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Management of Urinary Retention in Patients with Benign Prostatic Obstruction: A Systematic Review and Meta-analysis
dc.creator | Karavitakis M., Kyriazis I., Omar M.I., Gravas S., Cornu J.-N., Drake M.J., Gacci M., Gratzke C., Herrmann T.R.W., Madersbacher S., Rieken M., Speakman M.J., Tikkinen K.A.O., Yuan Y., Mamoulakis C. | en |
dc.date.accessioned | 2023-01-31T08:32:04Z | |
dc.date.available | 2023-01-31T08:32:04Z | |
dc.date.issued | 2019 | |
dc.identifier | 10.1016/j.eururo.2019.01.046 | |
dc.identifier.issn | 03022838 | |
dc.identifier.uri | http://hdl.handle.net/11615/74485 | |
dc.description.abstract | Context: Practice patterns for the management of urinary retention (UR) secondary to benign prostatic obstruction (BPO; UR/BPO) vary widely and remain unstandardized. Objective: To review the evidence for managing patients with UR/BPO with pharmacological and nonpharmacological treatments included in the European Association of Urology guidelines on non-neurogenic male lower urinary tract symptoms. Evidence acquisition: Search was conducted up to April 22, 2018, using CENTRAL, MEDLINE, Embase, ClinicalTrials.gov, and World Health Organization International Clinical Trials Registry Platform. This systematic review included randomized controlled trials (RCTs) and prospective comparative studies. Methods as detailed in the Cochrane handbook were followed. Certainty of evidence (CoE) was assessed using the Grading of Recommendations Assessment, Development, and Evaluation (GRADE) approach. Evidence synthesis: Literature search identified 2074 citations. Twenty-one studies were included (qualitative synthesis). The evidence for managing patients with UR/BPO with pharmacological or nonpharmacological treatments is limited. CoE for most outcomes was low/very low. Only α1-blockers (alfuzosin and tamsulosin) have been evaluated in more than one RCT. Pooled results indicated that α1-blockers provided significantly higher rates of successful trial without catheter compared with placebo [alfuzosin: 322/540 (60%) vs 156/400 (39%) (odds ratio {OR} 2.28, 95% confidence interval {CI} 1.55 to 3.36; participants = 940; studies = 7; I 2 = 41%; low CoE); tamsulosin: 75/158 (47%) vs 40/139 (29%) (OR 2.40, 95% CI 1.29 to 4.45; participants = 297; studies = 3; I 2 = 30%; low CoE)] with rare adverse events. Similar rates were achieved with tamsulosin or alfuzosin [51/87 (59%) vs 45/84 (54%) (OR 1.28, 95% CI 0.68 to 2.41; participants = 171; studies = 2; I 2 = 0%; very low CoE)]. Nonpharmacological treatments have been evaluated in RCTs/prospective comparative studies only sporadically. Conclusions: There is some evidence that usage of α1-blockers (alfuzosin and tamsulosin) may improve resolution of UR/BPO. As most nonpharmacological treatments have not been evaluated in patients with UR/BPO, the evidence is inconclusive about their benefits and harms. Patient summary: There is some evidence that alfuzosin and tamsulosin may increase the rates of successful trial without catheter, but little or no evidence on various nonpharmacological treatment options for managing patients with urinary retention secondary to benign prostatic obstruction. © 2019 European Association of UrologyAlfuzosin and tamsulosin appear to provide higher rates of successful trial without catheter. Most nonpharmacological treatment options have not been evaluated in patients with urinary retention secondary to benign prostatic obstruction. Consequently, the evidence is inconclusive regarding the efficacy of nonpharmacological interventions for the management of urinary retention secondary to benign prostatic obstruction. © 2019 European Association of Urology | en |
dc.language.iso | en | en |
dc.source | European Urology | en |
dc.source.uri | https://www.scopus.com/inward/record.uri?eid=2-s2.0-85061427449&doi=10.1016%2fj.eururo.2019.01.046&partnerID=40&md5=16389cfe57cc6057e7498ef1d33e06ff | |
dc.subject | alfuzosin | en |
dc.subject | doxazosin | en |
dc.subject | finasteride | en |
dc.subject | silodosin | en |
dc.subject | tamsulosin | en |
dc.subject | alfuzosin | en |
dc.subject | alpha 1 adrenergic receptor blocking agent | en |
dc.subject | quinazoline derivative | en |
dc.subject | benign prostatic obstruction | en |
dc.subject | bladder irrigation | en |
dc.subject | bladder training | en |
dc.subject | catheter removal | en |
dc.subject | comparative study | en |
dc.subject | GRADE approach | en |
dc.subject | hospitalization | en |
dc.subject | human | en |
dc.subject | intermittent catheterization | en |
dc.subject | International Prostate Symptom Score | en |
dc.subject | lower urinary tract symptom | en |
dc.subject | male | en |
dc.subject | meta analysis | en |
dc.subject | operation duration | en |
dc.subject | practice guideline | en |
dc.subject | priority journal | en |
dc.subject | prostate disease | en |
dc.subject | prostatectomy | en |
dc.subject | randomized controlled trial (topic) | en |
dc.subject | recurrence risk | en |
dc.subject | Review | en |
dc.subject | suprapubic catheterization | en |
dc.subject | systematic review | en |
dc.subject | transurethral microwave thermotherapy | en |
dc.subject | transurethral resection | en |
dc.subject | treatment outcome | en |
dc.subject | urethral catheterization | en |
dc.subject | urine retention | en |
dc.subject | bladder catheterization | en |
dc.subject | complication | en |
dc.subject | prostate hypertrophy | en |
dc.subject | urine retention | en |
dc.subject | Adrenergic alpha-1 Receptor Antagonists | en |
dc.subject | Humans | en |
dc.subject | Male | en |
dc.subject | Prostatectomy | en |
dc.subject | Prostatic Hyperplasia | en |
dc.subject | Quinazolines | en |
dc.subject | Randomized Controlled Trials as Topic | en |
dc.subject | Tamsulosin | en |
dc.subject | Urinary Catheterization | en |
dc.subject | Urinary Retention | en |
dc.subject | Elsevier B.V. | en |
dc.title | Management of Urinary Retention in Patients with Benign Prostatic Obstruction: A Systematic Review and Meta-analysis | en |
dc.type | other | en |
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