes after successful infrapopliteal intervention
CATHETERIZATION AND CARDIOVASCULAR INTERVENTIONS
2012; 80 (5): 861-871
Abstract
To clarify the clinical and angiographical variables related to delayed wound healing, major amputation and death after successful infrapopliteal intervention in critical limb ischemia patients with tissue loss.There is an underappreciation of adverse clinical outcomes after successful infrapopliteal intervention.Stent-assisted infrapopliteal angioplasty was successful in 106 limbs in 85 patients. Successful intervention was defined as revascularization of at least one straight-line flow to the foot.At 6 months and 1, 2, and 5 years, the repeat intervention-free rates were 55.0, 49.6, 44.4, and 36.1%, respectively; the amputation-free survival rates were 85.7, 68.0, 54.5, and 39.8%, respectively; and the limb salvage rates were 96.0, 92.4, 86.3, and 86.3%, respectively. An infectious wound was an independent predictor of major amputation after successful intervention. The complete wound healing rates were 36.8, 57.5, 67.9, and 73.6% at 3, 6, 9, and 12 months, respectively. In stepwise multivariate Cox analysis, diabetes mellitus, an infectious wound, and the pedal arch classification were identified as independent predictors of wound healing. The long-term survival rates at 6 months and 1, 2, and 5 years were 89.5, 73.8, 62.0, and 43.4%, respectively. Stepwise multivariate Cox analysis indentified end-stage renal disease (ESRD) on hemodialysis to be an independent predictor of death.An infectious wound, comorbidities of diabetes mellitus and ESRD on hemodialysis and classification of pedal arch can be predictors of adverse clinical outcomes after successful infrapopliteal intervention.
View details for DOI 10.1002/ccd.24370
View details for Web of Science ID 000310472300029
View details for PubMedID 22431493
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Clinical Feasibility of Higher-Frequency IVUS for Quantitative Measurements of Native Coronary Lesions: First-in-Human Experience with 60MHz versus 40MHz IVUS Imaging
Transcatheter Cardiovascular Therapeutics (TCT) Symposium
ELSEVIER SCIENCE INC. 2012: B81–B82
View details for Web of Science ID 000310210101088
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Impact of Stent Edge Plaque Burden on Lumen Preservation After DES Implantation: A 3D-IVUS Analysis from the J-DESsERT Trial
Transcatheter Cardiovascular Therapeutics (TCT) Symposium
ELSEVIER SCIENCE INC. 2012: B74–B74
View details for Web of Science ID 000310210101061
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Impact of Baseline Peri-Stent Plaque Volume on Positive Vessel Remodeling after Implantation of Paclitaxel Eluting Stents: A Pooled Volumetric Intravascular Ultrasound Analysis
Transcatheter Cardiovascular Therapeutics (TCT) Symposium
ELSEVIER SCIENCE INC. 2012: B85–B85
View details for Web of Science ID 000310210101098
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Myocardial Bridging Increases Diffuse and Focal Chronic Stent Recoil Following Drug-Eluting Stent Implantation
Transcatheter Cardiovascular Therapeutics (TCT) Symposium
ELSEVIER SCIENCE INC. 2012: B122–B122
View details for Web of Science ID 000310210101228
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Comparison of vascular response to the everolimus-eluting stent versus the paclitaxel-eluting stent: intravascular ultrasound results from the SPIRIT III trial
EUROINTERVENTION
2012; 8 (6): 724-731
Abstract
The purpose of this study was to investigate the vascular response of the everolimus-eluting stent (EES) compared with the paclitaxel-eluting stent (PES) using serial intravascular ultrasound (IVUS).Data were obtained from the SPIRIT III trial, a multicentre, 2:1 randomised, controlled study comparing EES and PES in de novo native coronary artery lesions. IVUS images were eligible for volumetric analysis at eight-month follow-up in 158 lesions (EES: 113, PES: 45). At eight months, EES had a smaller neointimal volume index (VI: mm3/mm) (EES: 0.4±0.4 vs. PES: 0.8±0.8 mm3/mm, p=0.002) and also a smaller % neointimal obstruction (EES: 7.1±6.7% vs. PES: 11.1±10.5%, p=0.005) compared with PES. While there was no significant change in vessel VI with EES, there was a significant increase in vessel VI in PES during eight-month follow-up (EES: 0.1±1.2 vs. PES: 1.2±0.8 mm3/mm, p=0.001). There were no statistical differences in the frequency of edge dissection or incomplete stent apposition between the two groups.Detailed IVUS analysis confirmed significantly less neointimal hyperplasia with EES compared with PES. While there was no increase in vessel volume with EES during the eight-month follow-up period, vessel enlargement was seen at the stented segment in PES.
View details for DOI 10.4244/EIJV8I6A112
View details for Web of Science ID 000312043500014
View details for PubMedID 23086791
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Intravascular Ultrasound Comparison of Small Coronary Lesions Between Novel Guidewire-Based Sirolimus-Eluting Stents and Conventional Sirolimus-Eluting Stents
JOURNAL OF INVASIVE CARDIOLOGY
2012; 24 (10): 489-493
Abstract
The Sparrow stent system (Biosensors International) consists of a self-expanding, ultra-thin nitinol stent mounted within a 0.014″ guidewire designed for small or tortuous coronary lesions. We compared the intravascular ultrasound (IVUS) findings between the novel self-expanding sirolimus-eluting stent (Sparrow-SES) and a conventional balloon-expandable sirolimus-eluting stent (Cypher-SES) in patients with small coronary disease.We examined 14 lesions treated with the Sparrow-SES from CARE II, compared with 22 small vessel lesions treated with Cypher-SES. IVUS examination was performed post-procedure and 8 months later. Volumetric data were standardized by length as volume index (VI; mm³/mm).While baseline stent VI trended smaller in Sparrow-SES, follow-up stent VI became similar between the 2 groups due to a significant increase of stent VI in self-expanding Sparrow-SES during the follow-up period. At 8 months, Sparrow-SES showed greater neointima than Cypher-SES (0.8 ± 0.6 mm³/mm vs 0.2 ± 0.2 mm³/mm; P<.001). However, the decrease in lumen VI was only 0.3 ± 0.7 mm³/mm in Sparrow-SES, as compared to 0.1 ± 0.3 mm³/mm in Cypher-SES (P=.259), since the late loss due to neointimal hyperplasia was partly counterbalanced by the chronic stent expansion in Sparrow-SES.While 8-month follow-up of Sparrow-SES revealed greater amounts of neointimal hyperplasia compared with conventional Cypher-SES, chronic stent expansion preserved the lumen by increasing stent volume. This novel, guidewire-based, self-expanding stent system designed to be delivered through complex anatomies may be useful to treat patients with small-caliber coronary lesions by offering sufficient lumen preservation at follow-up.
View details for Web of Science ID 000311028600014
View details for PubMedID 23043031
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Mid-Term Results of Everolimus-Eluting Stent in a Japanese Population Compared With a US Randomized Cohort: SPIRIT III Japan Registry With Harmonization by Doing
JOURNAL OF INVASIVE CARDIOLOGY
2012; 24 (9): 444-450
Abstract
To address safety concerns with first-generation drug-eluting stents (DESs), the everolimus-eluting stent (EES) has been developed as a second-generation DES. The study aim was to: (1) demonstrate that use of the EES in Japanese patients is non-inferior to use of the paclitaxel-eluting stent (PES) in US patients; and (2) compare vessel response to the EES in Japanese vs US patients.The SPIRIT III Japan Registry, a prospective single-arm multicenter study was a part of the SPIRIT III global clinical program using harmonization by doing. The primary endpoint was in-segment late loss at 8 months, compared to US PES.A total of 88 subjects were enrolled in the Japan EES group. Angiographic in-segment late loss was significantly less in Japan EES vs US PES (0.15 ± 0.34 mm vs 0.28 ± 0.48 mm, respectively; P=.0185; Pnon-inferio r<.0001), while target vessel failure (TVF; 8.0% vs 9.9%) and major adverse cardiac events (MACE) at 9 months (5.7% vs 8.8%) were not significantly different between the 2 groups. No differences were observed between Japan and US EES populations in terms of late loss, TVF, or MACE. Neointimal volume and postprocedural incomplete stent apposition rate were lower in Japan EES vs US EES/PES.The SPIRIT III Japan Registry met the primary endpoint of lower late loss in the Japan EES group vs the US PES group, with comparable results for EES between the Japanese and US patients.
View details for Web of Science ID 000310543300016
View details for PubMedID 22954564
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Evaluation of the peri-strut low intensity area following sirolimus- and paclitaxel-eluting stents implantation: Insights from an optical coherence tomography study in humans
INTERNATIONAL JOURNAL OF CARDIOLOGY
2012; 157 (1): 38-42
Abstract
Recent pathological studies have demonstrated that peri-strut low intensity area (PLIA) seen on optical coherence tomography (OCT) imaging represents the presence of fibrinogen and/or extracellular matrix. We sought to assess the clinical prevalence of PLIA and its relation to neointimal proliferation after the implantation of sirolimus- (SES) and paclitaxel-eluting stents (PES) in humans.Seventy patients underwent 6-months follow-up OCT after SES (43 stents) or PES (37 stents) implantation. PLIA was defined as a region around stent struts with homogenous lower intensity than surrounding tissue on OCT images without signal attenuation. The incidence of stent struts with PLIA (+PLIA struts) was calculated as the number of +PLIA struts/number of all struts (%).PES showed a higher incidence of stents with PLIA than SES (86% vs. 58%; p=0.005) with a higher prevalence of +PLIA struts (27.8±21.9% vs. 10.9±11.0%; p=0.0008). SES with PLIA showed a significantly greater neointimal thickness (NIT) than SES without PLIA (p=0.02), while PES showed a similar tendency (p=0.19). In a detailed strut basis analysis, average NIT on +PLIA struts were significantly greater than that on -PLIA struts in both SES and PES. In addition, average NIT was positively correlated with the prevalence of +PLIA struts (SES: Rho=0.73; p<0.0001, PES: Rho=0.58, p=0.0005) in both stents.The prevalence of PLIA was significantly higher in PES than in SES. The presence and extent of PLIA might be associated with intimal thickening after 1st-generation DES implantation.
View details for DOI 10.1016/j.ijcard.2010.11.006
View details for Web of Science ID 000303206800015
View details for PubMedID 21168926
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VESSEL RESPONSE TO NOVEL SIROLIMUS-ELUTING STENTS WITH ABSORBABLE POLYMER IN DE NOVO CORONARY LESIONS: FIRST-IN-HUMAN IVUS RESULTS FROM THE DESSOLVE-I 8-MONTH COHORT
61st Annual Scientific Session and Expo of the American-College-of-Cardiology (ACC)/Conference on ACC-i2 with TCT
ELSEVIER SCIENCE INC. 2012: E154–E154
View details for Web of Science ID 000302326700155
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IMPACT OF POST-DILATATION STRATEGIES ON ACUTE STENT EXPANSION: AN EXPERIMENTAL STUDY USING OPTICAL COHERENCE TOMOGRAPHY
61st Annual Scientific Session and Expo of the American-College-of-Cardiology (ACC)/Conference on ACC-i2 with TCT
ELSEVIER SCIENCE INC. 2012: E153–E153
View details for Web of Science ID 000302326700154
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EFFECTS OF INTER-STENT COMPRESSED INTIMAL VOLUME AFTER DRUG-ELUTING STENT TREATMENTS FOR BARE METAL IN-STENT RESTENOSIS: A VOLUMETRIC INTRAVASCULAR ULTRASOUND ANALYSIS
61st Annual Scientific Session and Expo of the American-College-of-Cardiology (ACC)/Conference on ACC-i2 with TCT
ELSEVIER SCIENCE INC. 2012: E113–E113
View details for Web of Science ID 000302326700114
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COMPARISON OF VASCULAR RESPONSE TO NOVOLIMUS-ELUTING STENT VERSUS ZOTAROLIMUS-ELUTING STENT IMPLANTATION: IVUS RESULTS FROM THE EXCELLA BD TRIAL
61st Annual Scientific Session and Expo of the American-College-of-Cardiology (ACC)/Conference on ACC-i2 with TCT
ELSEVIER SCIENCE INC. 2012: E210–E210
View details for Web of Science ID 000302326700211
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Consensus Standards for Acquisition, Measurement, and Reporting of Intravascular Optical Coherence Tomography Studies A Report From the International Working Group for Intravascular Optical Coherence Tomography Standardization and Validation
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY
2012; 59 (12): 1058-1072
Abstract
The purpose of this document is to make the output of the International Working Group for Intravascular Optical Coherence Tomography (IWG-IVOCT) Standardization and Validation available to medical and scientific communities, through a peer-reviewed publication, in the interest of improving the diagnosis and treatment of patients with atherosclerosis, including coronary artery disease.Intravascular optical coherence tomography (IVOCT) is a catheter-based modality that acquires images at a resolution of ~10 μm, enabling visualization of blood vessel wall microstructure in vivo at an unprecedented level of detail. IVOCT devices are now commercially available worldwide, there is an active user base, and the interest in using this technology is growing. Incorporation of IVOCT in research and daily clinical practice can be facilitated by the development of uniform terminology and consensus-based standards on use of the technology, interpretation of the images, and reporting of IVOCT results.The IWG-IVOCT, comprising more than 260 academic and industry members from Asia, Europe, and the United States, formed in 2008 and convened on the topic of IVOCT standardization through a series of 9 national and international meetings.Knowledge and recommendations from this group on key areas within the IVOCT field were assembled to generate this consensus document, authored by the Writing Committee, composed of academicians who have participated in meetings and/or writing of the text.This document may be broadly used as a standard reference regarding the current state of the IVOCT imaging modality, intended for researchers and clinicians who use IVOCT and analyze IVOCT data.
View details for DOI 10.1016/j.jacc.2011.09.079
View details for Web of Science ID 000301443000003
View details for PubMedID 22421299
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Intravascular ultrasound insights from the Cobalt Chromium Stent With Antiproliferative for Restenosis II (COSTAR II) trial comparing CoStar and Taxus paclitaxel-eluting stents.
Cardiovascular revascularization medicine : including molecular interventions
2012; 13 (2): 111-118
Abstract
Dedicated IVUS analyses of the second CObalt chromium STent with Antiproliferative for Restenosis (COSTAR II) trial have not been documented. We aim to compare IVUS findings between CoStar paclitaxel-eluting stent (PES) and Taxus PES in patients enrolled in the COSTAR II trial. We also attempted to examine the possible regional impact of multiple stenting.Among the 1700 patients enrolled, 238 were assigned to an IVUS cohort including 168 patients treated by provisional multiple stenting. At 9 months, qualitative and quantitative IVUS observations including incomplete stent apposition (ISA) and neointimal proliferation (neointimal obstruction: neointimal volume/stent volume ×100) were compared between CoStar and Taxus PESs.In qualitative analysis, late-acquired ISA was observed in 1 patient treated by Taxus PES. Impaired strut continuity suggestive of stent fracture was observed in 2 out of 33 patients treated by multiple CoStar, and 4 out of 21 patients treated by multiple Taxus (P=.14). No such findings were found in single-stented patients in either stent subset. Quantitative analysis showed greater neointimal obstruction in CoStar (19.7%±13.4%, n=52) than in Taxus (10.7%±9.9%, n=38), whereas no significant difference in neointimal obstruction was found between single and multiple stenting in either CoStar or Taxus PES.The CoStar PES exhibits greater neointimal proliferation compared with Taxus PES at 9 months but with similar qualitative outcomes including late-acquired ISA. IVUS findings suggestive of stent fracture were found only in multiple-stenting cases irrespective of the stent used.
View details for DOI 10.1016/j.carrev.2012.01.010
View details for PubMedID 22406056
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Intravascular Ultrasound Assessment of Postprocedural Incomplete Stent Apposition
JOURNAL OF INVASIVE CARDIOLOGY
2012; 24 (1): 13-16
Abstract
There has been no detailed intravascular ultrasound (IVUS) analysis to evaluate the degree to which stent underexpansion or reference vessel/stent size mismatch contributes to the occurrence of post-procedural incomplete stent apposition (post-ISA).We evaluated 238 lesions treated with everolimus-eluting stents (n = 110) or paclitaxel-eluting stents (n = 128). Reference lumen/stent area ratio was defined as the ratio of lumen area adjacent to the stent edge in the reference segment to stent area at the stent edge or at stent body ISA site.Post-ISA was observed in 36 of the 238 cases (15%) at the proximal stent edge, 15 of the 238 cases (6%) at the distal stent edge and 14 of the 238 cases (6%) at stent body. Reference lumen/stent area ratio was significantly greater in the ISA group compared with non-ISA in proximal edge (127 ± 20 vs. 99 ± 10%; P<.001), and greater reference lumen/stent area ratio (118 ± 18 vs. 94 ± 11%; P<.001) and higher presence of calcification (60 vs. 29%; P<0.001) were observed in distal edge ISA group compared with non-ISA. At the stent body, presence of calcification was more frequently observed in the ISA compared with the non-ISA group (86 vs. 42%; P=.002).Post-ISA at the stent edge was significantly associated with vessel/stent mismatch rather than stent underexpansion. IVUS-guided appropriate stent or balloon sizing might be useful to prevent post-ISA and optimize initial stent deployment.
View details for Web of Science ID 000299082000011
View details for PubMedID 22210583
- World Report: Up-to-Date. Stanford University Circulation Up-to-Date 2012; 7 (2): 164-166
- Intravascular ultrasound Catheter-Based Cardiovascular Interventions: A Knowledge-Based Approach 2012: 325-345
- Cardiovascular imaging for percutaneous coronary interventions Evidence Based Medicine: Treatment of Cardiovascular Disease 2012-2013 2012: 105-112
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Assessment of macro- and microcirculation in contemporary critical limb ischemia
CATHETERIZATION AND CARDIOVASCULAR INTERVENTIONS
2011; 78 (7): 1051-1058
Abstract
A paucity of data exists regarding manifestations of macro- and microcirculation in contemporary critical limb ischemia (CLI). The aim of this study was (1) to evaluate the differences in foot circulation based on angiographic findings, (2) to clarify the relationship between macro- and microcirculation, and (3) to investigate the effects of postural changes on micro as well as macrocirculation between the supine position to the dependent position.A total of 40 critically ischemic limbs in 29 patients were included in this study. Noninvasive evaluation of macrocirculation, based on the ankle brachial index (ABI) and ankle pressure, and microcirculation, using skin perfusion pressure (SPP), was performed in both the supine and dependent positions.There was no significant difference in macro- and microcirculations between any angiographical involvements. In the supine position, dorsal SPP correlated significantly with ABI (P = 0.021, r = 0.363) and ankle-pressure (P = 0.001, r = 0.495), whereas plantar SPP failed to correlate with ABI (P = 0.198, r = 0.208) or ankle-pressure (P = 0.185, r = 0.214). In the dependent position, however, SPP showed no significant correlation with ABI and ankle pressure. Postural change from the supine to dependent position yielded a significant increase in SPP (dorsal: 37.2 ± 16.2 to 77.9 ± 17.7 mm Hg, P < 0.001; plantar: 33.6 ± 17.3 to 75.7 ± 18.3 mm Hg, P < 0.001) as well as ABI and ankle-pressure (ABI: 0.70 ± 0.35 to 0.78 ± 0.42, P = 0.003; ankle-pressure; 108 ± 61 to 111 ± 60 mm Hg, P = 0.038). The effect of postural change on SPP showed no difference between patients with and without any clinical and angiographical complications.Of microcirculation assessed, only dorsal SPP correlated significantly with macrocirculation in the supine position. Furthermore, postural change from the supine to dependent position produced a dramatic improvement in microcirculation due to the effects of gravity.
View details for DOI 10.1002/ccd.23086
View details for Web of Science ID 000297203000015
View details for PubMedID 21805568
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Sex Differences in Neointimal Hyperplasia Following Zotarolimus-Eluting Stent Implantation: Potential Impact of Drug and Carrier Matrix
Scientific Sessions of the American-Heart-Association/Resuscitation Science Symposium
LIPPINCOTT WILLIAMS & WILKINS. 2011
View details for Web of Science ID 000299738704188
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IVUS Assessment of Patients with Early, Late and Very Late Stent Thrombosis after Sirolimus-Eluting Stent Implantation: Final IVUS Results From the RESTART Registry
LIPPINCOTT WILLIAMS & WILKINS. 2011
View details for Web of Science ID 000299738707094
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Arterial Response to Sirolimus Eluting Stents with Bioabsorbable Polymer: First IVUS Report from the DESSOLVE-I FIM Trial
23rd Annual Scientific Symposium of Transcatheter Cardiovascular Therapeutics (TCT)
ELSEVIER SCIENCE INC. 2011: B32–B32
View details for Web of Science ID 000296891900131
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First-In-Man IVUS Findings of the Prohealing PROTEX (TM) Coronary Stent System for the Treatment of Coronary Artery Disease
ELSEVIER SCIENCE INC. 2011: B63
View details for Web of Science ID 000296891900241
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Relative Dose and Vascular Response After Resolute Zotarolimus-Eluting Stunt Implantation: A Dosimetric 3D-Intravascular Ultrasound Study
23rd Annual Scientific Symposium of Transcatheter Cardiovascular Therapeutics (TCT)
ELSEVIER SCIENCE INC. 2011: B168–B169
View details for Web of Science ID 000296891900627
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Impact of Stent Size and Length on Neointimal Hyperplasia After Resolute Zotarolimus-Eluting Stent Implantation: Insights From RESOLUTE Trials
23rd Annual Scientific Symposium of Transcatheter Cardiovascular Therapeutics (TCT)
ELSEVIER SCIENCE INC. 2011: B62–B62
View details for Web of Science ID 000296891900240
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Contributions of Mechanical Factors and Biologic Response to Sirolimus-Eluting Stent Thrombosis: Final IVUS Results From the RESTART Registry
23rd Annual Scientific Symposium of Transcatheter Cardiovascular Therapeutics (TCT)
ELSEVIER SCIENCE INC. 2011: B186–B186
View details for Web of Science ID 000296891900690
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Discrepancy in the Assessment of Jailed Side Branch Lesions by Visual Estimation and Quantitative Coronary Angiographic Analysis: Comparison With Fractional Flow Reserve
CATHETERIZATION AND CARDIOVASCULAR INTERVENTIONS
2011; 78 (5): 720-726
Abstract
We sought to evaluate the variability in the assessment of jailed side branch (SB) lesions by visual estimation and quantitative coronary angiography (QCA) and to compare those results with fractional flow reserve (FFR).Twenty jailed SB lesions with available FFR (median 0.76; range, 0.39-0.94) were selected from the PRESSURE trial. Lesions were assessed by three independent QCA core laboratories with different QCA systems and by three different cardiologist groups (five European bifurcation club members, five Korean experts, and five trainees). Agreements of the continuous measurements were expressed as the intraclass correlation coefficient (ICC) and average coefficient of variance (CV), and those of the categorical values as kappa.Mean minimum lumen diameter (MLD) and % diameter stenosis differed among the three QCA systems up to 0.30 mm and 9.65%, respectively (P < 0.001). Three QCA systems showed fair agreement for the measurements of reference diameter, % diameter stenosis, MLD, and lesion length (ICC 0.346-0.686, CV 8.7-29.5%), and a poor agreement on stenosis of 75% or more (Fleiss κ 0.14 and mean κ 0.18). Agreements of visual estimation among the three groups were poor to fair (Fleiss κ 0.167-0.367). Sensitivity and specificity for predicting ischemia-inducible lesion (FFR < 0.75) were 64.7% and 48.0% for visual estimation and 56.6% and 56.6% by QCA, respectively. Visual estimation overestimated the % diameter stenosis and functional significance of the lesions compared with QCA (P < 0.001) and FFR (P = 0.036).Angiographic assessment of jailed SB lesions by both QCA and visual estimation showed variability. Visual estimation tended to overestimate the severity of jailed SB lesions compared to FFR and QCA.
View details for DOI 10.1002/ccd.23049
View details for Web of Science ID 000296412800012
View details for PubMedID 22025472
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Sex Differences in Neointimal Hyperplasia Following Endeavor Zotarolimus-Eluting Stent Implantation
AMERICAN JOURNAL OF CARDIOLOGY
2011; 108 (7): 912-917
Abstract
Inconsistent results in outcomes have been observed between the genders after drug-eluting stent implantation. The aim of this study was to investigate gender differences in neointimal proliferation for the Endeavor zotarolimus-eluting stent (ZES) and the Driver bare-metal stent (BMS). A total of 476 (n = 391 ZES, n = 85 BMS) patients whose volumetric intravascular ultrasound analyses were available at 8-month follow-up were studied. At 8 months, neointimal obstruction and maximum cross-sectional narrowing (CSN) were significantly lower in women than in men receiving ZES (neointimal obstruction 15.5 ± 9.5% vs 18.2 ± 10.9%, p = 0.025; maximum CSN 30.3 ± 13.2% vs 34.8 ± 15.0%, p = 0.007). Conversely, these parameters tended to be higher in women than in men receiving BMS (neointimal obstruction 36.3 ± 15.9% vs 27.5 ± 17.2%, p = 0.053; maximum CSN 54.3 ± 18.6% vs 45.6 ± 18.3%, p = 0.080). There was a significant interaction between stent type and gender regarding neointimal obstruction (p = 0.001) and maximum CSN (p = 0.003). Multivariate linear regression analysis revealed that female gender was independently associated with lower neointimal obstruction (p = 0.027) and maximum CSN (p = 0.004) for ZES but not for BMS. Compared to BMS, ZES were independently associated with a reduced risk for binary restenosis in both genders (odds ratio for women 0.003, p = 0.001; odds ratio for men 0.191, p <0.001), but the magnitude of this risk reduction with ZES was significantly greater in women than men (p = 0.015). In conclusion, female gender is independently associated with decreased neointimal hyperplasia in patients treated with ZES. The magnitude of risk reduction for binary restenosis with ZES is significantly greater in women than in men.
View details for DOI 10.1016/j.amjcard.2011.05.019
View details for Web of Science ID 000295863200002
View details for PubMedID 21784390
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Impact of Donor-Transmitted Atherosclerosis on Early Cardiac Allograft Vasculopathy: New Findings by Three-Dimensional Intravascular Ultrasound Analysis
TRANSPLANTATION
2011; 91 (12): 1406-1411
Abstract
The influence of donor-transmitted coronary atherosclerosis (DA) on plaque progression during the first year after cardiac transplantation (Tx) is unknown.Serial 3-dimensional intravascular ultrasound (IVUS) studies were performed within 8 weeks (baseline; BL) and at 1 year after Tx in 38 recipients. On the basis of maximum intimal thickness (MIT) at BL, recipients were divided into DA group (DA+; MIT≥0.5 mm, n=23) or non-DA group (DA-; MIT<0.5 mm, n=15). Plaque, lumen, and vessel volume indexes were calculated by volume/measured length (mm/mm) in the left anterior descending artery. Univariate and multivariate regression analyses were attempted to reveal clinical predictors of change in coronary dimensions.During the first year after Tx, plaque volume index increased significantly in DA+ group, but did not change in DA- Group (DA+, 3.0±1.5 to 4.1±1.5 mm/mm, P<0.0001: DA-, 1.2±0.4 to 1.3±0.5 mm/mm, P=0.53). In both groups vessel volume index decreased significantly (DA+, 16.3±3.6 to 14.6±3.3 mm/mm, P=0.003: DA-, 13.5±4.1 to 12.0±3.3 mm/mm, P=0.01), as did lumen volume index (DA+, 13.2±3.1 to 10.5±2.7 mm/mm, P<0.0001: DA-, 12.2±3.7 to 10.7±3.0 mm/mm, P=0.004). Univariate and multivariate regression analyses revealed that DA was one of the strongest predictors for plaque progression.DA was associated with significant plaque progression during the first year after Tx, and in conjunction with negative remodeling, may be an important determinant of cardiac allograft vasculopathy.
View details for DOI 10.1097/TP.0b013e31821ab91b
View details for PubMedID 21512436
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Impact of Polymer Formulations on Neointimal Proliferation After Zotarolimus-Eluting Stent With Different Polymers Insights From the RESOLUTE Trial
CIRCULATION-CARDIOVASCULAR INTERVENTIONS
2011; 4 (3): 248-255
Abstract
Polymer formulation may affect the efficacy of drug-eluting stents. Resolute, Endeavor, and ZoMaxx are zotarolimus-eluting stents with different stent platforms and different polymer coatings and have been tested in clinical trials. The aim of this analysis was to compare the efficacy of zotarolimus-eluting stents with different polymers.Data were obtained from the first-in man trial or first randomized trials of each stent, The Clinical RESpOnse EvaLUation of the MedTronic Endeavor CR ABT-578 Eluting Coronary Stent System in De Novo Native Coronary Artery Lesions (RESOLUTE), Randomized Controlled Trial to Evaluate the Safety and Efficacy of the Medtronic AVE ABT-578 Eluting Driver Coronary Stent in De Novo Native Coronary Artery Lesions (ENDEAVOR II), and ZoMaxx I trials. Follow-up intravascular ultrasound analyses (8 to 9 months of follow-up) were possible in 353 patients (Resolute: 88, Endeavor: 98, ZoMaxx: 82, Driver: 85). Volume index (volume/stent length) was obtained for vessel, stent, lumen, peristent plaque, and neointima. Cross-sectional narrowing was defined as neointimal area divided by stent area (%). Neointima-free frame ratio was calculated as the number of frames without intravascular ultrasound-detectable neointima divided by the total number of frames within the stent. At baseline, vessel, lumen, and peristent plaque volume index were not significantly different among the 4 stent groups. At follow-up, percent neointimal obstruction was significantly lower in Resolute compared with Endeavor, ZoMaxx, and Driver (Resolute: 3.7±4.0, Endeavor: 17.5±10.1, ZoMaxx: 14.6±8.1, Driver: 29.4±17.2%; P<0.001). Greater maximum cross-sectional narrowing and higher neointima-free frame ratio, suggesting less neointimal coverage, were observed in Resolute compared with other stent groups. Multiple regression analysis confirmed that the biodurable polymer used in Resolute independently correlated with neointimal suppression among 3 zotarolimus-eluting stents.The different polymer formulations significantly affect the relative amount of neointima for zotarolimus-eluting stents.URL: http://www.clinicaltrials.gov. Unique identifier: NCT00248079.
