Immediate or delayed trial without catheter in acute urinary retention in males: A systematic review.

alpha‐blocker benign prostatic hyperplasia catheterization trial without catheter urinary retention

Journal

BJUI compass
ISSN: 2688-4526
Titre abrégé: BJUI Compass
Pays: United States
ID NLM: 101764975

Informations de publication

Date de publication:
Aug 2024
Historique:
received: 30 11 2023
revised: 05 03 2024
accepted: 17 04 2024
medline: 19 8 2024
pubmed: 19 8 2024
entrez: 19 8 2024
Statut: epublish

Résumé

To compare the success of establishing spontaneous micturition following immediate trial without catheter (TWOC) to delayed TWOC in males catheterized for acute urinary retention. In this systematic review, we included studies reporting success rates of immediate TWOC or delayed TWOC (≤30 days) among males ≥18 years of age catheterized for acute urinary retention. We excluded studies on suprapubic catheterization, postoperative/perioperative catheterization and urinary retention related to trauma. We searched the following databases: MEDLINE, Embase, Cochrane Database of Systematic Reviews, Cochrane Central Register of Controlled Trials, Open Grey and Clinicaltrials.gov. The search was concluded on 30 November 2022. There were no restrictions on language or publication date. Risk of bias was assessed using the ROB 2.0 and ROBINS-I tools. We did random-effects restricted maximum likelihood model meta-analyses. Certainty of evidence was assessed using GRADE. We included 61 studies. In two randomized controlled trials (RCTs), both with some concerns for risk of bias, including in total 174 participants, the relative success rate was 1.22 (95% CI 0.84-1.76) favouring delayed TWOC. In two comparative cohort studies, both with serious risk of bias, including 642 participants, the relative success rate was 1.18 (0.94-1.47) favouring delayed TWOC. One study was excluded from this meta-analysis because of critically low quality. Four studies reporting success rates for cohorts with immediate TWOC, all with serious risk of bias, including 409 participants, had an overall success rate of 47% (29-66). Fifty-two studies reporting success rates for cohorts with delayed TWOC, all with serious risk of bias, including 12 489 participants, had an overall success rate of 53% (49-56). The certainty of the evidence was considered low for the RCTs and very low for the rest. There was a limited number of appropriately designed studies addressing the research question directly. The evidence favours neither approach.

Identifiants

pubmed: 39157169
doi: 10.1002/bco2.369
pii: BCO2369
pmc: PMC11327489
doi:

Types de publication

Journal Article Review

Langues

eng

Pagination

732-747

Informations de copyright

© 2024 The Authors. BJUI Compass published by John Wiley & Sons Ltd on behalf of BJU International Company.

Déclaration de conflit d'intérêts

The authors report no conflict of interests.

Auteurs

Veronika S Christensen (VS)

Faculty of Medicine University of Oslo Oslo Norway.

Marius Skow (M)

The Antibiotic Centre for Primary Care University of Oslo Oslo Norway.
Oslo Accident and Emergency Outpatient Clinic City of Oslo Health Agency Oslo Norway.

Signe A Flottorp (SA)

Department of General Practice University of Oslo Oslo Norway.
Division of Health Services Norwegian Institute of Public Health Oslo Norway.

Hilde Strømme (H)

Library of Medicine and Science University of Oslo Oslo Norway.

Ibrahimu Mdala (I)

Department of General Practice University of Oslo Oslo Norway.

Odd Martin Vallersnes (OM)

Oslo Accident and Emergency Outpatient Clinic City of Oslo Health Agency Oslo Norway.
Department of General Practice University of Oslo Oslo Norway.

Classifications MeSH