Bio


Jon Park, M.D., F.R.C.S.C is the Saunders Family Endowed Professor in Neurosurgery, the Chief of Spine Neurosurgery, Director of Spine Research Laboratory, and Director of Spine Fellowship Program at Stanford University Medical Center. His clinical practice specializes in surgically and non-surgically managing the spinal disorders that affect people's lives, such as debilitating pain and weakness that comes from spine disc problems, spine tumors, spine scoliosis, and spine trauma.

Dr. Park is an internationally recognized leader in the field of spine surgery. He is an active member of American Association of Neurosurgery, North American Spine Surgery, Scoliosis Research Society, and Cervical Spine Research Society. His research focuses on spinal disc regeneration in an effort to target the underlying causes using stem cells and mesenchymal stem cells for inter-vertebral disc regeneration. His research also pioneers in spinal bio-mechanics to apply mechanical principles to ensure spinal stability.

Clinical Focus


  • Minimally Invasive Spine surgery
  • Spine Trauma
  • Cyberknife Spine Tumor
  • Spine Tumor Surgery
  • Spine Deformity Surgery
  • Neurological Surgery

Academic Appointments


Administrative Appointments


  • Chief, Spine Neurosurgery, Stanford UMC. (2006 - Present)
  • Professor, Stanford University School of Medicine (2017 - Present)
  • Associate Professor, Stanford Univ. School of Medicine, Department of Neurosurgery (2010 - 2017)
  • Director, Comprehensive Spine Neurosurgery Program. Spine Fellowship and Spine Research Program, Stanford UMC. (2006 - Present)
  • Assistant Professor, Stanford Univ. School of Medicine, Department of Neurosurgery (2003 - 2009)
  • Assistant Professor, University of Washington School of Medicine, Neurological Surgery (2000 - 2003)
  • Clinical Instructor, UCLA School of Medicine, Neurological Surgery (1999 - 2000)

Honors & Awards


  • Stanford University School of Medicine Academic Grant Recipient, Stanford (2003-2004)
  • Saunders Family Endow Chair, Stanford Univsersity (2017)
  • President of Fellow's Society, Montreal Neurological Institute, Montreal Neurological Institute (1998-1999)
  • Kathleen Whipple Scholarship, University of Rochester School of Medicine (1990-1993)
  • Robert I. Weed Hematology Research Fellowship, Johns Hopkins University (1991)
  • HANA Graduate Merit Scholarship, Johns Hopkins University (1990)
  • Health Commendation Award, City of Baltimore (1986)

Professional Education


  • Fellowship: UCLA Medical Center Dept of Neurosurgery (2000) CA
  • Residency: Montreal Neurological Institute (1999) QC Canada
  • Residency: University of Washington Medical Center (1995) WA
  • Board Certification: American Board of Neurological Surgery, Neurological Surgery (2005)
  • Spine Fellowship, UCLA Medical Center, Neurological Surgery (2000)
  • Chief Resident, McGill University, Neurosurgery, Neurological Surgery (1999)
  • Fellowship, Lahey Hitchcock Medical Center, Interventional Neuroradiology (1997)
  • Intern & Resident, University of Washington, General Surgery (1995)
  • B.A., Johns Hopkins University, Biophysics (1989)

Current Research and Scholarly Interests


Non-fusion dynamic spinal stabilization, artificial disc technologies, and regenerative spinal technologies.

2024-25 Courses


Stanford Advisees


Graduate and Fellowship Programs


All Publications


  • Treatment Concept and Technical Considerations of Biportal Endoscopic Spine Surgery for Lumbar Spinal Stenosis. Asian spine journal Park, J., Ahn, D. K., Choi, D. J. 2023

    Abstract

    Decompression must be a major composure of surgical procedures for degenerative lumbar spinal stenosis. In addition to sufficient decompression for guarantee of relieving neurologic pain, compensating surgical instability after wider laminectomy and foraminotomy, and instrumentation with caging and fusion with grafting are performed for securing or restoring foraminal dimension, and correcting coronal/sagittal imbalance for expecting longer survival of adjacent segment. Endoscopic spinal surgery (ESS), full-endoscopic or biportal-, has been developed under a flag of successful decompression with preserving structural integrity as much as possible in helps of magnification and illumination, and gives a technical possibility and feasibility to solve LSS by decompression-alone. There come, recently, lots of endoscopic trials for overcoming conventional surgical treatment in need of wider dissection and escaping inevitable complications from surgical damage and compensating fusion technique. However, biportal-ESS till a recent era has been showing some technical limitations including clinical difficulties in accessibility for more moderate to severe stenosis and challenges for complicated conditions with segmental ventral slip, isthmic defect, stenosis combined with foraminal stenosis or foraminal disc rupture, or degenerative segmental scoliosis with disc height collapsing and endplate fatigue fracture. Because decompression-alone, itself, is just a skill for eliminating pathologies, and no protentional function of preserving degenerative structure young forever or stopping recurrency of disc degeneration or creeping subsidence foramen. The purpose of this review on clinical reports is to suggest potential possibility of Biportal-ESS for treating degenerative lumbar disorders by sufficient decompression, adequate elimination of various pathologies, and decreasing technical complications in deep considering of skillful tricks and trades, and in hope of being a basic skill for developing better innovative spinal surgical techniques in near future.

    View details for DOI 10.31616/asj.2023.0409

    View details for PubMedID 38130043

  • A neurovascular-unit-on-a-chip for the evaluation of the restorative potential of stem cell therapies for ischaemic stroke. Nature biomedical engineering Lyu, Z., Park, J., Kim, K., Jin, H., Wu, H., Rajadas, J., Kim, D., Steinberg, G. K., Lee, W. 2021

    Abstract

    The therapeutic efficacy of stem cells transplanted into an ischaemic brain depends primarily on the responses of the neurovascular unit. Here, we report the development and applicability of a functional neurovascular unit on a microfluidic chip as a microphysiological model of ischaemic stroke that recapitulates the function of the blood-brain barrier as well as interactions between therapeutic stem cells and host cells (human brain microvascular endothelial cells, pericytes, astrocytes, microglia and neurons). We used the model to track the infiltration of a number of candidate stem cells and to characterize the expression levels of genes associated with post-stroke pathologies. We observed that each type of stem cell showed unique neurorestorative effects, primarily by supporting endogenous recovery rather than through direct cell replacement, and that the recovery of synaptic activities is correlated with the recovery of the structural and functional integrity of the neurovascular unit rather than with the regeneration of neurons.

    View details for DOI 10.1038/s41551-021-00744-7

    View details for PubMedID 34385693

  • External validation of a predictive model of adverse events following spine surgery. The spine journal : official journal of the North American Spine Society Fatemi, P., Zhang, Y., Han, S. S., Purington, N., Zygourakis, C. C., Veeravagu, A., Desai, A., Park, J., Shuer, L. M., Ratliff, J. K. 2021

    Abstract

    BACKGROUND CONTEXT: We lack models that reliably predict 30-day postoperative adverse events (AEs) following spine surgery.PURPOSE: We externally validated a previously developed predictive model for common 30-day adverse events (AEs) after spine surgery.STUDY DESIGN/SETTING: This prospective cohort study utilizes inpatient and outpatient data from a tertiary academic medical center.PATIENT SAMPLE: We assessed a prospective cohort of all 276 adult patients undergoing spine surgery in the Department of Neurosurgery at a tertiary academic institution between April 1, 2018 and October 31, 2018. No exclusion criteria were applied.OUTCOME MEASURES: Incidence of observed AEs was compared with predicted incidence of AEs. Fifteen assessed AEs included: pulmonary complications, congestive heart failure, neurological complications, pneumonia, cardiac dysrhythmia, renal failure, myocardial infarction, wound infection, pulmonary embolus, deep venous thrombosis, wound hematoma, other wound complication, urinary tract infection, delirium, and other infection.METHODS: Our group previously developed the Risk Assessment Tool for Adverse Events after Spine Surgery (RAT-Spine), a predictive model of AEs within 30 days following spine surgery using a cohort of approximately one million patients from combined Medicare and MarketScan databases. We applied RAT-Spine to the single academic institution prospective cohort by entering each patient's preoperative medical and demographic characteristics and surgical type. The model generated a patient-specific overall risk score ranging from 0 to 1 representing the probability of occurrence of any AE. The predicted risks are presented as absolute percent risk and divided into low (<17%), medium (17-28%), and high (>28%).RESULTS: Among the 276 patients followed prospectively, 76 experienced at least one 30-day postoperative AE. Slightly more than half of the cohort were women (53.3%). The median age was slightly lower in the non-AE cohort (63 vs 66.5 years old). Patients with Medicaid comprised 2.5% of the non-AE cohort and 6.6% of the AE cohort. Spinal fusion was performed in 59.1% of cases, which was comparable across cohorts. There was good agreement between the predicted AE and observed AE rates, Area Under the Curve (AUC) 0.64 (95% CI 0.56-0.710). The incidence of observed AEs in the prospective cohort was 17.8% among the low-risk group, 23.0% in the medium-risk group, and 38.4% in the high risk group (p = 0.003).CONCLUSIONS: We externally validated a model for postoperative AEs following spine surgery (RAT-Spine). The results are presented as low-, moderate-, and high-risk designations.

    View details for DOI 10.1016/j.spinee.2021.06.006

    View details for PubMedID 34116215

  • Objective activity tracking in spine surgery: a prospective feasibility study with a low-cost consumer grade wearable accelerometer. Scientific reports Stienen, M. N., Rezaii, P. G., Ho, A. L., Veeravagu, A., Zygourakis, C. C., Tomkins-Lane, C., Park, J., Ratliff, J. K., Desai, A. M. 2020; 10 (1): 4939

    Abstract

    Patient-reported outcome measures (PROMs) are commonly used to estimate disability of patients with spinal degenerative disease. Emerging technological advances present an opportunity to provide objective measurements of activity. In a prospective, observational study we utilized a low-cost consumer grade wearable accelerometer (LCA) to determine patient activity (steps per day) preoperatively (baseline) and up to one year (Y1) after cervical and lumbar spine surgery. We studied 30 patients (46.7% male; mean age 57 years; 70% Caucasian) with a baseline activity level of 5624 steps per day. The activity level decreased by 71% in the 1st postoperative week (p<0.001) and remained 37% lower in the 2nd (p<0.001) and 23% lower in the 4th week (p=0.015). At no time point until Y1 did patients increase their activity level, compared to baseline. Activity was greater in patients with cervical, as compared to patients with lumbar spine disease. Age, sex, ethnic group, anesthesia risk score and fusion were variables associated with activity. There was no correlation between activity and PROMs, but a strong correlation with depression. Determining activity using LCAs provides real-time and longitudinal information about patient mobility and return of function. Recovery took place over the first eight postoperative weeks, with subtle improvement afterwards.

    View details for DOI 10.1038/s41598-020-61893-4

    View details for PubMedID 32188895

  • Association between Physician Industry Payments and Cost of Anterior Cervical Discectomy and Fusion in Medicare Beneficiaries. World neurosurgery Liu, C. n., Ahmed, K. n., Chen, C. L., Dudley, R. A., Gonzales, R. n., Orrico, K. n., Yerneni, K. n., Stienen, M. N., Veeravagu, A. n., Desai, A. n., Park, J. n., Ratliff, J. K., Zygourakis, C. C. 2020

    Abstract

    Neurosurgical spine specialists receive considerable amounts of industry support which may impact the cost of care. The aim of this study was to evaluate the association between industry payments received by spine surgeons and the total hospital and operating room (OR) costs of an anterior cervical discectomy and fusion (ACDF) procedure among Medicare beneficiaries.All ACDF cases were identified among the Medicare Carrier Files, from January 1, 2013, to December 31, 2014, and matched to the Medicare Inpatient Baseline File. The total hospital and OR charges were obtained for these cases. Charges were converted to cost using year-specific cost-to-charge ratios. Surgeons were identified among Open Payments database, which is used to quantify industry support. Analyses was performed to examine the association between industry payments received and ACDF costs.Matching resulting in the inclusion of 2,209 ACDF claims from 2013-2014. In 2013 and 2014, the mean total cost for an ACDF was $21,798 and $21,008, respectively; mean OR cost was $5,878 and $6,064, respectively. Mann-Whitney U test demonstrated no significant differences in the mean total or OR cost for an ACDF based on quartile of general industry payment received (p=0.21 and p=0.54), and linear regression found no association between industry general payments, research support, or investments on the total hospital cost (p=0.41, p=0.13, and p=0.25), or OR cost for an ACDF (p=0.35, p=0.24, and p=0.40).This study suggests that spine surgeons performing ACDF surgeries may receive industry support without impacting the cost of care.