View details for DOI 10.1161/CIRCINTERVENTIONS.110.957548
View details for Web of Science ID 000291592000012
View details for PubMedID 21586691
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GENDER-ASSOCIATED DIFFERENCES IN NEOINTIMAL VOLUME AFTER CORONARY ZOTAROLIMUS-ELUTING STENT IMPLANTATION: RELATIONSHIP TO RENAL FUNCTION
60th Annual Scientific Session and Expo of the American-College-of-Cardiology (ACC) / I2 Summit / ACCF/Herman K. Gold Young Investigator's Award in Molecular and Cellular Cardiology
ELSEVIER SCIENCE INC. 2011: E1902–E1902
View details for Web of Science ID 000291695101905
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NONPOLYMER-BASED BIOLIMUS-ELUTING STENT ACCELERATES OVERALL NEOINTIMAL COVERAGE: SHORT- AND MID-TERM INTRAVASCULAR ULTRASOUND RESULTS FROM STEALTH AND BIOFREEDOM TRIALS
60th Annual Scientific Session and Expo of the American-College-of-Cardiology (ACC) / I2 Summit / ACCF/Herman K. Gold Young Investigator's Award in Molecular and Cellular Cardiology
ELSEVIER SCIENCE INC. 2011: E1756–E1756
View details for Web of Science ID 000291695101759
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VESSEL RESPONSE TO THE NOVEL POLYMER-FREE BIOFREEDOM STENT VERSUS CONVENTIONAL DURABLE POLYMER COATING STENT: SHORT- AND MID-TERM INTRAVASCULAR ULTRASOUND RESULTS FROM THE BIOFREEDOM FIRST-IN-MAN TRIAL
60th Annual Scientific Session and Expo of the American-College-of-Cardiology (ACC) / I2 Summit / ACCF/Herman K. Gold Young Investigator's Award in Molecular and Cellular Cardiology
ELSEVIER SCIENCE INC. 2011: E1758–E1758
View details for Web of Science ID 000291695101761
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IMPROVED AUTOMATED LUMEN CONTOUR DETECTION BY A NOVEL MULTI-FREQUENCY PROCESSING ALGORITHM USING A CURRENT INTRAVASCULAR ULTRASOUND SYSTEM
60th Annual Scientific Session and Expo of the American-College-of-Cardiology (ACC) / I2 Summit / ACCF/Herman K. Gold Young Investigator's Award in Molecular and Cellular Cardiology
ELSEVIER SCIENCE INC. 2011: E1854–E1854
View details for Web of Science ID 000291695101857
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COMPARISON OF VESSEL RESPONSE TO SIROLIMUS-VS. PACLITAXEL-ELUTING STENT TREATMENTS FOR BARE METAL IN-STENT RESTENOSIS: A VOLUMETRIC INTRAVASCULAR ULTRASOUND ANALYSIS
60th Annual Scientific Session and Expo of the American-College-of-Cardiology (ACC) / I2 Summit / ACCF/Herman K. Gold Young Investigator's Award in Molecular and Cellular Cardiology
ELSEVIER SCIENCE INC. 2011: E1972–E1972
View details for Web of Science ID 000291695101975
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Intravascular Ultrasound Results From the NEVO ResElution-I Trial A Randomized, Blinded Comparison of Sirolimus-Eluting NEVO Stents With Paclitaxel-Eluting Taxus Liberte Stents in De Novo Native Coronary Artery Lesions
CIRCULATION-CARDIOVASCULAR INTERVENTIONS
2011; 4 (2): 146-U69
Abstract
The NEVO sirolimus-eluting stent (NEVO SES) is a novel cobalt-chromium stent combining sirolimus release from reservoirs with bioabsorbable polymer to reduce spatial and temporal polymer exposure. The aim of this study was to assess the arterial response to the NEVO SES in a randomized, blinded comparison versus the surface-coated TAXUS Liberte paclitaxel-eluting stent (TAXUS Liberté PES) in human native coronary lesions using intravascular ultrasound (IVUS).The NEVO ResElution-I IVUS substudy enrolled 100 patients (1:1 randomization). In addition to standard IVUS variables, uniformity of neointimal distribution within stents was evaluated in 3 dimensions by computing mean neointimal thickness within 12 equally spaced radial sectors on every 1-mm cross section along the stented segment. The NEVO SES showed significantly less neointimal proliferation (neointimal obstruction: 5.5±11.0% versus 11.5±9.7%, P=0.02), resulting in less late lumen area loss and smaller maximum cross-sectional narrowing at 6 months. The absolute variability of neointima distribution, assessed by the standard deviation of neointimal thickness within each stent, was significantly reduced with the NEVO SES compared with the TAXUS Liberté PES(0.04±0.04 mm versus 0.10±0.07 mm, P<0.0001). TAXUS Liberté PES showed significantly greater positive vessel remodeling than the NEVO SES (Δvessel volume index: 1.30±1.36 mm(3)/mm versus 0.36±0.63 mm(3)/mm, respectively, P=0.003).The NEVO SES with focal release of sirolimus from reservoirs achieved significantly greater and more consistent suppression of neointimal hyperplasia than the surface-coated TAXUS Liberté PES. This was associated with less positive remodeling and no increased morphological or morphometric abnormalities surrounding the stent or at the stent margins.URL: http://www.clinicaltrials.gov. Unique identifier: NCT00714883.
View details for DOI 10.1161/CIRCINTERVENTIONS.110.957175
View details for PubMedID 21386089
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Stent-Assisted Below-the-Ankle Angioplasty for Limb Salvage
JOURNAL OF ENDOVASCULAR THERAPY
2011; 18 (1): 32-42
Abstract
To report the clinical outcome of stent-assisted below-the-ankle angioplasty for limb salvage in the setting of critical limb ischemia (CLI).A retrospective single-center study was conducted of 40 critical ischemic limbs in 31 patients (mean age 67 ± 8 years, range 46-94) undergoing below-the-ankle stent-assisted angioplasty between April 2006 and April 2009. Coronary bare metal stents were implanted in cases of failed balloon angioplasty due to significant recoil, flow-limiting dissection, abrupt closure, or repeat early reocclusion.Technical success was 93% (37 limbs), with 3 failures to cross the occlusive lesions. Acute or subacute occlusion was evident in 9 (23%) limbs. The number of runoff vessels increased significantly (p < 0.001) from 0.6 ± 0.8 to 1.8 ± 0.8. During a clinical follow-up of 19.3 ± 11.4 months (range 1-48), the number of repeat interventions for limb salvage was 2.2 ± 1.6 (range 1-9), and a total of 1.6 ± 0.9 stents (range 1-3) were implanted in 8 dorsalis pedis arteries. Acute or subacute stent thrombosis after stenting was observed in 2 of these, and symptomatic in-stent restenosis was detected in 4, which were all treated by repeat intervention. At 6, 12, and 24 months, the freedom from repeat intervention was 39.6%, 39.6%, and 35.2%, respectively. Amputation-free survival was 80.0%, 69.7%, and 62.7%, and limb salvage was 94.7%, 91.4%, and 82.1% at the same time points. Patient survival rates were 77.4%, 71.0%, and 71.0%, respectively. During a mean follow-up of 13.4 ± 12.7 months (range 1-31 months) in 7 of the 8 stented arteries, all examined stents were deformed: stent compression was evident in 5 and stent fracture in 5. However, 7 limbs undergoing dorsalis pedis artery stenting showed complete wound healing; 1 limb had a resistant wound in the heel.Stent-assisted below-the-ankle angioplasty produced a satisfactory clinical outcome but with the need for repeat intervention. Thus, further refinement in endovascular technology is mandatory to reduce the need for repeat interventions and to resolve stent deformity issues.
View details for Web of Science ID 000287071700005
View details for PubMedID 21314346
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Study design and rationale of "Synergistic Effect of Combination Therapy with Cilostazol and ProbUcol on Plaque Stabilization and Lesion REgression (SECURE)" study: a double-blind randomised controlled multicenter clinical trial
TRIALS
2011; 12
Abstract
Probucol, a cholesterol-lowering agent that paradoxically also lowers high-density lipoprotein cholesterol has been shown to prevent progression of atherosclerosis. The antiplatelet agent cilostazol, which has diverse antiatherogenic properties, has also been shown to reduce restenosis in previous clinical trials. Recent experimental studies have suggested potential synergy between probucol and cilostazol in preventing atherosclerosis, possibly by suppressing inflammatory reactions and promoting cholesterol efflux.The Synergistic Effect of combination therapy with Cilostazol and probUcol on plaque stabilization and lesion REgression (SECURE) study is designed as a double-blind, randomised, controlled, multicenter clinical trial to investigate the effect of cilostazol and probucol combination therapy on plaque volume and composition in comparison with cilostazol monotherapy using intravascular ultrasound and Virtual Histology. The primary end point is the change in the plaque volume of index intermediate lesions between baseline and 9-month follow-up. Secondary endpoints include change in plaque composition, neointimal growth after implantation of stents at percutaneous coronary intervention target lesions, and serum levels of lipid components and biomarkers related to atherosclerosis and inflammation. A total of 118 patients will be included in the study.The SECURE study will deliver important information on the effects of combination therapy on lipid composition and biomarkers related to atherosclerosis, thereby providing insight into the mechanisms underlying the prevention of atherosclerosis progression by cilostazol and probucol.ClinicalTrials (NCT): NCT01031667.
View details for DOI 10.1186/1745-6215-12-10
View details for Web of Science ID 000287157800001
View details for PubMedID 21226953
View details for PubMedCentralID PMC3033833
- Intravascular ultrasound Textbook of Interventional Cardiology 2011: 793-808
- Optical coherence tomography for patient-specific 3D artery reconstruction and evaluation of wall shear stress in a left circumflex coronary artery Cardiovascular Engineering and Technology 2011; 2 (3): 212-227
- Coronary artery physiology: intracoronary ultrasonography, coronary flow velocity and pressure measurements McGraw-Hill Specialty Board Review: Cardiology 2011: 419-429
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Impact of Diabetes Mellitus on Vessel Response in the Drug-Eluting Stent Era: Pooled Volumetric Intravascular Ultrasound Analysis
LIPPINCOTT WILLIAMS & WILKINS. 2010
View details for Web of Science ID 000208231600752
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Very Late Stent Thrombosis After Sirolimus-Eluting Stent Implantation Is Associated With Expansive Vessel Remodeling
LIPPINCOTT WILLIAMS & WILKINS. 2010
View details for Web of Science ID 000208231601648
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Impact of Mechanical Factor and Biologic Response on Severe In-Stent Lumen Narrowing in Currently Approved Drug-Eluting Stents
LIPPINCOTT WILLIAMS & WILKINS. 2010
View details for Web of Science ID 000208231602056
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Intravascular Ultrasound Comparison of Small Coronary Lesions Between the CardioMind Coronary Stent and Conventional Sirolimus-Eluting Stent
LIPPINCOTT WILLIAMS & WILKINS. 2010
View details for Web of Science ID 000208231601636
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Awareness of Anatomical Variations for Infrapopliteral Intervention
CATHETERIZATION AND CARDIOVASCULAR INTERVENTIONS
2010; 76 (6): 888-894
Abstract
With the tremendous advancement and accumulated expertise of endovascular techniques, infrapopliteal intervention is emerging as an alternative therapeutic option to distal bypass surgery for limb salvage in the setting of critical limb ischemia (CLI). However, though much attention has been given to infrapopliteal intervention, the importance of identifying preprocedural infrapopliteal variants remains underappreciated. Becoming more aware of these anatomical variants will translate to increased clinical effectiveness for the patient with infrapopliteal artery disease. Therefore, this review will highlight the fundamental aspects of infrapopliteal variant anatomy for the catheter-based treatment of CLI patients with symptomatic infrapopliteal artery disease.
View details for DOI 10.1002/ccd.22673
View details for Web of Science ID 000284676100022
View details for PubMedID 20578165
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Neointimal hyperplasia in a thin-strut cobalt-chromium stent: Insights from detailed 3-D intravascular ultrasound analysis
INTERNATIONAL JOURNAL OF CARDIOLOGY
2010; 145 (1): 125-126
Abstract
The effect of current generation cobalt-chromium stents on neointimal proliferation has not been fully elucidated. IVUS images of 137 patients treated with a single thin-strut cobalt-chromium stent (Driver: DRI, n=74) or stainless steel stent (Multilink plus: ML, n=63) were selected. Although % neointima volume (neointimal volume divided by stent volume) were comparable, DRI showed significantly smaller maximum %cross-sectional narrowing (%CSN: neointimal area divided by stent area) (P=0.006) with significantly less %CSN>60 (percent stent length with %CSN>60%) than ML (P=0.04). In conclusion, the amount of neointimal hyperplasia after DRI implantation was comparable to that after ML. However, current generation cobalt-chromium DRI may show less and shorter severe narrowing than the stainless steel ML.
View details for DOI 10.1016/j.ijcard.2009.06.038
View details for Web of Science ID 000283727000070
View details for PubMedID 19619904
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Comparison of Vascular Response to Zotarolimus-Eluting Stent vs Paclitaxel-Eluting Stent Implantation - Pooled IVUS Results From the ZoMaxx I and II Trials
CIRCULATION JOURNAL
2010; 74 (11): 2334-2339
Abstract
The ZoMaxx I and II trials were randomized controlled studies of the zotarolimus-eluting, phosphorylcholine-coated, TriMaxx stent for the treatment of de novo coronary lesions. The aim of this study was to compare the vessel response between zotarolimus- (ZES) and paclitaxel-eluting stents (PES) using intravascular ultrasound (IVUS).Data were obtained from the ZoMaxx I and II trials, in which a standard IVUS parameter was available in 263 cases (baseline and 9-months follow up). Neointima-free frame ratio was calculated as the number of frames without IVUS-detectable neointima divided by the total number of frames within the stent. While an increase in vessel and plaque was observed in PES from baseline to follow up, there was no significant change in ZES. At follow up, % neointimal obstruction was significantly higher (15.4 ± 8.8% vs 11.3 ± 9.7%), and minimum lumen area at follow up was significantly smaller in ZES compared to PES. However, the incidence of IVUS-defined restenosis (maximum cross-sectional narrowing >60%) was similar in the 2 groups (3.2% vs 6.7%). Neointima-free frame ratio was significantly lower in ZES. There were 5 cases of late incomplete stent apposition in PES and none in ZES.These IVUS results demonstrate a similar incidence of severe narrowing between these 2 DES. There was a moderate increase in neointimal hyperplasia that was associated with a greater extent of neointimal coverage in ZES compared with PES.
View details for DOI 10.1253/circj.CJ-09-0850
View details for PubMedID 20890052
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Short- and Mid-Term Intravascular Ultrasound Analysis of the New Zotarolimus-Eluting Stent With Durable Polymer - Results From the RESOLUTE Trial -
CIRCULATION JOURNAL
2010; 74 (10): 2097-2102
Abstract
The Resolute stent is a newly developed system with a bio-histocompatible polymer that allows programmed drug delivery up to 180 days. The aim of this intravascular ultrasound (IVUS) analysis was to evaluate the short- (4 months) and mid-term (9 months) efficacy using the Resolute stent.Data were derived from the RESOLUTE trial, a prospective, multicenter, non-randomized, single-arm study to treat de novo native coronary artery lesions. This trial included 2 cohorts with different follow-up periods, and all enrollment patients in this trial received IVUS study. Follow-up IVUS was available in 24 patients (4-month group) and 88 patients (9-month group). Neointimal obstruction (%) was defined as neointimal volume divided by stent volume. Cross-sectional narrowing (CSN, %) was defined as neointimal area divided by stent area. No significant differences in vessel, lumen and stent volume at post-procedure were observed within stented segments between the 4- and 9-month follow-up groups. Although neointimal volume and % neointimal obstruction showed no significant difference between the 2 groups (% neointimal obstruction: 2.2 ± 2.5 vs 3.7 ± 4.0%, P=0.09), maximum CSN was significantly larger in the 9-month group. There were 7 cases of late incomplete stent apposition.These IVUS results showed minimum growth of neointimal proliferation by the Resolute stent throughout the stented segment up to 9 months follow up.
View details for DOI 10.1253/circj.CJ-10-0063
View details for Web of Science ID 000282562300015
View details for PubMedID 20689221
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Incidence of diffuse and focal chronic stent recoil after implantation of current generation bare-metal and drug-eluting stents
INTERNATIONAL JOURNAL OF CARDIOLOGY
2010; 144 (1): 132-134
View details for DOI 10.1016/j.ijcard.2008.12.117
View details for Web of Science ID 000282679000054
View details for PubMedID 19171393
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Intravascular Ultrasound Comparison of with Early, Late, and Very Late Stent Thrombosis After Sirolimus-Eluting Stent Implantation
ELSEVIER SCIENCE INC. 2010: B10
View details for Web of Science ID 000209824200043
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Intravascular Ultrasound Analysis of Small Coronary Lesions Treated with CardioMind Coronary Stent System: IVES Results of the CARE II Trial
ELSEVIER SCIENCE INC. 2010: B51–B52
View details for Web of Science ID 000209824200223
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Impact of Lumen Narrowing Within Drug-Eluting Stents and Bare-Metal Stents on Downstream Vessel Segments
ELSEVIER SCIENCE INC. 2010: B15
View details for Web of Science ID 000209824200062
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Impact of Bifurcation Angioplasty on Side Branch Ostium: Insights From BRANCH Trial
ELSEVIER SCIENCE INC. 2010: B2–B3
View details for Web of Science ID 000209824200010
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Vessel Response to Drug-Eluting Stents in PatientsVVith vs. Without Diabetes Mellitus: Pooled Volumetric Intravascular Ultrasound Analysis
ELSEVIER SCIENCE INC. 2010: B15
View details for Web of Science ID 000209824200061
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Comparison of Vessel Response to Sirolimus-Eluting NEVOTM Stents with Bioabsorbable Polymer Versus Sirolimus-Eluting CypherTM Steeds with Durable Polymer
ELSEVIER SCIENCE INC. 2010: B56
View details for Web of Science ID 000209824200241
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Comparison of Polymer -Free BioFreedo Struts with Polymer-BasedTABUS"' Liberte Stems: The 4-Nlonth lotravascular Ultrasound Results from the Bioireedoin First -In -Man Trial
ELSEVIER SCIENCE INC. 2010: B54
View details for Web of Science ID 000209824200232
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Angiographic findings of stent thrombosis cases after sirolimus-eluting stent implantation
OXFORD UNIV PRESS. 2010: 660
View details for Web of Science ID 000281531904271
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Comparison of Everolimus- Versus Paclitaxel-Eluting Stents Implanted in Patients With Diabetes Mellitus as Evaluated by Three-Dimensional Intravascular Ultrasound Analysis
AMERICAN JOURNAL OF CARDIOLOGY
2010; 106 (4): 492-497
Abstract
Previous reports have shown the advantage of paclitaxel compared to limus-derivative drugs for the treatment of diabetics. A total of 109 diabetics (115 lesions) treated with everolimus-eluting stents (EESs, n = 58) or paclitaxel-eluting stents (PESs, n = 55) undergoing 8 to 9 months of follow-up 3-dimensional intravascular ultrasound examinations were enrolled. In addition to the standard intravascular ultrasound parameters, the percentage of neointimal volume (neointimal volume/stent volume) and maximum percentage of cross-sectional narrowing (neointimal area/stent area) was calculated. EESs showed a lower percentage of neointimal volume (7.2 +/- 7.1% vs 11.7 +/- 11.0%; p = 0.01) and maximum percentage of cross-sectional narrowing (22.5 +/- 16.3% vs 29.4 +/- 19.2%; p = 0.04) than PESs. One case of severe narrowing (lesions with maximum percentage of cross-sectional narrowing >60%) in the EES group developed and 6 cases in the PESs group (p = 0.05). The EESs showed no serial changes for vessel or peri-stent plaque during the follow-up period, and PESs showed significant increases in vessel and peri-stent plaque. PESs showed significantly greater peri-stent plaque increase, with a tendency toward greater vessel enlargement than EESs. Late acquired incomplete stent apposition was observed in 2 PES cases. The major adverse cardiac event rate was comparable < or =2 years. In conclusion, EESs showed greater neointimal suppression without significant vessel expansion than PESs in diabetic patients. In this small cohort, no significant differences were observed in the major adverse cardiac event rate < or =2 years.
View details for DOI 10.1016/j.amjcard.2010.03.059
View details for Web of Science ID 000281174500007
View details for PubMedID 20691306
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Comparisons of Baseline Demographics, Clinical Presentation, and Long-Term Outcome Among Patients With Early, Late, and Very Late Stent Thrombosis of Sirolimus-Eluting Stents Observations From the Registry of Stent Thrombosis for Review and Reevaluation (RESTART)
CIRCULATION
2010; 122 (1): 52-U120
Abstract
Stent thrombosis (ST) after sirolimus-eluting stent implantation has not yet been adequately characterized, mainly because of its low incidence.The Registry of Stent Thrombosis for Review and Reevaluation (RESTART) is a Japanese nationwide registry of sirolimus-eluting stent-associated ST comprising 611 patients with definite ST (early [within 30 days; EST], 322 patients; late [between 31 and 365 days; LST], 105 patients; and very late [>1 year; VLST], 184 patients). Baseline demographics, clinical presentation, and long-term outcome of sirolimus-eluting stent-associated ST were compared among patients with EST, LST, and VLST. Baseline demographics were significantly different according to the timing of ST. Characteristic demographic factors for LST/VLST versus EST identified by multivariable model were hemodialysis, end-stage renal disease not on hemodialysis, absence of circumflex target, target of chronic total occlusion, prior percutaneous coronary intervention, and age <65 years. For LST versus VLST, they were hemodialysis, heart failure, insulin-dependent diabetes mellitus, and low body mass index. Patients with LST had a significantly higher rate of Thrombolysis in Myocardial Infarction grade 2/3 flow (36%) at the time of ST than those with EST (13%) (P<0.0001) and VLST (17%; P<0.0001). Mortality rate at 1 year after ST was significantly lower in patients with VLST (10.5%) compared with those with EST (22.4%; P=0.003) or LST (23.5%; P=0.009).ST timing-dependent differences in baseline demographic features, Thrombolysis in Myocardial Infarction flow grade, and mortality rate suggest possible differences in the predominant pathophysiological mechanisms of ST according to timing after sirolimus-eluting stent implantation.
View details for DOI 10.1161/CIRCULATIONAHA.109.903955
View details for Web of Science ID 000279560800008
View details for PubMedID 20566955
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Mechanism of lumen gain with a novel rotational aspiration atherectomy system for peripheral arterial disease: examination by intravascular ultrasound.
Cardiovascular revascularization medicine : including molecular interventions
2010; 11 (3): 155-158
Abstract
The purpose of this study was to evaluate the mechanism of luminal gain with a novel atheroablation system (Pathway PV) for the treatment of peripheral artery disease using intravascular ultrasound (IVUS).The atherectomy system is a rotational atherectomy device, which employs expandable rotating blades with ports that allow flushing and aspiration of the plaque material or thrombus. In this first-in-man clinical study, IVUS analysis was available in 6 patients with lower limb ischemia treated with this device. The treatment results were assessed using IVUS at pre and post atherectomy. Lumen beyond burr size (LBB) was defined as lumen gain divided by the estimated burr area determined by the burr-size.IVUS analysis was available in six patients (superficial femoral artery n=3, popliteal artery n=2, posterior tibial artery n=1). Atheroablation achieved a significant increase in lumen area (LA) (preintervention 3.9+/-0.4, postatheroablation 8.0+/-1.7 mm(2), P<.05), and significant reduction in plaque area (27.5+/-4.0, 23.7+/-3.1 mm(2), P=.001), while there was no change in the vessel area (31.3+/-4.2, 32.1+/-2.8 mm(2), P=.4). LBB was 57.4+/-51.3%.This novel rotational aspiration atherectomy device achieved significant luminal gain by debulking in the absence of vessel stretching. The LA was greater than burr-sized lumen expectancy at cross-sections along the treated segments, suggesting a complimentary role of aspiration in luminal gain in atherosclerotic peripheral artery lesions.
View details for DOI 10.1016/j.carrev.2009.05.001
View details for PubMedID 20599165
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Vascular responses to the multiple overlapped paclitaxel-eluting stents for the treatment of bare-metal in-stent restenotic lesions: angiographic and intravascular ultrasound analysis from the TAXUS-V ISR trial.
Cardiovascular revascularization medicine : including molecular interventions
2010; 11 (3): 140-148
Abstract
Although effective coverage of coronary diffuse in-stent restenosis (ISR) lesions has warranted the use of multiple drug-eluting stents, the vessel response to paclitaxel-eluting stent (PES) overlap is not fully understood.In the TAXUS-V ISR, i.e., comparing PES versus brachytherapy for the treatment of bare-metal ISR, angiographic analyses at 9-month follow-up were available in 184 ISR lesions treated with PES.In-stent late loss in entire stented segment of multiple PES (n=50) was 0.45+/-0.48 mm, whereas that of single PES (n=134) was 0.3+/-0.47 mm, P=.06. No aneurysm was observed at overlapping PES segments at 9 months. Stent thrombosis up to 9 months was observed in one in each group (single PES, 0.7% vs. multiple PES, 1.8%; P=.47). In a subset of 30 patients, volumetric intravascular ultrasound analysis demonstrated that in-stent net volume obstruction was 12.3+/-12.4 in single PES (n=20) and 14.9+/-9.8 in multiple PES (n=10), P=.60. The changes of vessel and lumen at the overlapping PES segment were similar to those of the adjacent 5-mm segments (Deltaminimum lumen area, mm(2): -1.2+/-1.0, -1.1+/-1.1, -0.8+/-0.9, P=.48; Deltavessel volume, mm(3)/mm: -0.2+/-1.4, 0.1+/-1.7, 0.3+/-1.3, P=.37; proximal, overlap, distal segment, respectively). There was no late incomplete stent apposition at overlapping PES segments.No in vivo evidence of adverse local vessel response at the site of overlapping PES for the treatment of bare-metal ISR has been demonstrated.
View details for DOI 10.1016/j.carrev.2009.07.004
View details for PubMedID 20599163
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SPIRIT III JAPAN Versus SPIRIT III USA: A Comparative Intravascular Ultrasound Analysis of the Everolimus-Eluting Stent
AMERICAN JOURNAL OF CARDIOLOGY
2010; 106 (1): 13-17
Abstract
The aim of this study was to evaluate the vascular response after everolimus-eluting stent (EES) implantation in the SPIRIT III Japan Registry (JAPAN) compared to EES implantation in the SPIRIT III United States (USA) trial using serial intravascular ultrasound (IVUS) analysis. Data were obtained from the JAPAN and the randomized EES arm of the USA trial. Serial (postprocedure and 8-month follow-up) IVUS analysis was available in 199 lesions (JAPAN 82, USA 117) of 183 patients (JAPAN 73, USA 110). Although no difference was observed in vessel size in the reference segment between the 2 groups, postprocedure minimum lumen area and stent volume index were significantly greater in the JAPAN arm (minimum lumen area 5.8 +/- 2.2 vs 5.1 +/- 1.5 mm(2), p = 0.03; stent volume index 7.0 +/- 2.4 vs 6.3 +/- 1.7 mm(3)/mm, p = 0.03). Postprocedure incomplete stent apposition (ISA) was less frequently observed in the JAPAN arm (15.9% vs 33.3%, p = 0.006), possibly related to higher maximum balloon pressure and/or more postdilatation without excess tissue prolapse or edge dissection. In the JAPAN arm, percent neointimal obstruction and maximum percent cross-sectional narrowing were significantly lower at 8-month follow-up (percent neointimal obstruction 3.5 +/- 4.2% vs 6.8 +/- 6.4%, p = 0.0004). Late acquired ISA was infrequent in the 2 arms. In conclusion, comparative IVUS analysis between the JAPAN and USA arms showed more optimal stent deployment in the JAPAN arm as evidenced by the lower incidence of postprocedure ISA and larger minimum lumen area after the procedure. Moreover, there was less neointimal hyperplasia in patients with EES implants from the JAPAN arm compared to the USA arm.
View details for DOI 10.1016/j.amjcard.2010.02.008
View details for PubMedID 20609640
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Vascular Response to Overlapping Everolimus-Eluting Stents - Comparison With Paclitaxel-Eluting Stents
CIRCULATION JOURNAL
2010; 74 (5): 1023-1025
Abstract
Overlapping drug-eluting stents might be associated with an adverse vessel response because of increased drug/polymer toxicity and lesion rigidity.Lesions treated with overlapping everolimus- (EES=36) or paclitaxel-eluting stents (PES=38) were analyzed for 8-9-months by 3-dimensional intravascular ultrasound. EES were associated with significantly greater neointimal suppression in the single-strut regions than PES, with a similar trend in the overlap region. PES had significant vessel expansion in all regions, whereas there were no changes with EES. Neither stent fracture nor late incomplete stent apposition (LISA) in the overlap region was observed.Overlapping EES appears to be effective without vessel expansion, stent fracture or LISA for up to 8-9 months.
View details for DOI 10.1253/circj.CJ-10-0052
View details for Web of Science ID 000277226100033
View details for PubMedID 20424338
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Anatomic and Functional Evaluation of Bifurcation Lesions Undergoing Percutaneous Coronary Intervention
CIRCULATION-CARDIOVASCULAR INTERVENTIONS
2010; 3 (2): 113-119
Abstract
We sought to investigate the mechanism of geometric changes after main branch (MB) stent implantation and to identify the predictors of functionally significant "jailed" side branch (SB) lesions.Seventy-seven patients with bifurcation lesions were prospectively enrolled from 8 centers. MB intravascular ultrasound was performed before and after MB stent implantation, and fractional flow reserve was measured in the jailed SB. The vessel volume index of both the proximal and distal MB was increased after stent implantation. The plaque volume index decreased in the proximal MB (9.1+/-3.0 to 8.4+/-2.4 mm(3)/mm, P=0.001), implicating plaque shift, but not in the distal MB (5.4+/-1.8 to 5.3+/-1.7 mm(3)/mm, P=0.227), implicating carina shifting to account for the change in vessel size (N=56). The mean SB fractional flow reserve was 0.71+/-0.20 (N=68) and 43% of the lesions were functionally significant. Binary logistic-regression analysis revealed that preintervention % diameter stenosis of the SB (odds ratio=1.05; 95% CI, 1.01 to 1.09) and the MB minimum lumen diameter located distal to the SB ostium (odds ratio=3.86; 95% CI, 1.03 to 14.43) were independent predictors of functionally significant SB jailing. In patients with > or =75% stenosis and Thrombolysis In Myocardial Infarction grade 3 flow in the SB, no difference in post-stent angiographic and intravascular ultrasound parameters was found between SB lesions with and without functional significance.Both plaque shift from the MB and carina shift contribute to the creation/aggravation of an SB ostial lesion after MB stent implantation. Anatomic evaluation does not reliably predict the functional significance of a jailed SB stenosis.
View details for DOI 10.1161/CIRCINTERVENTIONS.109.887406
View details for PubMedID 20407111
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ANGIOGRAPHIC FEATURES RELATED TO INCOMPLETE STENT APPOSITION IN SPIRIT III TRIAL. A QUANTITATIVE ANALYSIS OF VESSEL CURVATURE
ELSEVIER SCIENCE INC. 2010
View details for Web of Science ID 001045644801881
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MECHANISM OF SIDE BRANCH JAILING IN BIFURCATION LESION: PLAQUE OR CARINA SHIFT?
