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Methods of postoperative void trial management after urogynecologic surgery: a systematic review and meta-analysis

BACKGROUND: Voiding trials are used to identify women at risk for postoperative urinary retention while performing optimal voiding trial management with minimal burden to the patient and medical service team. We performed a systematic review and meta-analysis of postoperative void trials following u...

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Autores principales: Dong, Xue, Huang, Wu, Niu, Jinyang, Lei, Tingting, Tan, Xin, Guo, Tao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10327332/
https://www.ncbi.nlm.nih.gov/pubmed/37420310
http://dx.doi.org/10.1186/s13643-023-02233-1
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author Dong, Xue
Huang, Wu
Niu, Jinyang
Lei, Tingting
Tan, Xin
Guo, Tao
author_facet Dong, Xue
Huang, Wu
Niu, Jinyang
Lei, Tingting
Tan, Xin
Guo, Tao
author_sort Dong, Xue
collection PubMed
description BACKGROUND: Voiding trials are used to identify women at risk for postoperative urinary retention while performing optimal voiding trial management with minimal burden to the patient and medical service team. We performed a systematic review and meta-analysis of postoperative void trials following urogynecologic surgery to investigate (1) the optimal postoperative void trial methodology and (2) the optimal criteria for assessing void trial. METHOD: We searched PubMed, EMBASE, Cochrane Central Register of Controlled Trials, and relevant reference lists of eligible articles from inception to April 2022. We identified any randomized controlled trials (RCTs) in English that studied void trials in patients undergoing urogynecologic surgery. Study selection (title/abstract and full text), data extraction, and risk of bias assessment were conducted by two independent reviewers. Extracted study outcomes included the following: the correct passing rate, time to discharge, discharge rate without a catheter after the initial void trial, postoperative urinary tract infection, and patient satisfaction. RESULTS: Void trial methodology included backfill-assisted and autofill studies (2 RCTs, n = 95). Backfill assistance was more likely to be successful than autofill (RR 2.12, 95% CI 1.29, 3.47, P = 0.00); however, no significant difference was found in the time to discharge (WMDs =  − 29.11 min, 95% CI − 57.45, 1.23, P = 0.06). The criteria for passing void trial included subjective assessment of the urinary force of stream and objective assessment of the standard voiding trial (3 RCTs, n = 377). No significant differences were found in the correct passing rate (RR 0.97, 95% CI 0.93, 1.01, P = 0.14) or void trial failure rate (RR 0.78, 95% CI 0.52, 1.18, P = 0.24). Moreover, no significant differences were found in the complication rates or patient satisfaction between the two criteria. CONCLUSION: Bladder backfilling was associated with a lower rate of catheter discharge after urogynecologic surgery. The subjective assessment of FOS is a reliable and safe method for assessing postoperative voiding because it is less invasive. SYSTEMATIC REVIEW REGISTRATION: PROSPERO CRD42022313397 SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13643-023-02233-1.
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spelling pubmed-103273322023-07-08 Methods of postoperative void trial management after urogynecologic surgery: a systematic review and meta-analysis Dong, Xue Huang, Wu Niu, Jinyang Lei, Tingting Tan, Xin Guo, Tao Syst Rev Research BACKGROUND: Voiding trials are used to identify women at risk for postoperative urinary retention while performing optimal voiding trial management with minimal burden to the patient and medical service team. We performed a systematic review and meta-analysis of postoperative void trials following urogynecologic surgery to investigate (1) the optimal postoperative void trial methodology and (2) the optimal criteria for assessing void trial. METHOD: We searched PubMed, EMBASE, Cochrane Central Register of Controlled Trials, and relevant reference lists of eligible articles from inception to April 2022. We identified any randomized controlled trials (RCTs) in English that studied void trials in patients undergoing urogynecologic surgery. Study selection (title/abstract and full text), data extraction, and risk of bias assessment were conducted by two independent reviewers. Extracted study outcomes included the following: the correct passing rate, time to discharge, discharge rate without a catheter after the initial void trial, postoperative urinary tract infection, and patient satisfaction. RESULTS: Void trial methodology included backfill-assisted and autofill studies (2 RCTs, n = 95). Backfill assistance was more likely to be successful than autofill (RR 2.12, 95% CI 1.29, 3.47, P = 0.00); however, no significant difference was found in the time to discharge (WMDs =  − 29.11 min, 95% CI − 57.45, 1.23, P = 0.06). The criteria for passing void trial included subjective assessment of the urinary force of stream and objective assessment of the standard voiding trial (3 RCTs, n = 377). No significant differences were found in the correct passing rate (RR 0.97, 95% CI 0.93, 1.01, P = 0.14) or void trial failure rate (RR 0.78, 95% CI 0.52, 1.18, P = 0.24). Moreover, no significant differences were found in the complication rates or patient satisfaction between the two criteria. CONCLUSION: Bladder backfilling was associated with a lower rate of catheter discharge after urogynecologic surgery. The subjective assessment of FOS is a reliable and safe method for assessing postoperative voiding because it is less invasive. SYSTEMATIC REVIEW REGISTRATION: PROSPERO CRD42022313397 SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13643-023-02233-1. BioMed Central 2023-07-07 /pmc/articles/PMC10327332/ /pubmed/37420310 http://dx.doi.org/10.1186/s13643-023-02233-1 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Dong, Xue
Huang, Wu
Niu, Jinyang
Lei, Tingting
Tan, Xin
Guo, Tao
Methods of postoperative void trial management after urogynecologic surgery: a systematic review and meta-analysis
title Methods of postoperative void trial management after urogynecologic surgery: a systematic review and meta-analysis
title_full Methods of postoperative void trial management after urogynecologic surgery: a systematic review and meta-analysis
title_fullStr Methods of postoperative void trial management after urogynecologic surgery: a systematic review and meta-analysis
title_full_unstemmed Methods of postoperative void trial management after urogynecologic surgery: a systematic review and meta-analysis
title_short Methods of postoperative void trial management after urogynecologic surgery: a systematic review and meta-analysis
title_sort methods of postoperative void trial management after urogynecologic surgery: a systematic review and meta-analysis
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10327332/
https://www.ncbi.nlm.nih.gov/pubmed/37420310
http://dx.doi.org/10.1186/s13643-023-02233-1
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