    View details for DOI 10.1016/j.wneu.2020.08.023

    View details for PubMedID 32791230

  • Improving the Patient-Physician Relationship in the Digital Era - Transformation From Subjective Questionnaires Into Objective Real-Time and Patient-Specific Data Reporting Tools. Neurospine Maldaner, N., Desai, A., Gautschi, O. P., Regli, L., Ratliff, J. K., Park, J., Stienen, M. N. 2019; 16 (4): 712–14

    View details for DOI 10.14245/ns.1938400.200

    View details for PubMedID 31905462

  • Objective measures of functional impairment for degenerative diseases of the lumbar spine: a systematic review of the literature SPINE JOURNAL Stienen, M. N., Ho, A. L., Staartjes, V. E., Maldaner, N., Veeravagu, A., Desai, A., Gautschi, O. P., Bellut, D., Regli, L., Ratliff, J. K., Park, J. 2019; 19 (7): 1276–93
  • Patient Satisfaction and Press Ganey Scores for Spine Versus Nonspine Neurosurgery Clinics. Clinical spine surgery Chen, Y., Johnson, E., Montalvo, C., Stratford, S., Veeravagu, A., Tharin, S., Desai, A., Ratliff, J., Shuer, L., Park, J. 2019

    Abstract

    STUDY DESIGN: Retrospective survey review.OBJECTIVE: We seek to evaluate satisfaction scores in patients seen in neurosurgical spine versus neurosurgical nonspine clinics.SUMMARY OF BACKGROUND DATA: The Press Ganey survey is a well-established metric for measuring hospital performance and patient satisfaction. These measures have important implications in setting hospital policy and guiding interventions to improve patient perceptions of care.METHODS: Retrospective Press Ganey survey review was performed to identify patient demographics and patient visit characteristics from January 1st, 2012 to October 10th, 2017 at Stanford Medical Center. A total of 40 questions from the Press Ganey survey were investigated and grouped in categories addressing physician and nursing care, personal concerns, admission, room, meal, operating room, treatment and discharge conditions, visitor accommodations and overall clinic assessment. Raw ordinal scores were converted to continuous scores of 100 for unpaired student t test analysis. We identified 578 neurosurgical spine clinic patients and 1048 neurosurgical nonspine clinic patients.RESULTS: Spine clinic patients reported lower satisfaction scores in aggregate (88.2 vs. 90.1; P=0.0014), physician (89.5 vs. 92.6; P=0.0002) and nurse care (91.3 vs. 93.4; P=0.0038), personal concerns (88.2 vs. 90.9; P=0.0009), room (81.0 vs. 83.1; P=0.0164), admission (90.8 vs. 92.6; P=0.0154) and visitor conditions (87.0 vs. 89.2; P=0.0148), and overall clinic assessment (92.9 vs. 95.5; P=0.005).CONCLUSIONS: This study is the first to evaluate the relationship between neurosurgical spine versus nonspine clinic with regards to patient satisfaction. The spine clinic cohort reported less satisfaction than the nonspine cohort in all significant questions on the Press Ganey survey. Our findings suggest that efforts should be made to further study and improve patient satisfaction in spine clinics.LEVEL OF EVIDENCE: Level III.

    View details for DOI 10.1097/BSD.0000000000000825

    View details for PubMedID 30969193

  • Reliability of the 6-minute walking test smartphone application. Journal of neurosurgery. Spine Stienen, M. N., Gautschi, O. P., Staartjes, V. E., Maldaner, N. n., Sosnova, M. n., Ho, A. L., Veeravagu, A. n., Desai, A. n., Zygourakis, C. C., Park, J. n., Regli, L. n., Ratliff, J. K. 2019: 1–8

    Abstract

    Objective functional measures such as the 6-minute walking test (6WT) are increasingly applied to evaluate patients with degenerative diseases of the lumbar spine before and after (surgical) treatment. However, the traditional 6WT is cumbersome to apply, as it requires specialized in-hospital infrastructure and personnel. The authors set out to compare 6-minute walking distance (6WD) measurements obtained with a newly developed smartphone application (app) and those obtained with the gold-standard distance wheel (DW).The authors developed a free iOS- and Android-based smartphone app that allows patients to measure the 6WD in their home environment using global positioning system (GPS) coordinates. In a laboratory setting, the authors obtained 6WD measurements over a range of smartphone models, testing environments, and walking patterns and speeds. The main outcome was the relative measurement error (rME; in percent of 6WD), with |rME| < 7.5% defined as reliable. The intraclass correlation coefficient (ICC) for agreement between app- and DW-based 6WD was calculated.Measurements (n = 406) were reliable with all smartphone types in neighborhood, nature, and city environments (without high buildings), as well as with unspecified, straight, continuous, and stop-and-go walking patterns (ICC = 0.97, 95% CI 0.97-0.98, p < 0.001). Measurements were unreliable indoors, in city areas with high buildings, and for predominantly rectangular walking courses. Walking speed had an influence on the ME, with worse accuracy (2% higher rME) for every kilometer per hour slower walking pace (95% CI 1.4%-2.5%, p < 0.001). Mathematical adjustment of the app-based 6WD for velocity-dependent error mitigated the rME (p < 0.011), attenuated velocity dependence (p = 0.362), and had a positive effect on accuracy (ICC = 0.98, 95% CI 0.98-0.99, p < 0.001).The new, free, spine-specific 6WT smartphone app measures the 6WD conveniently by using GPS coordinates, empowering patients to independently determine their functional status before and after (surgical) treatment. Measurements of 6WD obtained for the target population under the recommended circumstances are highly reliable.

    View details for DOI 10.3171/2019.6.SPINE19559

    View details for PubMedID 31518975

  • Characterization of Brain Dysfunction Induced by Bacterial Lipopeptides That Alter Neuronal Activity and Network in Rodent Brains JOURNAL OF NEUROSCIENCE Kim, K., Zamaleeva, A. I., Lee, Y., Ahmed, M., Kim, E., Lee, H., Pothineni, V., Tao, J., Rhee, S., Jayakumar, M., Inayathullah, M., Sivanesan, S., Red-Horse, K., Palmer, T. D., Park, J., Madison, D. V., Lee, H., Rajadas, J. 2018; 38 (50): 10672–91
  • Posterior open reduction and internal fixation of C1 fractures: the C-clamp technique ACTA NEUROCHIRURGICA Gelinas-Phaneuf, N., Stienen, M., Park, J. 2018; 160 (12): 2451–57
  • Radiographic Rate and Clinical Impact of Pseudarthrosis in Spine Radiosurgery for Metastatic Spinal Disease. Cureus Zhang, M., Appelboom, G., Ratliff, J. K., Soltys, S. G., Adler, J. R., Park, J., Chang, S. D. 2018; 10 (11): e3631

    Abstract

    Purpose Pseudarthrosis within the spine tumor population is increased from perioperative radiation and complex stabilization for invasive and recurrent pathology. We report the radiographic and clinical rates of pseudarthrosis following multiple courses of instrumented fusion and perioperative stereotactic radiosurgery (SRS). Methods We performed a single institution review of 418 patients treated with non-isocentric SRS for spine between October 2002 and January 2013, identifying those with spinal instrumentation and greater than six months of follow-up. Surgical history, radiation planning, and radiographic outcomes were documented. Results Eleven patients whomet criteria for inclusion underwent 21 sessions of spinal SRS and 16 instrumented operations. Radiographic follow-up was 48.9 months; 3/11 (27%) were with radiographic hardware failure, and one (9%) separate case ultimately warranted externalization due to tumor recurrence. SRS was administered to treat progression of disease in 12/21 (57%) procedures, and residual lesions in 7/11 (64%) procedures. Following first and second SRS, 8/11 (73%) and 2/7 (29%) patients were with symptomatic improvement, respectively. Conclusion Risk of pseudarthrosis following SRS for patients with oncologic spinal lesions will become increasingly apparent with the optimized management of and survival from spinal pathologies. We highlight how the need for local control outpaces the risk of instrumentation failure.

    View details for PubMedID 30705790

  • Assessment of Biomechanical Changes After Sacroiliac Joint Fusion by Application of the 3-Dimensional Motion Analysis Technique WORLD NEUROSURGERY Jeong, J., Leasure, J. M., Park, J. 2018; 117: E538–E543

    Abstract

    Sacroiliac (SI) joint motion is complex and is poorly understood overall. In this study we evaluated a new biomechanical method developed to provide more insight into SI joint movement and to elucidate biomechanical changes after SI joint fusion surgery in a one-leg standing model.Eight lumbosacral cadaver specimens (L5-pelvis specimens, age 28-57 years, 6 female and 2 male) were used in this experiment. We analyzed the changes in range of motion (ROM) in single-plane motion and mobility in 3 groups of patients: intact, unilateral fusion, and bilateral fusion groups. For statistical analysis, we used repeated-measures analysis of variance to compare SI joint ROM among the 3 groups. iFuse implants were prepared using the standard posterior placement technique. Pure-moment multidirectional bending tests were performed in each direction (nutation and counternutation, axial rotation, and lateral bending).Average ROM in single-plane motion and mobility of the intact SI joint were 4.5 ± 3.3° and 4.8 ± 3.4°, respectively in nutation-counternutation; 2.9 ± 2.1° and 3.3 ± 2.3°, respectively, in axial rotation; and 1.5 ± 1.5° and 2.8 ± 2.5°, respectively, in lateral bending. We observed statistically significantly (P = 0.05) greater mobility in lateral moment testing than in single motion testing. Comparisons among the intact, unilateral fusion, and bilateral fusion groups showed statistically significant differences in the lateral moment test.This study suggests that our new biomechanical method for SI joint evaluation may provide improved insight into SI joint movement and biomechanical changes after SI joint fusion surgery in a one-leg standing model.

    View details for PubMedID 29933084

  • Predicting complication risk in spine surgery: a prospective analysis of a novel risk assessment tool. Journal of neurosurgery. Spine Veeravagu, A., Li, A., Swinney, C., Tian, L., Moraff, A., Azad, T. D., Cheng, I., Alamin, T., Hu, S. S., Anderson, R. L., Shuer, L., Desai, A., Park, J., Olshen, R. A., Ratliff, J. K. 2017: 1-11

    Abstract

    OBJECTIVE The ability to assess the risk of adverse events based on known patient factors and comorbidities would provide more effective preoperative risk stratification. Present risk assessment in spine surgery is limited. An adverse event prediction tool was developed to predict the risk of complications after spine surgery and tested on a prospective patient cohort. METHODS The spinal Risk Assessment Tool (RAT), a novel instrument for the assessment of risk for patients undergoing spine surgery that was developed based on an administrative claims database, was prospectively applied to 246 patients undergoing 257 spinal procedures over a 3-month period. Prospectively collected data were used to compare the RAT to the Charlson Comorbidity Index (CCI) and the American College of Surgeons National Surgery Quality Improvement Program (ACS NSQIP) Surgical Risk Calculator. Study end point was occurrence and type of complication after spine surgery. RESULTS The authors identified 69 patients (73 procedures) who experienced a complication over the prospective study period. Cardiac complications were most common (10.2%). Receiver operating characteristic (ROC) curves were calculated to compare complication outcomes using the different assessment tools. Area under the curve (AUC) analysis showed comparable predictive accuracy between the RAT and the ACS NSQIP calculator (0.670 [95% CI 0.60-0.74] in RAT, 0.669 [95% CI 0.60-0.74] in NSQIP). The CCI was not accurate in predicting complication occurrence (0.55 [95% CI 0.48-0.62]). The RAT produced mean probabilities of 34.6% for patients who had a complication and 24% for patients who did not (p = 0.0003). The generated predicted values were stratified into low, medium, and high rates. For the RAT, the predicted complication rate was 10.1% in the low-risk group (observed rate 12.8%), 21.9% in the medium-risk group (observed 31.8%), and 49.7% in the high-risk group (observed 41.2%). The ACS NSQIP calculator consistently produced complication predictions that underestimated complication occurrence: 3.4% in the low-risk group (observed 12.6%), 5.9% in the medium-risk group (observed 34.5%), and 12.5% in the high-risk group (observed 38.8%). The RAT was more accurate than the ACS NSQIP calculator (p = 0.0018). CONCLUSIONS While the RAT and ACS NSQIP calculator were both able to identify patients more likely to experience complications following spine surgery, both have substantial room for improvement. Risk stratification is feasible in spine surgery procedures; currently used measures have low accuracy.

    View details for DOI 10.3171/2016.12.SPINE16969

    View details for PubMedID 28430052

  • 3D patterned stem cell differentiation using thermo-responsive methylcellulose hydrogel molds. Scientific reports Lee, W., Park, J. 2016; 6: 29408

    Abstract

    Tissue-specific patterned stem cell differentiation serves as the basis for the development, remodeling, and regeneration of the multicellular structure of the native tissues. We herein proposed a cytocompatible 3D casting process to recapitulate this patterned stem cell differentiation for reconstructing multicellular tissues in vitro. We first reconstituted the 2D culture conditions for stem cell fate control within 3D hydrogel by incorporating the sets of the diffusible signal molecules delivered through drug-releasing microparticles. Then, utilizing thermo-responsivity of methylcellulose (MC), we developed a cytocompatible casting process to mold these hydrogels into specific 3D configurations, generating the targeted spatial gradients of diffusible signal molecules. The liquid phase of the MC solution was viscous enough to adopt the shapes of 3D impression patterns, while the gelated MC served as a reliable mold for patterning the hydrogel prepolymers. When these patterned hydrogels were integrated together, the stem cells in each hydrogel distinctly differentiated toward individually defined fates, resulting in the formation of the multicellular tissue structure bearing the very structural integrity and characteristics as seen in vascularized bones and osteochondral tissues.