ELSEVIER SCIENCE INC. 2010
View details for Web of Science ID 001045644801238
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IS THERE A DIFFERENCE IN VASCULAR RESPONSE BETWEEN BIODEGRADABLE POLYMER-BASED VERSUS NONPOLYMER-BASED BIOLIMUS-ELUTING STENT? SHORT-TERM INTRAVASCULAR ULTRASOUND RESULTS FROM STEALTH AND BIOFREEDOM TRIAL
ELSEVIER SCIENCE INC. 2010
View details for Web of Science ID 001045644801897
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FIRST-IN-MAN IVUS FINDINGS USING THE MEDTRONIC BIFURCATION STENT IN PATIENTS WITH CORONARY BIFURCATION LESIONS
ELSEVIER SCIENCE INC. 2010
View details for Web of Science ID 001045644802071
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INFLUENCE OF NON-UNIFORM STENT EXPANSION ON NEOINTIMAL HYPERPLASIA AFTER BARE-METAL AND ZOTAROLIMUS-ELUTING STENTS IMPLANTATION
ELSEVIER SCIENCE INC. 2010
View details for Web of Science ID 001045644802016
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FIRST-IN-MAN STUDY OF LOW-DOSE PACLITAXEL -ELUTING STENT WITH A NOVEL BIODEGRADABLE COATING
ELSEVIER SCIENCE INC. 2010
View details for Web of Science ID 001045644802258
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Sirolimus-eluting stent implantation in small coronary arteries: A three dimensional intravascular ultrasound study from the SIRIUS trial
INTERNATIONAL JOURNAL OF CARDIOLOGY
2010; 138 (2): 126-130
Abstract
To assess the efficacy of the sirolimus-eluting stent when implanted in smaller caliber vessels using three-dimensional intravascular ultrasound (IVUS) analysis.One hundred and twenty-three patients (69 sirolimus-coated Bx Velocity and 54 control) who underwent successful three-dimensional IVUS at follow up comprised this IVUS substudy from the SIRIUS (SIRolImUS-coated Bx Velocity stent in the treatment of patients with de novo coronary artery lesions) population. To evaluate the impact of vessel size, 2 groups were created using QCA reference vessel diameter (RVD; large vessel group: RVD>/=2.75 mm and small vessel group: RVD<2.75 mm).Sirolimus-eluting stents significantly reduced neointimal hyperplasia by the same relative magnitude within the stent in small vessels as well as in large vessels. Although sirolimus-eluting stents had favorable effects on lumen area at stent edges in larger vessels, the effect was less in smaller vessels, especially at the proximal edge. IVUS-detected adverse vessel response, such as late-acquired incomplete apposition, did not increase in smaller vessels even with relatively higher dose exposure.Sirolimus-eluting stents showed inhibition of neointimal hyperplasia in small vessels compared to bare metal stents with no increase of vascular complications.
View details for DOI 10.1016/j.ijcard.2008.08.006
View details for Web of Science ID 000273613300004
View details for PubMedID 18804877
- Plaque Characterization - IVUS, OCT Current Therapy 2010; 28 (5): 26-32
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Stent Expansion as a Mechanical Parameter to Predict Late Stent Patency Back to the Basics
JACC-CARDIOVASCULAR INTERVENTIONS
2009; 2 (12): 1276-1278
View details for DOI 10.1016/j.jcin.2009.10.013
View details for Web of Science ID 000275914400015
View details for PubMedID 20129556
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Preprocedural Inflammation Does Not Affect Neointimal Hyperplasia following Everolimus-Eluting Stent Implantation
JOURNAL OF INVASIVE CARDIOLOGY
2009; 21 (12): 613-617
Abstract
Preprocedual C-reactive protein (CRP) has been reported to correlate with in-stent restenosis following bare-metal stent implantation. The aim of this study was to investigate the impact of preprocedural inflammation on neointimal hyperplasia assessed by intravascular ultrasound (IVUS) following everolimus-eluting stent (EES) implantation.We identified 134 patients meeting the following criteria: 1) patients treated with EES; 2) those with stable or unstable angina; and 3) patients available for high-sensitivity (hs)-CRP before the procedure and volumetric IVUS analysis at follow up. We divided the patients into two groups on the basis of hs-CRP levels (< 3 or > or = 3 mg/L) before the procedure and compared IVUS parameters. Volume index (volume/length) was calculated for vessel (VVI), plaque (PVI), neointima (NIV), stent (SVI), and lumen (LVI). Percent neointimal volume (%NIV) was calculated as (NIV/SVI) x 100. Cross-sectional narrowing (CSN) was defined as neointimal area divided by stent area (%).There was no significant difference in VVI, PVI, or LVI at either baseline or 8-month follow up between the two groups. At 8-month follow up, there was also no significant difference in %NIV (4.93 +/- 5.66% vs. 4.98 +/- 5.25% p = 0.959) and maximum %CSN (16.81 +/- 13.62% vs. 18.14 +/- 13.91%; p = 0.608) as well as VVI, PVI, and LVI between the two groups. Furthermore, hs-CRP did not correlate with %NIV (r = 0.044; p = 0.610) and maximum %CSN (r = 0.086, p = 0.321) at follow up. There was no significant difference in incidence of late-acquired incomplete stent apposition between the two groups (1.2% vs. 0%; p = 0.512).Our results suggest that preprocedural inflammation does not affect neointimal hyperplasia following EES implantation.
View details for PubMedID 19966361
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Evaluation of the Peri-strut Low Intensity Area Following Sirolimus- and Paclitaxel-Eluting Stents Implantation: Insights From an Optical Coherence Tomography Study in Humans
82nd National Conference and Exhibitions and Scientific Sessions of the American-Heart-Association
LIPPINCOTT WILLIAMS & WILKINS. 2009: S1000–S1000
View details for Web of Science ID 000271831503408
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Comparison of Sirolimus-Eluting NEVO (TM) Stents With Paclitaxel-eluting CoStar (TM) Stents and Paclitaxel-eluting Taxus Liberte (TM) Stents: Insights From Intravascular Ultrasound Analysis of the Res-elution I and Costar II Trials
82nd National Conference and Exhibitions and Scientific Sessions of the American-Heart-Association
LIPPINCOTT WILLIAMS & WILKINS. 2009: S915–S915
View details for Web of Science ID 000271831503073
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Late-acquired incomplete stent apposition: morphologic characterization.
Cardiovascular revascularization medicine : including molecular interventions
2009; 10 (4): 236-246
Abstract
Incomplete stent apposition (ISA) is a lack of contact between stents and the underlying vessel wall, best described by intravascular ultrasound (IVUS). Late acquired incomplete apposition, defined as complete stent apposition at the time of procedure but ISA at follow-up, is an unusual IVUS finding reported in intracoronary brachytherapy, bare-metal stent (BMS), and drug-eluting stent (DES) implantation. Late-acquired ISA is observed relatively more frequently with DES implantation compared with BMS implantation. Possible mechanisms of this phenomenon include focal/extensive vascular remodeling and dissolution of thrombus. While there are conflicting reports regarding the possible impact of this IVUS finding on clinical outcomes, recent reports of DES have suggested its possible association with late adverse cardiac events including late stent thrombosis. In this paper, we review the incidence, location, underlying pathology, and possible clinical sequelae of late-acquired ISA, primarily focusing on that of DES.
View details for DOI 10.1016/j.carrev.2009.02.002
View details for PubMedID 19815171
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Impact of Lumen Narrowing Within Everolimus-Eluting Stents on Downstream Vessel Segments
21st Annual Transcatheter Cardiovascular Therapeutics Conference
EXCERPTA MEDICA INC-ELSEVIER SCIENCE INC. 2009: 18D–18D
View details for Web of Science ID 000269981600063
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Efficacy of Zotarolimus-Eluting Stent in Diabetes Patients: 3D-IVUS Analysis From the RESOLUTE Trial
EXCERPTA MEDICA INC-ELSEVIER SCIENCE INC. 2009: 62D
View details for Web of Science ID 000269981600175
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Serial Arterial Response to a Novel Drug-Eluting Stent with Novolimus, a Sirolimus Metabolite: IVUS Insights from the First Human Experience
EXCERPTA MEDICA INC-ELSEVIER SCIENCE INC. 2009: 63D
View details for Web of Science ID 000269981600178
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Vessel Behavior of Self-Expanding Biolimus A9-Eluting AXXESS Stent in Bifurcation Lesions Between Left Main Bifurcation vs. Non-Left Main Bifurcation: IVUS Findings of AXXENT and DIVERGE Trials
EXCERPTA MEDICA INC-ELSEVIER SCIENCE INC. 2009: 102D
View details for Web of Science ID 000269981600288
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Comparison of Sirolimus-Eluting NEVOTM Stents with Paclitaxel-eluting Taxus LieberteTM stents in De Novo Native Coronary Artery Lesions : Intravascular Ultrasound Results From the Reselution I Trial
EXCERPTA MEDICA INC-ELSEVIER SCIENCE INC. 2009: 133D
View details for Web of Science ID 000269981600373
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Vessel Response of the Low-Dose Paclitaxel-Eluting Coronary Stent System with Biodegradable Coating in de novo Coronary lesions-Results from the PLUS-ONE trial
EXCERPTA MEDICA INC-ELSEVIER SCIENCE INC. 2009: 152D–153D
View details for Web of Science ID 000269981600424
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Single Center, First-In-Man Study of the Elixir Novolimus Elating Coronary Stent System with Durable Polymer 24-Month Clinical Safety and Efficacy Results
21st Annual Transcatheter Cardiovascular Therapeutics Conference
EXCERPTA MEDICA INC-ELSEVIER SCIENCE INC. 2009: 158D–158D
View details for Web of Science ID 000269981600441
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Six-Month Volumetric IVUS Analysis in Diabetic and non-Diabetic Patients Treated with The Custom NX Biolimus-A9 Eluting stent: A Pooled Analysis of CUSTOM II and III Trials
21st Annual Transcatheter Cardiovascular Therapeutics Conference
EXCERPTA MEDICA INC-ELSEVIER SCIENCE INC. 2009: 63D–63D
View details for Web of Science ID 000269981600179
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Intravascular Ultrasound Results From the ENDEAVOR IV Trial Randomized Comparison Between Zotarolimus- and Paclitaxel-Eluting Stents in Patients With Coronary Artery Disease
JACC-CARDIOVASCULAR INTERVENTIONS
2009; 2 (8): 779-784
Abstract
The aim of this study was to compare the vessel response between zotarolimus-eluting stents (ZES) and paclitaxel-eluting stents (PES) using intravascular ultrasound.The ENDEAVOR IV (Randomized Comparison of Zotarolimus- and Paclitaxel-Eluting Stents in Patients With Coronary Artery Disease) trial was a randomized controlled study of zotarolimus-eluting, phosphorylcholine-coated, cobalt-alloy stents for the treatment of de novo coronary lesions compared with using PES for the same treatment.Data were obtained from patients with serial (baseline and 8-months follow-up) intravascular ultrasound analysis available (n = 198). Volumetric analysis was performed for vessel, lumen, plaque, stent, and neointima. Cross-sectional narrowing (given as percentage) was defined as neointimal area divided by stent area. Neointima-free frame ratio was calculated as the number of frames without intravascular ultrasound-detectable neointima divided by the total number of frames within the stent. Subsegment analysis was performed at every matched 1-mm subsegment throughout the stent.At follow-up, the ZES group showed significantly greater percentage of neointimal obstruction (16.6 +/- 12.0% vs. 9.9 +/- 8.9%, p < 0.01) and maximum cross-sectional narrowing (31.8 +/- 16.1% vs. 25.2 +/- 14.9%, p < 0.01) with smaller minimum lumen area than the PES group did. However, the incidence of maximum cross-sectional narrowing >50% was similar in the 2 groups. Neointima-free frame ratio was significantly lower in the ZES group. In overall analysis, whereas the PES group showed positive remodeling during follow-up (13.7 +/- 4.2 mm(3)/mm to 14.3 +/- 4.3 mm(3)/mm), the ZES group showed no significant difference (12.7 +/- 3.6 mm(3)/mm to 12.9 +/- 3.5 mm(3)/mm). In subsegment analysis, significant focal positive vessel remodeling was observed in 5% of ZES and 25% of PES cases (p < 0.05).There were different global and focal vessel responses for ZES and PES. Both drug-eluting stents showed a similar incidence of lesions with severe narrowing despite ZES having a moderate increase in neointimal hyperplasia compared with neointimal hyperplasia in PES. There was a relatively lower neointima-free frame ratio in ZES, suggesting a greater extent of neointimal coverage. (The ENDEAVOR IV Clinical Trial: A Trial of a Coronary Stent System in Coronary Artery Lesions; NCT00217269).
View details for DOI 10.1016/j.jcin.2009.05.015
View details for Web of Science ID 000278971500011
View details for PubMedID 19695548
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Drug-Eluting Stents - Insights From Invasive Imaging Technologies -
CIRCULATION JOURNAL
2009; 73 (8): 1371-1380
Abstract
Drug-eluting stents (DES) represent a revolutionary technology in their unique ability to provide both mechanical and biological solutions simultaneously to the target lesion. As a result of biological effects from the pharmacological agents and interaction of DES components with the arterial wall, considerable differences exist between DES and conventional bare metal stents (BMS), yet some of the old lessons learned in the BMS era remain clinically significant. In this context, contrast angiography provides very little information about in vivo device properties and their biomechanical effects on the arterial wall. In contrast, current catheter-based imaging tools, such as intravascular ultrasound, optical coherence tomography, and intracoronary angioscopy can offer unique insights into DES through direct assessment of the device and treated vessel in the clinical setting. This article reviews these insights from current DES with particular focus on performance and safety characteristics as well as discussing an optimal deployment technique, based upon findings obtained through the use of the invasive imaging technologies.
View details for Web of Science ID 000268433600003
View details for PubMedID 19574723
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A Novel Technique for Endovascular Detection and Removal of Radiographic Contrast during Angiography
JOURNAL OF INVASIVE CARDIOLOGY
2009; 21 (7): 314-318
Abstract
This study aims at in-vitro validation of the principles of endovascular detection of contrast medium and assessing the feasibility of in-vivo detection and removal of contrast during angiography.Contrast-induced nephropathy is a growing concern in current percutaneous interventions with increasing lesion complexity and patient comorbidity. To address this clinical problem, a novel method of endovascular detection and automatic removal of contrast has been developed, and is comprised of a catheter-based system with a reflectance-type optical sensor.Blood samples were obtained from ovine subjects to characterize the optical response of blood by measuring the reflectance spectrum at varying levels of hematocrit diluted by a contrast agent. The results from the in-vitro test were implemented into an in-vivo system. An aspiration catheter equipped with a fiberoptic sensor was inserted into the coronary sinus (CS) of 5 canines. Contrast was administered through the coronary artery and reflectance signals were recorded at the CS. The removal rate was analyzed through 20 specimen collections.A proportional relationship was found between hematocrit and reflectance intensity in in-vitro test. Upon in-vivo detection of contrast, the sensor signal showed a 79.5 +/- 9.9% (n = 33) drop from the pre-injection baseline. This was highly reproducible and beyond the noise level of baseline, (2.5 +/- 0.9%), enabling automatic activation of the aspiration system. The signal duration was 12.2 +/- 3.7 seconds. The removal rate of contrast was 59.3 +/- 11%.The present study validated the principles of endovascular contrast detection and demonstrated the feasibility of an in-vivo, catheter-based removal of contrast using reflectance technology.
View details for PubMedID 19571339
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A Prospective, Multicenter, Randomized Trial to Assess Efficacy of Pioglitazone on In-Stent Neointimal Suppression in Type 2 Diabetes POPPS (Prevention of In-Stent Neointimal Proliferation by Pioglitazone Study)
JACC-CARDIOVASCULAR INTERVENTIONS
2009; 2 (6): 524-531
Abstract
The aim of this study was to clarify whether pioglitazone suppresses in-stent neointimal proliferation and reduces restenosis and target lesion revascularization (TLR) after percutaneous coronary intervention (PCI).Previous single-center studies have demonstrated the anti-restenotic effect of a peroxisome proliferator-activated receptor gamma agonist, pioglitazone, after PCI.A total of 97 patients with type 2 diabetes mellitus (T2DM) undergoing PCI (bare-metal stents only) were enrolled. After PCI, patients were randomly assigned to either the pioglitazone group (n = 48) or the control group (n = 49). Angiographical and intravascular ultrasound (IVUS) imaging were performed at baseline and repeated at 6-month follow-up. Primary end points included angiographical restenosis and TLR at 6 months follow-up. Secondary end point was in-stent neointimal volume by IVUS.Baseline glucose level and glycosylated hemoglobin (HbA1c) level were similar between the pioglitazone group and the control group. Angiographical restenosis rate was 17% in the pioglitazone group and 35% in control group (p = 0.06). The TLR was significantly lower in pioglitazone group than in control group (12.5% vs. 29.8%, p = 0.04). By IVUS (n = 56), in-stent neointimal volume at 6 months showed a trend toward smaller in the pioglitazone group than in the control group (48.0 +/- 30.2 mm(3) vs. 62.7 +/- 29.0 mm(3), p = 0.07). Neointimal index (neointimal volume/stent volume x 100) was significantly smaller in the pioglitazone group than in the control group (31.1 +/- 14.3% vs. 40.5 +/- 12.9%, p = 0.01).Pioglitazone treatment might suppress in-stent neointimal proliferation and reduce incidence of TLR after PCI in patients with T2DM.
View details for DOI 10.1016/j.jcin.2009.04.007
View details for Web of Science ID 000278971200008
View details for PubMedID 19539256
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Local Determinants of Thrombus Formation Following Sirolimus-Eluting Stent Implantation Assessed by Optical Coherence Tomography
JACC-CARDIOVASCULAR INTERVENTIONS
2009; 2 (5): 459-466
Abstract
We conducted this study to assess the prevalence and determinants of subclinical thrombus after sirolimus-eluting stent (SES) implantation.Angioscopic analyses have demonstrated the presence of thrombus is more common than the clinical incidence of SES thrombosis.Fifty-three patients (53 lesions) underwent 6-month follow-up optical coherence tomography. A stent eccentricity index ([SEI] minimum/maximum stent diameter) was determined in each cross section. To evaluate unevenness of neointimal thickness, a neointimal unevenness score ([NUS] maximum neointimal thickness in the cross section/average neointimal thickness of the same cross section) was calculated for each cross section. Average SEI and NUS were calculated for each stent. Major adverse cardiac events were defined as a composite of death, myocardial infarction, and target vessel revascularization.Fourteen cases of thrombus (26%) were detected by optical coherence tomography (thrombus: n = 14 vs. nonthrombus: n = 39). The percentage of thrombus was associated with longer stents (36.4 +/- 20.2 mm vs. 25.1 +/- 9.8 mm; p = 0.008), a larger number of uncovered struts (17 +/- 16 vs. 8 +/- 11; p = 0.03), smaller average SEI (0.89 +/- 0.04 vs. 0.92 +/- 0.03; p = 0.001), and greater average NUS (2.22 +/- 0.24 vs. 2.00 +/- 0.33; p = 0.03). A significant relationship existed between average SEI and average NUS (p < 0.0001, R = 0.68), and between average SEI and the number of uncovered struts (p < 0.0006, R = 0.46). There was no significant difference in major adverse cardiac events during follow-up (median: 485 days, 7.1% vs. 12.8%; p > 0.99).Longer stents and greater asymmetric stent expansion may be important determinants of thrombus formation after SES implantation. In this small cohort, the presence of thrombus did not increase the risk of major adverse cardiac events.
View details for DOI 10.1016/j.jcin.2009.03.003
View details for Web of Science ID 000278971000014
View details for PubMedID 19463471
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Intraoperative Fluorescence Imaging System for On-Site Assessment of Off-Pump Coronary Artery Bypass Graft
JACC-CARDIOVASCULAR IMAGING
2009; 2 (5): 604-612
Abstract
The aim of this study was to evaluate the intraoperative fluorescence imaging (IFI) system in the real-time assessment of graft patency during off-pump coronary artery bypass graft.Intraoperative fluorescence imaging is an intraoperative angiography-like imaging modality using fluorescent indocyanine green excited with laser light. Recently, assessment of graft patency using the IFI system was introduced into clinical use. The feasibility and efficacy of IFI technology in off-pump coronary artery bypass graft has not been systematically compared with other conventional diagnostic modalities.Patients undergoing off-pump coronary artery bypass graft received IFI analysis, intraoperative transit time flowmetry, and postoperative X-ray angiography. In off-line IFI analysis, the graft washout was classified based on the number of heartbeats required for indocyanine green washout: fast washout (
15 beats).A total of 507 grafts in 137 patients received IFI analysis. Of all the IFI analyses, 379 (75%) grafts were visualized clearly up to the distal anastomosis. With regard to anastomosis location, anterior location was associated with a higher percentage of fully analyzable images (90%). More than 80% of images were analyzable, irrespective of graft type. Six grafts with acceptable transit time flowmetry results were diagnosed with graft failure by IFI, which required on-site graft revision. All revised grafts' patency was confirmed by post-operative X-ray angiography. Conversely, 21 grafts with unsatisfactory transit time flowmetry results demonstrated acceptable patency with IFI. Graft revision was considered unnecessary in these grafts, and 20 grafts (95%) were patent by post-operative X-ray angiography. Compared with slow washout, fast washout was associated with a higher preoperative ejection fraction, use of internal mammary artery grafts, and anterior anastomosis location.The IFI system enables on-site assessment of graft patency, providing both morphologic and functional information. This technique may help reduce procedure-related, early graft failures in off-pump bypass patients. View details for DOI 10.1016/j.jcmg.2008.12.028
View details for Web of Science ID 000287653200013
View details for PubMedID 19442948
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Relative Dose and Vascular Response After Drug-Eluting Stent Implantation: A Dosimetric 3D-Intravascular Ultrasound Study
58th Annual Scientific Session of the American-College-of-Cardiology
ELSEVIER SCIENCE INC. 2009: A9–A9
View details for Web of Science ID 000263864200036
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A Novel Technique For Endovascular Detection and Automated Removal of Radiographic Contrast During Angiography
ELSEVIER SCIENCE INC. 2009: A18
View details for Web of Science ID 000263864200071
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Intravascular Ultrasound Findings from the DIVERGE Trial: Serial Volumetric Analysis of the Biolimus A9-Eluting AXXESS Self-Expanding Stent for the Treatment of Bifurcation Coronary Lesions
ELSEVIER SCIENCE INC. 2009: A77
View details for Web of Science ID 000263864200319
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Intravascular Ultrasound Analysis of Vessel Response in Acute Coronary Syndrome Treated with Zotarolimus-Eluting Stents
58th Annual Scientific Session of the American-College-of-Cardiology
ELSEVIER SCIENCE INC. 2009: A15–A15
View details for Web of Science ID 000263864200059
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Gender Difference in Vessel Response in Coronary Artery Disease Treated with Zotarolimus-Eluting Stents
58th Annual Scientific Session of the American-College-of-Cardiology
ELSEVIER SCIENCE INC. 2009: A94–A94
View details for Web of Science ID 000263864200389
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Comparison of Vessel Response Between Zotarolimus- and Paclitaxel-eluting Stents: Global and Focal Vessel Responses as Assessed by Serial Intravascular Ultrasound
58th Annual Scientific Session of the American-College-of-Cardiology
ELSEVIER SCIENCE INC. 2009: A12–A12
View details for Web of Science ID 000263864200048
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Analysis of Left Main Coronary Artery Bifurcation Lesions Treated With Biolimus-Eluting DEVAX AXXESS Plus Nitinol Self-Expanding Stent: Intravascular Ultrasound Results of the AXXENT Trial
CATHETERIZATION AND CARDIOVASCULAR INTERVENTIONS
2009; 73 (1): 34-41
Abstract
To assess the efficacy of the AXXESS stent on the treatment of left main coronary artery (LMCA) bifurcation lesions using IVUS.The treatment of LMCA bifurcation lesions remains challenging even with the use of drug-eluting stents. The AXXESS system is a biolimus A9-eluting self-expanding stent, dedicated to the treatment of bifurcation lesions.Data were obtained from the AXXENT trial, a prospective, single-arm, multicenter study designed to evaluate the efficacy of the AXXESS stent on the treatment of LMCA bifurcation lesions. IVUS was available in 26 cases at 6-months follow-up. Volumetric and cross-sectional analyses within the AXXESS stent, and cross-sectional analyses at the ostia of left anterior descending (LAD) and left circumflex coronary arteries (LCX) were performed.Within the AXXESS stent, percent neointimal volume obstruction was (3.0 +/- 4.1)% with a minimal lumen area of 10.3 +/- 2.6 mm(2). AXXESS stent volume showed an 12.4% increase at follow-up compared with postprocedure (P = 0.04). Lumen area was significantly smaller in the LCX ostium compared with the LAD ostium at follow-up (3.6 +/- 1.3 mm(2) vs. 5.5 +/- 2.0 mm(2), P = 0.0112). There was greater neointimal formation in the LCX ostium compared with the LAD ostium (1.37 +/- 1.20 mm(2) vs. 0.30 +/- 0.36 mm(2), P = 0.0003).The AXXESS stent in the LMCA showed enlargement through 6-months follow-up and significant neointimal suppression. Greater neointimal formation and relatively inadequate stent expansion may contribute to luminal narrowing in the LCX ostium.
View details for DOI 10.1002/ccd.21765
View details for PubMedID 19089934
- Cardiovascular imaging: intravascular ultrasound Interventional Cardiology: Current Best Practice 2009: 206-211
- Drug-euting stents: current developments and future directions Journal of Clinical an Experimental Medicine 2009; 231 (6): 727-731
- Scieitific support for clinical trials: the role and system of core laboratories in clinical research Coronary Intervention 2009; 5 (6): 25-28
- IB-IVUS, Virtual Histology Journal of Clinical Echocardiography 2009; 10 (8): 792-802
- Primary PCI for STEMI: hypothermia and myocardial regeneration therapy Evidence Based Medicine: Treatment of Cardiovascular Disease 2010-2011 2009: 39-43
- Stent designs for bifurcation lesions: dedicated bifurcation stents Coronary Intervention 2009; 5 (3): 33-40
- Future directions of intravascular ultrasound The Lipid 2009; 20 (1): 90-99
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Intravascular Ultrasound Analysis of Small-Vessel Lesions Treated with Novel Ultra-Low Profile, Guidewire-Based Self-Expanding Stent System
JOURNAL OF INVASIVE CARDIOLOGY
2008; 20 (12): 647-650
Abstract
This study was performed to evaluate the long-term vascular response of the first series of patients treated by a novel ultra-low profile, guidewire-based self-expanding stent system (Sparrow stent) using serial intravascular ultrasound (IVUS).The long-term vascular response and stent geometry change after self-expanding stent implantation are not known.The CARE 1 trial was a single-arm feasibility study of the Sparrow stent in patients with small-vessel disease. Twenty patients were included in this prospective IVUS study, and serial volumetric IVUS analysis was performed after stent implantation and at 6- and 12-months follow up.Serial volumetric IVUS analysis was available in 13 cases between post-procedure and 6- month follow up and in 6 cases between 6- and 12-month follow up. At 6-month follow up, % neointimal volume was 34 +/- 9%. Stent volume index was increased by 13% , negating part of the luminal loss due to neointimal hyperplasia. There was no correlation between % neointimal volume index and % change in stent volume index (p = 0.7). No additional change occurred in any IVUS parameter between 6 and 12 months after stent implantation.In this small feasibility study, the use of a novel guidewire-based self-expanding stent was associated with the same degree of neointimal response as that seen with conventional bare-metal stents. Through serial analyses, the IVUS parameters of both the stent and the vessel remained unchanged beyond 6 months after stent implantation.
View details for Web of Science ID 000207739500007
View details for PubMedID 19057028
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Serial angiographic and intravascular ultrasound analysis of late stent strut fracture of sirolimus-eluting stents in native coronary arteries
INTERNATIONAL JOURNAL OF CARDIOLOGY
2008; 130 (2): 255-259
Abstract
Stent fracture in sirolimus-eluting stents (SES) has been reported to be associated with late adverse events. However, a suitable method to diagnose stent fracture is not fully elucidated.One hundred and two consecutive SES implantations were performed in 83 lesions in 56 patients and underwent serial angiography with intravascular ultrasound (IVUS) at baseline and at 6 months follow-up. Angiographic stent strut fracture was defined as stent bending with separation of stent struts. Angiographic hinge movement was defined as stent shaft deviation without separation of stent struts. IVUS stent strut dissociation was defined as the disappearance of stent struts in more than one cross-sectional image which were previously visualized at baseline.By angiography, no cases of stent fracture were detected at 6 months. One case of angiographic hinge movement was found at 12 months. However, three instances of stent fracture were detected by IVUS at 6 months. One case of stent fracture showed a patent lumen area at 6 months but subsequently developed late stent restenosis at 12 months. The other two cases were associated with in-stent restenosis at 6 months.Compared to angiography, IVUS can more reliably detect stent fracture during follow-up evaluation.
