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5 citation(s) found for "York, Justin M".

Efficacy of Short- vs Long-Course Antibiotics in Treatment of Hinchey Stage 3 and 4 Diverticulitis
Awad, Amir, Linnaus, Maria E., Theerman, Isaac, Yang, Theodore, York, Justin, Stephens, D. H., Jorge, Irving , Junker, Michelle S., Lara, Francisco J. Cardenas , Rich, Jennifer R. , Kooda, Kirstin , Awad, Abanoub A , Theerman, Isaac L, Jorge, Irving A , Cardenas Lara, Francisco J, Kooda, Kirstin J, Beckermann, Jason

Mayo Clinic

The American Surgeon™ | January 2, 2026 | Volume: 92 | Issue: 6 | Pages: 1701-1706

10.1177/00031348251409742 | PMID 41481278 Get It

Background This study aimed to evaluate outcomes of different antibiotic durations in patients with severe diverticulitis. Methods Initial electronic medical record review identified 2437 adult patients who underwent sigmoid colectomy. Manual chart review identified 133 patients who underwent sigmoid resection and proximal diversion for Hinchey stage 3 or 4 diverticulitis. Patients who received a short antibiotic course (SAC, ≤5 days) were compared with those who received a long antibiotic course (LAC, >5 days). The primary composite outcome included superficial, incisional, organ-space infections or death within 30 days post procedure. Results A total of 53 SAC patients and 55 LAC patients were identified. The composite outcome occurred more frequently in LAC patients than in SAC patients (40% vs 15%; P = .005). Organ-space infection occurred more frequently in LAC patients than in SAC patients (31% vs 13%; P = .04). Conclusions Extended duration of antibiotics after adequate source control does not improve outcomes even in the setting of extensive intra-abdominal contamination.
Optimizing Antibiotic Management for Adult Patients Presenting with Acute Perforated Appendicitis: A Quality Improvement Study
Gallego-Navarro, Carlos , Linnaus, Maria E., Swartz, Hayden J., Stewart, Shelby , York, Justin, Gassner, Ryan R , Kasal, Christopher A. , Seidel, Annaliese G., Wachter, Corey J., Kooda, Kirstin , Rich, Jennifer R. , Sawyer, Mark D. , Beckermann, Jason , York, Justin M, Kooda, Kirstin J

Mayo Clinic

Surgical Infections | November 12, 2024 | Volume: 26 | Issue: 3 | Pages: 143-149

10.1089/sur.2024.179 | PMID 40179309 Get It

Is There a Difference in Screw Accuracy, Robot Time Per Screw, Robot Abandonment, and Radiation Exposure Between the Mazor X and the Renaissance? A Propensity-Matched Analysis of 1179 Robot-Assisted Screws
Lee, Nathan J. , Buchanan, Ian A. , Boddapati, Venkat , Mathew, Justin , Robertson, Djani, Lakomkin, Nikita , Park, Paul , Leung, Eric , Lombardi, Joseph M. , Lehman, Ronald A. , Mathew, Justin , Leung, Eric , Zuckerman, Scott L. , Marciano, Gerard F.

Mayo Clinic

Global Spine Journal | July 8, 2021 | Volume: 13 | Issue: 5 | Pages: 1286-1292

10.1177/21925682211029867 | PMID 34235996 Get It

Study Design: Prospective single-cohort analysis. Objectives: To compare the outcomes/complications of 2 robotic systems for spine surgery. Methods: Adult patients (≥18-years-old) who underwent robot-assisted spine surgery from 2016-2019 were assessed. A propensity score matching (PSM) algorithm was used to match Mazor X to Renaissance cases. Preoperative CT scan for planning and an intraoperative O-arm for screw evaluation were preformed. Outcomes included screw accuracy, robot time/screw, robot abandonment, and radiation. Screw accuracy was measured using Vitrea Core software by 2 orthopedic surgeons. Screw breach was measured according to the Gertzbein/Robbins classification. Results: After PSA, a total of 65 patients (Renaissance: 22 vs. X: 43) were included. Patient/operative factors were similar between robot systems ( P > .05). The pedicle screw accuracy was similar between robots (Renaissance: 1.1%% vs. X: 1.3%, P = .786); however, the S2AI screw breach rate was significantly lower for the X (Renaissance: 9.5% vs. X: 1.2%, P = .025). Robot time per screw was not statistically different (Renaissance: 4.6 minutes vs. X: 3.9 minutes, P = .246). The X was more reliable with an abandonment rate of 2.3% vs. Renaissance:22.7%, P = .007. Radiation exposure were not different between robot systems. Non-robot related complications including dural tear, loss of motor/sensory function, and blood transfusion were similar between robot systems. Conclusion: This is the first comparative analyses of screw accuracy, robot time/screw, robot abandonment, and radiation exposure between the Mazor X and Renaissance systems. There are substantial improvements in the X robot, particularly in the perioperative planning processes, which likely contribute to the X’s superiority in S2AI screw accuracy by nearly 8-fold and robot reliability by nearly 10-fold.
Growth and alignment of the pediatric subaxial cervical spine following rigid instrumentation and fusion: a multicenter study of the Pediatric Craniocervical Society
Goldstein, Hannah E. , Neira, Justin A., Banu, Matei A. , Aldana, Philipp R. , Braga, Bruno P. , Brockmeyer, Douglas L. , DiLuna, Michael L. , Fulkerson, Daniel H. , Hankinson, Todd C. , Jea, Andrew, Lew, Sean M. , Limbrick, David D. , Martin, Jonathan E. , Rodriguez, Luis F. , Rozzelle, Curtis J. , Tuite, Gerald F. , Wetjen, Nicholas M. , Anderson, Richard C. E. , Limbrick, David D. , Pahys, Joshua M.