    View details for DOI 10.1038/srep29408

    View details for PubMedID 27381562

    View details for PubMedCentralID PMC4933913

  • Building an electronic health record integrated quality of life outcomes registry for spine surgery JOURNAL OF NEUROSURGERY-SPINE Azad, T. D., Kalani, M., Wolf, T., Kearney, A., Lee, Y., Flannery, L., Chen, D., Berroya, R., Eisenberg, M., Park, J., Shuer, L., Kerr, A., Ratliff, J. K. 2016; 24 (1): 176-185

    Abstract

    Demonstrating the value of spine care requires adequate outcomes assessment. Long-term outcomes are best measured as overall improvement in quality of life (QOL) after surgical intervention. Present registries often require parallel data entry, introducing inefficiencies and limiting compliance. The authors detail the methodology of constructing an integrated electronic health record (EHR) system to collect QOL metrics and demonstrate the effect of data collection on routine clinical workflow. A streamlined approach to collecting QOL data can capture patient data without requiring dual data entry and without increasing clinic visit times.Through extensive literature review, a combination of QOL assessments was selected, consisting of the Patient Health Questionnaire-2 and -9, Oswestry Disability Index, Neck Disability Index, and visual analog scale for pain. These metrics were used to provide assessment of QOL following spine surgery and were incorporated into standard clinic workflow by a multidisciplinary team of surgeons, advanced practice providers, and health care information technology specialists. A clinical dashboard tracking more than 25 patient variables was developed. Clinic flow was assessed and opportunities for improvement reviewed. Duration of clinic visits before and after initiation of QOL measure capture was recorded, with assessment of mean clinic visit times for the 12 months before and the 12 months after implementation.The integrated QOL capture was instituted for 3 spine surgeons in a tertiary care academic center. In the 12-month period prior to initiating collection of QOL data, 806 new patient visits were completed with an average visit time of 127.9 ± 51.5 minutes. In the 12 months after implementation, 1013 new patient visits were recorded, with 791 providing QOL measures with an average visit time of 117.0 ± 45.7 minutes. Initially the primary means of collecting patient outcome data was via paper form, with gradual transition to collection via entry into the electronic medical records system. To improve electronic data capture, paper forms were eliminated and an online portal used as part of the patient rooming process. This improved electronic capture to nearly 98% without decreasing the number of patients enrolled in the process.A systematic approach to collecting spine-related QOL data within an EHR system is feasible and offers distinct advantages over registries that require dual data entry. The process of data collection does not impact patients' clinical visit or providers' clinical workflow. This approach is scalable, and may form the foundation for a decentralized outcomes registry network.

    View details for DOI 10.3171/2015.3.SPINE141127

    View details for Web of Science ID 000367028000022

    View details for PubMedID 26431073

  • 3D patterned stem cell differentiation using thermo-responsive methylcellulose hydrogel molds Scientific Reports Lee, W., Park, J. 2016; 6: 29408

    Abstract

    Tissue-specific patterned stem cell differentiation serves as the basis for the development, remodeling, and regeneration of the multicellular structure of the native tissues. We herein proposed a cytocompatible 3D casting process to recapitulate this patterned stem cell differentiation for reconstructing multicellular tissues in vitro. We first reconstituted the 2D culture conditions for stem cell fate control within 3D hydrogel by incorporating the sets of the diffusible signal molecules delivered through drug-releasing microparticles. Then, utilizing thermo-responsivity of methylcellulose (MC), we developed a cytocompatible casting process to mold these hydrogels into specific 3D configurations, generating the targeted spatial gradients of diffusible signal molecules. The liquid phase of the MC solution was viscous enough to adopt the shapes of 3D impression patterns, while the gelated MC served as a reliable mold for patterning the hydrogel prepolymers. When these patterned hydrogels were integrated together, the stem cells in each hydrogel distinctly differentiated toward individually defined fates, resulting in the formation of the multicellular tissue structure bearing the very structural integrity and characteristics as seen in vascularized bones and osteochondral tissues.

    View details for DOI 10.1038/srep29408

    View details for PubMedCentralID PMC4933913

  • Clavicle pain and reduction of incisional and fascial pain after posterior cervical surgery. Journal of neurosurgery. Spine Duetzmann, S., Cole, T., Senft, C., Seifert, V., Ratliff, J. K., Park, J. 2015; 23 (6): 684-689

    Abstract

    Incisional pain after posterior cervical spine surgery can be severe and very unpleasant to the patient. Ongoing incisional pain is one of the key disadvantages of posterior over anterior surgical approaches to the cervical spine. It prolongs hospital stays and delays return to work. In this study, the hypothesized that incisional pain in the immediate postoperative period is caused partially by tension on the skin as well as on the deep cervical fascia and the fascia overlying the trapezius, which are usually sewn together during closure. Reduction of this tension through retraction of the shoulders should therefore reduce pain as well as the amount of pain medication used in the early postoperative period.In this prospective randomized controlled study, 30 patients who had undergone posterior cervical spine surgery were randomized into 2 groups who either wore or did not wear a clavicle brace to retract the shoulders. Patients in the brace group began wearing the brace on postoperative day (POD) 4 and wore it continuously throughout the 30-day study period. Outcome was assessed by two measures: 1) the daily level of self reported pain according to the visual analog scale (VAS) and 2) the number of pain pills taken during the 30-day postoperative period.Wearing a clavicle brace in the immediate postoperative period significantly reduced incisional pain and the amount of pain medication that patients took. Beginning on POD 4 and continuing until day POD 13, the mean daily VAS score for pain was significantly lower in the brace group than in the control group. Furthermore, patients who wore the clavicle brace took less pain medication from POD 4 to POD 12. At this point the difference lost significance until the end of the study period. Four patients were randomized but did not tolerate wearing the brace.Patients who tolerated wearing the clavicle brace after posterior cervical spine surgery had reduced pain and used less pain medication.

    View details for DOI 10.3171/2015.2.SPINE141118

    View details for PubMedID 26296190

  • Sacral Peak Pressure in Healthy Volunteers and Patients With Spinal Cord Injury With and Without Liquid-Based Pad NURSING RESEARCH Duetzmann, S., Forsey, L. M., Senft, C., Seifert, V., Ratliff, J., Park, J. 2015; 64 (4): 300-305

    Abstract

    The prevalence of sacral pressure ulcers in patients with spinal cord injuries is high. The sacral area is vulnerable to compressive pressure because of immobility and because the sacrum and posterior superior iliac prominence lie closely under the skin with no muscle layer in between.The aim of this study was to assess peak sacral pressure before and after use of PURAP, a liquid-based pad that covers only the sacral area and can be applied on any bed surface.Healthy volunteers (n = 12) and patients with spinal cord injuries (n = 10) took part; the patients had undergone spine surgery within 7 days before data collection. Participants were in bed, pretest pressure maps were generated, PURAP was placed for 15 minutes, and then posttest pressure maps were generated. Peak pressure was obtained every second and averaged over the entire period. Patients rated whether their comfort had improved when PURAP was in use.For healthy volunteers, mean pretest peak sacral pressure was 74.7 (SD = 16.2) mmHg; the posttest mean was 49.1 (SD = 7.5) mmHg (p < .001, Wilcoxon signed-rank test). For patients with spinal cord injuries, mean pretest peak sacral pressure was 105.7 (SD = 22.4) mmHg; the posttest mean was 81.4 (SD = 18.3) mmHg (p < .001, Wilcoxon signed-rank test). The pad reduced the peak sacral pressure in the patient group by 23% (range = 11%-42%) and in the volunteers by 32% (range = 19%-46%). Overall, 70% of the patients reported increased comfort with PURAP.Peak sacral pressure was reduced when PURAP was used. It covers only the sacral area but could help many patients with spinal cord injury because the prevalence of sacral pressure ulcers is high in this group. PURAP may be economically advantageous in countries and hospitals with limited financial resources needed for more expensive mattresses and cushions.

    View details for DOI 10.1097/NNR.0000000000000100

    View details for Web of Science ID 000357940700009

  • Sacral Peak Pressure in Healthy Volunteers and Patients With Spinal Cord Injury: With and Without Liquid-Based Pad. Nursing research Duetzmann, S., Forsey, L. M., Senft, C., Seifert, V., Ratliff, J., Park, J. 2015; 64 (4): 300-305

    Abstract

    The prevalence of sacral pressure ulcers in patients with spinal cord injuries is high. The sacral area is vulnerable to compressive pressure because of immobility and because the sacrum and posterior superior iliac prominence lie closely under the skin with no muscle layer in between.The aim of this study was to assess peak sacral pressure before and after use of PURAP, a liquid-based pad that covers only the sacral area and can be applied on any bed surface.Healthy volunteers (n = 12) and patients with spinal cord injuries (n = 10) took part; the patients had undergone spine surgery within 7 days before data collection. Participants were in bed, pretest pressure maps were generated, PURAP was placed for 15 minutes, and then posttest pressure maps were generated. Peak pressure was obtained every second and averaged over the entire period. Patients rated whether their comfort had improved when PURAP was in use.For healthy volunteers, mean pretest peak sacral pressure was 74.7 (SD = 16.2) mmHg; the posttest mean was 49.1 (SD = 7.5) mmHg (p < .001, Wilcoxon signed-rank test). For patients with spinal cord injuries, mean pretest peak sacral pressure was 105.7 (SD = 22.4) mmHg; the posttest mean was 81.4 (SD = 18.3) mmHg (p < .001, Wilcoxon signed-rank test). The pad reduced the peak sacral pressure in the patient group by 23% (range = 11%-42%) and in the volunteers by 32% (range = 19%-46%). Overall, 70% of the patients reported increased comfort with PURAP.Peak sacral pressure was reduced when PURAP was used. It covers only the sacral area but could help many patients with spinal cord injury because the prevalence of sacral pressure ulcers is high in this group. PURAP may be economically advantageous in countries and hospitals with limited financial resources needed for more expensive mattresses and cushions.

    View details for DOI 10.1097/NNR.0000000000000100

    View details for PubMedID 26126064

  • Biomechanical Analysis of a Novel Pedicle Screw Anchor Designed for the Osteoporotic Population WORLD NEUROSURGERY Gates, T. A., Moldavsky, M., Salloum, K., Dunbar, G. L., Park, J., Bucklen, B. 2015; 83 (6): 965-969

    Abstract

    The biomechanical study was performed to investigate the effect of a novel pedicle screw anchor in increasing the pullout strength of pedicle screws.Ten lumbar vertebral bodies with a weighted average T-score of -2.13 were used. Pedicle screws of 4.5 mm diameter and 25 mm length were inserted in to one pedicle randomly and matched with an anchor in the corresponding pedicle. Fatigue testing was performed by applying an axial load of ±200N to the screw tulip, along the axis of the rod, at a rate of 0.5 Hz for 1,000 cycles. After fatigue loading was completed, all screws underwent axial pullout testing at a rate of 0.1 mm/sec until failure. A paired two sample for means t-test was performed to determine a significant difference between the two groups (p ≤ 0.05).Following fatigue testing, the axial displacement at the 1,000 cycle point for the anchor and non-anchor group was 1.4 ± 0.7mm and 2.9 ± 1.2mm, respectively. The anchor group had significantly lower axial displacement compared to the non-anchor group (p ≤ 0.01). The group with the anchor reached an average maximum load of 702 ± 373N. The average yield load for the non-anchor group was 421 ± 293N. The anchor group yield load was significantly greater than the non-anchor group (p ≤ 0.01).A novel anchor for standard pedicle screws resulted in significantly less axial movement during fatigue and a greater failure force compared a screw with no anchor. The anchor may provide a stronger bone-to-screw interface, than a non-anchor screw, without the complications of cement augmentation.

    View details for DOI 10.1016/j.wneu.2015.01.057

    View details for Web of Science ID 000356138800016

    View details for PubMedID 25779853

  • Biomechanical Comparisons of Pull Out Strengths After Pedicle Screw Augmentation with Hydroxyapatite, Calcium Phosphate, or Polymethylmethacrylate in the Cadaveric Spine WORLD NEUROSURGERY Yi, S., Rim, D., Park, S. W., Murovic, J. A., Lim, J., Park, J. 2015; 83 (6): 976-981

    Abstract

    In vertebrae with low bone mineral densities pull out strength is often poor, thus various substances have been used to fill screw holes before screw placement for corrective spine surgery. We performed biomechanical cadaveric studies to compare nonaugmented pedicle screws versus hydroxyapatite, calcium phosphate, or polymethylmethacrylate augmented pedicle screws for screw tightening torques and pull out strengths in spine procedures requiring bone screw insertion.Seven human cadaveric T10-L1 spines with 28 vertebral bodies were examined by x-ray to exclude bony abnormalities. Dual-energy x-ray absorptiometry scans evaluated bone mineral densities. Twenty of 28 vertebrae underwent ipsilateral fluoroscopic placement of 6-mm holes augmented with hydroxyapatite, calcium phosphate, or polymethylmethacrylate, followed by transpedicular screw placements. Controls were pedicle screw placements in the contralateral hemivertebrae without augmentation. All groups were evaluated for axial pull out strength using a biomechanical loading frame.Mean pedicle screw axial pull out strength compared with controls increased by 12.5% in hydroxyapatite augmented hemivertebrae (P = 0.600) and by 14.9% in calcium phosphate augmented hemivertebrae (P = 0.234), but the increase was not significant for either method. Pull out strength of polymethylmethacrylate versus hydroxyapatite augmented pedicle screws was 60.8% higher (P = 0.028).Hydroxyapatite and calcium phosphate augmentation in osteoporotic vertebrae showed a trend toward increased pedicle screw pull out strength versus controls. Pedicle screw pull out force of polymethylmethacrylate in the insertion stage was higher than that of hydroxyapatite. However, hydroxyapatite is likely a better clinical alternative to polymethylmethacrylate, as hydroxyapatite augmentation, unlike polymethylmethacrylate augmentation, stimulates bone growth and can be revised.

