Jonathan Matthews
University of North Carolina at Chapel Hill
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The Journal of Urology | 2014
Angela B. Smith; Allison M. Deal; Hyeon Yu; Brian A. Boyd; Jonathan Matthews; Eric Wallen; Raj S. Pruthi; Michael Woods; Hyman B. Muss; Matthew E. Nielsen
PURPOSE Patients undergoing radical cystectomy face substantial but highly variable risks of major complications. Risk stratification may be enhanced by objective measures such as sarcopenia. Sarcopenia (loss of skeletal muscle mass) has emerged as a novel biomarker associated with adverse outcomes in many clinical contexts relevant to cystectomy. Based on these data we hypothesized that sarcopenia would be associated with increased 30-day major complications and mortality after radical cystectomy for bladder cancer. MATERIALS AND METHODS We performed a retrospective study of patients treated with radical cystectomy at our institution from 2008 to 2011. Sarcopenia was assessed by measuring cross-sectional area of the psoas muscle (total psoas area) on preoperative computerized tomography. Cutoff points were developed and evaluated using ROC curves to determine predictive ability in men and women for outcomes of major complications and survival. RESULTS Of 224 patients with bladder cancer 200 underwent preoperative computerized tomography within 1 month of surgery. Total psoas area was calculated with a mean score of 712 and 571 cm2/m2 in men and women, respectively. A clear association was noted between major complications and lower total psoas area in women using a cutoff of 523 cm2/m2 to define sarcopenia (AUC 0.70). Sarcopenia was not significantly associated with complications in men. There was a nonsignificant trend of sarcopenia with worse 2-year survival. CONCLUSIONS Sarcopenia in women was a predictor of major complications after radical cystectomy. Further research confirming sarcopenia as a useful predictor of complications would support the development of targeted interventions to mitigate the untoward effects of sarcopenia before cancer surgery.
BJUI | 2014
David C. Johnson; Matthew E. Nielsen; Jonathan Matthews; Michael Woods; Eric Wallen; Raj S. Pruthi; Matthew I. Milowsky; Angela B. Smith
To determine whether neoadjuvant chemotherapy (NAC) is a predictor of postoperative complications, length of stay (LOS), or operating time after radical cystectomy (RC) for bladder cancer.
Urology | 2014
J. Patrick Selph; William M. Whited; Angela B. Smith; Jonathan Matthews; Raj S. Pruthi; Eric Wallen; Matthew E. Nielsen; Michael Woods
OBJECTIVE To elucidate whether metabolic syndrome (MS) has an effect on outcomes after nephrectomy, prostatectomy, or cystectomy. METHODS Using the American College of Surgeons National Surgical Quality Improvement Programs database, patients undergoing cystectomy, nephrectomy, or prostatectomy between 2005 and 2011 were reviewed to assess for the presence of MS and a variety of perioperative complications. RESULTS The overall complication rate for cystectomy, nephrectomy, and prostatectomy was 52.4%, 20.2%, and 8.7%, respectively. On multivariate analysis controlling for age, sex, body mass index, cardiac comorbidity, functional status, surgical approach (prostatectomy and nephrectomy), and surgery within 30 days, MS was not associated with perioperative complications in patients undergoing cystectomy (odds ratio [OR], 0.760; 95% confidence interval [CI], 0.476-1.213). On multivariate analysis, the presence of MS was a significant predictor of perioperative complications after radical nephrectomy (adjusted OR, 1.489; 95% CI, 1.146-1.934). With regards to prostatectomy, MS was not a significant predictor of complications (OR, 1.065; 95% CI, 0.739-1.535). CONCLUSION Patients in this cohort with MS undergoing cystectomy or prostatectomy did not experience a higher rate of complications compared with patients without MS, although patients with MS undergoing nephrectomy had a higher complication rate. It may be warranted to preoperatively counsel patients with MS undergoing nephrectomy that complication rates may be higher.