View details for DOI 10.1016/j.ijcard.2007.08.082
View details for Web of Science ID 000260757600021
View details for PubMedID 18096257
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Impact of Additional Ballooning on Plaque Prolapse After Stent Implantation in Patients With Acute Myocardial Infarction
JACC-CARDIOVASCULAR IMAGING
2008; 1 (6): 815-815
View details for DOI 10.1016/j.jcmg.2008.09.003
View details for Web of Science ID 000207650100017
View details for PubMedID 19356522
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SPIRIT III Japan: Eight-Month IVUS Analysis of Everolimus-Elurting Stent Compared to the US Arm
81st Annual Scientific Session of the American-Heart-Association
LIPPINCOTT WILLIAMS & WILKINS. 2008: S1044–S1044
View details for Web of Science ID 000262104504150
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Characteristics of Late Incomplete Stent Apposition: A Comparison with Sirolimus-, Paclitaxel- and Zotarolimus-Eluting Stents
LIPPINCOTT WILLIAMS & WILKINS. 2008: S1045
View details for Web of Science ID 000262104504155
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Role of Stent Expansion on Hemodynamic Profile in Bifurcation Lesions
LIPPINCOTT WILLIAMS & WILKINS. 2008: S742
View details for Web of Science ID 000262104502440
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Role of Self-Expanding Drug-Eluting Axxess Stent In Bifurcation Lesions: Intravascular Ultrasound Findings of AXXESS, AXXENT and DIVERGE Trials
LIPPINCOTT WILLIAMS & WILKINS. 2008: S901
View details for Web of Science ID 000262104503320
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Arterial Responses at Proximal and Distal Edges of Everolimus-Eluting Stents: Insights from the Spirit III Randomized Controlled Trial
81st Annual Scientific Session of the American-Heart-Association
LIPPINCOTT WILLIAMS & WILKINS. 2008: S1045–S1045
View details for Web of Science ID 000262104504153
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Efficacy Of The Everolimus-eluting Stent in Diabetic Patients: Comparison With The Paclitaxel-eluting Stent
81st Annual Scientific Session of the American-Heart-Association
LIPPINCOTT WILLIAMS & WILKINS. 2008: S1042–S1042
View details for Web of Science ID 000262104504143
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Local Determinants and Clinical Significance of Thrombus Formation Following Sirolimus-Eluting Stent Implantation: Insights from Optical Coherence Tomography Analysis
81st Annual Scientific Session of the American-Heart-Association
LIPPINCOTT WILLIAMS & WILKINS. 2008: S896–S896
View details for Web of Science ID 000262104503300
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Impact of Pre-procedural C-reactive Protein on Intravascular Ultrasound Parameters following Everolimus-eluting Stent Implantation: Results from the SPIRIT III Trial
81st Annual Scientific Session of the American-Heart-Association
LIPPINCOTT WILLIAMS & WILKINS. 2008: S1051–S1051
View details for Web of Science ID 000262104504174
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IVUS Analysis in the SPIRIT III Japan Treated with XIENCE (TM) V Everolimus-Eluting Stent Compared to the SPIRIT III US Arm
20th Annual Transcatheter Cardiovascular Therapeutics Conference
EXCERPTA MEDICA INC-ELSEVIER SCIENCE INC. 2008: 138I–138I
View details for Web of Science ID 000260094700332
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Long-term Intravascular Ultrasound Analysis of Small Vessel Lesions Treated with Novel Ultra-low Profile, Guidewire based Self-expanding Stent System
EXCERPTA MEDICA INC-ELSEVIER SCIENCE INC. 2008: 180I
View details for Web of Science ID 000260094700444
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Incidence of Diffuse and Focal Chronic Stent Recoil after Implantation of Current Generation Bare-metal and Drug-eluting Stents
EXCERPTA MEDICA INC-ELSEVIER SCIENCE INC. 2008: 197I
View details for Web of Science ID 000260094700486
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Vascular Response to Overlapping Everolimus-eluting stents: Comparison with Paclitaxel-eluting Stents
20th Annual Transcatheter Cardiovascular Therapeutics Conference
EXCERPTA MEDICA INC-ELSEVIER SCIENCE INC. 2008: 170I–170I
View details for Web of Science ID 000260094700421
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Pooled Analysis of CUSTOM II and III Trials: Six-Month IVUS Analysis of Very Long Lesions Treated with the Custom NX Biolimus-A9 Eluting Stent
20th Annual Transcatheter Cardiovascular Therapeutics Conference
EXCERPTA MEDICA INC-ELSEVIER SCIENCE INC. 2008: 137I–137I
View details for Web of Science ID 000260094700330
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Effect of Pioglitazone on Plaque Regression in Diabetic Patients with Coronary Artery Disease following Bare Metal Stent Implantation: Results from the POPPS Trial
20th Annual Transcatheter Cardiovascular Therapeutics Conference
EXCERPTA MEDICA INC-ELSEVIER SCIENCE INC. 2008: 232I–232I
View details for Web of Science ID 000260094700584
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Comparison of Vascular Response to Zotarolimus-Eluting Stent Versus Paclitaxel-Eluting Stent Implantation: IVUS Results From the ENDEAVOR IV Trial
20th Annual Transcatheter Cardiovascular Therapeutics Conference
EXCERPTA MEDICA INC-ELSEVIER SCIENCE INC. 2008: 146I–146I
View details for Web of Science ID 000260094700353
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Six-Month IVUS Analysis of Pimecrolimus and Dual Pimecrolimus/Paclitaxel Eluting Stents: Results of the GENESIS Trial
20th Annual Transcatheter Cardiovascular Therapeutics Conference
EXCERPTA MEDICA INC-ELSEVIER SCIENCE INC. 2008: 139I–140I
View details for Web of Science ID 000260094700336
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Two-Year Intravascular Ultrasound Observations in Diabetic Patients Treated with Single and Double Dose Sirolimus-Eluting Stents: Results of the Double Dose Diabetes (3D) Study
JOURNAL OF INVASIVE CARDIOLOGY
2008; 20 (8): 411-416
Abstract
Diabetes has been reported as an independent predictor of restenosis after drug-eluting stent implantation. The purpose of this study was to assess the long-term impact of increased drug dose in sirolimus-eluting stents (SES) on neointimal hyperplasia (NIH) in diabetic patients using volumetric intravascular ultrasound analysis.The 3D trial is a multicenter, prospective, randomized, feasibility study of double-dose (280 microg/cm2) or conventional single-dose (140 microg/cm2) SES for the treatment of de novo coronary lesions in diabetic patients. To evaluate long-term efficacy, complete serial volumetric analyses (baseline, 6-month and 2-year follow up) were performed in 39 diabetic patients (17 single-dose, 22 double-dose). Each volume was divided by stent length to acquire volume index, expressed as mm3/mm. Percent neointimal volume was calculated as (neointimal volume/stent volume) x 100 at follow up.Volumetric analysis showed similar results over time between the 2 stent groups (p = NS for all). At 2-year follow up, minimal increases in NIH area and percent NIH were observed in both groups, which translated into a decrease in lumen volume index compared to baseline (p < 0.05 for all). No late-acquired incomplete stent apposition was observed in either group.The current single dose of sirolimus in SES is effective in inhibiting NIH in diabetic patients up to 2 years. In this patient subset, double-dose SES did not confer additional NIH suppression at 2-year follow up compared to conventional single-dose SES.
View details for Web of Science ID 000207739100009
View details for PubMedID 18688066
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Novel guidewire-based stent-delivery system: Examination by intravascular ultrasound
CATHETERIZATION AND CARDIOVASCULAR INTERVENTIONS
2008; 72 (1): 47-51
Abstract
This report describes the first-in-man experience with a novel 0.014-in. guidewire-based, self-expanding stent delivery system designed for small or tortuous coronary arteries that may be difficult to access with conventional stent-delivery systems.
View details for DOI 10.1002/ccd.21562
View details for Web of Science ID 000257306300010
View details for PubMedID 18412249
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Impact of coronary artery bending at stent edges on subsequent plaque proliferation: A serial volumetric intravascular ultrasound analysis.
EXCERPTA MEDICA INC-ELSEVIER SCIENCE INC. 2008: 37C
View details for Web of Science ID 000255009600087
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Frontiers in intravascular Imaging technologies
CIRCULATION
2008; 117 (15): 2024-2037
View details for DOI 10.1161/CIRCULATIONAHA.105.551804
View details for Web of Science ID 000254966200014
View details for PubMedID 18413510
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Effect of lumen narrowing within sirolimus-eluting stents on proximal and distal vessel segments
CIRCULATION JOURNAL
2008; 72 (4): 534-537
Abstract
Flow dynamics and shear stress may influence downstream vessel segments. The aim of this study was to investigate the potential impact of lumen narrowing within sirolimus-eluting stents (SES) on vessel response at adjacent reference sites.In 135 patients after SES implantation, minimal lumen area (MLA) within the stent and average lumen area at distal or proximal adjacent reference segments (5 mm) were obtained at baseline and follow up. In the smaller in-stent MLA group (MLA <3 mm(2)), lumen area decreased significantly at the distal reference compared with the larger in-stent MLA group (MLA >or=3 mm(2)), although no significant difference was seen at the proximal reference.In-stent lumen patency may influence vascular responses at adjacent reference segments after SES implantation.
View details for Web of Science ID 000254468800005
View details for PubMedID 18362421
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Overlapping drug-eluting stents: Intravascular ultrasound insights from cobalt chromium stent with antiproliferative for restenosis II (COSTAR II) trial
57th Annual Scientific Session of the American-College-of-Cardiology
ELSEVIER SCIENCE INC. 2008: B41–B41
View details for Web of Science ID 000253997200167
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Proximal calcification may influence performance of polymer-based drug-eluting stents: A detailed intravascular ultrasound analysis
ELSEVIER SCIENCE INC. 2008: B41
View details for Web of Science ID 000253997200169
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Eight-month volumetric IVUS analysis in DIM and non-DM patients treated with XIENCE V everolimus-eluting coronary stent
57th Annual Scientific Session of the American-College-of-Cardiology
ELSEVIER SCIENCE INC. 2008: B43–B43
View details for Web of Science ID 000253997200176
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Untitled
AMERICAN HEART JOURNAL
2008; 155 (3)
View details for DOI 10.1016/j.ahj.2007.10.048
View details for Web of Science ID 000253798100032
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Coronary risk factors and coronary atheroma burden at severely narrowing segments
INTERNATIONAL JOURNAL OF CARDIOLOGY
2008; 124 (1): 124-126
Abstract
While only few data exist correlating cardiovascular risk factors with volumetric measurements of coronary atheroma burden in patients with coronary artery disease, a recent report using intravascular ultrasound (IVUS) demonstrated independent predictors of atherosclerotic burden in a native coronary artery with relatively mild narrowing (20-50% diameter stenosis by visual estimation). The purpose of this study was to examine whether cardiovascular risk factors can predict atherosclerotic burden at severely narrowing segments (>50% diameter stenosis).Patients who met the criteria (high-quality, automated pull-back IVUS images of severely narrowing segments prior to intervention) were identified from the IVUS database of the Cardiovascular Core Analysis Laboratory at Stanford University. Using commercially available planimetry software, lumen and vessel inside external elastic membrane areas were manually traced at every 0.5-mm interval in diseased segments. Using Simpson's method, vessel, lumen, and plaque (vessel minus lumen) volumes were calculated, and average area was calculated as volume data divided by length. Percent plaque volume was computed as plaque volume divided by vessel volume. Multiple linear regression analysis with backward selection was used to determine the risk factors for atherosclerotic burden.For percent plaque volume, diabetes or hypertension were predictors of more severe disease. For average plaque area, male gender or diabetes were predictors of more severe disease. These variables were also independent predictors in multivariate regression models.Male gender, hypertension, and diabetes are also strong independent predictors of atherosclerotic burden in coronary disease patients, though analyzed segments and disease severity were different.
View details for DOI 10.1016/j.ijcard.2006.11.194
View details for Web of Science ID 000253546900022
View details for PubMedID 17350700
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Comparison of vascular response to zotarolimus-eluting stent versus sirolimus-eluting stent: Intravascular ultrasound results from ENDEAVOR III
AMERICAN HEART JOURNAL
2008; 155 (1): 108-113
Abstract
The purpose of this study was to investigate the vascular response of zotarolimus-eluting stent (ZES) and sirolimus-eluting stent (SES) using serial intravascular ultrasound (IVUS).Data were obtained from the Endeavor Drug-Eluting Coronary Stent System Versus the Center Siromlimus-Eluting Coronary Stent System in De Novo Native Coronary Artery Lesions (ENDEAVOR) III trial, a randomized study comparing ZES and SES for the treatment of de novo native coronary artery lesions. Serial (baseline and 8-month follow-up) IVUS was available in 258 patients (190 ZES, 68 SES).At 8 months, ZES had greater percentage of neointimal volume index (ZES 1.1 +/- 0.8 mm3/mm vs SES 0.2 +/- 0.1 mm3/mm, P < .01), resulting in smaller lumen volume index (6.0 +/- 2.0 mm3/mm vs 7.0 +/- 2.1 mm3/mm, P < .05). Zotarolimus-eluting stents showed larger IVUS-detectable neointimal coverage over stent surface (50.2% vs 10.5%, P < .01) and greater mean neointimal thickness (0.19 +/- 0.07 mm vs 0.10 +/- 0.06 mm, P < .01). Zotarolimus-eluting stents had a significantly lower incidence of late-acquired incomplete stent apposition.Zotarolimus-eluting stent is associated with a significantly greater amount of neointimal hyperplasia compared with SES. This amount of hyperplasia in ZES is distributed throughout the stent at 8-month follow-up.
View details for DOI 10.1016/j.ahj.2007.08.008
View details for PubMedID 18082499
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Characterization of late incomplete stent apposition: a comparison among bare-metal stents, intracoronary radiation and sirolimus-eluting stents.
journal of invasive cardiology
2007; 19 (12): 515-518
Abstract
Late incomplete stent apposition (LISA) develops following implantation of conventional bare-metal stents (BMS) or drug-eluting stents, or after adjunctive intracoronary radiation (IR). However, no study has systematically compared the morphology of LISA seen with various treatment modalities.To compare the morphometric features of LISA accompanying BMS, IR or sirolimus-eluting stents (SES) using serial intravascular ultrasound (IVUS).A query of Stanford University's IVUS database of the Cardiovascular Core Analysis Laboratory was performed to identify LISA cases. Dedicated software programs were used for volumetric IVUS analyses.In 30 LISA cases (12 BMS, 6 IR and 12 SES), there was no intertreatment difference in the degree of LISA (lumen area minus stent area at follow up). Serial analyses of LISA segments showed that vessel area of SES and IR showed significant increase at follow up as compared with post procedure, while there was no significant change in plaque area. In contrast, the BMS group showed no increase in vessel area, whereas plaque area revealed significant reduction. Eight of 12 BMS cases were treated by directional atherectomy before stenting; however, there was no difference in the area change between patients with or without pre-stent atherectomy. Post-procedure plaque thickness beneath the stent struts of LISA was thinner for SES as compared with BMS.Plaque reduction primarily contributes to LISA after BMS, whereas vessel expansion is the predominant factor in LISA development for IR and SES. Thus, the mechanism of LISA may vary among different interventional treatments.
View details for PubMedID 18180522
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Analysis of bifurcation lesions treated with novel drug-eluting dedicated bifurcation stent system: Intravascular ultrasound results of the AXXESS PLUS trial
CATHETERIZATION AND CARDIOVASCULAR INTERVENTIONS
2007; 70 (7): 952-957
Abstract
The aim of this intravascular ultrasound (IVUS) study was to assess the efficacy of the AXXESS Plus stent system for the treatment of bifurcation coronary lesions.The AXXESS Plus is a novel bifurcation drug-eluting stent, comprised of a self-expanding flare-shaped stent platform and bioabsorbable polymer coating that releases Biolimus A9.Data were obtained from the AXXESS PLUS trial, a prospective, multicenter, nonrandomized, single-arm study to evaluate safety and efficacy. Six-month follow-up IVUS analysis was available in 49 cases. Volumetric analysis using Simpson's method within the AXXESS stent, and cross-sectional analysis at the ostium of main branch and/or side branch was performed. Impact of bifurcation angle on stent expansion at the carina was also evaluated. Results: Within the AXXESS stent, neointimal volume obstruction percentage was 2.3% +/- 2.2%, with a minimum lumen area of 7.9 +/- 2.6 mm(2). Lumen area was 5.2 +/- 1.7 mm(2) at main branch ostium, and 4.0 +/- 1.5 mm(2) at side branch ostium. In two cases, incomplete stent apposition was observed at the proximal edge of the AXXESS stent. In one case, a gap between the AXXESS stent and an additional stent was observed. Greater bifurcation angle inversely correlated with smaller stent area at side branch ostium (r = -0.54, P = 0.03) but not at main branch ostium (r = -0.2, P = 0.29).This novel self-expanding, drug-eluting bifurcation stent demonstrated effective lesion coverage along with significant neointimal suppression equivalent to current generation balloon-expandable drug-eluting stent technology.
View details for DOI 10.1002/ccd.21269
View details for Web of Science ID 000251442900009
View details for PubMedID 18044777
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Efficacy of reduced-dose sirofimus-eluting stems on the human coronary artery: Serial IVUS analysis of neointimal hyperplasia and luminal dimension
CATHETERIZATION AND CARDIOVASCULAR INTERVENTIONS
2007; 70 (7): 946-951
Abstract
Using serial intravascular ultrasound (IVUS), the efficacy of reduced-dose sirolimus-eluting stents (SESs) in the prevention of neointimal hyperplasia (NH) and maintenance of luminal patency in human coronary arteries was evaluated.In the animal model, a broad therapeutic window regarding sirolimus doses in suppressing NH has been reported.Serial cross-sectional and volumetric IVUS analyses were performed in 44 patients treated with SES that contained lower sirolimus doses (either 45% or 70%) than standard SES. For cross-sectional analysis, minimum lumen area (MLA) was measured. Percent (%) NH volumetric obstruction was calculated as 100 x NH volume/stent volume.IVUS measurements were similar between the two drug-dose groups. At 12 months follow-up, only one case developed late incomplete stent apposition. Between 4 and 12 months, a slight increase of in-stent % area loss and % NH obstruction was noted (3.5% +/- 10.4% to 6.7% +/- 10.7% and 1.9% +/- 5.0% to 4.4% +/- 8.0%, respectively). The majority of studied cases, however, sustained less than a 10% volumetric (93% of studied cases) and area loss (75% of studied cases) in the stented segment up to 12 months. At 12 months, % area loss within the stented segments and 5-mm reference segments were comparable (7.0% +/- 19.6% versus 6.7% +/- 10.7%).Although slight increases of NH were noted, SESs, delivering two reduced drug doses, appeared to be effective for maintaining luminal patency during 12 months follow-up.
View details for DOI 10.1002/ccd.21272
View details for Web of Science ID 000251442900008
View details for PubMedID 17621671
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Determinants of lumen loss between years 1 and 2 after cardiac transplantation
TRANSPLANTATION
2007; 84 (9): 1097-1102
Abstract
We previously reported that negative remodeling, not plaque progression, correlated with lumen loss during the first year after cardiac transplantation and that cytomegalovirus antibody seropositivity correlated with increased negative remodeling and greater lumen loss. Whether these findings persist between years 1 and 2 after transplantation is unknown.Serial 3-dimensional intravascular ultrasound analysis in the left anterior descending coronary artery was performed in 30 cardiac transplant recipients at year 1 and 2 after transplantation. Vessel, lumen, and plaque area were determined at 0.5-mm axial intervals in the first 50 mm of the left anterior descending coronary artery, and volumes were computed using Simpson's method. Univariate and multivariate regression analyses were performed to identify clinical predictors of change in coronary dimensions.Although mean vessel area did not change (13.6+/-3.4 to 13.4+/-3.3 mm/mm(3), P=0.45), mean plaque area increased (3.4+/-2.3 to 3.8+/-2.2 mm/mm(3), P=0.012), resulting in significant mean lumen area loss (10.3+/-2.5 to 9.6+/-2.3 mm/mm(3), P=0.016). However, the degree of luminal change strongly correlated with the degree of change in vessel size (R=0.81, P<0.0001), but not with change in plaque amount (R=-0.19, P=0.32). In fact, in 57% of the patients who demonstrated lumen loss, negative remodeling contributed more to lumen loss than did plaque progression. Diabetes at 2 years was the only significant independent clinical predictor of plaque progression and lumen loss.Despite significant plaque progression, negative remodeling correlated with coronary lumen loss between years 1 and 2 after cardiac transplantation.
View details for DOI 10.1097/01.tp.0000285987.27033.65
View details for PubMedID 17998863
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Design criteria for the ideal drug-eluting Stent
AMERICAN JOURNAL OF CARDIOLOGY
2007; 100 (8B): 3M-9M
Abstract
The deployment of drug-eluting stents (DESs) is an integral treatment option for patients with coronary artery disease. Although the development and testing of the first-generation DESs focused to a considerable degree on efficacy parameters, including restenosis, recent concerns over late clinical events have prompted a refinement of the design criteria for succeeding generations of these devices. This review assesses design criteria for the ideal DES from 3 complementary perspectives: deliverability, efficacy, and safety. Most new investigational balloon-expandable DES systems have lowered crossing profiles by thinning stent struts using a cobalt chromium alloy, while investigational self-expanding DESs often use nitinol as the platform material. Stents designed to be fully biodegradable are also being developed, with deliverability and performance to be determined in future clinical trials. Refinements in bifurcation-dedicated stents will secure branch accessibility to offer better deliverability in complex lesion morphologies. Experimentation in stent design is already realizing multiple-lesion stenting and the in situ customization of stent length. Rather than simply targeting further reductions in restenosis rates, efforts to improve efficacy are shifting toward a lesion-specific approach, including the design of stents dedicated to bifurcation lesions. Another future direction is a disease-specific approach, or an approach using DESs as local drug-delivery devices. The identification of long-term safety issues with the first-generation DESs has reignited clinical interest in the development of stents that are more biologically based, including fully biodegradable stents and stents using biomimetic and biodegradable polymers. Important performance criteria for future DES agents include more cell-type specificity, broader safety margins, and greater facility at promoting endothelialization and healing.
View details for DOI 10.1016/j.amjcard.2007.08.016
View details for Web of Science ID 000250759000002
View details for PubMedID 17950830
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Intravascular ultrasound findings in ENDEAVOR II and ENDEAVOR III
AMERICAN JOURNAL OF CARDIOLOGY
2007; 100 (8B): 71M-76M
Abstract
The results of 2 randomized controlled trials of the Endeavor zotarolimus-eluting stent (ZES; Medtronic Vascular, Santa Rosa, CA) were recently reported: ENDEAVOR II, in which the Endeavor stent was compared with the Driver bare metal stent (BMS; Medtronic Vascular), and ENDEAVOR III, in which the Endeavor stent was compared with the first-generation Cypher sirolimus-eluting stent (SES; Cordis Corporation, Miami Lakes, FL). To examine in detail the vascular responses to the Endeavor stent, serial intravascular ultrasound (IVUS) analyses were performed in subsets of patients in the 2 trials at baseline and 8-month follow-up. The investigators report results for various IVUS parameters and compare those with published results for the first-generation SES and paclitaxel-eluting stent (PES). The ZES demonstrated significantly improved effectiveness and equivalent safety compared with the BMS in ENDEAVOR II. Although the ZES seems to be slightly less effective at inhibiting intimal hyperplasia than the SES and PES, early results are indicative of an acceptable safety profile. This finding may be due in part to the relatively complete and uniform neointimal coverage associated with the ZES.
View details for DOI 10.1016/j.amjcard.2007.08.025
View details for Web of Science ID 000250759000010
View details for PubMedID 17950835
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Six-month IVUS analysis of complex coronary artery lesions treated with Biolimus-A9 eluting XTENT stent: Results of the CUSTOM II trial
EXCERPTA MEDICA INC-ELSEVIER SCIENCE INC. 2007: 155L
View details for Web of Science ID 000250393900388
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Analysis of left main coronary artery bifurcation lesions treated with biolimus-eluting DEVAX AXXESS plus nitinol self-expanding stent: Intravascular ultrasound results of the AXXENT trial
EXCERPTA MEDICA INC-ELSEVIER SCIENCE INC. 2007: 18L
View details for Web of Science ID 000250393900035
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Short- and mid-term intravascular ultrasound analysis of the new ENDEAVOR CR zotarolimus-eluting stent: Insights from the RESOLUTE trial
EXCERPTA MEDICA INC-ELSEVIER SCIENCE INC. 2007: 19L–20L
View details for Web of Science ID 000250393900040
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Comparison of vascular response to zotarolimus-eluting Stent versus paclitaxel-eluting stent implantation: IVUS results from the Zomaxx I trial
EXCERPTA MEDICA INC-ELSEVIER SCIENCE INC. 2007: 62L
View details for Web of Science ID 000250393900136
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Six-month IVUS analysis of long coronary artery lesions treated with Biolimus-A9 eluting XTENT interdigitating stent with bioabsorbable polymer: Results of the CUSTOM II trial
LIPPINCOTT WILLIAMS & WILKINS. 2007: 616
View details for Web of Science ID 000250394302774
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Post-procedural incomplete stent apposition after implantation of everolimus-eluting or paclitaxel-eluting stents: Insights from the randomized SPIRIT III trial
LIPPINCOTT WILLIAMS & WILKINS. 2007: 361
View details for Web of Science ID 000250394301638
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Comparison of everolimus-eluting Stents with paclitaxel-eluting Stents in de novo native coronary artery lesions: Intravascular ultrasound results from the SPIRIT III trial
LIPPINCOTT WILLIAMS & WILKINS. 2007: 615
View details for Web of Science ID 000250394302772
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Impact of polymer formulations on neointimal proliferation following zotarolimus-eluting stent with a different polymer: Results of a 3D intravascular ultrasound analysis
LIPPINCOTT WILLIAMS & WILKINS. 2007: 615–16
View details for Web of Science ID 000250394302773
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Detailed intravascular ultrasound analysis of Zotarolimus-eluting phosphorylcholine-coated cobalt-chromium alloy stent in de Novo Coronary lesions (results from the ENDEAVOR II trial)
AMERICAN JOURNAL OF CARDIOLOGY
2007; 100 (5): 818-823
Abstract
Zotarolimus-eluting phosphorylcholine-coated cobalt-chromium alloy Driver stents (ZES) demonstrated significant reductions in target lesion revascularization rate with few apparent adverse events compared with bare metal stents (BMS; uncoated Driver stents) in a prospective, multicenter, double-blind, randomized controlled trial in de novo coronary lesions. The aim of this study was to examine detailed vascular responses to ZES compared with BMS using serial intravascular ultrasound analysis. A total of 343 patients (ZES n = 178, BMS n = 165) were enrolled in this formal, prespecified intravascular ultrasound substudy of the Randomized Controlled Trial to Evaluate the Safety and Efficacy of the Medtronic AVE Zotarolimus-Eluting Driver Coronary Stent in de Novo Native Coronary Artery Lesions (ENDEAVOR II), a prospective, multicenter, double-blind, randomized controlled trial to compare ZES and BMS in de novo native coronary artery lesions. Quantitative and qualitative intravascular ultrasound analyses were performed postprocedurally and at 8-month follow-up in stented and reference segments. ZES showed significantly less neointima, with a larger lumen than BMS at 8 months (percentage neointimal volume 17.6 +/- 10.1% vs 29.4 +/- 17.2%, p <0.0001; maximum percentage neointimal area 32.9 +/- 13.0% vs 47.6 +/- 18.6%, p <0.0001; minimum luminal area 4.9 +/- 1.6 vs 4.0 +/- 1.7 mm(2), p <0.0001) and no unfavorable edge effect. In the 18-mm single stents, ZES showed evenly inhibited neointima compared with BMS. Neither persistent stent-edge dissection nor late-acquired incomplete stent apposition was observed in either group. In conclusion, ZES showed evenly inhibited neointima with no apparent adverse vascular response in stented and reference segments at 8 months compared with BMS.
View details for DOI 10.1016/j.amjcard.2007.04.016
View details for Web of Science ID 000249226100013
View details for PubMedID 17719326
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Neointimal progression and luminal narrowing in sirolimus-eluting stent treatment for bare metal in-stent restenosis: A quantitative intravascular ultrasound analysis
AMERICAN HEART JOURNAL
2007; 154 (2): 361-365
Abstract
Recurrent restenosis may occur after drug-eluting stent implantation for in-stent restenosis (ISR) of bare metal stents (BMSs), especially in areas involving drug-eluting stent gaps.To investigate the details of neointimal progression and luminal narrowing after the treatment of ISR using sirolimus-eluting stents (SESs), serial intravascular ultrasound analysis was performed in 65 patients with ISR at postintervention and at 6-month follow-up. The total stented segment was categorized into 3 compartments: new SES (N), new SES and old BMS overlap (N/O), and old BMS (O). In each of the 190 compartments, serial intravascular ultrasound parameters were analyzed at the cross section of the maximum change in neointimal area (delta neointimal area) from postintervention to follow-up or the minimum lumen area at follow-up if delta neointimal area was 0. Minimum lumen area in each compartment was also investigated serially.At postintervention, lumen area was the smallest in compartment N/O (N 5.8 +/- 1.5, N/O 5.1 +/- 1.3, O 6.0 +/- 1.4 mm2, P = .005). Not only the average of maximum delta neointimal area (N 0.2 +/- 0.4, N/O 0.2 +/- 0.4, O 0.8 +/- 1.0 mm2, P < .0001) but also the frequency of minimum lumen area decreasing from > or = 4.0 mm2 at postintervention to < 4.0 mm2 at follow-up (N 4.0%, N/O 5.1%, O 23.5%, P = .012) was the largest in compartment O.Neointimal progression and consequent luminal narrowing tend to occur where BMS is uncovered with SES in treatment of ISR, even in the absence of an obvious stenosis at postintervention.
View details for DOI 10.1016/j.ahj.2007.04.023
View details for Web of Science ID 000248511000025
View details for PubMedID 17643589
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The risks and benefits of drug-eluting stents.
The American heart hospital journal
2007; 5 (3): 146-150
View details for PubMedID 17673855
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Comparison of nonuniform strut distribution between two drug-eluting stent platforms.
journal of invasive cardiology
2007; 19 (6): 244-246
Abstract
To compare the difference of strut distribution between two clinically available drug-eluting stent platforms (Bx Velocity and Express II stents) using intravascular ultrasound (IVUS).Nonuniform strut distribution (NSD) has been shown to be associated with increased intimal hyperplasia after drug-eluting stent implantation.IVUS imaging was performed on Bx Velocity (n = 6) and Express II stents (n = 6) after inflation pressures of 10, 16, and 26 atm in a bench test model. Percent NSD was defined as the length of segments with NSD (interstrut angle > 90 degrees) divided by stent length. NSD was also assessed in postprocedure IVUS images in 53 clinical cases (32 Cypher, 21 Taxus) using 3-dimensional IVUS analysis.Frequency of NSD segment and %NSD were lower in Bx Velocity stents than in Express II stents at the inflation pressures of 16 and 26 atm (%NSD: 16 atm, 0% vs. 13.8 +/- 9.4%; p < 0.005; 26 atm, 1.1 +/- 2.6% vs. 19.9 +/- 6.9% p < 0.0001). In postprocedural images from clinical cases, the frequency of NSD segment and %NSD were lower in Cypher stents than in Taxus stents (%NSD: 0.5 +/- 1.6 vs. 6.8 +/- 7.2; p < 0.0001).NSD segment was observed less in Bx Velocity stents than in Express II stents.
View details for PubMedID 17541122
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Changes in coronary anatomy and physiology after heart transplantation
AMERICAN JOURNAL OF CARDIOLOGY
2007; 99 (11): 1603-1607
Abstract
Cardiac allograft vasculopathy (CAV) is a progressive process involving the epicardial and microvascular coronary systems. The timing of the development of abnormalities in these 2 compartments and the correlation between changes in physiology and anatomy are undefined. The invasive evaluation of coronary artery anatomy and physiology with intravascular ultrasound, fractional flow reserve, coronary flow reserve, and the index of microcirculatory resistance (IMR) was performed in the left anterior descending coronary artery during 151 angiographic evaluations of asymptomatic heart transplant recipients from 0 to >5 years after heart transplantation (HT). There was no angiographic evidence of significant CAV, but during the first year after HT, fractional flow reserve decreased significantly (0.89 +/- 0.06 vs 0.85 +/- 0.07, p = 0.001), and percentage plaque volume derived by intravascular ultrasound increased significantly (15.6 +/- 7.7% to 22.5 +/- 12.3%, p = 0.0002), resulting in a significant inverse correlation between epicardial physiology and anatomy (r = -0.58, p <0.0001). The IMR was lower in these patients compared with those > or =2 years after HT (24.1 +/- 14.3 vs 29.4 +/- 18.8 units, p = 0.05), suggesting later spread of CAV to the microvasculature. As the IMR increased, fractional flow reserve increased (0.86 +/- 0.06 to 0.90 +/- 0.06, p = 0.0035 comparing recipients with IMRs < or =20 to those with IMRs > or =40), despite no difference in percentage plaque volume (21.0 +/- 11.2% vs 20.5 +/- 10.5%, p = NS). In conclusion, early after HT, anatomic and physiologic evidence of epicardial CAV was found. Later after HT, the physiologic effect of epicardial CAV may be less, because of increased microvascular dysfunction.