    View details for DOI 10.1016/j.wneu.2015.01.056

    View details for Web of Science ID 000356138800018

    View details for PubMedID 25769482

  • Spinal Sealant System Provides Better Intraoperative Watertight Closure Than Standard of Care During Spinal Surgery A Prospective, Multicenter, Randomized Controlled Study SPINE Wright, N. M., Park, J., Tew, J. M., Kim, K. D., Shaffrey, M. E., Cheng, J., Choudhri, H., Krishnaney, A. A., Graham, R. S., Mendel, E., Simmons, N. 2015; 40 (8): 505-513

    Abstract

    Prospective, 3:1 randomized, single-blind, multicenter investigational study.To assess the safety and efficacy of a low-swell spinal sealant when used as an adjunct to sutured dural repair compared with standard of care methods to obtain watertight dural closure in subjects undergoing spinal surgery.Watertight dural closure is paramount in spinal surgery to avoid complications of cerebrospinal fluid leak. Prior reports have proven the efficacy of a synthetic, absorbable polyethylene glycol (PEG) hydrogel sealant in spinal surgery compared with standard of care. Given the potential concerns of swelling in spinal applications, the hydrogel was modified to a low-swell formulation.The primary endpoint was success rate in obtaining intraoperative watertight dural closure in subjects receiving PEG hydrogel sealant versus a control group of subjects receiving any standard method designed to provide intraoperative watertight closure. Subjects were evaluated at discharge and at 30 and 90 days postprocedure for cerebrospinal fluid leaks, surgical site infections, and adverse events.Between May 2007 and May 2009, 98 subjects (74 PEG hydrogel spinal sealant, 24 control) were randomized at 14 clinical sites in the United States. Patients treated with the PEG hydrogel spinal sealant had a significantly higher rate of watertight closure than the control (98.6% vs. 79.2%, P = 0.003). No statistical differences were seen in postoperative cerebrospinal fluid, infection, and wound healing. No neurological deficits were seen attributable to the sealant.The low-swell PEG hydrogel spinal sealant evaluated in this study has been proven safe and effective for providing watertight closure when used as an adjunct to sutured closure of intentional durotomies during spinal surgery. PEG hydrogel sealants have again proved superior to other standard of care technologies for safe, efficacious dural closure.2.

    View details for DOI 10.1097/BRS.0000000000000810

    View details for Web of Science ID 000352787100011

    View details for PubMedID 25646746

  • Biomechanical Comparison of Cervical Fixation via Transarticular Facet Screws without Rods versus Lateral Mass Screws with Rods WORLD NEUROSURGERY Yi, S., Rim, D., Nam, K., Keem, S., Murovic, J. A., Lim, J., Park, J. 2015; 83 (4): 548-552

    Abstract

    Transarticular facet screws restore biomechanical stability to the cervical spine when posterior cervical anatomy has been compromised. This study compares the more recent, less invasive, and briefer transarticular facet screw system without rods with the lateral mass screw system with rods.For this study, 6 human cervical spines were obtained from cadavers. Transarticular facet screws without rods were inserted bilaterally into the inferior articular facets at the C5-C6 and C5-C6-C7 levels. Lateral mass screws with rods were inserted bilaterally at the same levels using Magerl's technique. All specimens underwent range of motion (ROM) testing by a material testing machine for flexion, extension, lateral bending, and axial rotation.Both fixation methods, transarticular facet screws without rods and lateral mass screws with rods, reduced all ROM measurements and increased spinal stiffness. No statistically significant differences between the 2 stabilization methods were found in ROM measurements for 1-level insertions. However, in 2-level insertions, ROM for the nonrod transarticular facet screw group was significantly increased for flexion-extension and lateral bending.Transarticular facet screws without rods and lateral mass screws with rods had similar biomechanical stability in single-level insertions. For 2-level insertions, transarticular facet screws without rods are a valid option in cervical spine repair.

    View details for DOI 10.1016/j.wneu.2014.12.008

    View details for Web of Science ID 000353039500032

    View details for PubMedID 25514614

  • Does a Medial Retraction Blade Transmit Direct Pressure to Pharyngeal/Esophageal Wall During Anterior Cervical Surgery? SPINE Han, I. H., Lee, S. H., Lee, J. M., Kim, H. S., Nam, K. H., Duetzmann, S., Park, J., Choi, B. K. 2015; 40 (1): E18-E22

    Abstract

    A prospective study of 25 patients who underwent anterior cervical surgery.To assess retraction pressure and the exposure of pharyngeal/esophageal (P/E) wall to the medial retractor blade to clarify whether medial retraction causes direct pressure transmission to the P/E wall.Retraction pressure on P/E walls has been used to explain the relation between the retraction pressure and dysphagia or the efficacies of new retractor blades. However, it is doubtful whether the measured pressure represent real retraction pressure on the P/E wall because exposure of the P/E in the surgical field could be reduced by the shielding effect of thyroid cartilage.Epi- and endoesophageal pressures were serially measured using online pressure transducers 15 minutes before retraction, immediately after retraction, and 30 minutes after retraction. To measure the extent of P/E wall exposure to pressure transducer, we used posterior border of thyroid cartilage as a landmark. Intraoperative radiograph was used to mark the position of the posterior border of thyroid cartilage. We checked out the marked location on retractors by measuring the distance from distal retractor tip.The mean epiesophageal pressure significantly increased after retraction (0 mmHg: 88.7 ± 19.6 mmHg: 81.9 ± 15.3 mmHg). The mean endoesophageal pressure minimally changed after retraction (9.0 ± 6.6 mmHg: 15.7 ± 13.8 mmHg: 17.0 ± 14.3 mmHg). The mean location of the posterior border of thyroid cartilage was 7.3 ± 3.5 mm on the retractor blade from the tip, which means epiesophageal pressure was measured against the posterior border of thyroid cartilage, not against the P/E wall.We suggest that a medial retraction blade does not transmit direct pressure on P/E wall due to minimal wall exposure and intervening thyroid cartilage. Our result should be considered when measuring retraction pressure during anterior cervical surgery or designing novel retractor systems.

    View details for DOI 10.1097/BRS.0000000000000649

    View details for PubMedID 25341988

  • Biornechanical Analysis of Disc Pressure and Facet Contact Force After Simulated Two-Level Cervical Surgeries (Fusion and Arthroplasty) and Hybrid Surgery WORLD NEUROSURGERY Park, J., Shin, J. J., Lim, J. 2014; 82 (6)

    Abstract

    The objective of this study was designed to compare 2-level cervical disc surgery (2-level anterior cervical discectomy and fusion [ACDF] or disc arthroplasty) and hybrid surgery (ACDF/arthroplasty) in terms of postoperative adjacent-level intradiscal pressure (IDP) and facet contact force (FCF).Twenty-four cadaveric cervical spines (C3-T2) were tested in various modes, including extension, flexion, and bilateral axial rotation, to compare adjacent-level IDP and FCF after specified treatments as follows: 1) C5-C6 arthroplasty using ProDisc-C (Synthes Spine, West Chester, Pennsylvania, USA) and C6-C7 ACDF, 2) C5-C6 ACDF and C6-C7 arthroplasty using ProDisc-C, 3) 2-level C5-C6/C6-C7 disc arthroplasties, and 4) 2-level C5-C6/C6-C7 ACDF. IDPs were recorded at anterior, central, and posterior disc portions.After 2-level cervical arthrodesis (ACDF), IDP increased significantly at the anterior annulus of distal adjacent-level disc during flexion and axial rotation and at the center of proximal adjacent-level disc during flexion. In contrast, after cervical specified treatments, including disc arthroplasty (2-level disc arthroplasties and hybrid surgery), IDP decreased significantly at the anterior annulus of distal adjacent-level disc during flexion and extension and was unchanged at the center of proximal adjacent-level disc during flexion. Two-level cervical arthrodesis also tended to adversely impact facet loads, increasing distal rather than proximal adjacent-level FCF.Both hybrid surgery and 2-level arthroplasties seem to offer significant advantages over 2-level arthrodesis by reducing IDP at adjacent levels and approximating FCF of an intact spine. These findings suggest that cervical arthroplasties and hybrid surgery are an alternative to reduce IDP and facet loads at adjacent levels.

    View details for DOI 10.1016/j.wneu.2014.06.013

    View details for Web of Science ID 000347635900130

    View details for PubMedID 24937596

  • Directed Axonal Outgrowth Using a Propagating Gradient of IGF-1. Advanced materials Lee, W., Frank, C. W., Park, J. 2014; 26 (29): 4936-4940

    Abstract

    The temporospatial regulation of axon outgrowth is useful for guiding de novo connectivity or re-connectivity of neurons in neurological injury or disease. Here we report the successful construction of a biocompatible guidance device, in which a linear propagation of IGF-1 gradient sequentially directs axon outgrowth. We observe the extensive in vitro axonal extension over 5 mm with a desired growth rate of ∼1 mm/day.

    View details for DOI 10.1002/adma.201305995

    View details for PubMedID 24664530

  • Directed axonal outgrowth using a propagating gradient of IGF-1 ADVANCED MATERIALS Lee, W., Frank, C. W., Park, J. 2014; 26: 4936–4940

    Abstract

    The temporospatial regulation of axon outgrowth is useful for guiding de novo connectivity or re-connectivity of neurons in neurological injury or disease. Here we report the successful construction of a biocompatible guidance device, in which a linear propagation of IGF-1 gradient sequentially directs axon outgrowth. We observe the extensive in vitro axonal extension over 5 mm with a desired growth rate of ∼1 mm/day.

    View details for DOI 10.1002/adma.201305995

  • Minimally Invasive Surgery for Lumbar Decompression in Obese Patients. J Spine Smith, Z. A. 2014; 3 (181)
  • Primary surgical management by reduction and fixation of unstable hangman's fractures with discoligamentous instability or combined fractures: clinical article. Journal of neurosurgery. Spine Shin, J. J., Kim, S. H., Cho, Y. E., Cheshier, S. H., Park, J. 2013; 19 (5): 569-575

    Abstract

    Several controversial issues arise in the management of unstable hangman's fractures. Some surgeons perform external reduction and immobilize the patient's neck in a halo vest, while others perform surgical reduction and internal fixation. The nonsurgical treatments with rigid collar or halo vest immobilization present problems, including nonunion, pseudarthrosis, skull fracture, and scalp laceration and may also fail to achieve anatomical realignment of the local C2-3 kyphosis. With recent advances in surgical technique and technology, surgical intervention is increasingly performed as the primary treatment in high cervical fractures. The outcomes of such surgeries are often superior to those of conservative treatment. The authors propose that surgical intervention as a primary management for hangman's fracture may avoid risks inherent in conservative management when severe circumferential discoligamentous instability is present and may reduce the risk of catastrophic results at the fracture site. The purposes of this study were to assess fracture healing following expedient reduction and surgical fixation and to propose a guideline for treatment of unstable hangman's fractures.From April 2006 to December 2011, the authors treated 105 patients with high cervical fractures. This study included 23 (21.9%) of these patients (15 men and 8 women; mean age 46.4 years) with Type II, IIa, and III hangman's fractures according to the Levine and Edwards classification. The patient's age, sex, mechanism of injury, associated injuries, neurological status, and complications were ascertained. The authors retrospectively assessed the clinical outcome (Neck Disability Index), radiological findings (disc height, translation, and angulation), and bony healing.The average follow-up period was 28.9 months (range 12-63.2 months). The overall average Neck Disability Index score at the time of this study was 6.6 ± 2.3. The average duration of hospitalization was 20.3 days, and fusion was achieved in all cases by 14.8 ± 1.6 weeks after surgery, as demonstrated on dynamic radiographs and cervical 3D CT scans. The mean pretreatment translation was 6.9 ± 3.2 mm, and the mean postoperative translation was 1.6 ± 1.8 mm (mean reduction 5.2 ± 3.1 mm). The initial angulation was 4.7° ± 5.3° and the postoperative angulation was 2.5° ± 1.8° (mean reduction 6.1° ± 5.3°). The preoperative and postoperative values for translation and angulation differed significantly (p < 0.05). The overall C2-3 disc height was 6.7 ± 1.2 mm preoperatively, whereas 3 months after surgery it was 6.4 ± 1.1 mm. These values did not differ significantly (p = 0.0963).The authors observed effective reduction and bony healing in cases of unstable hangman's fractures after fixation, and all patients experienced favorable clinical outcomes with neck pain improvement. The protocols allowed for physiological reconstruction of the fractured deformities and avoided external fixation. The authors suggest that posterior reduction and screw fixation should be used as a primary treatment to promote stability of hangman's fracture in the presence of discoligamentous instability or combined fractures.