The Journal of Sexual Medicine | 2015
E. Will Kirby; Daniel Verges; Jonathan Matthews; Culley C. Carson; Robert M. Coward
INTRODUCTION Low testosterone (T) has been suggested as a risk factor for Peyronies disease (PD) that may correlate with disease severity. Low T is common in men with sexual dysfunction but its role in the pathogenesis of PD remains unclear. AIM The aim of this study was to compare the prevalence of low T (<300 ng/dL) in patients presenting with PD or erectile dysfunction (ED), as well as disease severity between men with PD and either low T or normal T (≥300 ng/dL). METHODS Retrospective review of 300 men with either PD or ED was conducted. Men were excluded for combined PD and ED, psychogenic ED, or prior T use. For men with PD, plaque size, degree of curvature, and surgical correction rate were compared. MAIN OUTCOME MEASURES The main outcome measures were (i) mean T levels in men with PD or ED and (ii) plaque size, degree of curvature, and surgical correction rates among men with PD and either low T or normal T. RESULTS Eighty-seven men with PD and 98 men with ED were identified. Men with PD had mean total T and free T of 328 ng/dL and 11.5 ng/dL, while men with ED had mean levels of 332 ng/dL and 12.1 ng/dL, respectively (P > 0.05). Of PD men, 52.9% had low T, compared with 45.9% of men with ED (P = 0.35). T levels did not correlate with plaque size or degree of curvature in the PD group (P > 0.05). CONCLUSIONS Men with sexual dysfunction characterized by either PD or ED had similarly low T levels, and low T did not correlate with PD severity or surgical correction rate. The comparable prevalence of low T in men with PD or ED suggests the high rate of low T in PD men may be related to a common process among men with abnormal erectile physiology and not specifically causative in plaque formation.
World Journal of Urology | 2015
David C. Johnson; Stephen B. Riggs; Matthew E. Nielsen; Jonathan Matthews; Michael Woods; Eric Wallen; Raj S. Pruthi; Angela B. Smith
Journal of Clinical Oncology | 2015
Kimberley S. Mak; Angela Smith; Alec Eidelman; R.H. Clayman; Jed-Sian Cheng; Jonathan Matthews; Andrzej Niemierko; Matthew E. Nielsen; Adam S. Feldman; Richard J. Lee; Anthony L. Zietman; William U. Shipley; Ronald C. Chen; Matthew I. Milowsky; Jason A. Efstathiou
International Journal of Radiation Oncology Biology Physics | 2015
Kimberley S. Mak; Angela B. Smith; Alec Eidelman; R.H. Clayman; Andrzej Niemierko; Jed Sian Cheng; Jonathan Matthews; Michael Drumm; Matthew E. Nielsen; Adam S. Feldman; Richard J. Lee; Anthony L. Zietman; Ronald C. Chen; William U. Shipley; Matthew I. Milowsky; Jason A. Efstathiou
World Journal of Urology | 2015
Daniel T. McMillan; Anthony J. Viera; Jonathan Matthews; Mathew C. Raynor; Michael Woods; Raj S. Pruthi; Eric Wallen; Matthew E. Nielsen; Angela B. Smith
Urologic Oncology-seminars and Original Investigations | 2014
Sarah A. Gallagher; Angela B. Smith; Jonathan Matthews; Clarence W. Potter; Michael Woods; Mathew C. Raynor; Eric Wallen; W.Kimryn Rathmell; Young E. Whang; William Y. Kim; Paul A. Godley; Ronald C. Chen; Andrew Z. Wang; Chaochen You; Daniel A. Barocas; Raj S. Pruthi; Matthew E. Nielsen; Matthew I. Milowsky
Journal of The American College of Surgeons | 2013
David A. Johnson; E. Will Kirby; Jed Ferguson; Angela B. Smith; Jonathan Matthews; Michael Woods; Matthew E. Nielsen; Mathew C. Raynor; Raj S. Pruthi; Eric Wallen