View details for DOI 10.1016/j.amjcard.2007.01.039
View details for PubMedID 17531589
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Serial intravascular ultrasonic study of outcomes of coronary culprit lesions with plaque rupture following bare metal stent implantation in patients with angina pectoris
AMERICAN JOURNAL OF CARDIOLOGY
2007; 99 (10): 1394-1398
Abstract
Coronary culprit lesions with plaque rupture (PR) have been treated with different coronary interventions. However, it is unknown whether the presence of PR affects the restenotic process after coronary intervention. One hundred forty-two patients undergoing coronary bare metal stent implantation were enrolled in the present retrospective analysis. Case selection was based on availability of intravascular ultrasound (IVUS) and quantitative coronary angiographic examinations at baseline (before and after intervention) and at follow-up. Serial comparative analyses included qualitative and quantitative features of the culprit lesion and reference segments. PR was defined as an intraplaque cavity in communication with the lumen in the presence of a residual, disrupted cap. Patients were categorized according to the presence/absence of PR. Pre-interventional IVUS detected PR in 54 patients (38%). Baseline patient demographics were similar between the +PR and -PR groups. Quantitative IVUS analysis showed higher rates of positive remodeling and larger vessel and plaque areas in the +PR compared with -PR lesions (p <0.001 for all). At follow-up (7.2 +/- 2.6 months), no statistically significant difference was observed between the 2 groups in quantitative coronary angiographic or IVUS measurements. In conclusion, culprit lesions with PR exhibited larger plaque mass and higher rates of positive remodeling at preintervention IVUS examination. However, when treated with bare metal stents, the absence/presence of preintervention PR was not found to affect the rate or severity of in-stent restenosis in these culprit lesions.
View details for DOI 10.1016/j.amjcard.2006.12.067
View details for Web of Science ID 000246715900010
View details for PubMedID 17493467
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Drug delivery via nano-, micro and macroporous coronary stent surfaces
EXPERT OPINION ON DRUG DELIVERY
2007; 4 (3): 287-295
Abstract
Drug-eluting stents (DESs) have revolutionized the treatment of occlusive coronary artery disease via marked reduction of in-stent restenosis. One critical feature for successful DESs is the sustained release of drugs, which is achieved using a polymer coating in the present generation of DESs. However, recent studies have raised a concern that polymers may trigger allergic reactions and/or prolonged inflammation in some patients. These untoward reactions may eventually lead to undesirable clinical events, including stent thrombosis and sudden cardiac death. A new drug delivery technology, using a porous stent surface, may offer desirable drug elution properties without the use of polymers, and may translate into an improved safety profile for the next-generation DESs.
View details for DOI 10.1517/17425247.4.3.287
View details for Web of Science ID 000252856900008
View details for PubMedID 17489655
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Comparison of vessel response following sirolimus-eluting stent implantation as assessed by serial 3-D intravascular ultrasound study.
journal of invasive cardiology
2007; 19 (4): 171-173
Abstract
Recent sirolimus-eluting stent (SES) studies have suggested higher rates of restenosis in non-left anterior descending (LAD) artery lesions. The aim of this study was to evaluate differential vessel response (LAD versus non-LAD) to SES implantation using serial intravascular ultrasound (IVUS). A total of 94 patients who underwent SES implantation and serial (post-PCI and 8 months) 3-dimensional IVUS were enrolled from our database. Volumetric analysis was performed throughout the stent as well as the adjacent reference segment (up to 5 mm). Volume index (volume/length) was calculated for vessel (VVI), lumen (LVI), and plaque (PVI). Cross-sectional narrowing (CSN) was defined as neointimal area divided by stent area (%). With respect to the in-stent segment, VVI, PVI, and LVI at post-PCI were not significantly different between the LAD (n = 41) and non-LAD (n = 53) lesions. At follow up, however, maximum CSN was significantly greater in the non-LAD lesions (18.3 +/- 15.2% versus 12.2 +/- 10.0%; p = 0.029). At the proximal reference segment, the non-LAD lesions showed a significantly greater LVI decrease than the LAD lesions (p <0.05), primarily due to mild vessel shrinkage observed in the non-LAD lesions. There were no significant differences at the distal reference segment between the LAD and non-LAD lesions. This detailed IVUS analysis suggests that there are minimal differences in the vessel responses following SES implantation. These findings may have potential implications for mechanical and pharmacokinetic properties of next-generation drug-eluting stent technology.
View details for PubMedID 17404402
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Impact of gender on neointimal hyperplasia following coronary artery stenting
AMERICAN JOURNAL OF CARDIOLOGY
2007; 99 (4): 491-493
Abstract
Whether gender affects long-term outcomes after bare metal stent implantation remains controversial. The aim of this study was to examine the impact of gender on neointimal hyperplasia in a large cohort of patients after stent implantation using 3-dimensional intravascular ultrasound. Lumen and stent areas were manually traced at 0.5-mm intervals throughout the stented segment. Using Simpson's method, lumen, stent, and neointimal (stent - lumen) volumes were calculated and standardized by stent length. Women were older, presented more often with hyperlipidemia or hypertension, and had smaller reference vessel diameter and mean stent area, compared with men. Although neointimal hyperplasia and neointimal thickness in women were similar to that in men, the percentage of neointimal hyperplasia (neointimal area divided by stent area) was higher in women due to the smaller stent area. After adjusting for stent area, the percentage of neointimal hyperplasia did not differ by gender. In conclusion, the results of this study indicate that neointimal hyperplasia after bare metal stent implantation in women is similar to that seen in men. Despite the similarity in outcome, there are several gender-specific differences in baseline characteristics.
View details for DOI 10.1016/j.amjcard.2006.09.094
View details for Web of Science ID 000244514500014
View details for PubMedID 17293191
- Intravascular ultrasound Cardiovasuclar Medicine 2007: 1797-1810
- Future directions of drug-eluting stents in the treatment of acute coronary syndrome Coronary Intervention 2007; 3 (1): 94-99
- Intravascular ultrasound Textbook of Interventional Cardiology 2007: 1115-1142
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Comparison of the efficacy of direct coronary stenting with sirolimus-eluting stents versus stenting with predilation by intravascular ultrasound imaging (from the DIRECT trial)
AMERICAN JOURNAL OF CARDIOLOGY
2006; 98 (11): 1464-1467
Abstract
A direct coronary stenting technique using drug-eluting stents may decrease drug-eluting stent efficacy due to possible damage to the surface coating of the stent. The DIRECT is a multicenter, prospective, nonrandomized trial designed to evaluate the direct stenting strategy for the sirolimus-eluting Bx-Velocity stent compared with the historical control (SIRIUS trial, stenting with predilation). Volumetric and cross-sectional intravascular ultrasound analyses at 8-month follow-up were performed in 115 patients (DIRECT n= 64, control n = 51). Patient and lesion characteristics were comparable between groups. The DIRECT group achieved an equivalent uniform expansion index, defined as minimum stent area/maximum stent area x 100, compared with the control group (65.9 +/- 11.7 vs 63.1 +/- 12.7, p = NS). At 8-month follow-up, vessel, stent, lumen, and neointimal volume index (volume in cubic millimeters/length in millimeters) and percent neointimal volume were similar between the DIRECT and control groups (vessel volume index 13.9 +/- 4.40 vs 15.0 +/- 3.83; stent volume index 6.83 +/- 2.02 vs 6.94 +/- 2.04; lumen volume index 6.71 +/- 2.04 vs 6.81 +/- 2.07; neointimal volume index 0.14 +/- 0.24 vs 0.16 +/- 0.23; percent neointimal volume 3.73 +/- 6.97 vs 3.14 +/- 5.32, p = NS for all). In addition, in-stent neointimal hyperplasia distribution was significantly smaller near the distal stent edge (0.22 vs 0.098 mm(3)/mm, p = 0.01 for an average neointimal volume index within 3 mm from the distal stent edge). In conclusion, direct coronary stenting with the sirolimus-eluting Bx-Velocity stent is equally effective in terms of uniform stent expansion and long-term quantitative intravascular ultrasound results compared with conventional stenting using predilation. This strategy appears to be associated with less neointimal hyperplasia near the distal stent edge.
View details for DOI 10.1016/j.amjcard.2006.06.046
View details for Web of Science ID 000242595300010
View details for PubMedID 17126651
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Negative remodeling is primarily responsible for coronary artery lumen loss early after cardiac transplantation: Role of cytomegalovirus
LIPPINCOTT WILLIAMS & WILKINS. 2006: 533
View details for Web of Science ID 000241792803413
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A randomized comparison of paclitaxel-eluting stents vs. intra-coronary brachytherapy in the treatment of in-stent restenosis: Intravascular ultrasound results from the TAXUS-V ISR trial
LIPPINCOTT WILLIAMS & WILKINS. 2006: 547
View details for Web of Science ID 000241792803476
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Novel intra-operative fluorescence imaging system for on-site assessment of off-pump coronary artery bypass graft
18th Annual Transcatheter Cardiovascular Therapeutics Symposium
EXCERPTA MEDICA INC-ELSEVIER SCIENCE INC. 2006: 247M–248M
View details for Web of Science ID 000241442800631
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Intravascular ultrasound observation of "Black hole" appearance: Porcine carotid artery model with artificial focal stenosis
EXCERPTA MEDICA INC-ELSEVIER SCIENCE INC. 2006: 100M
View details for Web of Science ID 000241442800237
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Influence of intra-luminal tissue on myocardial injury after stent implantation with intravascular ultrasound observation
EXCERPTA MEDICA INC-ELSEVIER SCIENCE INC. 2006: 100M
View details for Web of Science ID 000241442800236
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A novel expandable rotational atherectomy/aspiration system: An intravascular ultrasound study of the first human cases
EXCERPTA MEDICA INC-ELSEVIER SCIENCE INC. 2006: 122M
View details for Web of Science ID 000241442800294
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Intravascular ultrasound analysis of bifurcation lesions treated with a novel drug-eluting dedicated bifurcation stent system: Intravascular ultrasound results of the AXXESS Plus trial
EXCERPTA MEDICA INC-ELSEVIER SCIENCE INC. 2006: 41M
View details for Web of Science ID 000241442800088
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Predictors of recurrent in-stent restenosis after beta-radiation: An analysis from the START 40/20 trial.
Journal of interventional cardiology
2006; 19 (5): 376-380
Abstract
The purpose of this study was to identify potential predictors, including clinical, procedural, angiographic, and intravascular ultrasound (IVUS) parameters, for recurrent in-stent restenosis (ISR) following beta-radiation 90Strontium/Yttrium (90Sr/Y) in a large multicenter trial.Although adjunct brachytherapy reduces recurrent ISR after primary catheter-based intervention, recurrence of stenosis after brachytherapy still occurs.We analyzed 185 IVUS cohort patients in the STent And Restenosis Therapy (START) 40/20 trial where a 40-mm, 90Sr/Y, radioactive source train was exclusively used for treatment of ISR to be treatable with a 20-mm balloon.Thirty-nine patients underwent target lesion revascularization. Preliminary univariate analysis showed that age, smoking, balloon/artery ratio, geographic miss, minimum lumen diameter, and diameter stenosis at baseline were associated with target lesion revascularization, while none of IVUS variables were (minimum lumen area, minimum stent area, or residual plaque burden). The multivariate logistic regression analysis showed that younger age, lower balloon/artery ratio, and presence of geographic miss were independent predictors of target lesion revascularization.Even with adjunct beta-radiation therapy, initial mechanical optimization, such as appropriate balloon sizing and positioning, may be critical for the prevention of recurrent ISR.
View details for PubMedID 17020560
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Axial plaque redistribution after coronary stent deployment.
journal of invasive cardiology
2006; 18 (8): E225-6
Abstract
We report a case of axial plaque redistribution after coronary stent deployment assessed by intravascular ultrasound (IVUS) as well as coronary angiography. A 72-year-old male with a history of hypertension, hyperlipidemia and a nuclear stress test demonstrating anterior and lateral ischemia was admitted for cardiac catheterization. Coronary angiography and IVUS examination revealed eccentric stenoses in the left anterior descending artery (LAD) and the left circumflex artery (LCx), just before the bifurcation of the first obtuse marginal branch. After successful LAD stent placement, the LCx was also stented, jailing the obtuse marginal branch. Immediately after dilatation, however, the coronary angiogram showed a new significant stenosis at the distal adjacent segment. IVUS examination after administration of nitroglycerin revealed a secondary critical lesion that was not observed before the interventional procedure. A significant plaque increase at the new lesion site presumably resulted from axial plaque redistribution (extrusion from the stented segment, otherwise known as plaque shift). After additional stenting, the patient had an uneventful course.
View details for PubMedID 16877793
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Intravascular ultrasonic analysis of atherosclerotic vessel remodeling and plaque distribution of stenotic left anterior descending coronary arterial bifurcation lesions upstream and downstream of the side branch
AMERICAN JOURNAL OF CARDIOLOGY
2006; 98 (2): 193-196
Abstract
Bifurcation lesions remain a challenging lesion subset, even in the era of drug-eluting stents. The aim of this study was to investigate the longitudinal remodeling pattern and cross-sectional plaque location of bifurcation lesions. Seventy-four preintervention intravascular ultrasound studies of left anterior descending bifurcation lesions were analyzed, in which the lesion was located proximal (type A, n=32) or distal (type B, n=42) to the side branch. Vessel area and plaque area at the lesion (VAlesion and PAlesion) and at the reference site (VAreference and PAreference) were measured. The remodeling ratio was defined as VAlesion/VAreference, and the vessel compensation ratio was defined as (VAlesion-VAreference)/(PAlesion-PAreference). The geometric center of the lumen at the lesion site was identified, and the lesion site was divided into circumferential equal arcs to compare the cross-sectional distribution of percentage plaque area (100x[PAlesion/VAlesion]) between the 2 groups. The remodeling ratio (1.03+/-0.15 vs 0.94+/-0.14, p=0.01) and the vessel compensation ratio (0.0+/-0.36 vs -0.37+/-0.61, p<0.01) were significantly greater in type A than in type B lesions. The circumferential distribution pattern of percentage plaque area was significantly different between the groups (analysis of variance p<0.005), with greater percentage plaque area for the vessel wall opposite from the side branch in type B lesions (46.3+/-18.0% vs 54.6+/-15.4%, type A vs type B lesions, p<0.05). In conclusion, these results suggest that a major side branch may affect longitudinal lesion remodeling as well as the circumferential location of atherosclerotic plaque.
View details for DOI 10.1016/j.amjcard.2006.01.073
View details for PubMedID 16828591
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Safety of beta radiation exposure to the non-target segment: an intravascular ultrasound dosimetric analysis.
journal of invasive cardiology
2006; 18 (7): 309-312
Abstract
The use of longer radioactive seed trains to avoid geographic miss may lead to greater radiation exposure to distal vasculature due to the natural tapering of coronary arteries. The aim of this study was to use IVUS-based dosimetric analysis to evaluate the effect of beta-radiation on angiographically normal, noninjured distal segments.We analyzed 17 in-stent restenosis cases (stent length: 20 +/- 8 mm) treated with a 40 mm 90Sr/Y source train. The prescribed dose was 18.4 Gy (reference less than or equal to 3.3 mm) or 23 Gy (reference > 3.3 mm) at 2 mm from the source. Noninjured, but fully radiated, distal reference sites were determined by angiography. Based upon the three-dimensional vessel contours obtained at baseline, the minimum dose delivered to 90% of plaque volume (Dv90) was determined. Vessel, plaque and lumen volumes and Dv90 were computed in every 2 mm subsegment (n = 52).On average, no significant serial change was observed in plaque area (5.0 +/- 2.5 mm3/mm post-treatment to 5.6 +/- 3.1 mm3/mm at 8-month follow up; p = 0.09), vessel area (10.2 +/- 3.7 to 10.3 +/- 4.0 mm3/mm; p = 0.84), or lumen area (5.2 +/- 2.0 to 4.7 +/- 1.8 mm3/mm; p = 0.19). Subsegment analysis, however, revealed a wide range of dose distribution, with a significant positive correlation between Dv90 and plaque increase (p = 0.008), as well as vessel change (p < 0.001), representing dose-dependent positive vessel remodeling following beta radiation. Consequently, no significant relationship was observed between Dv90 and lumen change.Detailed IVUS-based dosimetric analysis demonstrated that beta radiation promoted positive remodeling, preventing lumen loss despite a mild increase in plaque mass on angiographically normal, noninjured distal segments.
View details for PubMedID 16816435
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Influence of plaque calcium on neointimal hyperplasia following bare metal and drug-eluting stent implantation
CATHETERIZATION AND CARDIOVASCULAR INTERVENTIONS
2006; 67 (6): 866-869
Abstract
To examine the influence of vessel wall calcium on neointimal hyperplasia (NIH) following bare metal stent (BMS) and drug-eluting stent (DES) implantation.While procedural complications with coronary stenting in calcified lesions are well reported, little is known about subsequent NIH on plaque calcium following either BMS or DES implantation.In the Study to COmpare REstenosis Rate between QueST and QuaDDS-QP2 (SCORE) trial, 6 months follow-up volumetric intravascular ultrasound data were available for 41 lesions (BMS, 19; DES, 22). NIH thicknesses on superficial, deep, and noncalcified plaque were calculated at every 0.5 mm intervals over the stented segment. Calcified and less-calcified cross-sections were defined as those containing arcs of plaque calcium > or = 90 degrees and < 90 degrees , respectively.In BMS, mean NIH thickness on both superficial (0.24 +/- 0.23 mm) and deep calcium (0.25 +/- 0.21 mm) was significantly smaller than that of noncalcified plaque (0.31 +/- 0.22 mm) (P < 0.0005). NIH area was significantly smaller in calcified cross-sections compared to less-calcified cross-sections (2.1 +/- 1.2 mm2 vs. 3.1 +/- 1.9 mm2, P < 0.0001). While in contrast, in DES, mean NIH thickness was similar, irrespective of the presence or location of calcium (0.03 +/- 0.05 mm vs. 0.03 +/- 0.06 mm vs. 0.03 +/- 0.05 mm, superficial vs. deep vs. noncalcified plaque, P = NS). NIH area was also similar between calcified and less-calcified cross-sections (0.3 +/- 0.6 mm2 vs. 0.3 +/- 0.6 mm2, P = NS).These results suggest that while plaque calcium may influence NIH following BMS implantation, NIH suppression using DES does not appear to be affected by the presence or location of calcium.
View details for DOI 10.1002/ccd.20708
View details for PubMedID 16649232
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Mechanisms of lumen narrowing of saphenous vein bypass grafts 12 months after implantation: An intravascular ultrasound study
AMERICAN HEART JOURNAL
2006; 151 (3): 726-729
Abstract
Previous long-term (>1 year) studies have suggested that saphenous vein bypass grafts (SVGs) undergo vascular remodeling similar to native coronary arteries. However, early morphologic stages of SVG remodeling have not been characterized in vivo.Thirty SVGs were studied 12 months after implantation using an intravascular ultrasound automated pullback system. Intravascular ultrasound images were analyzed between 10 and 60 mm from the tip of the guide. Lumen area (LA), intima area (IA), and vessel area (VA, defined as the area within the outer border of a hypoechoic intimal layer) were computed at 3 cross sections: the minimum LA (MLA) site and the proximal and distal reference sites. Area changes (Delta) were calculated as the MLA site minus the average of the reference sites.In this cohort, 70% of the MLA sites had a smaller VA than the average references. On average, MLA sites had significantly smaller VA (9.7 +/- 2.9 vs 10.7 +/- 3.2 mm2, P < .01) and larger IA (2.5 +/- 2.1 vs 1.2 +/- 1.3 mm2, P < .01) than at the reference sites. The relative contribution of DeltaVA (-1.0 +/- 1.4 mm2) and DeltaIA (1.3 +/- 1.3 mm2) to lumen compromise (-2.3 +/- 1.4 mm2) were 43% and 57%, respectively. On the other hand, simple linear regression analysis revealed a significant positive correlation between DeltaIA and DeltaVA (y = -1.7 + 0.52x, r = 0.50, P < .01).Within the first year, the mechanism of lumen compromise in SVG is a combination of negative remodeling and intimal hyperplasia. Positive remodeling is seen in a minority of cases. However, the direction and extent of remodeling correlated with change in intimal thickness.
View details for DOI 10.1016/j.ahj.2005.05.011
View details for Web of Science ID 000236353900027
View details for PubMedID 16504641
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Twelve-month intravascular ultrasound results from STEALTH-1: A randomized first in man trial of Biolimus A9 eluting stents
i2 Summit 2006 on Innovation in Intervention
ELSEVIER SCIENCE INC. 2006: 39B–39B
View details for Web of Science ID 000235530500166
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Nonuniform strut distribution is associated with more neointimal hyperplasia after ABT-578 eluting stent implantation: A 3-D IVUS analysis from the ENDEAVOR 2 trial
ELSEVIER SCIENCE INC. 2006: 2B
View details for Web of Science ID 000235530500008
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Comparison of vascular response to ABT-578 versus sirolimus eluting stent implantation: Intravascular ultrasound results from ENDEAVOR 3
ELSEVIER SCIENCE INC. 2006: 21B–22B
View details for Web of Science ID 000235530500093
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Heterogeneity of neointimal distribution of in-stent restenosis in patients with diabetes mellitus
AMERICAN JOURNAL OF CARDIOLOGY
2006; 97 (3): 340-342
Abstract
Diabetes mellitus is an independent predictor of restenosis after percutaneous coronary intervention. The pattern of restenosis after bare metal stent implantation in diabetic patients was examined with 3-dimensional intravascular ultrasound analysis. Lumen and stent were manually traced at every 0.5-mm interval in stented segments. Using Simpson's method, stent, luminal, and neointimal (stent minus lumen) volumes were calculated and average area was calculated as volume data divided by length. To measure the cross-sectional and longitudinal severities of luminal encroachment by the neointima, percent neointimal area (neointimal area divided by stent area) and neointimal hyperplasia 50 (IH50) (defined as percent stent length with percent neointimal area >50%) were calculated. In 278 patients (68 with diabetes and 210 without diabetes), there was a significantly higher percentage of maximal percent neointimal area with significantly longer percent stent length that was severely encroached by the neointima in diabetic patients. Diabetic patients showed a more heterogenous pattern of the neointima after bare metal stenting, resulting in longer high-grade obstruction segments. This may have important implications for stent design and pharmacokinetic properties of next-generation drug-eluting technology for this complex patient subset.
View details for DOI 10.1016/j.amjcard.2005.08.067
View details for Web of Science ID 000235265400009
View details for PubMedID 16442392
- Intravascular imaging techniques Cardiac Catheterization, Angioplasty and Intervention 2006: 371-394
- Next generation drug-eluting stents Drug-Eluting Stent 2 2006: 100-105
- Available transcatheter mitral valve repair techniques: CS method Transcathter Valve Repair 2006: 285-294
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Transient left ventricular dysfunction under severe stress: Brain-heart relationship revisited
AMERICAN JOURNAL OF MEDICINE
2006; 119 (1): 10-17
Abstract
Transient left ventricular dysfunction in patients under emotional or physical stress, also known as tako-tsubo-like left ventricular dysfunction, has been recently been recognized as a distinct clinical entity. The aims of this review are to define this phenomenon and to explore its similarities to the left ventricular dysfunction seen in patients with acute brain injury.MEDLINE database, bibliographies of each citation for relevant articles, and consultation with clinical experts were used to examine the clinical picture of tako-tsubo-like left ventricular dysfunction.We identified case series and a systematic review that report on patients with this syndrome. This phenomenon occurs predominantly in female patients, presenting with a variety of ST-T segment changes and mildly elevated cardiac enzymes that mimic an acute coronary syndrome. The left ventricular dysfunction, typically showing a hyperkinetic basal region and an akinetic apical half of the ventricle, occurs in the absence of obstructed epicardial coronary arteries. The ventricular dysfunction usually resolves within weeks with a generally favorable prognosis. This phenomenon has similarities to that seen in patients with acute brain injury with regard to clinical presentation, pathology, and its reversible nature.Transient left ventricular dysfunction occurs in the absence of obstructive epicardial coronary artery disease. In its broadest sense, this phenomenon may encompass a range of disorders including left ventricular dysfunction after central nervous system injury.
View details for DOI 10.1016/j.amjmed.2005.08.022
View details for Web of Science ID 000234912000005
View details for PubMedID 16431176
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Impact of asymmetric stent expansion on neointimal hyperplasia following sirolimus-eluting stent implantation
AMERICAN JOURNAL OF CARDIOLOGY
2005; 96 (10): 1404-1407
Abstract
To assess whether asymmetric stent expansion affects suppression of neointimal hyperplasia after sirolimus-eluting stent implantation, 64 patients in the SIRolImUS-coated Bx Velocity stent trial who underwent single 18-mm stent implantation and 3-dimensional intravascular ultrasonography at 8-month follow-up were enrolled. To assess the longitudinal stent asymmetric expansion, 2 cross sections with a maximal/minimal stent area were chosen in each patient. To assess for tomographic stent asymmetric expansion, stent eccentricity was determined by dividing the minimum stent diameter by the maximum stent diameter. At the 2 cross sections with a maximal/minimal stent area, a sirolimus-eluting stent reduced neointimal hyperplasia significantly with no interaction between the treatment and stent areas. A sirolimus-eluting stent also significantly reduced neointimal hyperplasia in the concentric and eccentric stent groups.
View details for DOI 10.1016/j.amjcard.2005.07.044
View details for Web of Science ID 000233509900012
View details for PubMedID 16275187
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Predictors of edge stenosis following sirolimus-eluting stent deployment (A quantitative intravascular ultrasound analysis from the SIRIUS trial)
AMERICAN JOURNAL OF CARDIOLOGY
2005; 96 (9): 1251-1253
Abstract
To study the interaction of the sirolimus-eluting stent and vessel margins, we analyzed the intravascular ultrasound parameters in 317 edges of 167 stents having 18 edge stenoses at 8 months of follow-up from the SIRIUS trial. Of the baseline parameters, a larger reference percentage of plaque area and a larger edge stent area/reference minimum lumen area were associated with edge stenosis in the sirolimus-eluting stent cohort compared with the incidence of edge stenosis in the bare metal stent cohort. Thus, full lesion coverage and matching the stented segment properly to the adjacent segment using intravascular ultrasound guidance may improve sirolimus-eluting stent implantation efficacy further.
View details for DOI 10.1016/j.amjcard.2005.06.066
View details for Web of Science ID 000233343500015
View details for PubMedID 16253592
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Impact of intravascular ultrasound lesion characteristics on neointimal hyperplasia following sirolimus-eluting stent implantation
AMERICAN JOURNAL OF CARDIOLOGY
2005; 96 (9): 1237-1241
Abstract
The effect of lesion characteristics on neointimal hyperplasia after sirolimus-eluting stent implantation was examined in 45 patients who underwent successful preinterventional intravascular ultrasound. There were no differences in neointimal hyperplasia between the moderate/severe calcified lesion group (calcium arc >120 degrees ) and the non/mild calcified lesion group or between the positive vessel remodeling group (external elastic membrane area at the minimal lumen area site larger than that at the proximal reference site) and negative vessel remodeling group. No correlation between preinterventional plaque burden and neointimal hyperplasia was found. In patients who have coronary artery disease, sirolimus-eluting stents continue to demonstrate striking suppression of neointimal proliferation, irrespective of lesion characteristics previously associated with greater restenotic risk.
View details for DOI 10.1016/j.amjcard.2005.06.063
View details for Web of Science ID 000233343500012
View details for PubMedID 16253589
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Characteristics of late incomplete stent apposition: A comparison among bare metal stents, intracoronary radiation, and drug-eluting stents
78th Annual Scientific Session of the American-Heart-Association
LIPPINCOTT WILLIAMS & WILKINS. 2005: U800–U800
View details for Web of Science ID 000232956405106
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Sirolimus-eluting stents vs. intracoronary brachytherapy for the treatment of in-stent restenosis: A serial intravascular ultrasound analysis
LIPPINCOTT WILLIAMS & WILKINS. 2005: U834
View details for Web of Science ID 000232956405253
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Sirolimus-eluting stent implantation in small coronary arteries: Predictors of long-term stent patency and neointimal hyperplasia
LIPPINCOTT WILLIAMS & WILKINS. 2005: U800
View details for Web of Science ID 000232956405105
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Vascular response after overlapping sirolimus-eluting stent implantation: Serial intravascular ultrasound analysis
LIPPINCOTT WILLIAMS & WILKINS. 2005: U834
View details for Web of Science ID 000232956405251
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Safety and feasibility of novel guidewire-based self-expanding stent delivery system
17th Annual Transcatheter Cardiovascular Therapeutics Symposium/4th Annual Transcatheter Cardiovascular Therapeutics Inflammation Summit
EXCERPTA MEDICA INC-ELSEVIER SCIENCE INC. 2005: 33H–33H
View details for Web of Science ID 000232725200069
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Prospective comparison of sirolimus-eluting stents vs. intracoronary brachytherapy for the treatment of in-stent restenosis
EXCERPTA MEDICA INC. 2005: 98H
View details for Web of Science ID 000232725200236
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Intravascular ultrasound analysis of sirolimus-eluting stents for the treatment of in-stent restenosis: Results from the TROPICAL trial
17th Annual Transcatheter Cardiovascular Therapeutics Symposium/4th Annual Transcatheter Cardiovascular Therapeutics Inflammation Summit
EXCERPTA MEDICA INC-ELSEVIER SCIENCE INC. 2005: 95H–95H
View details for Web of Science ID 000232725200226
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Late incomplete stent apposition after sirolimus-eluting stent implantation - A serial intravascular ultrasound analysis
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY
2005; 46 (6): 1002-1005
Abstract
We sought to identify the frequency of incomplete stent apposition (ISA) in sirolimus-eluting stents (SES) and clarify its findings and clinical sequelae.Late-acquired ISA has been reported in bare-metal stents (BMS) and brachytherapy and recently in drug-eluting stents. However, the characteristics of late ISA in SES have not been clarified.From the SIRIUS trial, a randomized, multicenter study comparing SES and BMS, serial qualitative intravascular ultrasound (IVUS; at stent implantation and eight-month follow-up) was available in 141 patients (BMS: n = 61; SES: n = 80). The IVUS images were reviewed for the presence of ISA.Incomplete stent apposition at follow-up was observed in 19 patients (BMS: n = 6 [9.8%]; SES: n = 13 [16.3%]; p = NS). Among these, 12 had ISA after intervention and at follow-up (persistent ISA). Late-acquired ISA was seen in the remaining seven cases, all from the SES group (BMS: n = 0; SES: n = 7 [8.7%]; p < 0.05). In late-acquired ISA, there was an increase in external elastic membrane area (after intervention: 16.2 +/- 2.7 m2; follow-up: 18.9 +/- 3.6 mm2; p < 0.05). The location of stent-vessel wall separation was primarily at the stent edges in persistent ISA cases, whereas late-acquired ISA in SES occurred mostly in the mid portion of the stent. There were no negative clinical events reported for any ISA cases at 12-month clinical follow-up.Late ISA was observed in 8.7% of patients after SES implantation. There were no negative clinical events associated with this IVUS finding at 12-month clinical follow-up; however, careful long-term follow-up will be necessary.
View details for DOI 10.1016/j.jacc.2005.05.068
View details for Web of Science ID 000231991600009
View details for PubMedID 16168282
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Effect of lumen narrowing within coronary stents on proximal and distal vessel segments following bare metal stent implantation
AMERICAN JOURNAL OF CARDIOLOGY
2005; 96 (3): 376-378
Abstract
Adjacent reference vessel response to smaller lumens at stented segments was examined with 3-dimensional intravascular ultrasound analysis. In 128 patients after bare metal stent implantation, minimal lumen area (MLA) within the stent and average lumen area at distal/proximal adjacent reference segments (5 mm) were obtained at baseline and follow-up. In the smaller in-stent MLA group (MLA <3 mm2), lumen area decreased significantly at the distal edge compared with the larger in-stent MLA group (MLA > or =3 mm2), although no significant difference was seen at the proximal edge. In-stent lumen patency may influence vascular responses at adjacent reference segments after bare metal stent implantation.