    View details for DOI 10.3171/2013.8.SPINE12948

    View details for PubMedID 24033304

  • Primary surgical management by reduction and fixation of unstable hangman's fractures with discoligamentous instability or combined fractures JOURNAL OF NEUROSURGERY-SPINE Shin, J. J., Kim, S. H., Cho, Y. E., Cheshier, S. H., Park, J. 2013; 19 (5): 569-575

    Abstract

    Several controversial issues arise in the management of unstable hangman's fractures. Some surgeons perform external reduction and immobilize the patient's neck in a halo vest, while others perform surgical reduction and internal fixation. The nonsurgical treatments with rigid collar or halo vest immobilization present problems, including nonunion, pseudarthrosis, skull fracture, and scalp laceration and may also fail to achieve anatomical realignment of the local C2-3 kyphosis. With recent advances in surgical technique and technology, surgical intervention is increasingly performed as the primary treatment in high cervical fractures. The outcomes of such surgeries are often superior to those of conservative treatment. The authors propose that surgical intervention as a primary management for hangman's fracture may avoid risks inherent in conservative management when severe circumferential discoligamentous instability is present and may reduce the risk of catastrophic results at the fracture site. The purposes of this study were to assess fracture healing following expedient reduction and surgical fixation and to propose a guideline for treatment of unstable hangman's fractures.From April 2006 to December 2011, the authors treated 105 patients with high cervical fractures. This study included 23 (21.9%) of these patients (15 men and 8 women; mean age 46.4 years) with Type II, IIa, and III hangman's fractures according to the Levine and Edwards classification. The patient's age, sex, mechanism of injury, associated injuries, neurological status, and complications were ascertained. The authors retrospectively assessed the clinical outcome (Neck Disability Index), radiological findings (disc height, translation, and angulation), and bony healing.The average follow-up period was 28.9 months (range 12-63.2 months). The overall average Neck Disability Index score at the time of this study was 6.6 ± 2.3. The average duration of hospitalization was 20.3 days, and fusion was achieved in all cases by 14.8 ± 1.6 weeks after surgery, as demonstrated on dynamic radiographs and cervical 3D CT scans. The mean pretreatment translation was 6.9 ± 3.2 mm, and the mean postoperative translation was 1.6 ± 1.8 mm (mean reduction 5.2 ± 3.1 mm). The initial angulation was 4.7° ± 5.3° and the postoperative angulation was 2.5° ± 1.8° (mean reduction 6.1° ± 5.3°). The preoperative and postoperative values for translation and angulation differed significantly (p < 0.05). The overall C2-3 disc height was 6.7 ± 1.2 mm preoperatively, whereas 3 months after surgery it was 6.4 ± 1.1 mm. These values did not differ significantly (p = 0.0963).The authors observed effective reduction and bony healing in cases of unstable hangman's fractures after fixation, and all patients experienced favorable clinical outcomes with neck pain improvement. The protocols allowed for physiological reconstruction of the fractured deformities and avoided external fixation. The authors suggest that posterior reduction and screw fixation should be used as a primary treatment to promote stability of hangman's fracture in the presence of discoligamentous instability or combined fractures.

    View details for DOI 10.3171/2013.8.SPINE12948

    View details for Web of Science ID 000325956500006

    View details for PubMedID 24033304

  • Radiofrequency Ablation of Spine An Experimental Study in an Ex Vivo Bovine and In Vivo Swine Model for Feasibility in Spine Tumor SPINE You, N. K., Lee, H. Y., Shin, D. A., Choi, G. H., Yi, S., Kim, K. N., Yoon, D. H., Park, J. 2013; 38 (18): E1121-E1127

    Abstract

    Study Design. An experimental study of radiofrequency ablation of spine in an ex vivo bovine and in vivo swine animal model.Objective. To study the feasibility of radiofrequency ablation for spine tumors close to the spinal cord, to examine the safety and efficacy of radiofrequency ablation, and to suggest quantitative guidelines for clinical application.Summary of Background Data. Radiofrequency ablation has received increased attention as an effective and minimally invasive method for treating soft tissue tumors. However, there is currently only anecdotal evidence to support radiofrequency ablation of spinal tumors and only a few experimental studies have been conducted.Methods. We performed ex vivo experiments by producing 10 radiofrequency ablation zones in extracted bovine spines and an in vivo study by producing eight radiofrequency ablation zones in a swine spine using internally cooled electrodes. The volume and diameter of ablation zones were evaluated and analyzed by the corresponding energy and ablation times.Results. In the ex vivo study, the average diameters of the ablation zones were 3.05 cm, 1.85 cm, and 1.26 cm, for the D1, D2, and D3 zones, respectively, and the average ablation volume was 4.19 cm. In the in vivo study, the average diameters were 2.51 cm, 2.05 cm, and 1.28 cm, respectively, and the ablation volume was 6.80 cm. The ablation zones demonstrated a positive correlation with ablation time, but the coefficients were 0.942 ex vivo and 0.257 in vivo. The temperature in the ex vivo study was inversely proportional to distance, with a maximal temperature of 63.7°C at 10 mm; however, the maximum temperature was 38.2°C in the in vivo study.Conclusion. This study demonstrated that sufficient radiofrequency ablation zone volume could be induced, which suggests that radiofrequency ablation is feasible and safe for application to human spinal tumors with predictability.

    View details for DOI 10.1097/BRS.0b013e31829c2e12

    View details for Web of Science ID 000330365000001

    View details for PubMedID 23698575

  • Modified Polyaxial S1 Screw Placement in Patients with Difficult Sacral Anatomy - Technical Report Cureus 5(1): e83. doi:10.7759/cureus.83 M Kalani, G Li, S Mindea, J Park 2013
  • The Design of a Heterocellular 3D Architecture and its Application to Monitoring the Behavior of Cancer Cells in Response to the Spatial Distribution of Endothelial Cells ADVANCED MATERIALS Lee, W., Park, J. 2012; 24 (39): 5339-5344

    Abstract

    The spatial cell distribution is one of the critical features for governing cellular interactions and their consequent behaviors. Here we suggest a novel method of building a hierarchical cellular structure by stacking cell-attached microplate structures with specific configurations within hydrogel layers. This method is applied to the reconstruction of the 3D architecture of a liver lobule and the development of an experimental model of the various phases of cancer angiogenesis.

    View details for DOI 10.1002/adma.201200687

    View details for Web of Science ID 000309405200006

    View details for PubMedID 22927197

  • Morbidity and Mortality of C2 Fractures in the Elderly: Surgery and Conservative Treatment NEUROSURGERY Chen, Y., Boakye, M., Arrigo, R. T., Kalanithi, P. S., Cheng, I., Alamin, T., Carragee, E. J., Mindea, S. A., Park, J. 2012; 70 (5): 1055-1059

    Abstract

    Closed C2 fractures commonly occur after falls or other trauma in the elderly and are associated with significant morbidity and mortality. Controversy exists as to best treatment practices for these patients.To compare outcomes for elderly patients with closed C2 fractures by treatment modality.We retrospectively reviewed 28 surgically and 28 nonsurgically treated cases of closed C2 fractures without spinal cord injury in patients aged 65 years of age or older treated at Stanford Hospital between January 2000 and July 2010. Comorbidities, fracture characteristics, and treatment details were recorded; primary outcomes were 30-day mortality and complication rates; secondary outcomes were length of hospital stay and long-term survival.Surgically treated patients tended to have more severe fractures with larger displacement. Charlson comorbidity scores were similar in both groups. Thirty-day mortality was 3.6% in the surgical group and 7.1% in the nonsurgical group, and the 30-day complication rates were 17.9% and 25.0%, respectively; these differences were not statistically significant. Surgical patients had significantly longer lengths of hospital stay than nonsurgical patients (11.8 days vs 4.4 days). Long-term median survival was not significantly different between groups.The 30-day mortality and complication rates in surgically and nonsurgically treated patients were comparable. Elderly patients faced relatively high morbidity and mortality regardless of treatment modality; thus, age alone does not appear to be a contraindication to surgical fixation of C2 fractures.

    View details for DOI 10.1227/NEU.0b013e3182446742

    View details for Web of Science ID 000303390400013

    View details for PubMedID 22157549

  • Charlson Score is a Robust Predictor of 30-Day Complications Following Spinal Metastasis Surgery SPINE Arrigo, R. T., Kalanithi, P., Cheng, I., Alamin, T., Carragee, E. J., Mindea, S. A., Boakye, M., Park, J. 2011; 36 (19): E1274-E1280

    Abstract

    Retrospective chart review.To identify predictors of 30-day complications after the surgical treatment of spinal metastasis.Surgical treatment of spinal metastasis is considered palliative with the aim of reducing or delaying neurologic deficit. Postoperative complication rates as high as 39% have been reported in the literature. Complications may impact patient quality of life and increase costs; therefore, an understanding of which preoperative variables best predict 30-day complications will help risk-stratify patients and guide therapeutic decision making and informed consent.We retrospectively reviewed 200 cases of spinal metastasis surgically treated at Stanford Hospital between 1999 and 2009. Multiple logistic regression was performed to determine which preoperative variables were independent predictors of 30-day complications.Sixty-eight patients (34%) experienced one or more complications within 30 days of surgery. The most common complications were respiratory failure, venous thromboembolism, and pneumonia. On multivariate analysis, Charlson Comorbidity Index score was the most significant predictor of 30-day complications. Patients with a Charlson score of two or greater had over five times the odds of a 30-day complication as patients with a score of zero or one.After adjusting for demographic, oncologic, neurologic, operative, and health factors, Charlson score was the most robust predictor of 30-day complications. A Charlson score of two or greater should be considered a surgical risk factor for 30-day complications, and should be used to risk-stratify surgical candidates. If complications are anticipated, medical staff can prepare in advance, for instance, scheduling aggressive ICU care to monitor for and treat complications. Finally, Charlson score should be controlled for in future spinal metastasis outcomes studies and compared to other comorbidity assessment tools.

    View details for DOI 10.1097/BRS.0b013e318206cda3

    View details for Web of Science ID 000294207500005

    View details for PubMedID 21358481

  • Biomechanical analysis of Goel technique for C1-2 fusion JOURNAL OF NEUROSURGERY-SPINE Park, J., Scheer, J. K., Lim, T. J., Deviren, V., Ames, C. P. 2011; 14 (5): 639-646

    Abstract

    The Goel technique, in which C1-2 intraarticular spacers are used, may be performed to restore stability to a disrupted atlantoaxial complex in conjunction with the Harms technique of placing polyaxial screws and bilateral rods. However, it has yet to be determined biomechanically whether the addition of the C1-2 joint spacers increases the multiaxial rigidity of the fixation construct. The goal of this study was to quantify changes in multiaxial rigidity of the combined Goel-Harms technique with the addition of C1-2 intraarticular spacers.Seven cadaveric cervical spines (occiput-C2) were submitted to nondestructive flexion-extension, lateral bending, and axial rotation tests in a material testing machine spine tester. The authors applied 1.5 Nm at a rate of 0.1 Nm/second and held it constant for 10 seconds. The specimens were loaded 3 times, and data were collected on the third cycle. Testing of the specimens was performed for the following groups: 1) intact (I); 2) with the addition of C-1 lateral mass/C-2 pedicle screws and rod system (I+SR); 3) with C1-2 joint capsule incision, decortication (2 mm on top and bottom of each joint [that is, the C-1 and C-2 surface) and addition of bilateral C1-2 intraarticular spacers at C1-2 junction to the screws and rods (I+SR+C); 4) after removal of the posterior rods and only the bilateral spacers in place (I+C); 5) after removal of spacers and further destabilization with simulated odontoidectomy for a completely destabilized case (D); 6) with addition of posterior rods to the destabilized case (D+SR); and 7) with addition of bilateral C1-2 intraarticular spacers at C1-2 junction to the destabilized case (D+SR+C). The motion of C-1 was measured by a 3D motion tracking system and the motion of C-2 was measured by the rotational sensor of the testing system. The range of motion (ROM) and neutral zone (NZ) across C-1 and C-2 were evaluated.For the intact spine test groups, the addition of screws/rods (I+SR) and screws/rods/cages (I+SR+C) significantly reduced ROM and NZ compared with the intact spine (I) for flexion-extension and axial rotation (p < 0.05) but not lateral bending (p > 0.05). The 2 groups were not significantly different from each other in any bending mode for ROM and NZ, but in the destabilized condition the addition of screws/rods (D+SR) and screws/rods/cages (D+SR+C) significantly reduced ROM and NZ compared with the destabilized spine (D) in all bending modes (p < 0.05). Furthermore, the addition of the C1-2 intraarticular spacers (D+SR+C) significantly reduced ROM (flexion-extension and axial rotation) and NZ (lateral bending) compared with the screws and rods alone (D+SR).Study result indicated that both the Goel and Harms techniques alone and with the addition of the C1-2 intraarticular spacers to the Goel-Harms technique are advantageous for stabilizing the atlantoaxial segment. The Goel technique combined with placement of a screw/rod construct appears to result in additional construct rigidity beyond the screw/rod technique and appears to be more useful in very unstable cases.