Mayo Clinic

Journal of Neurosurgery: Pediatrics | April 20, 2018 | Volume: 22 | Issue: 1 | Pages: 81-88

10.3171/2018.1.peds17551 | PMID 29676682 Get It

OBJECTIVEThe long-term effects of surgical fusion on the growing subaxial cervical spine are largely unknown. Recent cross-sectional studies have demonstrated that there is continued growth of the cervical spine through the teenage years. The purpose of this multicenter study was to determine the effects of rigid instrumentation and fusion on the growing subaxial cervical spine by investigating vertical growth, cervical alignment, cervical curvature, and adjacent-segment instability over time.METHODSA total of 15 centers participated in this multi-institutional retrospective study. Cases involving children less than 16 years of age who underwent rigid instrumentation and fusion of the subaxial cervical spine (C-2 and T-1 inclusive) with at least 1 year of clinical and radiographic follow-up were investigated. Charts were reviewed for clinical data. Postoperative and most recent radiographs, CT, and MR images were used to measure vertical growth and assess alignment and stability.RESULTSEighty-one patients were included in the study, with a mean follow-up of 33 months. Ninety-five percent of patients had complete clinical resolution or significant improvement in symptoms. Postoperative cervical kyphosis was seen in only 4 patients (5%), and none developed a swan-neck deformity, unintended adjacent-level fusion, or instability. Of patients with at least 2 years of follow-up, 62% demonstrated growth across the fusion construct. On average, vertical growth was 79% (4-level constructs), 83% (3-level constructs), or 100% (2-level constructs) of expected growth. When comparing the group with continued vertical growth to the one without growth, there were no statistically significant differences in terms of age, sex, underlying etiology, surgical approach, or number of levels fused.CONCLUSIONSContinued vertical growth of the subaxial spine occurs in nearly two-thirds of children after rigid instrumentation and fusion of the subaxial spine. Failure of continued vertical growth is not associated with the patient’s age, sex, underlying etiology, number of levels fused, or surgical approach. Further studies are needed to understand this dichotomy and determine the long-term biomechanical effects of surgery on the growing pediatric cervical spine.
Relief and Recurrence of Congestion During and After Hospitalization for Acute Heart Failure
Lala, Anuradha , McNulty, Steven E., Mentz, Robert J. , AbouEzzeddine, Omar F. , DeVore, Adam D. , Khazanie, Prateeti , Redfield, Margaret M. , Goldsmith, Steven R., Bart, Bradley A. , Anstrom, Kevin J. , Felker, G. Michael , Hernandez, Adrian F. , Stevenson, Lynne W. , Dunlay, Shannon M. , Vader, Justin M, Vader, Justin M. , Hernandez, Adrian , Mentz, Robert J , AbouEzzeddine, Omar F

Mayo Clinic

Circulation: Heart Failure | June 4, 2015 | Volume: 8 | Issue: 4 | Pages: 741-748

10.1161/circheartfailure.114.001957 | PMID 26041600 Get It

Background— Congestion is the most frequent cause for hospitalization in acute decompensated heart failure. Although decongestion is a major goal of acute therapy, it is unclear how the clinical components of congestion (eg, peripheral edema, orthopnea) contribute to outcomes after discharge or how well decongestion is maintained. Methods and Results— A post hoc analysis was performed of 496 patients enrolled in the Diuretic Optimization Strategy Evaluation in Acute Decompensated Heart Failure (DOSE-AHF) and Cardiorenal Rescue Study in Acute Decompensated Heart Failure (CARRESS-HF) trials during hospitalization with acute decompensated heart failure and clinical congestion. A simple orthodema congestion score was generated based on symptoms of orthopnea (≥2 pillows=2 points, <2 pillows=0 points) and peripheral edema (trace=0 points, moderate=1 point, severe=2 points) at baseline, discharge, and 60-day follow-up. Orthodema scores were classified as absent (score of 0), low-grade (score of 1–2), and high-grade (score of 3–4), and the association with death, rehospitalization, or unscheduled medical visits through 60 days was assessed. At baseline, 65% of patients had high-grade orthodema and 35% had low-grade orthodema. At discharge, 52% patients were free from orthodema at discharge (score=0) and these patients had lower 60-day rates of death, rehospitalization, or unscheduled visits (50%) compared with those with low-grade or high-grade orthodema (52% and 68%, respectively; P =0.038). Of the patients without orthodema at discharge, 27% relapsed to low-grade orthodema and 38% to high-grade orthodema at 60-day follow-up. Conclusions— Increased severity of congestion by a simple orthodema assessment is associated with increased morbidity and mortality. Despite intent to relieve congestion, current therapy often fails to relieve orthodema during hospitalization or to prevent recurrence after discharge. Clinical Trial Registration— URL: http://www.clinicaltrials.gov . Unique identifiers: NCT00608491, NCT00577135.