View details for DOI 10.1016/j.amjcard.2005.03.079
View details for Web of Science ID 000231057000011
View details for PubMedID 16054461
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Impact of different definitions on the interpretation of coronary remodeling determined by intravascular ultrasound
CATHETERIZATION AND CARDIOVASCULAR INTERVENTIONS
2005; 65 (2): 233-239
Abstract
The objective of this study was to compare the categorizations and determinants related to remodeling by the three definitions commonly used. Several morphological and intravascular ultrasound (IVUS) studies have demonstrated the fundamental importance of arterial remodeling in atherosclerosis. However, lack of consensus on how to define remodeling has led to conflicting analyses of factors that influence this process. Analysis of pre-interventional IVUS images of 514 lesions in native coronary arteries was performed. Arterial remodeling was defined as outward by definition 1, when [cross-sectional area (CSA) of the external elastic membrane (EEM) at the lesion site (EEM(lesion))]/[EEM CSA either at the proximal (EEM(prox ref)) or distal (EEM(distal ref)) reference site with the least amount of plaque] was > 1.05, intermediate when this ratio was between 0.95 and 1.05, and inward when < 0.95. Remodeling was defined as outward by definition 2 when EEM(lesion) > both EEM(prox ref) and EEM(distal ref), inward when EEM(lesion) < both EEM(prox ref) and EEM(distal ref), and intermediate when EEM(lesion) was intermediate between EEM(prox ref) and EEM(distal ref). By definition 3, vessel remodeling was defined as outward when EEM(lesion) > (EEM(prox ref) + EEM(distal ref))/2 and intermediate/inward when EEM(lesion) < or = (EEM(prox ref) + EEM(distal ref))/2. The frequency of outward remodeling was significantly higher by definitions 1 and 3 than by definition 2, whereas a higher frequency of inward remodeling was observed in definition 1, resulting in significantly different remodeling distributions between the three definitions (P < 0.0001). By multivariate logistic analysis, the only clinical determinants related to outward remodeling was younger age, and only by definition 3. IVUS determinants varied significantly between the three definitions. The only consistent determinants among the three definitions were smaller lumen CSA at the reference site and larger plaque + media CSA at the lesion site. This study demonstrates the significant impact of different remodeling definitions on the incidence and determinants of remodeling patterns. The marked variability in categorization of remodeling underscores the importance of developing a standard methodology.
View details for DOI 10.1002/ccd.20366
View details for Web of Science ID 000229557600015
View details for PubMedID 15812811
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Transient left ventricular apical ballooning
ANNALS OF INTERNAL MEDICINE
2005; 142 (8): 678-678
View details for Web of Science ID 000228410400019
View details for PubMedID 15838081
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Assessment of fibrous cap thickness in lipid-rich plaques by optical coherence tomography assisted with attenuation signal analysis
54th Annual Scientific Session of the American-College-of-Cardiology
ELSEVIER SCIENCE INC. 2005: 45A–45A
View details for Web of Science ID 000226808200192
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Intravascular ultrasound assessment of the safety and efficacy of heparin-coated sirolimus-eluting stent in small vessel stenting
54th Annual Scientific Session of the American-College-of-Cardiology
ELSEVIER SCIENCE INC. 2005: 72A–72A
View details for Web of Science ID 000226808200308
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Efficacy of reduced sirolimus doses on neointimal hyperplasia: Serial IVUS analyses from the REDOX trial
54th Annual Scientific Session of the American-College-of-Cardiology
ELSEVIER SCIENCE INC. 2005: 43A–44A
View details for Web of Science ID 000226808200185
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High resolution ex vivo magnetic resonance imaging of human coronary arteries: A comparison with intravascular ultrasound imaging
54th Annual Scientific Session of the American-College-of-Cardiology
ELSEVIER SCIENCE INC. 2005: 77A–77A
View details for Web of Science ID 000226808200331
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Impending coronary perforation after cutting balloon angioplasty.
Heart
2005; 91 (1)
View details for PubMedID 15604315
View details for PubMedCentralID PMC1768613
- Future directions of drug-eluting stent technology Coronary Intervention 2005; 1 (1): 96-101
- New treatment technologies for coronary artery disease: other techniques Practical Cardiology: Coronary Artery Disease II 2005; 5: 158-164
- Percutaneous coronary sinus repair of mitral regurgitation Interventional Cardiology: Current Best Practice 2005: 69-86
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Time course of neointimal hyperplasia growth in de novo human coronary lesions treated with the ABT-578 eluting phosphorylcholine-coated Stent implantation
77th Scientific Meeting of the American-Heart-Association
LIPPINCOTT WILLIAMS & WILKINS. 2004: 379–79
View details for Web of Science ID 000224783502120
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Relation between stent area, length, and 8-month neointimal hyperplasia after sirolimus-eluting stent implantation in small coronary arteries
LIPPINCOTT WILLIAMS & WILKINS. 2004: 734–35
View details for Web of Science ID 000224783503846
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One year results of intravascular ultrasound analysis for the ABT-578 eluting phosphorylcholine-coated stent implantation in de novo coronary lesions
77th Scientific Meeting of the American-Heart-Association
LIPPINCOTT WILLIAMS & WILKINS. 2004: 758–58
View details for Web of Science ID 000224783504085
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Atherosclerotic plaque distribution and remodeling of bifurcation lesions upstream and downstream of the side branch.
16th Annual Transcatheter Cardiovascular Therapeutics Symposium
EXCERPTA MEDICA INC-ELSEVIER SCIENCE INC. 2004: 183E–183E
View details for Web of Science ID 000224406500391
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Lumen narrowing within stent determines the vessel response in the distal adjacent reference segment after bare metal stent implantation.
EXCERPTA MEDICA INC. 2004: 157E
View details for Web of Science ID 000224406500337
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Impact of final Stent dimensions on long-term results following sirolimus-eluting stent implantation - Serial intravascular ultrasound analysis from the SIRIUS trial
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY
2004; 43 (11): 1959-1963
Abstract
We assessed the predictive value of minimum stent area (MSA) for long-term patency of sirolimus-eluting stents (SES) implantation compared to bare metal stents (BMS).Although MSA is a consistent predictor of in-stent restenosis, its predictive value in BMS is still limited because of biologic variability in the restenosis process.From the SIRolImUS (SIRIUS) trial, 122 cases (SES: 72; BMS: 50) with complete serial intravascular ultrasound (IVUS) (baseline and 8-month follow-up) were analyzed. Postprocedure MSA and follow-up minimum lumen area (MLA) were obtained. Based on previous physiologic studies, adequate stent patency at follow-up was defined as MLA >4 mm(2).In both groups, a significant positive correlation was observed between baseline MSA and follow-up MLA (SES: p < 0.0001, BMS: p < 0.0001). However, SES showed higher correlation than BMS (0.8 vs. 0.65) with a higher regression coefficient (0.92 vs. 0.59). The sensitivity and specificity curves identified different optimal thresholds of MSA to predict adequate follow-up MLA: 5 mm(2) for SES and 6.5 mm(2) for BMS. The positive predictive values with these cutoff points were 90% and 56%, respectively.In this SIRIUS IVUS substudy, SES reduced both biologic variability and restenosis, resulting in increased predictability of long-term stent patency with postprocedure MSA. In addition, SES had a considerably lower optimal MSA threshold compared to BMS.
View details for DOI 10.1016/j./jacc.2004.01.044
View details for Web of Science ID 000221715800006
View details for PubMedID 15172398
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Validation of a thermographic guidewire for endoluminal mapping of atherosclerotic disease: An in vitro study
CATHETERIZATION AND CARDIOVASCULAR INTERVENTIONS
2004; 62 (2): 221-229
Abstract
Temperature heterogeneity along the inner surface of an artery may be a surrogate marker of impending plaque rupture and has been associated with an increased likelihood of future coronary events. Initial studies using catheter-based thermographic devices have demonstrated that the changes in temperature are subtle, while the effects of coronary flow on measured temperature have not yet been examined. A novel guidewire-based system (ThermoCoil, Imetrx) designed to measure surface temperature in coronary arteries was used to study the effects of heat source intensity and flow on measured temperature. An in vitro model of a focal, eccentric, heat-generating lesion demonstrated that a guidewire-based system can detect changes in surface temperature with a precision of less than 0.08 degrees C. In this model, temperature measurements increased linearly with source temperature and decreased with increases in flow by an exponent of -0.33 (P < 0.001 for both). Flow rates and heat source properties can significantly influence the measurement and interpretation of thermographic data. The incorporation of 2D thermographic images may contribute further to the characterization of metabolically active plaques likely to cause acute coronary syndromes.
View details for DOI 10.1002/ccd.10750
View details for PubMedID 15170716
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Six- and twelve-month results from first human experience using everolimus-eluting stents with bioabsorbable polymer
CIRCULATION
2004; 109 (18): 2168-2171
Abstract
Everolimus, an active immunosuppressive and antiproliferative agent of the same family as sirolimus (rapamycin), has demonstrated significant reduction of neointimal proliferation in animal studies. The First Use To Underscore restenosis Reduction with Everolimus (FUTURE) I trial was the first in-human experience to evaluate the safety and efficacy of everolimus-eluting stents (EES), coated with a bioabsorbable polymer, compared with bare metal stents (BMS).FUTURE I was a prospective, single-blind, randomized trial that enrolled 42 patients with de novo coronary lesions (EES 27, BMS 15). Patient and lesion characteristics were comparable between the groups. Major adverse cardiac event rates were low at 30 days and 6 months, without any early or late stent thrombosis for either group (P=NS). Between 6 and 12 months, there were no additional reports of major adverse cardiac events. The 6-month angiographic in-stent restenosis rate was 0% versus 9.1% (1 patient) (P=NS), with an associated late loss of 0.11 mm versus 0.85 mm (P<0.001), and the in-segment restenosis rate was 4% (1 patient) and 9.1% (1 patient) (P=NS) for EES and BMS, respectively. Intravascular ultrasound analysis revealed a significant reduction of percent neointimal volume in EES compared with BMS (2.9+/-1.9 mm3/mm versus 22.4+/-9.4 mm3/mm, P<0.001). There was no late stent malapposition in either group. The safety and efficacy of the EES appeared to be sustained at 12 months.In this initial clinical experience, EES with bioabsorbable polymer demonstrated a safe and efficacious method to reduce in-stent neointimal hyperplasia and restenosis.
View details for DOI 10.1161/01.CIR.0000128850.84227.FD
View details for Web of Science ID 000221322600003
View details for PubMedID 15123533
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Conditions associated with ST-segment elevation
NEW ENGLAND JOURNAL OF MEDICINE
2004; 350 (11): 1152-1153
View details for Web of Science ID 000220110100023
View details for PubMedID 15014192
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Impact of stent implantation techniques on stent edge neointimal hyperplasia following sirolimus-eluting stenting
53rd Annual Scientific Session of the American-College-of-Cardiology
ELSEVIER SCIENCE INC. 2004: 84A–85A
View details for Web of Science ID 000189388500355
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Longitudinal vessel remodeling pattern following. sirolimus-eluting stent implantation: Analysis of vessel integrity throughout target segment
ELSEVIER SCIENCE INC. 2004: 66A
View details for DOI 10.1016/S0735-1097(04)90275-6
View details for Web of Science ID 000189388500277
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Impact of coronary artery bending at stent edges on subsequent plaque proliferation: A serial volumetric itravascular ultrasound analysis
ELSEVIER SCIENCE INC. 2004: 85A
View details for DOI 10.1016/S0735-1097(04)90354-3
View details for Web of Science ID 000189388500356
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First human experience with the ABT-578 eluting phosphorylcholine polymer stent: A serial volumetric intravascular ultrasound analysis from the PREFER trial
ELSEVIER SCIENCE INC. 2004: 67A
View details for Web of Science ID 000189388500280
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Impact of periprocedural plaque/thrombus reduction on myocardial injury after stent deployment
ELSEVIER SCIENCE INC. 2004: 55A
View details for DOI 10.1016/S0735-1097(04)90231-8
View details for Web of Science ID 000189388500233
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Effect of everolimus-eluting stents in preventing neointimal hyperplasia: An intravascular ultrasound analysis from the FUTURE II trial
53rd Annual Scientific Session of the American-College-of-Cardiology
ELSEVIER SCIENCE INC. 2004: 66A–66A
View details for Web of Science ID 000189388500278
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Morphological characteristics of de novo coronary lesions presenting with plaque rupture: An intravascular ultrasound study
53rd Annual Scientific Session of the American-College-of-Cardiology
ELSEVIER SCIENCE INC. 2004: 73A–73A
View details for Web of Science ID 000189388500304
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Intravascular ultrasound analysis of the new ABT-578 eluting phosphorylcholine-coated stent implantation to de novo human coronary lesions: The ENDEAVOR I trial
53rd Annual Scientific Session of the American-College-of-Cardiology
ELSEVIER SCIENCE INC. 2004: 85A–85A
View details for Web of Science ID 000189388500358
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An intravascular ultrasound analysis from FUTURE I, the first human experience using everolimus-eluting stents: Six- and 12-month results
53rd Annual Scientific Session of the American-College-of-Cardiology
ELSEVIER SCIENCE INC. 2004: 85A–86A
View details for Web of Science ID 000189388500359
- Paclitaxel-eluting stent Drug-Eluting Stent 2004: 74-82
- Other drug-eluting stents Drug-Eluting Stent 2004: 105-110
- Dexamethasone-eluting stent (Dexamet?) Drug-Eluting Stent 2004: 83-88
- Sirolimus-eluting stent (CYPHER?) Drug-Eluting Stent 2004: 63-73
- Left main coronary disease: an IVUS perspective Coronary Intervention 2004; 3 (2): 16-22
- Estradiol-eluting stent Drug-Eluting Stent 2004: 101-104
- Drug-eluting stent: basic components Drug-Eluting Stent 2004: 40-50
- ABT-578-eluting stent Drug-Eluting Stent 2004: 98-100
- Drug-eluting stent for the treatment of in-stent restenosis Drug-Eluting Stent 2004: 116-122
- Paclitaxel-eluting stent Jpn J Cardiovasc Ther 2004; 4 (2): 148-153
- Thrombectomy and distal protection: protection of coronary microcirculation and myocardium Coronary Intervention 2004: 199-206
- Lessons from failed drug-eluting stents Drug-Eluting Stent 2004: 111-115
- IVUS observations of drug-eluting stents Drug-Eluting Stent 2004: 128-138
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Tako-tsubo-like left ventricular dysfunction
CIRCULATION
2003; 108 (23): E158
View details for DOI 10.1161/01.CIR.0000102942.24174.AE
View details for Web of Science ID 000187070100004
View details for PubMedID 14662694
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Late incomplete stent apposition and focal vessel expansion after bare metal stenting
AMERICAN JOURNAL OF CARDIOLOGY
2003; 92 (10): 1217-1219
Abstract
Late incomplete stent apposition was observed in 2.4% of the 412 stented segments studied by serial intravascular ultrasound analyses. Most of these phenomena and all late vessel expansions with incomplete stent apposition developed in vessels in which lesions were treated by atherectomy before stenting, suggesting a potential association between mechanical injury from debulking and these phenomena.
View details for Web of Science ID 000186638600019
View details for PubMedID 14609603
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Risk factors for neointimal hyperplasia following sirolimus-eluting stent implantation
76th Annual Scientific Session of the American-Heart-Association
LIPPINCOTT WILLIAMS & WILKINS. 2003: 702–
View details for Web of Science ID 000186360603237
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Sirolimus-eluting stent: Effect on instent and edge neointimal proliferation in small vessels
LIPPINCOTT WILLIAMS & WILKINS. 2003: 702
View details for Web of Science ID 000186360603238
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Impact of asymmetric stent expansion on neointimal hyperplasia after sirolimus-eluting stent implantation
15th Annual Transcatheter Cardiovascular Therapeutics Symposium
EXCERPTA MEDICA INC-ELSEVIER SCIENCE INC. 2003: 187L–187L
View details for Web of Science ID 000185385600444
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Everolimus-eluting stents are effective in preventing neointimal hyperplasia regardless of the vessel diameter: An intravascular ultrasound subanalysis of the FUTURE I trial
EXCERPTA MEDICA INC. 2003: 184L
View details for Web of Science ID 000185385600435
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Plaque burden is not a risk factor for neointimal growth after sirolimus-eluting stent implantation
EXCERPTA MEDICA INC. 2003: 187L
View details for Web of Science ID 000185385600443
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Late incomplete apposition with excessive remodeling of the stented coronary artery following intravascular brachytherapy
AMERICAN JOURNAL OF CARDIOLOGY
2003; 92 (5): 587-590
Abstract
Intravascular brachytherapy may cause "exaggerated" vessel remodeling with late incomplete apposition in segments that have little disease, which are exposed to higher radiation doses. The long-term clinical impact of this finding is unclear.
View details for DOI 10.1016/S0002-9149(03)00728-8
View details for PubMedID 12943881
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Stent thrombosis - An issue revisited in a changing world
CIRCULATION
2003; 108 (1): 2-5
View details for DOI 10.1161/01.CIR.0000075929.79964.D8
View details for Web of Science ID 000183991600012
View details for PubMedID 12847051
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High prevalence of silent myocardial ischemia amongst Asian Americans
Asia Pacific Scientific Forum on New Discoveries in Cardiovascular Disease and Stroke
LIPPINCOTT WILLIAMS & WILKINS. 2003: E158–E158
View details for Web of Science ID 000183014500163
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Coronary vasodilation by noninvasive transcutaneous ultrasound - An in vivo canine study
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY
2003; 41 (9): 1623-1627
Abstract
We evaluated the coronary vasodilatory effects of transcutaneous low-frequency (27-kHz) ultrasound (USD).Ultrasound has been shown to affect vascular function.Ultrasound energy was administered transcutaneously to 12 dogs. Coronary arterial dimensions were assessed using intravascular coronary ultrasound (IVUS) and quantitative coronary angiography (QCA).The IVUS mid-left anterior descending (LAD) luminal area was 6.77 +/- 1.27 mm(2) at baseline. After 30 s of ultrasound, this area increased by 9% (7.40 +/- 1.44 mm(2), p < 0.05), after 3 min by 19% (8.05 +/- 1.72 mm(2), p < 0.05) and after 5 min increased by 21% (8.16 +/- 1.29 mm(2), p < 0.05). The mean coronary diameter (2.69 +/- 0.33 mm) at baseline (QCA of three segments of LAD and three segments of left circumflex coronary artery) increased by 19.3% (3.21 +/- 0.28 mm) after 5 min of USD exposure. After a 90-min observation period there was a return to baseline values (p = NS). Intracoronary nitroglycerin (NTG) administered to five dogs revealed a similar magnitude of vasodilation as USD.Noninvasive, transthoracic low-frequency USD energy results in coronary artery vasodilation within seconds of exposure. The vasodilation is reversible and is similar in magnitude to that induced by NTG. Further evaluation is needed to assess its potential applications in humans.
View details for DOI 10.1016/S0735-1097(03)00412-1
View details for Web of Science ID 000182631800030
View details for PubMedID 12742306
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Noninvasive transcutaneous ultrasound augments thrombolysis in the left circumflex coronary artery - an in vivo canine study
THROMBOSIS RESEARCH
2003; 110 (2-3): 149-158
Abstract
Ultrasound has the potential to augment chemical thrombolysis.Thrombotic occlusions in the left circumflex artery (LCx) were induced in 27 dogs. Sixty minutes later, tissue-type plasminogen activator (t-PA) was given intravenously over 90 min. Thrombotic occlusions (n = 20) were treated with concomitant transcutaneous low frequency (27 kHz), continuous wave (CW) (n = 10) or pulsed wave (PW) (n = 10) ultrasound. Tissue-type plasminogen activator plus ultrasound (n = 20) vs. tissue-type plasminogen activator alone (n=7) resulted in more frequent Thrombolysis in Myocardial Infarction (TIMI) 3 flow (90% vs. 43%, P = 0.024) and less reocclusion (11% vs. 67%, P = 0.080). At 60 min, median TIMI grade flow for tissue-type plasminogen activator alone was 2 (mean: 1.43 +/- 1.40) compared to 3 (mean: 2.70 +/- 0.95) for tissue-type plasminogen activator plus continuous as well as pulsed wave ultrasound (P = 0.035). Continuous wave and pulsed wave ultrasound were equally effective in augmenting thrombolysis. Histologically, no ultrasound-mediated injury to the myocardium or coronary arteries occurred.Both transcutaneous low frequency continuous wave ultrasound and pulsed wave ultrasound enhance tissue-type plasminogen activator-mediated thrombolysis of the posterior circulation with higher TIMI 3 flow rates and less reocclusion than with tissue-type plasminogen activator alone. In addition, at the energy levels used, low frequency ultrasound appears safe.
View details for DOI 10.1016/S0049-3848(03)00335-9
View details for Web of Science ID 000184729400011
View details for PubMedID 12893030
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An optimal diagnostic threshold of minimum stent area to predict long-term stent patency following sirolimus-eluting stent implantation: Serial intravascular ultrasound analysis from the SIRIUS trial
52nd Annual Scientific Session of the American-College-of-Cardiology
ELSEVIER SCIENCE INC. 2003: 80A–80A
View details for Web of Science ID 000181669500347
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Qualitative assessment of coronary lesions treated with sirolimus-eluting stents: Serial intravascular ultrasound analysis from the SIRIUS trial
ELSEVIER SCIENCE INC. 2003: 81A
View details for Web of Science ID 000181669500350
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Exaggeration of neointimal formation associated with the critical segment in bare metal stenting
ELSEVIER SCIENCE INC. 2003: 81A
View details for Web of Science ID 000181669500352
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Incidence and characteristics of ruptured plaque in femoro-popliteal arteries
52nd Annual Scientific Session of the American-College-of-Cardiology
ELSEVIER SCIENCE INC. 2003: 303A–304A
View details for Web of Science ID 000181669501331
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Overlapping sirolimus-eluting stents: Intravascular ultrasound analysis from the SIRIUS trial
52nd Annual Scientific Session of the American-College-of-Cardiology
ELSEVIER SCIENCE INC. 2003: 81A–81A
View details for Web of Science ID 000181669500351
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Effects of sirolimus-eluting stents in diabetic patients volumetric intravascular ultrasound analysis from the SIRIUS trial
52nd Annual Scientific Session of the American-College-of-Cardiology
ELSEVIER SCIENCE INC. 2003: 73A–73A
View details for Web of Science ID 000181669500317
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Late incomplete stent apposition following sirolimus-eluting stent: Serial quantitative intravascular ultrasound analysis from the SIRIUS trial
52nd Annual Scientific Session of the American-College-of-Cardiology
ELSEVIER SCIENCE INC. 2003: 33A–33A
View details for Web of Science ID 000181669500144
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Taxol-based eluting stents from theory to human validation: clinical and intravascular ultrasound observations.
journal of invasive cardiology
2003; 15 (3): 109-114
Abstract
Treatment with antiproliferative drugs via coated stents appears to be a promising approach to both mechanically remodel target lesions and biologically reduce neointimal hyperplasia. Drug-eluting stents can maximize local drug effects and minimize the potential for systemic toxic effects. The purpose of this review is to describe the effects of a lipophilic microtubular inhibitor, paclitaxel, a strong antiproliferative agent under clinical investigation, and to define the vascular response to taxol-based eluting stents by intravascular ultrasound.
View details for PubMedID 12612382
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Relationship between neointimal regrowth and mechanism of acute lumen gain during the treatment of in-stent restenosis with or without supplementary intravascular radiation
CATHETERIZATION AND CARDIOVASCULAR INTERVENTIONS
2003; 58 (2): 162-167
Abstract
We investigated whether neointimal regrowth is related to the mechanism of acute lumen gain during the treatment of in-stent restenosis (ISR) lesions both with and without adjunct intravascular brachytherapy. From the WRIST (Washington Radiation for In-Stent Restenosis Trial) cohort, 54 ISR patients ((192)Ir, 29; placebo, 25) were treated with nonrepeat stenting percutaneous interventions (excimer laser, rotational atherectomy, and/or balloon angioplasty) prior to (192)Ir or placebo therapy. Using Simpson's method, serial volumetric intravascular ultrasound (IVUS) analyses (pre- and posttreatment and 6-month follow-up) were analyzed to obtain stent, lumen, and intimal hyperplasia (IH) volumes that were then adjusted for stent length to create stent, lumen, and IH volume indexes. In the placebo group, the acute reduction of neointima (1.6 +/- 1.4 mm(3)/mm) was counteracted by intimal regrowth (2.1 +/- 1.7 mm(3)/mm). The amount of intimal regrowth correlated directly with the intimal reduction due to the intervention (r = 0.76; P < 0.001), but not with the amount of additional stent expansion. In the (192)Ir-treated group, intimal regrowth was significantly less than in the placebo group (-0.3 +/- 0.1 vs. 2.1 +/- 1.7 mm(3)/mm; P < 0.001) despite a similar initial intimal reduction (1.3 +/- 0.9 vs. 1.6 +/- 1.4 mm(3)/mm; P = NS). No correlation was found between intimal reduction at the time of the procedure and intimal regrowth in the (192)Ir group. In this study, neointimal regrowth following treatment of ISR lesions correlates directly with the extent of acute intimal volume reduction, but not with the extent of additional stent expansion. This relation is not seen in ISR segments treated with radiation, where intimal regrowth is substantially inhibited.
View details for DOI 10.1002/ccd.10405
View details for Web of Science ID 000182814600005
View details for PubMedID 12552537
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Impact of deep vessel wall injury on acute response and remodeling of coronary artery segments after cutting balloon angioplasty
AMERICAN JOURNAL OF CARDIOLOGY
2003; 91 (1): 6-11
Abstract
Deep vessel wall injury is believed to affect vessel dimension following coronary intervention. The cutting balloon is designed to treat coronary artery stenoses with dilatation and surgical incisions, thereby reducing excess vessel injury. This study examines the effect of deep vessel wall injury on acute and late coronary arterial response after cutting balloon angioplasty. Serial volumetric intravascular ultrasound (IVUS) analyses were performed in 63 lesions treated with cutting balloon angioplasty alone. Before intervention, the longitudinal range of the lesion segment that included the smallest lumen area (LA) was determined as LA <4 mm(2) and/or LA stenosis >60%. The exact corresponding site at postintervention and follow-up was aligned using peri- and intravascular landmarks. Average vessel area (VA), plaque area (PA), and LA were measured. Lesion segments were categorized as with or without deep vessel wall injury, which was defined as the presence of plaque/vessel wall fracture extending to the sonolucent (medial) layer. Before intervention, the lesion vessel size of deep injury group was smaller than that of the nondeep injury group (p <0.05 for average VA and PA), whereas average lesion LA, lesion length, and reference vessel size did not differ. Immediately after cutting balloon angioplasty, the deep injury group showed a significant increase in VA (p <0.0001) and a lesser decrease in PA (p <0.01) compared with the nondeep injury group. During follow-up, the increase of VA tended to be greater in the deep injury group than in the nondeep injury group (p = 0.06), whereas the change of PA did not differ. Consequently, LA decrease was less in the deep injury group than in the nondeep injury group (p <0.05). From these results, it is suggested that deep vessel wall injury tends to occur in lesions with relatively small size and such lesions show favorable vessel response after cutting balloon angioplasty.
View details for Web of Science ID 000180201000002
View details for PubMedID 12505563
- What do cardiologists want from vascular ultrasound? Vascular Ultrasound 2003: 3-27
- New technologies for the treatment of acute myocardial infarction: ongoing clinical trials in the United States and Europe Cardioangiology 2003; 54: 70-79
- Percutaneous intervention by the coronary venous route Heart View 2003; 7 (2): 58-64
- IVUS guided stenting - optimizing outcomes Coronary Intervention 2003; 2 (2): 26-30
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Efficacy and feasibility of helixcision for debulking neointimal hyperplasia for in-stent restenosis
CATHETERIZATION AND CARDIOVASCULAR INTERVENTIONS
2002; 57 (4): 460-466
Abstract
The Helixcision system is a novel 6 Fr-compatible catheter designed to debulk tissue for in-stent restenosis lesions. The purpose of this study was to determine the efficacy and feasibility of this new system for removing neointimal hyperplasia. A total of 32 in-stent restenosis lesions in 32 patients were treated with helixcision followed by balloon angioplasty. Debulking efficacy was assessed with serial baseline intravascular ultrasound (IVUS) in a subset of 18 lesions. To investigate longitudinal efficacy, 3D analysis was also performed in 12 lesions with automated pullback to calculate average cross-sectional areas across the stent. Prior to procedure, the angiographic reference diameter was 2.60 +/- 0.46 mm. Immediately after procedure, minimum lumen diameter improved from 0.84 +/- 0.33 to 2.19 +/- 0.41 mm (P < 0.0001). IVUS showed a significant reduction of intimal area (IA) after helixcision (from 4.95 +/- 2.04 to 2.88 +/- 1.48 mm(2); P < 0.001). Adjunctive balloon angioplasty further improved lumen area (LA) mainly by stent expansion rather than IA reduction at the site of minimum lumen area. The degrees of IA reduction and LA improvement were closely similar in volumetric analysis. Thirty-day and 6-month clinical follow-up were available in 97% (n = 31) and 72% (n = 23) of the enrolled patients, respectively. At 30-day follow-up, no major adverse cardiac event was reported except for periprocedural CK elevation in two patients (6%). Target legion revascularization within 6 months was performed in six patients (26%). Preliminary results of helixcision indicate that this system is safe and feasible for the treatment of in-stent restenosis. The concordant results between 2D and 3D IVUS analyses suggest that this unique technology can achieve uniform longitudinal debulking throughout the stent. The long-term outcomes appeared to be favorable, considering the relatively diffuse lesion morphology.
View details for DOI 10.1002/ccd.10352
View details for Web of Science ID 000182814400006
View details for PubMedID 12455079
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Quantitative and spatial relation of baseline atherosclerotic plaque burden and subsequent in-stent neointimal proliferation as determined by intravascular ultrasound
AMERICAN JOURNAL OF CARDIOLOGY
2002; 90 (10): 1164-?