    View details for DOI 10.3171/2011.1.SPINE10446

    View details for Web of Science ID 000289914100014

    View details for PubMedID 21332283

  • Biomechanical Evaluations of Various C1-C2 Posterior Fixation Techniques SPINE Sim, H. B., Lee, J. W., Park, J. T., Mindea, S. A., Lim, J., Park, J. 2011; 36 (6): E401-E407

    Abstract

    A biomechanical in vitro study using human cadaveric spine.To compare the biomechanical stability of pedicle screws versus various established posterior atlantoaxial fixations used to manage atlantoaxial instability.Rigid screw fixation of the atlantoaxial complex provides immediate stability and excellent fusion success though has a high risk of neurovascular complications. Some spine surgeons thus insert shorter C2 pedicle or pars/isthmus screws as alternatives to minimize the latter risks. The biomechanical consequences of short pedicle screw fixation remain unclear, however.Seven human cadaveric cervical spines with the occiput attached (C0-C3) had neutral zone (NZ) and range of motion (ROM) evaluated in three modes of loading. Specimens were tested in the following sequence: initially (1) the intact specimens were tested, after destabilization of C1-C2, then the specimens underwent (2) C1 lateral mass and C2 short pedicle screw fixation (PS-S), (3) C1 lateral mass and C2 long pedicle screw fixation (PS-L), (4) C1 lateral mass and C2 intralaminar screw fixation (ILS), (5) Sonntag's modified Gallie fixation (MG) and (6) C1-C2 transarticular screw fixation with posterior wiring (TAS 1 MG). (7) The destabilized spine was also tested.All instrumented groups were significantly stiffer in NZ and ROM than the intact spines, except in lateral bending, which was statistically significantly increased in the TAS 1 MG group. The MG group's NZ and ROM values were statistically significantly weaker than those of the PS-S, PS-L, and the ROM values of the TAS 1 MG groups. The ILS group's NZ values were higher than those of the TAS 1 MG group and for ROM, than that of the PS-S and PS-L groups. In flexion, the NZ and ROM values of the TAS 1 MG group were significantly less than those of the PS-S, PS-L, ILS, and MG groups. In axial rotation, the NZ and ROM values of the MG group were statistically significantly higher than those of the PS-S, PS-L, ISL and TAS 1 MG groups.The TAS 1 MG procedures provided the highest stability. The MG method alone may not be adequate for atlantoaxial arthrodesis, because it does not provide sufficient stability in lateral bending and rotation modes. The C2 pedicle screw and C2 ILS techniques are biomechanically less stable than the TAS 1 MG. In the C1 lateral mass-C2 pedicle screw fixation, the use of a short pedicle screw may be an alternative when other screw fixation techniques are not feasible.

    View details for DOI 10.1097/BRS.0b013e31820611ba

    View details for PubMedID 21372651

  • Open Posterior Reduction and Stabilization of a C1 Burst Fracture Using Mono-axial Screws SPINE Chung, S. K., Park, J. T., Lim, J., Park, J. 2011; 36 (5): E301-E306

    View details for DOI 10.1097/BRS.0b013e31820644cd

    View details for Web of Science ID 000287446300002

    View details for PubMedID 21325928

  • Predictors of Survival After Surgical Treatment of Spinal Metastasis NEUROSURGERY Arrigo, R. T., Kalanithi, P., Cheng, I., Alamin, T., Carragee, E. J., Mindea, S. A., Park, J., Boakye, M. 2011; 68 (3): 674-681

    Abstract

    Surgery for spinal metastasis is a palliative treatment aimed at improving patient quality of life by alleviating pain and reversing or delaying neurologic dysfunction, but with a mean survival time of less than 1 year and significant complication rates, appropriate patient selection is crucial.To identify the most significant prognostic variables of survival after surgery for spinal metastasis.Chart review was performed on 200 surgically treated spinal metastasis patients at Stanford Hospital between 1999 and 2009. Survival analysis was performed and variables entered into a Cox proportional hazards model to determine their significance.Median overall survival was 8.0 months, with a 30-day mortality rate of 3.0% and a 30-day complication rate of 34.0%. A Cox proportional hazards model showed radiosensitivity of the tumor (hazard ratio: 2.557, P<.001), preoperative ambulatory status (hazard ratio: 2.355, P=.0001), and Charlson Comorbidity Index (hazard ratio: 2.955, P<.01) to be significant predictors of survival. Breast cancer had the best prognosis (median survival, 27.1 months), whereas gastrointestinal tumors had the worst (median survival, 2.66 months).We identified the Charlson Comorbidity Index score as one of the strongest predictors of survival after surgery for spinal metastasis. We confirmed previous findings that radiosensitivity of the tumor and ambulatory status are significant predictors of survival.

    View details for DOI 10.1227/NEU.0b013e318207780c

    View details for Web of Science ID 000287242300036

    View details for PubMedID 21311295

  • Lumbar disc rehydration postimplantation of a posterior dynamic stabilization system JOURNAL OF NEUROSURGERY-SPINE Cho, B. Y., Murovic, J., Park, K. W., Park, J. 2010; 13 (5): 576-580

    Abstract

    Biological attempts at disc regeneration are promising; however, disc degeneration is closely related to other predisposing factors such as alteration of disc height, intradiscal pressure, load distribution, and motion. The restoration of the physiological status of the affected spinal segment is thus necessary prior to attempts at disc regeneration. Dynamic stabilization systems now offer the potential of a mechanical approach to intervertebral disc regeneration. The authors used decompression and placement of the BioFlex dynamic stabilization device to treat a young male patient with disc degeneration. This patient underwent follow-up, and he was found to gradually improve both neurologically and radiographically. On MR imaging performed 1 year postoperatively, he had an increase in disc height and disc rehydration. This case and the concept of disc rehydration are presented in this paper.

    View details for DOI 10.3171/2010.5.SPINE08418

    View details for Web of Science ID 000283473600005

    View details for PubMedID 21039146

  • Biomechanical Analysis of the Range of Motion After Placement of a Two-Level Cervical ProDisc-C Versus Hybrid Construct SPINE Cho, B. Y., Lim, J., Sim, H. B., Park, J. 2010; 35 (19): 1769-1776

    Abstract

    The study design was that of an in vitro human cadaveric biomechanical analysis.The objective of this study was the biomechanical analysis of the range of motion (ROM) of a 2-level intact spine control versus total, then operative- and adjacent-segment ROM after (1) 2-level ProDisc-C placement (PP), (2) anterior cervical discectomy and fusions (ACDFs), and (3) hybrid constructs of both. Follower load and multidirectional testing were performed in each instance.With in vivo cervical arthroplasties gaining in popularity, limited biomechanical data are available, which highlight changes in the adjacent-level biomechanics after multilevel procedures.Biomechanical testing for ROM was performed using 7 cadaveric C4-T1 spine specimens. Moments up to 2 Nm with a 100 N follower load were applied in flexion/extension (F/E), right and left lateral bending (LB), and right and left axial rotation (AR). Specimens were tested in the intact state and then with a combination of ProDisc-C arthroplasty and ACDF at C5-C6 and C6-C7.In the 2-level PP group, the increase in ROM in F/E, LB, and AR of C4-T1 occurs due to an increased ROM at the operative level. The ROM of the level adjacent to the operative levels showed no significant change, except at C4-C5 in LB. For the latter level, the ROM of C4-C5 in each direction showed increases for each parameter. In the 2-level fusion C5-C6 and C6-C7 fusion (FF) group, the ROM in F/E, LB, and AR of C4-T1 was decreased because of a decrease in ROM primarily at the fused levels, and the ROM of adjacent levels was increased. In the ProDisc-C/Fusion (PF) and Fusion/ProDisc-C (FP) groups undergoing placements of a 1-level ProDisc-C/1-level fusion with cage and plate, both groups showed no significant ROM change of C4-T1 when compared with the control and no significant change at adjacent levels, with the exception of C4-C5 in LB.(1) Two-level ACDFs decrease whereas 2-level PPs increase the entire C4-T1 ROM. (2) ACDF/ProDisc-C hybrid operations do not alter the C4-T1 ROM. (3) For the ACDF/ProDisc-C hybrid operative groups, the combined ROM of the operative levels showed no significant difference when compared with that of the intact spine. (4) Regarding adjacent-level ROM, a 2-level ACDF increases ROM, but 2-level ProDisc-C and hybrid ACDF/PPs do not show significant change except for LB at C4-C5. (5) When the segmental distribution of C4-T1 ROM is plotted as the percentage of total motion, it demonstrates that for PF and FP groups, the combined ROM of the C5-C6 and C6-C7 operative levels are similar to that of the intact spine in EF and LB. For the PP group, the combined ROM of the operative levels increased, whereas the combined ROM for the FF group is decreased. The decrease or increase of the adjacent C4-C5 or C7-T1 level ROM compensates for the operative levels.

    View details for DOI 10.1097/BRS.0b013e3181c225fa

    View details for Web of Science ID 000281656400005

    View details for PubMedID 20395885

  • Biomechanical comparison of single-level posterior versus transforaminal lumbar interbody fusions with bilateral pedicle screw fixation: segmental stability and the effects on adjacent motion segments Laboratory investigation JOURNAL OF NEUROSURGERY-SPINE Sim, H. B., Murovic, J. A., Cho, B. Y., Lim, T. J., Park, J. 2010; 12 (6): 700-708

    Abstract

    Both posterior lumbar interbody fusion (PLIF) and transforaminal lumbar interbody fusion (TLIF) have been frequently undertaken for lumbar arthrodesis. These procedures use different approaches and cage designs, each of which could affect spine stability, even after the addition of posterior pedicle screw fixation. The objectives of this biomechanical study were to compare PLIF and TLIF, each accompanied by bilateral pedicle screw fixation, with regard to the stability of the fused and adjacent segments.Fourteen human L2-S2 cadaveric spine specimens were tested for 6 different modes of motion: flexion, extension, right and left lateral bending, and right and left axial rotation using a load control protocol (LCP). The LCP for each mode of motion utilized moments up to 8.0 Nm at a rate of 0.5 Nm/second with the application of a constant compression follower preload of 400 N. All 14 specimens were tested in the intact state. The specimens were then divided equally into PLIF and TLIF conditions. In the PLIF Group, a bilateral L4-5 partial facetectomy was followed by discectomy and a single-level fusion procedure. In the TLIF Group, a unilateral L4-5 complete facetectomy was performed (and followed by the discectomy and single-level fusion procedure). In the TLIF Group, the implants were initially positioned inside the disc space posteriorly (TLIF-P) and the specimens were tested; the implants were then positioned anteriorly (TLIF-A) and the specimens were retested. All specimens were evaluated at the reconstructed and adjacent segments for range of motion (ROM) and at the adjacent segments for intradiscal pressure (IDP), and laminar strain.At the reconstructed segment, both the PLIF and the TLIF specimens had significantly lower ROMs compared with those for the intact state (p < 0.05). For lateral bending, the PLIF resulted in a marked decrease in ROM that was statistically significantly greater than that found after TLIF (p < 0.05). In flexion-extension and rotation, the PLIF Group also had less ROM, however, unlike the difference in lateral bending ROM, these differences in ROM values were not statistically significant. Variations in the position of the implants within the disc space were not associated with any significant differences in ROM values (p = 0.43). Analyses of ROM at the adjacent levels L2-3, L3-4, and L5-S1 showed that ROM was increased to some degree in all directions. When compared with that of intact specimens, the ROMs were increased to a statistically significant degree at all adjacent segments in flexion-extension loads (p < 0.05); however, the differences in values among the various operative procedures were not statistically significant. The IDP and facet contact force for the adjacent L3-4 and L5-S1 levels were also increased, but these values were not statistically significantly increased from those for the intact spine (p > 0.05).Regarding stability, PLIF provides a higher immediate stability compared with that of TLIF, especially in lateral bending. Based on our findings, however, PLIF and TLIF, each with posterolateral fusions, have similar biomechanical properties regarding ROM, IDP, and laminar strain at the adjacent segments.

    View details for DOI 10.3171/2009.12.SPINE09123

    View details for Web of Science ID 000278024300017

    View details for PubMedID 20515358

  • A biomechanical study of the instrumented and adjacent lumbar levels after In-Space interspinous spacer insertion Laboratory investigation JOURNAL OF NEUROSURGERY-SPINE Park, S. W., Lim, T. J., Park, J. 2010; 12 (5): 560-569

    Abstract

    Interspinous process implants are becoming more common for the treatment of lumber disc degeneration. The authors undertook this study to evaluate the effect of the In-Space interspinous spacer on the biomechanics of the lumbosacral spine.Seven L2-S1 cadaver spines were physiologically loaded in extension, flexion, lateral bending, and axial rotation modes. The range of motion (ROM) and intervertebral disc pressure (DP) at the level implanted with an In-Space device and at adjacent levels were measured under 4 experimental conditions. Biomechanical testing was carried out on 7 sequentially prepared specimens in the following states: 1) the intact L2-S1 cadaver spine and 2) the L2-S1 cadaver specimen implanted with an In-Space interspinous spacer at L3-4 (Group 1), 3) after an additional L3-4 discectomy (with the In-Space interspinous spacer still in place) (Group 2), and finally, 4) after removal of the In-Space interspinous spacer, leaving only the discectomized (that is, destabilized) spine model (Group 3).The extension ROM at the implanted level after experimental conditions 2 and 3 above was statistically significantly reduced. An increase of ROM at the adjacent levels compensated for the reduction at the implanted level. However, there was no statistically significant change in ROM in any of the other modes of motion at any of the levels studied. Likewise, the DP reduction at L3-4 during extension was statistically significant, but in all other modes of motion, there was no statistically significant change in DP at any measured level. The In-Space interspinous spacer statistically significantly reduced the ROM of the L3-4 motion segment in Groups 1 and 2 (extension: 67%, p = 0.018 and 70%, p = 0.018; flexion: 72%, p = 0.028 and 80%, p = 0.027). After placement of the In-Space interspinous spacer, the DP was decreased at L3-4 in extension for Groups 1 and 2 in the posterior anular region (63%, p = 0.028; 59%, p = 0.043), Group 2 in the center region (73%, p = 0.028), and Groups 1 and 2 in the anterior anular region (57%, p = 0.018; 60%, p = 0.018).The In-Space interspinous spacer both stabilizes the spine and reduces the intervertebral DP at the instrumented level during extension. The biomechanics for other modes of motion and at the adjacent levels are not affected statistically significantly, however. The device thus performed as intended. It significantly stabilized the motion segments at the instrumented level, but not at the segment adjacent to the instrumented level.

    View details for DOI 10.3171/2009.11.SPINE08668

    View details for Web of Science ID 000277132000017

    View details for PubMedID 20433305

  • DRIVING WITH POLYNEUROPATHY MUSCLE & NERVE Cho, S. C., Katzberg, H. D., Rama, A., Kim, B., Roh, H., Park, J., Katz, J., So, Y. T. 2010; 41 (3): 324-328

    Abstract

    Polyneuropathy may result in pain, numbness, and weakness, which may in turn affect driving ability. Medications used to treat neuropathic pain may alter cognition, which may further affect driving. Although such impairments have engendered questions about the driving safety in this group of patients, the rate of motor vehicle accidents (MVAs) in patients with neuropathy has not been studied rigorously. We surveyed patients with neuropathy from three medical centers for reported accident rate, and we analyzed variables related to increased risk for accidents compared to National Highway Traffic Safety Administration data. Surveys from 260 subjects demonstrated that 40.6% were involved in traffic accidents (0.11 accidents/year). Their accident rate was 10.8 MVAs per million vehicle miles traveled (MVA/MVMT), compared to 3.71 MVA/MVMT in 55-59-year-old drivers and 3.72 in 60-64-year-olds (National Highway Traffic Safety Administration data). In all, 72.4% cited their neuropathy and 55.2% cited their medications as playing a role in their accidents, and 51.6% changed their driving habits after developing neuropathy. Independently, elevated levels of pain, motor weakness, and ambulation difficulty met statistical significance for increased MVA frequency. We conclude that accident frequency and discomfort with driving are higher in neuropathy patients compared to age-matched national statistics. However, most patients seem to change habits according to their ability to drive; as such, driving issues should be addressed with caution and on a case-by-case basis.

    View details for DOI 10.1002/mus.21511

    View details for PubMedID 19882633

  • Surgical strategies for managing foraminal nerve sheath tumors: the emerging role of CyberKnife ablation EUROPEAN SPINE JOURNAL Murovic, J. A., Cho, S. C., Park, J. 2010; 19 (2): 242-256

    Abstract

    Sixteen Stanford University Medical Center (SUMC) patients with foraminal nerve sheath tumors had charts reviewed. CyberKnife radiosurgery was innovative in management. Parameters were evaluated for 16 foraminal nerve sheath tumors undergoing surgery, some with CyberKnife. Three neurofibromas had associated neurofibromatosis type 1 (NF1). Eleven patients had one resection; others had CyberKnife after one (two) and two (three) operations. The malignant peripheral nerve sheath tumor (MPNST) had prior field-radiation and adds another case. Approaches included laminotomy and laminectomies with partial (three) or total (two) facetectomies/fusions. Two cases each had supraclavicular, lateral extracavitary, retroperitoneal and Wiltze and costotransversectomy/thoracotomy procedures. Two underwent a laminectomy/partial facetectomy, then CyberKnife. Pre-CyberKnife, one of two others had a laminectomy/partial facetectomy, then total facetectomy/fusion and the other, two supraclavicular approaches. The MPNST had a hemi-laminotomy then laminectomy/total facetectomy/fusion, followed by CyberKnife. Roots were preserved, except in two. Of 11 single-operation-peripheral nerve sheath tumors, the asymptomatic case remained stable, nine (92%) improved and one (9%) worsened. Examinations remained intact in three (27%) and improved in seven (64%). Two having a single operation then CyberKnife had improvement after both. Of two undergoing two operations, one had symptom resolution post-operatively, worsened 4 years post-CyberKnife then has remained unchanged after re-operation. The other such patient improved post-operatively, had no change after re-operation and improved post-CyberKnife. The MPNST had presentation improvement after the first operation, worsened and after the second surgery \and CyberKnife, the patient expired from tumor spread. In conclusion, surgery is beneficial for pain relief and function preservation in foraminal nerve sheath tumors. Open surgery with CyberKnife is an innovation in these tumors' management.

    View details for DOI 10.1007/s00586-009-1160-0

    View details for Web of Science ID 000274545200006

    View details for PubMedID 19798517

    View details for PubMedCentralID PMC2899818

  • "Mini-transthoracic supradiaphragmatic approach to the thoracolumbar junction" Korean J Spine Chang JC, Park HK, Doh JW, Park J 2010; 7 (4): 249-254
  • Imaging correlation of the degree of degenerative L4-5 spondylolisthesis with the corresponding amount of facet fluid JOURNAL OF NEUROSURGERY-SPINE Cho, B. Y., Murovic, J. A., Park, J. 2009; 11 (5): 614-619

    Abstract

    The aim of this study was to correlate the degree of L4-5 spondylolisthesis on plain flexion-extension radiographs with the corresponding amount of L4-5 facet fluid visible on MR images.Patients underwent evaluation at the Neurosurgical Spine Clinics of Stanford University Medical Center and National Health Insurance Medical Center (Goyang, South Korea) between January 2006 and December 2007. Only patients who were diagnosed with L4-5 degenerative spondylolisthesis (DS) and who had both lumbosacral flexion-extension radiographs and MR images available for review were eligible for this study. Each patient's dynamic motion index (DMI) was measured using the lateral lumbosacral plain radiograph and was the percentage of the degree of anterior slippage seen on flexion versus that seen on extension. Axial T2-weighted MR images of the L4-5 facet joints obtained in each patient was analyzed for the amount of facet fluid, using the image showing the widest portion of the facets. The facet fluid index was calculated from the ratio of the sum of the amounts of facet fluid found in the right plus left facets over the sum of the average widths of the right plus left facet joints.Fifty-four patients with L4-5 DS were included in this study. Of these 54 patients, facet fluid was noted on MR images in 29 patients (53.7%), and their mean DMI was 6.349 +/- 2.726. Patients who did not have facet fluid on MR imaging had a mean DMI of 1.542 +/- 0.820; this difference was statistically significant (p < 0.001). There was a positive linear association between the facet fluid index and the DMI in the group of patients who exhibited facet fluid on MR images (Pearson correlation coefficient 0.560, p < 0.01). In the subgroup of 29 patients with L4-5 DS who showed facet fluid on MR images, flexion-extension plain radiographs in 10 (34.5%) showed marked anterolisthesis, while the corresponding MR images did not.There is a linear correlation between the degree of segmental motion seen on flexion-extension plain radiography in patients with DS at L4-5 and the amount of L4-5 facet fluid on MR images. If L4-5 facet fluid in patients with DS is seen on MR images, a corresponding anterolisthesis on weight-bearing flexion-extension lateral radiographs should be anticipated. Obtaining plain radiographs will aid in the diagnosis of anterolisthesis caused by an L4-5 hypermobile segment, which may not always be evident on MR images obtained in supine patients.

    View details for DOI 10.3171/2009.6.SPINE08413

    View details for Web of Science ID 000271244200023

    View details for PubMedID 19929367

  • Fracture-related Thoracic Kyphotic Deformity Correction by Single-stage Posterolateral Vertebrectomy With Circumferential Reconstruction and Stabilization Outcomes in 30 Cases JOURNAL OF SPINAL DISORDERS & TECHNIQUES Yoo, C., Ryu, S. I., Park, J. 2009; 22 (7): 492-501

    Abstract

    This paper is a retrospective chart review.This study assesses single-stage thoracic vertebrectomy with circumferential reconstruction and stabilization. Preoperative and postoperative thoracic kyphotic angles and other outcomes are analyzed.Pathologic and traumatic thoracic vertebral body fracture deformity can be corrected by an anterior vertebral body corpectomy and reconstruction. If the pathology is primarily posterior, then laminectomy and posterolateral instrumentation may be preferred. In some patients, simultaneous anterior and posterior correction of instability and fracture is necessary and is now possible with a single-stage Stanford University Medical Center (SUMC) technique with similar results to the traditional 2-stage approach.Thirty patients who underwent 31 single-stage thoracic vertebrectomies with circumferential reconstructions for thoracic spine fractures between 2004 and 2006 at SUMC were retrospectively reviewed. All surgeries were performed prone; operative technical details are reported. The preoperative and postoperative thoracic kyphotic angles were measured by Cobb angle evaluation using lateral chest plain films and magnetic resonance imaging. Other outcome measures evaluated included operative time, blood loss, neurologic and functional outcomes, postoperative pain, and treatment complications.The mean follow-up was 17.21 months (range: 9 to 30 mo) and preoperative kyphosis was 20.4 degrees (range: 6.0 to 57.9 degrees). The average postoperative kyphosis was 8.3 degrees (range: 1.8 to 2.67 degrees) and correction of kyphosis was 16.2 degrees (range: 6 to 30 degrees). The median estimated blood loss was 1411.67 mL (range: 300 to 4000 mL) and mean operating time was 4.8 hours (range: 2.8 to 8.6 h). Complications included 2 hardware failures requiring revision, 2 infections, and 1 dural laceration. Pain, Frankel Grade, and functional status were improved in all, except 1 preoperatively bedridden patient.Thoracic kyphotic correction is possible through a prone single-stage simultaneous anterior vertebrectomy and posterior reconstruction. Sufficient anterior and posterior correction of instability and fracture using the SUMC technique is possible with similar results to the traditional 2-stage approach.

    View details for DOI 10.1097/BSD.0b013e31818f0ec3

    View details for Web of Science ID 000279665400006

    View details for PubMedID 20075812

  • FORAMINAL NERVE SHEATH TUMORS: INTERMEDIATE FOLLOW-UP AFTER CYBERKNIFE RADIOSURGERY NEUROSURGERY Murovic, J. A., Gibbs, I. C., Chang, S. D., Mobley, B. C., Park, J., Adler, J. R. 2009; 64 (2): A33-A43

    Abstract

    To conduct a retrospective review of outcomes in 15 patients with 18 foraminal tumors, including 17 benign peripheral nerve sheath tumors and 1 malignant peripheral nerve sheath tumor, who underwent CyberKnife (Accuray, Inc., Sunnyvale, CA) radiosurgery at Stanford University Medical Center from 1999 to 2006.Symptoms and findings, neurofibromatosis (NF) association, previous radiation, imaging, dosimetry, tumor volume, central necrosis, and the relation of these factors to outcomes were evaluated.Before treatment, 1 asymptomatic patient had radiculopathic findings, 3 patients experienced local pain with intact neurological examinations, and 7 patients had radiculopathic complaints with intact (1 patient), radiculopathic (4 patients), or radiculomyelopathic examinations (2 patients). Five patients had myelopathic complaints and findings. Three patients had NF1-associated neurofibromas, 1 patient with NF2 had a schwannoma, and 1 patient had a schwannomatosis-related lesion. Two likely radiation-induced lesions, a neurofibroma and a malignant peripheral nerve sheath tumor, were observed. Prescribed doses ranging from 16 to 24 Gy, delivered in 1 to 3 fractions of 6 to 20 Gy, resulted in maximum tumor doses ranging from 20.9 to 30 Gy. Target volumes ranged from 1.36 to 16.9 mL. After radiosurgery, the asymptomatic case remained asymptomatic, and neurological findings improved. Thirteen of 15 symptomatic patients with (12 patients) or without (3 patients) neurological findings improved (3 cases after resection) or remained stable, and 2 patients worsened. Symptoms and examinations remained stable or improved in 8 (80%) of 10 patients with schwannomas and 3 (60%) of 5 patients with neurofibromas. Tumor volumes decreased in 12 (67%) of 18 tumors and increased in 3 tumors. Tumor volumes decreased in 8 of 10 schwannomas and 3 of 7 neurofibromas. Central necrosis developed in 8 (44%) of 18 tumors.CyberKnife radiosurgery resulted in pain relief and functional preservation in selected foraminal peripheral nerve sheath tumors and a malignant peripheral nerve sheath tumor. Symptomatic and neurological improvements were more noticeable with schwannomas. Myelopathic symptoms may necessitate surgical debulking before radiosurgery.