View details for Web of Science ID 000179262600027
View details for PubMedID 12423727
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Beneficial effects of coronary debulking prior to stenting in LAD ostial lesion: A volumetric IVUS substudy from the DESIRE trial
American-Heart-Association Abstracts From Scientific Sessions
LIPPINCOTT WILLIAMS & WILKINS. 2002: 586–87
View details for Web of Science ID 000179142702936
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Serial stent edge analysis following sirolimus eluting stent implantation: Interim IVUS results from the SIRIUS trial
LIPPINCOTT WILLIAMS & WILKINS. 2002: 519
View details for Web of Science ID 000179142702602
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Incidence of incomplete stent apposition at baseline and follow-up: Interim analysis from the SIRIUS trial
LIPPINCOTT WILLIAMS & WILKINS. 2002: 520
View details for Web of Science ID 000179142702608
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Neointimal distribution within sirolimus-eluting stents: A 3-D IVUS interim analysis from the SIRIUS trial
American-Heart-Association Abstracts From Scientific Sessions
LIPPINCOTT WILLIAMS & WILKINS. 2002: 391–91
View details for Web of Science ID 000179142701984
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Effect of sirolimus eluting stents an neointimal hyperplasia: A serial in-stent IVUS interim analysis from the SIRIUS trial
American-Heart-Association Abstracts From Scientific Sessions
LIPPINCOTT WILLIAMS & WILKINS. 2002: 520–20
View details for Web of Science ID 000179142702607
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In vivo mechanisms of saphenous vein graft patency following intraoperative cell-cycle blockade with E2F decoy: An IVUS substudy from PREVENT II
LIPPINCOTT WILLIAMS & WILKINS. 2002: 69
View details for Web of Science ID 000179142700385
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In vitro surface temperature images from a guidewire-based thermography system
LIPPINCOTT WILLIAMS & WILKINS. 2002: 591
View details for Web of Science ID 000179142702959
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Delivered dose and vascular response after beta-radiation for in-stent restenosis - Retrospective dosimetry and volumetric intravascular ultrasound analysis
CIRCULATION
2002; 106 (18): 2334-2339
Abstract
Observations from previous intracoronary radiation therapy trials noted a considerable discrepancy between the prescribed radiation dose and the dose actually delivered. The aims of this study were to investigate the effect of actual delivered dose on vascular changes and to test the appropriateness of the current dose prescription.Serial volumetric intravascular ultrasound (IVUS) analysis was performed in 30 in-stent restenosis cases treated with a 40-mm (90)Sr/Y source train. The fixed dose was prescribed at 2 mm from the centerline of the source train (18.4 Gy at 2 mm for reference diameter < or =3.35 mm and 23 Gy for diameter > or =3.36 mm). Only stent segments with full radiation coverage and device injury were enrolled and divided into 2-mm-long subsegments (n=202). D(S90)EEM (the minimum dose absorbed by 90% of the external elastic membrane surface) was calculated as the delivered dose corresponding to each segment, assuming that the radiation catheter occupied the same position in the vessel as the IVUS catheter. Mean D(S90)EEM of 23.5+/-5.82 Gy (range 12.3 to 41.7 Gy) was delivered to these subsegments. Overall, intimal hyperplasia volume remained constant from postintervention to follow-up (2.23+/-1.10 to 2.32+/-1.09 mm3/m; P=NS). Regression analysis revealed there was no correlation between delivered dose intensity and changes in intimal hyperplasia volume. No particular dose-dependent complications were appreciated in this delivered dose range.The current dose-prescription protocol of (90)Sr/Y radiation to native in-stent restenosis lesions may provide substantial inhibition of neointimal reproliferation regardless of the actual delivered dose intensity.
View details for DOI 10.1161/01.CIR.0000036367.17043.03
View details for Web of Science ID 000179046600017
View details for PubMedID 12403663
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7-hexanoyltaxol-eluting stent for prevention of neointimal growth - An intravascular ultrasound analysis from the study to COmpare REstenosis rate between QueST and QuaDS-QP2 (SCORE)
CIRCULATION
2002; 106 (14): 1788-1793
Abstract
Inhibition of neointimal tissue growth has been demonstrated in preliminary human feasibility studies with a stent-based polymer sleeve delivering 7-hexanoyltaxol. The Study to COmpare REstenosis rate between QueST and QuaDS-QP2 (SCORE) trial is a human, randomized, multicenter trial comparing 7-hexanoyltaxol (QP2)-eluting stents (qDES) with bare metal stents (BMS) in the treatment of de novo coronary lesions. The purpose of this substudy was to evaluate the acute expansion property and long-term neointimal responses of qDES compared with BMS as assessed by intravascular ultrasound (IVUS).A total of 122 (qDES 66, BMS 56) patients were enrolled into the IVUS substudy. All IVUS images (immediately after the procedure and at 6-month follow-up) were analyzed at an independent core laboratory in a blind manner. At baseline, qDES achieved stent expansion similar to BMS. At follow-up, qDES showed reduced neointimal growth by 70% at the tightest cross section and by 68% over the stented segment (P<0.0001 for both), resulting in a significantly larger lumen in qDES than in BMS. Unlike intracoronary brachytherapy, there was no evidence of negative edge effects, unhealed dissections, or late stent-vessel wall malapposition over the stented and adjacent references segments in either group.Detailed IVUS analysis revealed that qDES had comparable acute mechanical and superior long-term biological effects to BMS. Although the long-term benefits and limitations of this technology require further investigation, the reduction in neointimal thickenings demonstrated that local delivery of 7-hexanoyltaxol through polymer sleeves augments conventional mechanical treatment of atherosclerotic disease.
View details for Web of Science ID 000178385700012
View details for PubMedID 12356631
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New catheter-based technology for the treatment of restenosis.
Journal of interventional cardiology
2002; 15 (5): 371-379
Abstract
Catheter-based vascular interventions have been in development worldwide for several decades, leading to remarkable progress in device technology. Mechanical interventional devices, such as angioplasty balloons, atherectomy devices, and stents, were invented and have contributed greatly to the treatment of atherosclerotic vascular stenosis. However, mechanical approaches do not effectively prevent subsequent intimal growth. Recently, several biological approaches, including radiation therapy and drug-eluting stents, have shown striking inhibition of intimal growth. These significant results are likely to change the treatment strategy in the field of interventional cardiology. Furthermore, additional catheter-based technologies for vascular interventions are presently being evaluated. These latest technologies designed to prevent intimal proliferation include intravascular sonotherapy, cryotherapy, photoangioplasty, and soft X ray. To date, intravascular sonotherapy has proven its efficacy in animal studies and safety in human studies. Cryotherapy, the application of cold thermal energy during angioplasty, enhances the acute effects of conventional dilation while decreasing the likelihood of restenosis. Photoangioplasty has a unique property based on its selective mechanism of action to treat atheromatous plaque. Soft X ray systems provide convenient device handling and well-controlled radiation dose. Some of these technologies may play an important role in vascular interventions in the near future.
View details for PubMedID 12440180
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Long-term angiographic outcome after biosensors S-stent implantation.
EXCERPTA MEDICA INC. 2002: 98H–99H
View details for Web of Science ID 000178077400247
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Effect of sirolimus eluting stents on neointimal hyperplasia: A serial in-stent intravascular ultrasound interim analysis from the SIRIUS trial
EXCERPTA MEDICA INC. 2002: 1H–2H
View details for Web of Science ID 000178077400004
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Polymer sleeve-based 7-hexanolytaxol-eluting stent implantation: A 3-dimensional intravascular ultrasound analysis characterizing neointimal patterns.
EXCERPTA MEDICA INC. 2002: 70H
View details for Web of Science ID 000178077400168
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Plaque prolapse after current generation stent implantation: An intravascular ultrasound study.
EXCERPTA MEDICA INC. 2002: 89H
View details for Web of Science ID 000178077400218
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Images in cardiovascular medicine. "Arteries within the artery" after Kawasaki disease: a lotus root appearance by intravascular ultrasound.
Circulation
2002; 106 (7): 887-?
View details for PubMedID 12176965
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"Arteries within the artery" after Kawasaki disease - A lotus root appearance by intravascular ultrasound
CIRCULATION
2002; 106 (7): 887-887
View details for DOI 10.1161/01.CIR.0000030708.86783.92
View details for Web of Science ID 000177530700034
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Late vascular response to repeat stenting for in-stent restenosis with and without radiation - An intravascular ultrasound volumetric analysis
CIRCULATION
2002; 105 (21): 2465-2468
Abstract
Re-stenting of in-stent restenosis (ISR) improves acute angiographic results. Methods and Results- Volumetric intravascular ultrasound analysis was performed in 70 ISR lesions that received either placebo (n=36) or (192)Ir radiation (n=34). ISR lesions treated by re-stenting were divided into 3 groups: old stent not re-stented (A), old/new stent overlap (B), and new stent only (C). ISR lesions treated without re-stenting were categorized as D. In placebo patients, postintervention lumen volume index (LVI) was significantly greater in re-stented segments B and C than in non-re-stented segment A (P<0.05).At follow-up, however, LVI was similar in all 4 segments secondary to the increased intimal hyperplasia (IH) reaccumulation within the re-stented segments. In patients treated with (192)Ir radiation, LVI was maintained from baseline to follow-up only in non-re-stented segments A and D. Conversely, there was a significant decrease in LVI in re-stented segments B and C (P<0.05). Qualitatively, 79% of patients in the irradiated group had stent struts with undetectable neointimal versus only 27% in the placebo group (P<0.001). Coefficient of variation of IH reaccumulation was greater in re-stented segments of (192)Ir patients (B=57.3% and C=58.9%) than in re-stented segments in placebo patients (B=27.3% and C 26.8%) and non-re-stented segments in irradiated patients.Additional lumen gain from re-stenting ISR lesions is counteracted by exaggerated neointimal proliferation in placebo patients. Maximum effectiveness and safety of radiation can be achieved for ISR lesions when treated without re-stenting. Thus, regardless of supplementary intravascular brachytherapy, repeat stenting strategies provided little long-term advantage.
View details for DOI 10.1161/01.CIR.0000018949.39445.40
View details for Web of Science ID 000175927500011
View details for PubMedID 12034650
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Intraoperative cell-cycle blockade therapy using E2F decoy for prevention of early atherosclerosis in coronary bypass vein grafts: A volumetric IVUS subanalysis from a prospective randomized double blind clinical trial
ELSEVIER SCIENCE INC. 2002: 228A
View details for Web of Science ID 000174106701017
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Excessive beta-radiation exposure to the non-target segment: An intravascular ultrasound dosimetric analysis
ELSEVIER SCIENCE INC. 2002: 13A
View details for Web of Science ID 000174106700056
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Three-dimensional relationship between peri-stent plaque and neointimal proliferation throughout the stented segment: A novel intravascular ultrasound approach
ELSEVIER SCIENCE INC. 2002: 34A
View details for Web of Science ID 000174106700148
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Feasibility and safety of a novel cryoangioplasty system
ELSEVIER SCIENCE INC. 2002: 57A
View details for Web of Science ID 000174106700248
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Mechanisms of lumen narrowing of saphenous vein bypass grafts 12 months after implantation: An intravascular ultrasound study
ELSEVIER SCIENCE INC. 2002: 60A
View details for Web of Science ID 000174106700259
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Three-dimensional IVUS assessment of edge effects following drug-eluting stent implantation
ELSEVIER SCIENCE INC. 2002: 70A
View details for Web of Science ID 000174106700307
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Optimal endpoint for drug-eluting stent: Predictive value of minimum stent area for long-term stent patency
ELSEVIER SCIENCE INC. 2002: 71A
View details for Web of Science ID 000174106700309
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Peri-stent remodeling and neointimal response following intracoronary radiation therapy: A volumetric intravascular ultrasound study
ELSEVIER SCIENCE INC. 2002: 71A–72A
View details for Web of Science ID 000174106700312
- Intravascular ultrasound observations for stented and non-stented procedures Vascular Brachytherapy 2002: 581-603
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Impact of insulin resistance on neointimal tissue proliferation after coronary stent implantation - Intravascular ultrasound studies
International Symposium on Insulin Resistance and Atherosclerosis
ELSEVIER SCIENCE INC. 2002: 50–55
Abstract
Serial intravascular ultrasound (IVUS) studies in 55 nondiabetic patients showed that neointimal tissue proliferation after stent implantation in patients with impaired glucose tolerance (IGT) was greater than that in patients with normal glucose tolerance at follow-up. Multiple regression analysis showed that the sum of insulin levels was the best predictor of the greater neointimal index at follow-up. Another group of serial IVUS studies were performed in 62 stented lesions in 52 patients with Type 2 diabetes mellitus (DM). The study patients were randomized into a troglitazone group and a control group. The neointimal tissue proliferation at follow-up in the troglitazone group was significantly smaller than that in the control group.
View details for Web of Science ID 000174300400011
View details for PubMedID 11872367
- Prevention of restenosis: sonotheraphy, photoangioplasty and cryotherapy Cardiology New Trends: New Trends in Coronary Intervention 2002: 138-147
- Intravascular ultrasound Textbook of Interventional Cardiology 2002: 893-917
- Combining a drug-eluting stent and platelet glycoprotein IIb/IIIa inhibition in a patient with acute coronary syndrome J Invasive Cardiol 2002; 4 (16)
- New technology for the treatment of acute myocardial infarction: how to protect coronary microcirculation and myocardium Coronary Intervention 2002; 1 (4): 99-105
- New technology for the treatment of acute myocardial infarction: how to protect coronary microcirculation and myocardium Coronary Intervention 2002; 1 (4): 99-105
- Coronary intravascular ultrasonography PanVascular Medicine: Integrated Clinical Management 2002: 667-678
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Intravascular ultrasound and quantitative coronary angiography
CATHETERIZATION AND CARDIOVASCULAR INTERVENTIONS
2002; 55 (1): 118-128
View details for Web of Science ID 000172956000024
View details for PubMedID 11793508
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Predictors and outcomes of stent thrombosis - An intravascular ultrasound registry
EUROPEAN HEART JOURNAL
2002; 23 (2): 124-132
Abstract
To investigate whether intravascular ultrasound provides additional information regarding the prediction of stent thrombosis, a retrospective multicentre registry was designed to enrol patients with stent thrombosis following stent deployment under ultrasound guidance.A total of 53 patients were enrolled (mean age 61+/-9 years) with stable angina (43%), unstable angina (36%), and post-infarct angina (21%) who underwent intracoronary stenting. The majority had balloon angioplasty alone prior to stenting (94%) with 6% also undergoing rotational atherectomy. The indication for stenting was elective (53%), suboptimal result (32%) and bailout (15%). There were 1.6+/-0.8 stents/artery with 87% undergoing high-pressure dilatation (> or =14 atmospheres). The minimum stent area was 7.7+/-2.8 mm(2)with a mean stent expansion of 81.5+/-21.9%. Overall, 94% of cases demonstrated one abnormal ultrasound finding (stent under-expansion, malapposition, inflow/outflow disease, dissection, or thrombus). Angiography demonstrated an abnormality in only 32% of cases (chi-square=30.0, P<0.001). Stent thrombosis occurred at 132+/-125 h after deployment. Myocardial infarction occurred in 67% and there was an overall mortality of 15%.On comparison with angiography, the vast majority of stents associated with subsequent thrombosis have at least one abnormal feature by intravascular ultrasound at the time of stent deployment.
View details for DOI 10.1053/euhj.2001.2707
View details for Web of Science ID 000173390100009
View details for PubMedID 11785994
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Efficacy of postdeployment balloon dilatation for current generation stents as assessed by intravascular ultrasound
AMERICAN JOURNAL OF CARDIOLOGY
2001; 88 (10): 1114-1119
Abstract
Adjunctive balloon dilatation strategy has been shown to improve optimal stent deployment. As improvements in current stent designs evolve, less adjunctive balloon dilatation may be needed. However, few data currently exist to support this practice. We evaluated 88 native coronary lesions treated with single stent implantation (Nir, Tristar or S670). Serial intravascular ultrasound was performed after successful stent deployment and again after adjunctive balloon dilatation. To investigate further the precise expansion characteristics of the stents, serial volumetric intravascular ultrasound analyses were performed in 40 patients with automated pullback. After adjunctive balloon dilatation, minimal stent area increased significantly, from 6.4 +/- 2.1 to 7.4 +/- 2.2 mm(2) (p <0.001). Volumetric analysis showed a corresponding increase in stent volume index (6.6 +/- 1.8 to 7.5 +/- 2.0 mm(3)/mm, p <0.001). In the analysis of cross sections at 0.5-mm axial intervals, the percentage of cross sections, where stent area was > or =80% of the average reference lumen area, increased from 51% to 78% (p <0.001). Similarly, the percentage of cross sections, where stent area was > or =90% of the average reference lumen area, increased from 29% to 56% (p <0.001) with postdilatation. Postdeployment high- pressure balloon dilatation improved minimal stent area and volumetric expansion throughout the stented segment.
View details for Web of Science ID 000172412300006
View details for PubMedID 11703954
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The renaissance of directional coronary atherectomy: a second look from the inside.
journal of invasive cardiology
2001; 13 (11): 748-751
View details for PubMedID 11689719
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Does arterial remodeling before debulking affect restenosis following directional coronary atherectomy?
LIPPINCOTT WILLIAMS & WILKINS. 2001: 508–
View details for Web of Science ID 000171895002385
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Late vascular response to repeat stent deployment for treatment of in-stent restenosis with or without radiation: An intravascular ultrasound volumetric analysis
LIPPINCOTT WILLIAMS & WILKINS. 2001: 545
View details for Web of Science ID 000171895002559
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Relationship between plaque burden debulking and long-term stent patency: A three-dimenshional IVUS analysis
LIPPINCOTT WILLIAMS & WILKINS. 2001: 616-+
View details for Web of Science ID 000171895002889
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Effect of deep vessel wall injury on late arterial response after cutting balloon angioplasty
LIPPINCOTT WILLIAMS & WILKINS. 2001: 616–17
View details for Web of Science ID 000171895002891
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Prevention of restenosis by a new drug eluting stent: An intravascular ultrasound substudy of the SCORE trial
LIPPINCOTT WILLIAMS & WILKINS. 2001: 701
View details for Web of Science ID 000171895003280
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Intravascular ultrasound stent edge analysis following drug eluting stent implantation: "Candy without the wrapper"
LIPPINCOTT WILLIAMS & WILKINS. 2001: 770–71
View details for Web of Science ID 000171895003600
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Patterns of in-stent restenosis assessed by 3-dimensional intravascular ultrasound.
EXCERPTA MEDICA INC. 2001: 92G–93G
View details for Web of Science ID 000170893600240
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The impact of drug eluting stent to prevent coronary restenosis: A volumetric intravascular ultrasound analysis from the SCORE (Study to compare restenosis rate between QueST and QuaDDS-QP2) trial.
EXCERPTA MEDICA INC. 2001: 15G–16G
View details for Web of Science ID 000170893600042
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Diabetes as a predictor for intravascular ultrasound-guided post-dilatation after angiographically successful stent implantation: An observational study from the CRUISE (Can routine ultrasound influence stent expansion) trial.
EXCERPTA MEDICA INC. 2001: 40G
View details for Web of Science ID 000170893600100
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An optimal diagnostic threshold for minimal stent area to predict target lesion revascularization following stent implantation in native coronary lesions
AMERICAN JOURNAL OF CARDIOLOGY
2001; 88 (3): 301-?
View details for Web of Science ID 000170090500020
View details for PubMedID 11472713
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Novel drug-delivery stent - Intravascular ultrasound observations from the first human experience with the QP2-eluting polymer stent system
CIRCULATION
2001; 104 (4): 380-383
Abstract
The aim of this study was to use serial intravascular ultrasound (IVUS) to evaluate the long-term effect of stent-based 7-hexanoyltaxol (QP2, a taxane analogue) delivery on neointimal tissue growth within the stent and on vessel dimensions at the adjacent reference segments.Serial IVUS analyses (immediately after intervention and at follow-up at 8.3 months) were performed in 15 native coronary lesions treated with the QuaDS-QP2 stent. IVUS measurements were performed at 8 cross-sections in each target segment (4 cross-sections within the stent and 2 cross-sections in each reference segment). At baseline, no significant plaque protrusion or thrombus was detected in the target segment. Mild incomplete stent apposition and edge dissection were observed in one and two cases, respectively. Percent expansion of the stent (minimum stent area/average reference lumen area) was 96.0+/-21.7%. At follow-up, mean neointimal area within the stent was 1.2+/-1.3 mm(2), and mean cross-sectional narrowing (neointimal area/stent area) was 13.6+/-14.9%. At the vessel segments immediately adjacent to the stent, a significant increase in plaque area (1.9+/-2.6 mm(2), P=0.001) was observed, but vessel area remained unchanged. However, no patients showed clinically significant in-stent or edge restenosis (diameter stenosis >/=50%) during the follow-up period.The first human experience with the new drug-delivery stent showed a minimal amount of neointimal proliferation in the stented segment. Late lumen loss at the reference sites adjacent to the stent was acceptable and predominantly due to plaque proliferation.
View details for Web of Science ID 000170116200003
View details for PubMedID 11468196
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Impact of peri-stent remodeling on restenosis - A volumetric intravascular ultrasound study
CIRCULATION
2001; 103 (17): 2130-2132
Abstract
Vessel remodeling is an important mechanism of late lumen loss after nonstent coronary interventions. However, its impact on in-stent restenosis has not been systematically investigated.Serial volumetric intravascular ultrasound analyses (poststent and follow-up) were performed in 55 lesions treated with a balloon-expandable stent (ACS MultiLink) using standard stent deployment techniques. The vessel volume (VV), lumen volume (LV), and volume bordered by the stent (SV) were measured using Simpson's method. The volume of plaque and neointima outside the stent (peri-stent volume, PSV) and volume of neointima within the stent (intrastent volume) were also measured. The change of each parameter during the follow-up period (follow-up minus poststent) was calculated and then divided by SV to normalize these values (designated as percent change [%]). As expected, %PSV directly correlated with %VV (P<0.0001, r=0.935), with no significant SV. A highly significant inverse correlation was seen between %PSV and the percent change of intrastent volume (P<0.0001, r=0.517). Consequently, %LV significantly correlated with peri-stent remodeling, as measured by %VV (P<0.0001, r=0.602).Positive remodeling of the vessel exterior to a coronary stent occurs to a variable degree after stent implantation. There is a distinct trade-off between positive remodeling and in-stent hyperplasia: in segments in which the degree of peri-stent remodeling is less, intrastent neointimal proliferation is greater and accompanied by more significant late lumen loss.
View details for Web of Science ID 000168583700002
View details for PubMedID 11331251
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Long-term vessel response to a self-expanding coronary stent: A serial volumetric intravascular ultrasound analysis from the ASSURE trial
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY
2001; 37 (5): 1329-1334
Abstract
We sought to investigate the in vivo mechanical properties of a new self-expanding coronary stent (RADIUS) and, particularly, the subsequent vessel response over time.Preclinical studies have suggested that self-expanding stents may produce less vessel wall injury at initial deployment, leading to larger follow-up lumens than with balloon-expandable stents. However, the influence of the chronic stimulus from self-expanding stents on the vessel wall remains unknown.Sixty-two patients were randomly assigned to either the RADIUS self-expanding stent group (n = 32) or the Palmaz-Schatz balloon-expandable stent group (n = 30). Intravascular ultrasound was performed after stent deployment and at six-month follow-up.At follow-up, the RADIUS stents had increased 23.6% in overall volume, while the Palmaz-Schatz stents had remained unchanged. Due to the greater mean neointimal area (3.0 +/- 1.7 mm2 vs. 1.9 +/- 1.2 mm2, p = 0.02) in the RADIUS group, no significant difference in net late lumen loss was observed between the two groups. On the other hand, analysis at the peristent margins demonstrated that mean late loss was significantly smaller in the RADIUS group than it was in the Palmaz-Schatz group (0.1 +/- 2.1 mm2 vs. 1.9 +/- 2.4 mm2, p = 0.02).Serial volumetric IVUS revealed that the RADIUS stents continued to enlarge during the follow-up period. In this stent implantation protocol, this expansion was accompanied by a greater amount of neointima than the Palmaz-Schatz stents, resulting in similar late lumen loss in both configurations. In the peristent margins, however, late lumen loss was minimized with the RADIUS stents.
View details for Web of Science ID 000167901700027
View details for PubMedID 11300443
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Is the use of fractional flow reserve to guide coronary interventions cost-effective?
ELSEVIER SCIENCE INC. 2001: 12A–12A
View details for Web of Science ID 000166914400053
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Regrowth of neointimal effect of in-stent restenosis: A volumetric analysis of the effects of radiation
ELSEVIER SCIENCE INC. 2001: 41A–42A
View details for Web of Science ID 000166914400189
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Relationship between vessel size and late lumen loss following intracoronary beta- and gamma-radiation therapy
ELSEVIER SCIENCE INC. 2001: 57A
View details for Web of Science ID 000166914400263
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A novel drug-delivery stent: Intravascular ultrasound observations from the first human experience with the QUANAM QuaDS-QP2 stent system
ELSEVIER SCIENCE INC. 2001: 14A
View details for Web of Science ID 000166914400065
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Higher doses of intracoronary adenosine are necessary for FFR-based stent optimization
ELSEVIER SCIENCE INC. 2001: 12A
View details for Web of Science ID 000166914400054
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The cold edge effect: Mechanisms of edge narrowing following stenting without radiation
ELSEVIER SCIENCE INC. 2001: 57A–58A
View details for Web of Science ID 000166914400265
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Acute and chronic vessel responses to direct stenting vs stenting with predilatation: A serial intravascular ultrasound study
ELSEVIER SCIENCE INC. 2001: 26A–26A
View details for Web of Science ID 000166914400118
- The role of IVUS in the prevention and treatment of restenosis Restenosis: A Guide to Therapy 2001: 77-95
- Principles of intravascular ultrasound Clinical Echocardiography 2001: 252-259
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The effect of intracoronary gamma-radiation therapy for in-stent restenosis: an intravascular ultrasound study.
Cardiovascular radiation medicine
2001; 2 (1): 54-?
View details for PubMedID 11068265
- The role of intravascular ultrasound in clinical trials Clinical Echocardiography 2001: 265-267
- Stanford University Journal of Clinical Echocardiography 2001
- Vascular brachytherapy: from theory to practice Coronary Angioplasty and Intravascular Ultrasound for Brachytherapy 2001: 121-141
- Future direction of intravascular ultrasound Clinical Echocardiography 2001: 267-275
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Longitudinal plaque redistribution during stent expansion
AMERICAN JOURNAL OF CARDIOLOGY
2000; 86 (10): 1069-1072
Abstract
The purpose of this study was to clarify the 3-dimensional behavior of plaque during coronary stent expansion. Serial intravascular ultrasound (IVUS) studies, preintervention, and poststenting were evaluated in 32 patients treated with a single-balloon expandable tubular stent. External elastic membrane (EEM), lumen, stent, and plaque + media cross-sectional area were measured at 1-mm intervals through the entire stent as well as proximal and distal reference segments 5 mm from the stent edge. Volumetric calculations were based on Simpson's rule. Overall, the plaque + media volume through the entire lesion did not change during stent expansion (218 +/- 51 vs 217 +/- 47 mm3, p = 0.69). However, EEM and lumen volume increased significantly (EEM volume, 391 +/- 84 vs 448 +/- 87 mm3 [p < 0.0001]; lumen volume, 173 +/- 52 vs 231 +/- 54 mm3 [p < 0.0001]). The change in lumen volume correlated strongly with the change in EEM volume (r = 0.85, p < 0.0001), but poorly with the change in plaque + media volume (r = 0.37, p = 0.03). Plaque + media volume decreased in the midstent zone (59 +/- 14 vs 53 +/- 11 mm3, p = 0.0005), and increased in the distal stent zone (40 +/- 11 vs 44 +/- 9 mm3, p = 0.003), but did not change in either the proximal stent zone or reference segments. The mechanism of stent expansion is a combination of vessel stretch and plaque redistribution, translating disease accumulation from the midstent zone to the distal stent zone.
View details for Web of Science ID 000165185500003
View details for PubMedID 11074201
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Troglitazone reduces neointimal tissue proliferation after coronary stent implantation in patients with non-insulin dependent diabetes mellitus - A serial intravascular ultrasound study
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY
2000; 36 (5): 1529-1535
Abstract
The aim of the present study was to determine whether troglitazone reduces neointimal tissue proliferation after coronary stent implantation in patients with non-insulin dependent diabetes mellitus (NIDDM).Increased in-stent restenosis in patients with diabetes mellitus is due to accelerated neointimal tissue proliferation after coronary stent implantation. Troglitazone inhibits intimal hyperplasia in experimental animal models.We studied 62 stented lesions in 52 patients with plasma glucose levels (PG) > or = 11.1 mmol/liter at 2 h after 75 g oral glucose load. The study patients were randomized into two groups: the troglitazone group of 25 patients with 29 stents, who were treated with 400 mg of troglitazone, and the control group of 27 patients with 33 stents. All patients underwent oral glucose tolerance tests before and after their six-month treatment period. The sum of PG (sum of PG) and the sum of insulin levels (sum of IRI) were measured. Serial (postintervention and at six-month follow-up) intravascular ultrasound studies were performed. Cross-sectional images within stents were taken at every 1 mm, using an automatic pullback. Stent areas (SA), lumen areas (LA), and intimal areas (IA = SA - LA) were measured and averaged over a number of selected image slices. The intimal index was calculated as intimal index = averaged IA/averaged SA x 100%.There were no differences between the two groups before treatment in sum of PG (31.35 +/- 3.07 mmol/liter vs. 32.89 +/- 4.87 mmol/liter, respectively, p = 0.2998) and sum of IRI (219.6 +/- 106.2 mU/liter vs. 209.2 +/- 91.6 mU/liter, respectively, p = 0.8934). However, reductions in sum of PG at the six-month follow-up in the troglitazone group were significantly greater than those in the control group (-21.4 +/- 8.8% vs. -4.5 +/- 7.4%, respectively, p < 0.0001). Likewise, decreases in sum of IRI were greater in the troglitazone-treated group (-31.4 +/- 17.9% vs. -1.9 +/- 15.1%, respectively, p < 0.0001). Although, there were no differences between the two groups in SA at postintervention (7.4 +/- 2.2 mm2 vs. 7.3 +/- 1.7 mm2, respectively, p = 0.9482) and at follow-up (7.3 +/- 2.3 mm2 vs. 7.3 +/- 1.8 mm2, respectively, p = 0.2307), the LA at follow-up in the troglitazone group was significantly greater than that in the control group (5.3 +/- 1.7 mm2 vs. 3.7 +/- 1.7 mm2, respectively, p = 0.0002). The IA at follow-up in the troglitazone group was significantly smaller than that in the control group (2.0 +/- 0.9 mm2 vs. 3.5 +/- 1.8 mm2, respectively, p < 0.0001). This was also true for intimal index (27.1 +/- 11.5% vs. 49.0 +/- 14.4%, respectively, p < 0.0001).Serial intravascular ultrasound assessment shows that administration of troglitazone reduces neointimal tissue proliferation after coronary stent implantation in patients with NIDDM.
View details for Web of Science ID 000165171500013
View details for PubMedID 11079654
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Effects of post intervention atherosclerotic plaque burden on neointimal proliferation
LIPPINCOTT WILLIAMS & WILKINS. 2000: 690-?
View details for Web of Science ID 000090072303328
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Is the luminal position of an intracoronary catheter reproducible? An intravascular ultrasound investigation
LIPPINCOTT WILLIAMS & WILKINS. 2000: 635–36
View details for Web of Science ID 000090072303074
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An optimal cut-off value for minimal stent area to predict target vessel revascularization following stent implantation in native coronary lesions
LIPPINCOTT WILLIAMS & WILKINS. 2000: 692
View details for Web of Science ID 000090072303336
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In-stent restenosis: Can neointimal tissue reduction improve long-term outcome? A serial volumetric intravascular ultrasound study.
EXCERPTA MEDICA INC. 2000: 119I
View details for Web of Science ID 000165269800310
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Sirolimus (rapamycin) halts and reverses progression of allograft vascular disease in non-human primates
TRANSPLANTATION
2000; 70 (6): 969-975
Abstract
Current immunosuppressive protocols fail to prevent chronic rejection often manifested as graft vascular disease (GVD) in solid organ transplant recipients. Several new immunosuppressants including sirolimus, a dual function growth factor antagonist, have been discovered, but studies of drug efficacy have been hampered by the lack of a model of GVD in primates, as a prelude to clinical trials. As described earlier, we have developed a novel non-human primate model of GVD where progression of GVD is quantified by intravascular ultrasound (IVUS).Twelve cynomolgus monkeys underwent aortic transplantation from blood group compatible but mixed lymphocyte reaction-mismatched donors. To allow the development of GVD in the allograft, no treatment was administered for the first 6 weeks. Six monkeys were treated orally with sirolimus from day 45 after transplantation to day 105.Progression of GVD measured as change in intimal area from day 42 to 105 was halted in sirolimus-treated monkeys compared to untreated monkeys (P<0.001, general linear model). On day 105, the intimal area +/- SEM was 3.7+/-1.0 and 6.4+/-0.5 mm2, respectively (P<0.05, t test). The magnitude of allograft intimal area on day 105 correlated inversely with sirolimus trough levels (R2=0.67, P<0.05). Regression of the intimal area was seen in four of six sirolimus-treated monkeys, which was significantly different from the untreated monkeys (P<0.05).Our results in the first non-human primate model of GVD showed that treatment with sirolimus not only halted the progression of preexisting GVD but also was associated with partial regression. Sirolimus trough blood levels were correlated with efficacy. Therefore, sirolimus has the potential to control clinical chronic allograft rejection.
View details for Web of Science ID 000089710700014
View details for PubMedID 11014651
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Hyperinsulinemia during oral glucose tolerance test is associated with increased neointimal tissue proliferation after coronary stent implantation in nondiabetic patients - A serial intravascular ultrasound study
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY
2000; 36 (3): 731-738
Abstract
The purpose of this study was to determine whether hyperinsulinemia during the oral glucose tolerance test is associated with increased neointimal tissue proliferation after coronary stent implantation in nondiabetic patients.Although hyperinsulinemia induces increased vascular smooth muscle cell proliferation in experimental models, it has not been determined whether hyperinsulinemia is associated with increased neointimal tissue proliferation after coronary stent implantation.Serial (postintervention and six-month follow-up) intravascular ultrasound (IVUS) was used to study 67 lesions treated with Palmaz-Schatz stents in 55 nondiabetic patients. Cross-sectional images within stents were taken at every 1 mm, using an automatic pullback, and a neointimal index was calculated as the ratio between the averaged neointimal area and averaged stent area. All patients underwent a 75-g oral glucose tolerance test. Plasma glucose (PG) and immunoreactive insulin (IRI) levels were measured at baseline and 1 and 2 h after the glucose load. The sum of PGs (sigmaPG) and the sum of IRIs (sigmaIRI) were calculated. Body mass index (BMI), lipid levels, and glycosylated hemoglobin levels were measured.There were 27 patients with normal glucose tolerance, and 28 patients with impaired glucose tolerance (IGT). The neointimal index in patients with IGT was greater than that in patients with normal glucose tolerance (42.9 +/- 14% vs. 24.9 +/- 8.3%, respectively, p < 0.0001). Linear regression analysis showed that the neointimal index at follow-up correlated well with sigmaPG (p < 0.0001), fasting IRI (p < 0.0001), sigmaIRI (p < 0.0001), triglyceride level (p = 0.018), and BMI (p < 0.0001). Multiple regression analysis revealed that sigmaIRI (p = 0.0002) and sigmaPG (p = 0.0034) were the best predictors of the greater neointimal index at follow-up.Serial IVUS assessment shows that hyperinsulinemia during an oral glucose tolerance test is associated with increased neointimal tissue proliferation after coronary stent implantation in nondiabetic patients.
View details for Web of Science ID 000089152100012
View details for PubMedID 10987592
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Multidimensional assessment of graft vascular disease (GVD) in aortic grafts by serial intravascular ultrasound in rhesus monkeys
TRANSPLANTATION
2000; 70 (3): 420-429
Abstract
Graft vascular disease (GVD) is an incompletely understood process and the primary cause of late allograft failure. A nonhuman primate model was established to study the progression of GVD by using serial intravascular ultrasound (IVUS).Aortic allografts were transplanted below the inferior mesenteric arteries (IMA) into 6 rhesus monkeys. Removed and re-implanted aortic segments between renal arteries, and the inferior mesenteric arteries served as autografts. IVUS was performed at days 0, 24, 52, 80, and 98 after transplantation. Vessel area (VA) and lumen area (LA) were measured from each cross-section at 0.5 mm intervals. Intimal index (II=100x (VA-LA/VA)) and corresponding vessel volumes were calculated for the whole grafts. Histologic features were assessed from autopsy samples using computerized morphometric method and a score from 0 to 3 for GVD (0=none, 3=severe).In allografts, vessel volume and luminal volume decreased significantly (P<0.05 for both) and the intimal index increased from 12% to 59% by day 98. These parameters remained unchanged in autografts. Histologic analysis of allografts showed concentric intimal hyperplasia and scattered mononuclear cell accumulations, whereas the autografts had only occasional eccentric intimal changes. The GVD-scores were significantly higher in allografts than in autografts (median 3 vs. 1, P=0.042).We introduce a nonhuman primate model of GVD that enables serial IVUS assessments of multiple parameters of GVD. Concentric intimal proliferation and decrease of vessel dimensions was observed in allografts as a consequence of alloimmunity. This is a potential new model for studying new therapies to prevent GVD or halt its progression.
View details for Web of Science ID 000088863300006
View details for PubMedID 10949182
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Impact of coronary debulking prior to stenting versus conventional stenting on early outcome: Initial IVUS findings
ELSEVIER SCIENCE INC. 2000: 94A–94A
View details for Web of Science ID 000085209700362
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Vessel wall distance variation between centered and non-centered radiation: Cross-sectional and longitudinal analysis by intravascular ultrasound
ELSEVIER SCIENCE INC. 2000: 7A
View details for Web of Science ID 000085209700026
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Extent of neointima predicts subsequent neointimal proliferation in in-stent restenosis: A volumetric intravascular ultrasound study
ELSEVIER SCIENCE INC. 2000: 95A
View details for Web of Science ID 000085209700367
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Efficacies of sirolimus (rapamycin) and cyclosporine in allograft vascular disease in non-human primates: trough levels of sirolimus correlate with inhibition of progression of arterial intimal thickening.
Transplant international
2000; 13: S314-20
Abstract
We investigated the efficacies of sirolimus (rapamycin) and cyclosporine for inhibition of graft vascular disease (GVD) in cynomolgus monkey recipients of aortic allografts. Increases in arterial intimal thickening in the midgraft (six consecutive cross-sections) after transplantation were quantified by serial intravascular ultrasound (IVUS) from day 21 to day 105. These data enabled correlations between changes in intimal indexes [II = (intimal area/vessel area) x 100] and trough levels of sirolimus and cyclosporine to be determined. Eighteen recipients received no immunosuppression for 6 weeks to allow alloimmune injury to occur. On day 45, monkeys were treated daily with sirolimus (n = 6) or cyclosporine (n = 6); six monkeys remained untreated. II increased significantly from day 63 to day 105 in untreated monkeys and monkeys treated with cyclosporine, whereas monkeys treated with sirolimus did not have a significant increase in II (P = 0.008, P = 0.006, P = NS; paired t-test). The change in II from days 63 to 105 was significantly greater in untreated monkeys compared to sirolimus-treated monkeys (P = 0.13; one-way ANOVA, P = 0.012 Tukey's post hoc test); other post hoc pairwise comparisons were not significant. Mean sirolimus and cyclosporine levels +/- SEM were 43 +/- 7 ng/ml and 562 +/- 20 ng/ml, respectively. Sirolimus trough levels, but not cyclosporine levels, correlated inversely with changes in II from day 42 to 105 (r2 = 0.73, P = 0.03). This non-human primate study shows that inhibition of intimal thickening by sirolimus depends on trough levels and provides the rationale for clinical trials of sirolimus for the control of GVD in organ transplant recipients.
View details for PubMedID 11112022
- Intravascular ultrasound Diagnosis of Coronary Artery Disease 2000: 104-115
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Feasibility of in vivo intravascular ultrasound tissue characterization in the detection of early vascular transplant rejection
CIRCULATION
1999; 100 (21): 2127-2130
Abstract
Unprocessed ultrasound radiofrequency (RF) signal analysis has been shown to distinguish different tissue structures more reliably than gray-scale interpretation of conventional ultrasound images.The objective of this study was to test the feasibility of in vivo intravascular ultrasound (IVUS) RF signal analysis in an animal model of allograft rejection. Six cynomolgus monkeys underwent transplantation of 3-cm aortic allograft segments distal to the renal arteries from immunologically mismatched donors. IVUS imaging with a 30-MHz system was performed 84 to 105 days after the operation. RF signals were acquired from cross sections of the recipient and the allograft aortas in real time with a digitizer at 500 MHz with 8-bit resolution. Sixty-five cross sections and 68 regions of interest (31 in host aorta and 37 in allograft) were analyzed in the adventitial layer with a total number of 8568 vectors processed. For each region of interest, a weighted-average attenuation was calculated on the basis of the attenuation and length for each individual vector. Histological examination was performed at every cross section imaged by IVUS. When the gray-scale images of conventional IVUS scored by an independent observer were compared, no distinction between adventitia of the native aorta and allograft was possible. Analysis of the average RF backscatter power also showed no significant difference (70.32+/-3.55 versus 70.72+/-3.38 dB). However, the average attenuation of allografts was significantly lower than that of the host aortas (2.64+/-1.38 versus 4.02+/-1.16 dB/mm, P<0.001). Histology demonstrated a marked adventitial inflammatory response in all allografts, with no inflammation observed in the host aortas.In vivo IVUS tissue characterization can be performed during routine imaging. In this model of transplant vasculopathy, RF attenuation measurements were more sensitive than visual or quantitative gray-scale analysis.
View details for Web of Science ID 000083945000005
View details for PubMedID 10571969
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Impact of residual plaque burden on clinical outcomes of coronary interventions
CATHETERIZATION AND CARDIOVASCULAR INTERVENTIONS
1999; 46 (3): 265-276
Abstract
In this study, we summarize the role of residual plaque burden, as determined by intravascular ultrasound, on the development of restenosis following percutaneus coronary interventions. Several clinical trials have shown that the amount of residual plaque is a consistent and independent predictor of subsequent restenosis. The impact of residual plaque burden on late lumen loss is particularly augmented by negative vessel remodeling that is commonly seen after balloon angioplasty and atherectomy. However, early evidence suggests that the importance of plaque burden also applies in the context of stenting. The cotreatment of debulking may further improve the long-term outcome of stenting by maximizing an acute lumen gain with less vessel stretching, preventing stent edge problems and possibly reducing the cell source involved in the intimal hyperplastic process. Evaluation of residual plaque burden with on-line intravascular ultrasound could lead to definitive therapies via risk stratification of the treated segments.
View details for Web of Science ID 000079175800003
View details for PubMedID 10348121
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Development of models of graft vascular disease in nonhuman primates: Evaluation of GVD by intravascular ultrasound in a new cynomolgus model with arterial allograft exchange
XVIIth World Congress of the Transplantation-Society
ELSEVIER SCIENCE INC. 1999: 687–87
View details for Web of Science ID 000078960600305
View details for PubMedID 10083296
- Intravascular ultrasound Textbook of Interventional Cardiology 1999: 801-818
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A new large-animal model for research of graft vascular disease
3rd International Conference on New Trends in Clinical and Experimental Immunosuppression
ELSEVIER SCIENCE INC. 1998: 4023–23
View details for Web of Science ID 000077593000033
View details for PubMedID 9865284
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Sirolimus (rapamycin) reverses the progression of graft vascular disease in primate aortic allografts
LIPPINCOTT WILLIAMS & WILKINS. 1998: 751–51
View details for Web of Science ID 000076594403954
- Stanford University Medical Center The Circulation Frontier 1998; 2 (3): 81-84
- Quantitative Assessment of Cardiac Hemodynamics by Doppler Echocardiography 1998
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Impact of vessel wall injury on vascular response after directional coronary atherectomy: A serial intravascular ultrasound study
AMER HEART ASSOC. 1997: 3265
View details for Web of Science ID A1997YC88003246
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Exaggerated plaque proliferation in diabetes mellitus following deep wall excision by directional coronary atherectomy: A serial intravascular ultrasound study
AMER HEART ASSOC. 1997: 856
View details for Web of Science ID A1997YC88000858
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Time course of vascular response following deep wall excision by DCA: One-year follow-up of the ABACAS trial
EXCERPTA MEDICA INC. 1997: TC203
View details for Web of Science ID A1997YC88500200
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Impact of curve distortion errors on intravascular ultrasound measurements and three-dimensional reconstructions
AMERICAN JOURNAL OF CARDIOLOGY
1997; 79 (3): 384-?
Abstract
Intravascular ultrasound distortion errors and longitudinal reconstructions are primarily determined by the angle of curvature. The error in commonly encountered angles is relatively small.
View details for Web of Science ID A1997WG53700029
View details for PubMedID 9036768
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Longitudinal redistribution of plaque is an important mechanism for lumen expansion in stenting
ELSEVIER SCIENCE INC. 1997: 99448
View details for Web of Science ID A1997WF76101198
- The value of IVUS guidance in directional atherectomy Current Review of Interventional Cardiology 1997: 1-11
- Phonocardiography Evidence Based Medicine 1997: 478-481
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Late vessel expansion after directional atherectomy is related to sonolucent zone cutting: Initial observations from the adjunctive balloon angioplasty following coronary atherectomy study (ABACAS)
AMER HEART ASSOC. 1996: 780
View details for Web of Science ID A1996VN11900778
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Use of intravascular ultrasound for in vivo assessment of changes in intimal thickness of angiographically normal saphenous vein grafts one year after aortocoronary bypass surgery
HEART
1996; 76 (4): 317-320
Abstract
To use intravascular ultrasound in vivo to evaluate changes in the intimal thickness of angiographically normal saphenous vein grafts one year after implantation.Fifteen saphenous vein grafts in 12 patients were examined one month and 12 months after aortocoronary bypass graft surgery with intravascular ultrasound using a 30 MHz transducer. None of the grafts examined showed any angiographic abnormalities. The intimal thickness and intimal area of the graft in the proximal portion were measured on intravascular ultrasound images obtained one month and 12 months after operation.General hospital.Twelve patients who underwent aortocoronary bypass graft surgery.The ultrasound images showed a thin-walled graft with a thin intima one month after operation (mean (SD)) (0.31 (0.09) mm). The intimal thickness of the graft increased significantly to 0.65 (0.08) mm (P < 0.001) 12 months after operation. The intimal area of the graft was 0.90 (0.80) mm2 one month after operation. 12 months after operation the intimal area had increased significantly to 5.26 (1.38) mm2 (P < 0.001).Intravascular ultrasound in vivo showed that one year after implantation angiographically normal saphenous vein grafts had a thicker intima than one month after implantation.
View details for Web of Science ID A1996VL97100008
View details for PubMedID 8983677
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[Prognostic value of serial Doppler echocardiographic follow-up of transmitral flow patterns in patients with congestive heart failure who presented with pulmonary edema].
Journal of cardiology
1996; 27 (6): 321-327
Abstract
The predictive value of serial Doppler echocardiographic follow-up of transmitral flow patterns for the prognosis of patients with congestive heart failure who presented with pulmonary edema was evaluated in 80 consecutive patients with decreased left ventricular systolic function (ejection fraction < 40%). Restrictive patterns [peak early diastolic filling velocity (E)/peak late diastolic filling velocity (A) ratio (E/A) > 2 and/or deceleration time for E wave to decline to baseline (DcT) < 150 msec] were observed in 72 patients (90%) on admission. After intensive therapy, DcT showed a nonrestrictive pattern in 38 of 72 patients (53%). The survival rates at 1 year was 50% for the restrictive group, and 97% for the nonrestrictive group. E/A showed a nonrestrictive pattern in 37 of 56 patients (66%). The survival rates at 1 year was 86% for the restrictive group, and 58% for the nonrestrictive group. Serial Doppler echocardiographic follow-up of transmitral flow patterns is useful in predicting the prognosis in patients with congestive heart failure who presented with pulmonary edema.
View details for PubMedID 9062593
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[Phasic flow velocity characteristics of the right coronary artery in patients with aortic stenosis: a Doppler guide wire study].
Journal of cardiology
1996; 27 (5): 255-259
Abstract
This study investigated the characteristics of the phasic flow velocity pattern of the right coronary artery and the relationship to hemodynamic parameters in patients with aortic stenosis. Coronary flow velocities were recorded at the proximal (segment 1) and the distal (segment 4PD) portion of the right coronary artery using a Doppler guide wire (0.014-in, 15 MHz) in 10 patients with aortic stenosis and 8 control subjects with normal coronary arteries. The diastolic to systolic peak velocity ratio at both the proximal and distal portion were significantly greater in patients with aortic stenosis than in control subjects. Systolic flow reversal was not seen in the right coronary artery in control subjects, but it was observed in 5 patients (50%) at the proximal portion and in 10 patients (100%) at the distal portion. Peak velocity of flow reversal at the distal portion showed a significant correlation with mean pressure gradient across the aortic valve (y = -1.3x + 37.3, r = 0.71, p = 0.02). Systolic flow reversal is characteristic in the right coronary artery, especially at the distal portion, in patients with aortic stenosis. This may be related to the pressure difference across the aortic valve through the posterior descending artery.
View details for PubMedID 8642513
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[Evaluation of left ventricular volume and ejection fraction using three-dimensional transesophageal echocardiography].
Journal of cardiology
1996; 27 (4): 207-210
Abstract
Left ventricular (LV) volume and ejection fraction (EF) derived from three-dimensional echocardiography using a multiplane transesophageal probe (3D-TEE) were compared with LV volume and EF obtained from left ventriculography (LVG) in 14 patients (mean age: 61 years). Left ventricular volumes were calculated using a summation of disks algorithm based on multiple reconstructed short-axis cross-sections from 3D data. Left ventricular volume (end-diastole and end-systole) and EF from 3D-TEE were compared with those from LVG using linear regression analysis. Three-dimensional TEE demonstrated excellent correlations with LVG for measuring LV volume (r = 0.97, SEE = 11 ml) and EF (r = 0.95, SEE-4%), respectively. Three-dimensional TEE is useful for the measurement of LV volume and EF in the clinical setting.
View details for PubMedID 8642507
- Value and limitations of 'aortic valve resistance' in assessing severity of aortic stenosis in patients with low pressure gradient : a clinical study using dobutamine stress echocardiography Jpn J Med Ultrasonics 1996; 23 (4): 287
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[Value and limitations of valve resistance in assessing prosthetic aortic valve function: clinical study using dobutamine stress doppler echocardiography].
Journal of cardiology
1996; 27 (1): 9-13
Abstract
Hemodynamic resistance may be a useful index for the severity of valvular aortic stenosis, but little is known about the utility of valve resistance in assessing the prosthetic aortic valve function. This study investigated whether valve resistance is useful in assessing prosthetic valve function in 13 patients with normally functioning CarboMedics prosthetic aortic valves. Transvalvular pressure gradient, effective orifice area and valve resistance derived from two-dimensional and Doppler echocardiography were calculated before and after dobutamine infusion. Dobutamine was infused incrementally (3-12 micrograms/kg/min) under echocardiographic imaging. Transvalvular pressure gradient (24 +/- 7-->53 +/- 18 mmHg, p < 0.01) and valve resistance (102 +/- 32-->140 +/- 57 dynes.sec.cm-5, p < 0.01) significantly increased after dobutamine infusion. However, effective orifice area did not increase significantly (1.1 +/- 0.5-->1.2 +/- 0.5 cm2). These findings indicate that transvalvular pressure gradient and valve resistance are flow-dependent and should be treated with caution when assessing prosthetic valve function.
View details for PubMedID 8683434
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[Intravascular ultrasound scanning assessment of plaque distribution in the left anterior descending coronary artery just distal to the bifurcation].
Journal of cardiology
1995; 26 (6): 325-329
Abstract
Coronary plaque has a distinct spatial distribution with the peak incidence on the outer wall around the bifurcation of the left main coronary artery. Intravascular ultrasound scanning was used to evaluate the distribution of the plaque in the proximal site of the left anterior descending coronary artery in 16 patients. Coronary angiography showed the examined sites were normal in all patients. A cross-sectional coronary scan was recorded in the left anterior descending coronary artery just distal to the bifurcation using a 4.3 Fr, 30 MHz intravascular ultrasound catheter. The thickness of the plaque was measured at 0, 90, 180, and 270 degrees, where 0 degree indicates the left circumflex coronary artery branching direction. The scan was divided into four areas of 90 degrees and labeled 1 to 4 in the counterclockwise direction (site 1 was the left circumflex coronary artery branching direction). The thickness and area of the plaque were measured in each site. The percentage plaque fraction was calculated as (plaque area in each site)/(plaque area of all) x 100. In 15 (94%) of the 16 patients, images of crescent shaped plaques were obtained. The mean thicknesses of the plaque at sites 1-4 were 0.25 +/- 0.07 mm, 0.46 +/- 0.21 mm, 0.82 +/- 0.19 mm, and 0.42 +/- 0.23 mm, respectively. The mean percentage plaque fractions were 7.9 +/- 3.6% (site 1), 18.1 +/- 7.2% (site 2), 55.0 +/- 8.1% (site 3), 18.7 +/- 6.9% (site 4), respectively. In site 3, opposite to the left circumflex coronary artery branching, the thickness and percentage plaque fraction were significantly greater than the remaining three sites (p < 0.001). In vivo intravascular ultrasound scanning revealed that coronary plaque in angiographically normal left anterior descending coronary artery just distal to the bifurcation has a distinct distribution with a peak incidence opposite to the left circumflex coronary artery branching.
View details for PubMedID 8558410
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3-DIMENSIONAL MEASUREMENT OF LEFT-VENTRICULAR VOLUMES AND EJECTION FRACTION USING MULTIPLANE TRANSESOPHAGEAL ECHOCARDIOGRAPHY IN HUMAN-SUBJECTS
AMER HEART ASSOC. 1995: 1321
View details for Web of Science ID A1995TB48001314
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DYNAMIC 3-DIMENSIONAL IMAGING OF MITRAL-VALVE PROLAPSE USING MULTIPLANE TRANSESOPHAGEAL ECHOCARDIOGRAPHY
AMER HEART ASSOC. 1995: 3460
View details for Web of Science ID A1995TB48003438
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[Pseudoxanthoma elasticum associated with unstable angina and Leriche syndrome: a case report].
Journal of cardiology
1995; 26 (1): 43-49
Abstract
A 64-year-old man with a history of intermittent claudication presented with chest pain. On admission, he had yellowish papules with a "plucked chicken" appearance on his neck. Histological examination of the biopsy specimen of the lesion revealed degeneration and calcification of elastic fibers in the dermis. His daughter also had similar histological changes in the skin. The diagnosis was pseudoxanthoma elasticum. Fundoscopic examination revealed angioid streaks. Electrocardiography showed inverted T waves in V2-V6, and echocardiography revealed hypokinesis in the anterior wall of the left ventricle. Emergency catheterization showed 90% stenosis in the left anterior descending coronary artery, total occlusion of the abdominal aorta, and severe stenosis in the right subclavian artery. He was treated medically and had no recurrent episodes of chest pain. A careful examination for cardiovascular diseases should be considered in patients with pseudoxanthoma elasticum.
View details for PubMedID 7666344
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[Detection of hibernating myocardium in patients with myocardial infarction by low-dose dobutamine echocardiography: comparison with thallium-201 scintigraphy with reinjection].
Journal of cardiology
1995; 25 (4): 155-161
Abstract
The identification of hibernating myocardium is important for selecting patients who will benefit from coronary revascularization. The relationship between echocardiographic and radioisotopic markers of hibernating myocardium and postrevascularization recovery of myocardial function was investigated in 21 patients who underwent successful revascularization. Each patient underwent low-dose dobutamine stress echocardiography and thallium-201 (201Tl) scintigraphy with reinjection before revascularization. The presence of contractile reserve in dobutamine stress echocardiography and Tl uptake in 201Tl scintigraphy with reinjection were defined as markers of hibernating myocardium. Follow-up echocardiograms were evaluated for improved regional wall motion in all patients at a mean of 8.6 months after revascularization. Sensitivity, specificity, and positive and negative predictive values of low-dose dobutamine stress echocardiography for indicating recovery of function after revascularization were 75.0%, 77.8%, 81.8%, and 70.0%, respectively. Sensitivity, specificity, and positive and negative predictive values of 201Tl scintigraphy with reinjection for indicating recovery of function after revascularization were 91.7%, 55.6%, 73.3%, and 83.3%, respectively. There were no statistical differences between low-dose dobutamine echocardiography and 201Tl scintigraphy in predicting postrevascularization recovery of function patients with hibernating myocardium.
View details for PubMedID 7752049
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[Relationship between regional flow reserve supplied by the great saphenous vein graft and regional left ventricular wall motion: a Doppler guide wire study].
Journal of cardiology
1995; 25 (2): 83-88
Abstract
The relationship between regional flow reserve supplied by a great saphenous vein graft and myocardial infarction and anterior wall motion assessed by left ventriculography was studied in 28 patients with no stenosis in the great saphenous vein graft and the peripheral site of the recipient left anterior descending coronary arteries. The proximal segment to the anastomosis was totally or subtotally occluded. The resting graft blood flow velocity was measured using a Doppler guide wire, then 0.56 mg/kg of dipyridamole was injected for 4 minutes intravenously and the resultant increase in graft blood flow velocity was recorded. The regional flow reserve of the anterior wall supplied by great saphenous vein grafts in 11 patients with anterior myocardial infarction (MI group) was significantly lower than that in 17 patients without myocardial infarction (non-MI group) (1.5 +/- 0.3 vs 2.6 +/- 0.7, p < 0.01). The flow reserve supplied by great saphenous vein grafts in 11 patients with normal anterior wall motion was 2.8 +/- 0.7, 10 with hypokinesis 1.9 +/- 0.3, and with akinesis 1.3 +/- 0.3. Reduced anterior wall motion induced a significant decrease in the flow reserve of the anterior wall supplied by the great saphenous vein graft (p < 0.01). The anterior wall motion score of four segments assessed by left ventriculography showed a significant correlation with the flow reserve of the anterior wall supplied by the great saphenous vein graft (y = -0.24 x + 3.7, r = 0.75, p < 0.001). The results show infarcted myocardium was an important influence on coronary flow reserve.
View details for PubMedID 7897611
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[Assessment of coronary stenosis severity using a Doppler guide wire in vivo: is the continuity equation applicable to moderate to severe coronary artery stenosis?].
Journal of cardiology
1995; 25 (1): 1-7
Abstract
The usefulness of a Doppler guide wire was evaluated in the estimation of coronary stenosis severity in patients with moderate to severe coronary stenosis using the continuity equation. The maximal coronary flow velocities (V) proximal to the stenosis (p), at the stenosis (s), and distal to the stenosis (d) were measured using a Doppler guide wire (12-MHz, 0.018-in) in 12 patients with mild coronary stenosis (less than 50% diameter stenosis: group A) and 12 patients with moderate to severe coronary stenosis (more than 50% diameter stenosis: group B). Percent diameter stenosis (%DS) was calculated from Vp/Vs by: %DS = (1 - square root of Vp/Vs) x 100 (%) (Vp = the maximal velocity proximal to the stenosis; Vs = the peak velocity at the stenotic site) Percent DS was calculated from Vd/Vs by: %DS = (1 - square root of Vd/Vs) x 100 (%) (Vd = the peak velocity distal to the stenosis) Regression of Doppler-derived %DS from Vp/Vs compared to quantitative coronary angiographic % DS were: Group A: y = 0.83x + 3.0 (r = 0.79), Group B: y = 0.63x + 9.4 (r = 0.81), Overall: y = 0.63x + 9.6 (r = 0.91) Regression of Doppler-derived %DS from Vd/Vs compared to quantitative coronary angiographic %DS were: Group A: y = 0.98x - 1.0 (r = 0.81), Group B: y = 0.67x + 14.6 (r = 0.84), Overall: y = 0.79x + 7.6 (r = 0.91) The continuity equation method using a Doppler guide wire underestimates coronary stenosis severity in patients with moderate to severe coronary stenosis, although Doppler-derived %DS is correlated with angiographic %DS.
View details for PubMedID 7877097
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IMPROVED VISUALIZATION OF PULMONARY VENOUS FLOW DOPPLER SIGNAL BY INTRAVENOUS-INJECTION OF SONICATED ALBUMIN
AMER HEART ASSOC. 1994: 555
View details for Web of Science ID A1994PN41703024
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A NEW METHOD FOR DETERMINING CARDIAC-OUTPUT BY FLOW VELOCITY VECTOR PROFILE DERIVED FROM COLOR-FLOW MAPPING
AMER HEART ASSOC. 1994: 495
View details for Web of Science ID A1994PN41702698
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[Usefulness and limitations of dobutamine stress echocardiography for detection of coronary artery disease].
Journal of cardiology
1994; 24 (5): 347-355
Abstract
The value of dobutamine stress echocardiography for detecting coronary artery disease was evaluated in 67 patients with normal left ventricular wall motion at rest who also underwent quantitative angiography. The overall sensitivity and specificity of dobutamine stress echocardiography for detecting coronary artery disease were 83% and 70%, respectively. The sensitivities for detecting multivessel disease and single vessel disease were 92% and 76%, respectively. The sensitivity of dobutamine stress echocardiography was 91% in patients treated without beta-blocker, and 70% in patients treated with beta-blocker (p < 0.001). The relatively low peak heart rate during dobutamine infusion in patients treated with beta-blocker seems to affect the sensitivity of dobutamine stress echocardiography. There were no severe complications during dobutamine infusion. Dobutamine stress echocardiography is a safe and accurate method for detecting coronary artery disease. However, an additional technique to increase peak heart rate in patients treated with beta-blocker such as injection of atropin should be considered.
View details for PubMedID 7932068
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QUANTITATION OF LEFT-TO-RIGHT SHUNTS IN SECUNDUM ATRIAL SEPTAL-DEFECT - A CLINICAL-APPLICATION OF 2-DIMENSIONAL CONTRAST ECHOCARDIOGRAPHY WITH USE OF SONICATED ALBUMIN
ELSEVIER SCIENCE INC. 1994: A468
View details for Web of Science ID A1994PP51801854
- Aortic dissection: early diagnosis and treatment Gendai-Iryo 1994; 26 (1): 233-238
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[Clinical characteristics and surgical treatment of atrial septal defect in adults].
Japanese circulation journal
1994; 58: 1250-1254
View details for PubMedID 7699769
- Intravascular ultrasound imaging in renal bifurcation with a reference to the location and development of atherosclerosis Jpn J Med Ultrasonics 1994; 21: 451-454
- Syndrome X and coronary angiography Practical Cardiology 1994; 2: 94-96
- The effect of a trackball-derived region of interest on left ventricular volume using an acoustic quantification method Jpn J Med Ultrasonics 1994; 21: 489-494