    View details for DOI 10.1227/01.NEU.0000341632.39692.9E

    View details for Web of Science ID 000262797700010

    View details for PubMedID 19165072

  • Imaging Correlation of the Degree of Degenerative L4-L5 Spondylolisthesis with the Corresponding Amount of the Facet Fluid. Journal of Neurosurgery: Spine Cho BY, Park J 2009; 11: 614-619
  • Stem Cell Regeneration of the Intervertebral Disc-Cellular and Molecular Challenges Neurosurgery Focus Jandial R, Aryan HE, Park J, Taylor WT, Snyder EY 2008; 24 (E:20)
  • Requests for 692 transfers to an academic Level I trauma center: Implications of the Emergency Medical Treatment and Active Labor Act 65th Annual Meeting of the American-Association-for-the-Surgery-of-Trauma Spain, D. A., Bellino, M., Kopelman, A., Chang, J., Park, J., Gregg, D. L., Brundage, S. I. LIPPINCOTT WILLIAMS & WILKINS. 2007: 63–67

    Abstract

    The Emergency Medical Treatment and Active Labor Act (EMTALA) effectively requires Level I trauma centers (TC) to accept all transfers for a higher level of care if capacity exists. We hypothesized that EMTALA would burden a Level I TC by a selective referral of a poor payer mix of primarily nonoperative patients.All transfer calls (December 2003 and September 2005) to our Level I TC are handled by a dedicated transfer center. Calls were reviewed for age, surgical service requested, and outcome of request. The trauma registry was queried to compare Injury Severity Scale (ISS) score, hospital stay (LOS), operations, mortality, and payer status for transfer and primary catchment patients.In all, 821 calls were received; 77 calls were cancelled by the referring hospital and 52 were for consultation only. Of the 692 transfer requests, 534 (77%) were accepted, 134 (19%) were denied for no capacity, and only 24 (4%) were declined by TC as not clinically indicated. Transferred patients were younger (32.0 +/- 1.49 versus 38.9 +/- 0.51, p < 0.05), had similar ISS scores (13.6 +/- 0.62 versus 13.7 +/- 0.26) and LOS (7.0 +/- 0.70 versus 7.4 +/- 0.25), but were somewhat more likely to require an operation than direct admissions (58% versus 51%, p < 0.05). Although trauma (24%) and neurosurgery (24%) were the most commonly requested services, followed by orthopedics (20%), orthopedics accounted for 60% of operations on transferred patients compared with 10% to 13% for trauma and neurosurgery (mostly spine). There was no difference in the payer status of transfer and direct admit patients.Contrary to our assumptions, EMTALA patients had an identical payer mix and similar operative need compared with our primary catchment patients. They do represent a large additional patient load (20% of admissions) and differentially impact specialists, mostly operative for orthopedics and complex nonoperative care for trauma and neurosurgery. These data suggest that the primary motivations for transfer are specialist availability and complexity of care rather than financial concerns. As TCs provide backup specialty call coverage for a wide geographic area, this further supports the need for trauma systems development.

    View details for DOI 10.1097/TA.0b013e31802d9716

    View details for Web of Science ID 000243490100012

    View details for PubMedID 17215734

  • Treatment of Fracture-Related Thoracic Kyphosis by Circumferential Reconstruction and Stabilization via a Prone Extracavitary Costotransversectomy Approach The Spine Journal Yoo C, Ryu C, Park J 2007; 7 (Supplement): 120S-121S
  • Posterior Dynamic Stabilization Systems Korean Journal of Spine Park SW, Park J 2007; 4 (4): 171-187
  • The Effect of a Posterior Dynamic Stabilization Device on Extension Using Finite Element Analysis Korean Journal of Spine Min SW, Park J 2007; 4 (Suppl. 1): 58-59
  • Biomechanical comparison: stability of lateral-approach anterior lumbar interbody fusion and lateral fixation compared with anterior-approach anterior lumbar interbody fusion and posterior fixation in the lower lumbar spine JOURNAL OF NEUROSURGERY-SPINE Kim, S. M., Lim, T. J., Paterno, J., Park, J., Kim, D. H. 2005; 2 (1): 62-68

    Abstract

    The stability of lateral lumbar interbody graft-augmented fusion and supplementary lateral plate fixation in human cadavers has not been determined. The purpose of this study was to investigate the immediate biomechanical stabilities of the following: 1) femoral ring allograft (FRA)-augmented anterior lumbar interbody fusion (ALIF) after left lateral discectomy combined with additional lateral MACS HMA plate and screw fixation; and 2) ALIF combined with posterior transpedicular fixation after anterior discectomy.Sixteen human lumbosacral spines were loaded with six modes of motion. The intervertebral motion was measured using a video-based motion-capturing system. The range of motion (ROM) and the neutral zone (NZ) in each loading mode were compared with a maximum of 7.5 Nm. The ROM values for both stand-alone ALIF approaches were similar to those of the intact spine, whereas NZ measurements were higher in most loading modes. No significant intergroup differences were found. The ROM and NZ values for lateral fixation in all modes were significantly lower than those of intact spine, except when NZ was measured in lateral bending. All ROM and NZ values for transpedicular fixation were significantly lower than those for stand-alone anterior ALIF. Transpedicular fixation conferred better stabilization than lateral fixation in flexion, extension, and lateral bending modes.Neither approach to stand-alone FRA-augmented ALIF provided sufficient stabilization, but supplementary instrumentation conferred significant stabilization. The MACS HMA plate and screw fixation system, although inferior to posterior transpedicular fixation, provided adequate stability compared with the intact spine and can serve as a sound alternative to supplementary spinal stabilization.

    View details for PubMedID 15658128

  • Expandable Cage for Cervical Spine Reconstruction J Korean Neurosurgery Ho Yeol Zhang, Thongtrangan I, Le H, Park J, Kim, DH 2005; Soc 38: 435-441
  • A biomechanical comparison of three surgical approaches in bilateral subaxial cervical facet dislocation JOURNAL OF NEUROSURGERY-SPINE Kim, S. M., Lim, J., Paterno, J., Park, J., Kim, D. H. 2004; 1 (1): 108-115

    Abstract

    In bilateral cervical facet dislocation, biomechanical stabilities between anterior locking screw/plate fixation after anterior cervical discectomy and fusion (ACDFP) and posterior transpedicular screw/rod fixation after anterior cervical discectomy and fusion (ACDFTP) have not been compared using the human cadaver, although ACDFP has been performed frequently. In this study the stability of ACDFP, a posterior wiring procedure after ACDFP (ACDFPW), and ACDFTP for treatment of bilateral cervical facet dislocation were compared.Spines (C3-T1) from 10 human cadavers were tested in the intact state, and then after ACDFP, ACDFPW, and ACDFTP were performed. Intervertebral motion was measured using a video-based motion capture system. The range of motion (ROM) and neutral zone (NZ) were compared for each loading mode to a maximum of 2 Nm. The ROM for spines treated with ACDFP was below that of the intact spine in all loading modes, with statistical significance in flexion and extension, but NZs were decreased in flexion and extension and slightly increased in bending and axial rotation; none of these showed statistical significance. The ACDFPW produced statistically significant additional stability in axial rotation ROM and in flexion NZ than ACDFP. The ACDFTP provided better stability than ACDFP in bending and axial rotation, and better stability than ACDFPW in bending for both ROM and NZ. There was no significant difference in extension with either ROM or NZ for the three fixation methods.The spines treated with ACDFTP demonstrated the most effective stabilization, followed by those treated with ACDFPW, and then ACDFP. The spines receiving ACDFP also revealed a higher stability than the intact spine in most loading modes; thus ACDFP can also provide a relatively effective stabilization in bilateral cervical facet dislocation, but with the aid of a brace.

    View details for PubMedID 15291030

  • Cauda equina syndrome in patients with low lumbar fractures. Neurosurgical focus Thongtrangan, I., Le, H., Park, J., Kim, D. H. 2004; 16 (6)

    Abstract

    Symptoms of cauda equina syndrome (CES) can include low-back pain, sciatica, lower-extremity weakness, sensory deficit, perineal hypesthesia or anesthesia, and loss of bowel or bladder function. Several causes of the syndrome are recognized, but its optimal treatment remains controversial and has been broadly based on data gathered from series involving herniated discs. Information on the treatment of CES caused by low lumbar traumatic injuries has not been well documented.Between January 2000 and December 2003, 17 consecutive cases of CES caused by low lumbar traumatic injuries at L2-5 were identified. The traumatic injuries consisted of gun shot wound in two cases, motor vehicle accident in 11, and a fall from height in four. Conus medullaris injuries causing CES were excluded from this review. Presenting symptoms, mechanisms of injury, radiographic images, timing of surgery, surgical approaches, and neurological status at the final follow up were documented. All patients underwent follow up of at least 12 months. Fourteen of 17 patients had satisfactory outcomes. Despite undergoing surgery within the first 24 hours postinjury, three patients had what was classified as a poor outcome given their residual deficits and included two cases with gunshot injuries. Recovery of leg weakness occurred within 4 months, whereas bladder and bowel function recovered within 3 months. All patients in this series underwent decompression within less than 48 hours after syndrome onset. Overall, the authors found no difference regarding timing of surgery between patients in the satisfactory outcome group and those in the poor outcome group.Based on the evidence in this study, the severity of a patient's condition on initial presentation is the most crucial factor in predicting outcome following CES due to low lumbar injuries. Although the matter of the timing of surgery remains controversial, the authors of this study recommend that surgery be performed within 48 hours of syndrome onset.

    View details for PubMedID 15202876

  • Minimally invasive spinal surgery: a historical perspective. Neurosurgical focus Thongtrangan, I., Le, H., Park, J., Kim, D. H. 2004; 16 (1): E13-?

    Abstract

    The concept of minimally invasive spinal surgery embodies the goal of achieving clinical outcomes comparable to those of conventional open surgery, while minimizing the risk of iatrogenic injury that may be incurred during the exposure process. The development of microscopy, laser technology, endoscopy, and video and image guidance systems provided the foundation on which minimally invasive spinal surgery is based. Minimally invasive treatments have been undertaken in all areas of the spinal axis since the 20th century. Lumbar disc disease has been treated using chemonucleolysis, percutaneous discectomy, laser discectomy, intradiscal thermoablation, and minimally invasive microdiscectomy techniques. The initial use of thoracoscopy for thoracic discs and tumor biopsies has expanded to include deformity correction, sympathectomy, vertebrectomy with reconstruction and instrumentation, and resection of paraspinal neurogenic tumors. Laparoscopic techniques, such as those used for appendectomy or cholecystectomy by general surgeons, have evolved into procedures performed by spinal surgeons for anterior lumbar discectomy and fusion. Image-guided systems have been adapted to facilitate pedicle screw placement with increased accuracy. Over the past decade, minimally invasive treatment of cervical spinal disorders has become feasible by applying technologies similar to those developed for the thoracic and lumbar spine. Endoscope-assisted transoral surgery, cervical laminectomy, discectomy, and foraminotomy all represent the continual evolution of minimally invasive spinal surgery. Further improvement in optics and imaging resources, development of biological agents, and introduction of instrumentation systems designed for minimally invasive procedures will inevitably lead to further applications in minimally invasive spine surgery.

    View details for PubMedID 15264791

  • Surgical treatment of tumors involving the cervicothoracic junction. Neurosurgical focus Le, H., Balabhadra, R., Park, J., Kim, D. 2003; 15 (5): E3-?

    Abstract

    Tumors involving the cervicothoracic junction can have a high propensity for causing instability, with kyphosis and spinal cord compression resulting. Treatment with decompression only can lead to further instability and worsening neurological status. In this article, the authors review their surgical experience in the treatment of 19 patients with tumors involving the cervicothoracic junction. The various approaches and instrumentation techniques involved in decompression and stabilization of the cervicothoracic junction are also reviewed.Aggressive instrumentation-augmented fusion after decompression of the cervicothoracic region can provide for immediate stabilization and early rehabilitation. Recent development of new hardware such as dual-diameter transition rods, polyaxial screws, and interlocking devices have enhanced the ability to fashion a strong construct for stabilization of the cervicothoracic junction.Familiarity with complex instrumentation techniques and various surgical approaches to the cervicothoracic junction will be required for effective treatment of tumors causing instability of this region.

    View details for PubMedID 15323460

  • Vertebral body replacement with an expandable cage for reconstruction after spinal tumor resection. Neurosurgical focus Thongtrangan, I., Balabhadra, R. S., Le, H., Park, J., Kim, D. H. 2003; 15 (5): E8-?

    Abstract

    The authors report their clinical experience with expandable cages used to stabilize the spine after vertebrectomy. The objectives of surgical treatment for spine tumors include a decrease in pain, decompression of the neural elements, mechanical stabilization of the spine, and wide resection to gain local control of certain primary tumors. Most of the lesions occur in the anterior column or vertebral body (VB). Anterior column defects following resection of VBs require surgical restoration of anterior column support. Recently, various expandable cages have been developed and used clinically for VB replacement (VBR).Between January 2001 and June 2003, the authors treated 15 patients who presented with primary spinal tumors and metastatic lesions from remote sites. All patients underwent vertebrectomy, VBR with an expandable cage, and anterior instrumentation with or without posterior instrumentation, depending on the stability of the involved segment. The correction of kyphotic angle was achieved at an average of 20 degrees. Pain scores according to the visual analog scale decreased from 8.4 to 5.2 at the last follow-up review. Patients whose Frankel neurological grade was below D attained at least a one-grade improvement after surgery. All patients achieved immediate stability postsurgery and there were no significant complications related to the expandable cage.The advantage of the expandable cage is that it is easy to use because it permits optimal fit and correction of the deformity by in vivo expansion of the device. These results are promising, but long-term follow up is required.

    View details for PubMedID 15323465

  • Surgical Treatment of Tumors Involving Cervicothoracic Junction Neurosurgery Focus Le H, Balahadra RSV, Park J, Kim DH 2003: E3
  • Effect of Frameless Stereotaxy on Accuracy of C1-C2 Transarticular Screw Placement J Neurosurgery Bloch O, Holly LT, Park J 2001; 95: 74-79
  • Thoracolumbar Vertebral Reconstruction for Metastatic Spine Tumors Neurosurgery Villavicencio AT, Oskouian RJ, Roberson C, Stokes J, Park J, Shaffrey CI, Johnson JP 2000; 47: 530-531