Efficacy of Electroacupuncture in the Treatment of Mild to Moderate Female Stress Urinary Incontinence: Protocol for a Systematic Review and Network Meta-Analysis.

IF 1.4 Q3 HEALTH CARE SCIENCES & SERVICES JMIR Research Protocols Pub Date : 2024-11-04 DOI:10.2196/55870
JiaNi Shi, Peiqi Li, Yifan Wu, Jiawei Li, Yuchen Zhang, Bin Xiao
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Abstract

Background: Stress urinary incontinence (SUI), the most common form of urinary incontinence, is a condition that affects many women. It is characterized by involuntary urine leakage during activities that increase abdominal pressure, such as sneezing, coughing, or physical exertion, according to the International Continence Society. SUI affects patients' quality of life and causes depression and emotional disorders, which negatively influences physical and mental health. The participants in the studies in this review comprised women with mild to moderate SUI, because there are more female patients than male patients, and most patients with severe SUI are treated surgically. Moreover, after retrieval, there were no systematic reviews or network meta-analyses (NMAs) of conservative treatments, such as electroacupuncture (EA), in women with mild to moderate SUI.

Objective: This study aims to investigate the efficacy of electroacupuncture among women with mild to moderate SUI using an NMA.

Methods: Randomized clinical trials related to conservative treatments for SUI will be searched in 5 English and 3 Chinese literature databases: EMBASE, PubMed, Cochrane, Web of Science, ClinicalTrials.gov, Chinese National Knowledge Infrastructure (CNKI), WanFang, and the Chinese BioMedical Literature Database. The search period for these 8 electronic databases will be from 2002 to 2022. The PROSPERO database and the International Platform of Registered Systematic Review and Meta-Analysis Protocols (INPLASY) database will also be searched. Two reviewers will independently complete the research selection. After screening the studies, 2 other researchers will extract the data, and the quality of the included studies will be evaluated according to the quality standards specified in the Cochrane Collaboration Tool (version 2). The primary outcomes will be the change in urine leakage determined by a 1-hour pad test and International Consultation on Incontinence Questionnaire Short Form (ICIQ-SF) scores at baseline and at the conclusion of the follow-up. The secondary outcomes will be 72-hour incontinence episodes, residual bladder volume, effective rate, urodynamic indexes, and other reported measurements. Stata (version 14.0; StataCorp) and Review Manager (RevMan version 5.3; Cochrane) will be implemented for data synthesis and meta-analysis.

Results: The results are not yet accessible because this is a protocol for a systematic review and meta-analysis. The protocol was registered on INPLASY on February 22, 2023. By April 6, 2023, we had completed the literature search of the 8 databases and completed the selection and data extraction of the articles.

Conclusions: The results of this systematic review will demonstrate the efficacy of EA among women with mild to moderate SUI. The results will provide evidence for clinicians and guideline makers to choose suitable treatments for SUI.

Trial registration: International Platform of Registered Systematic Review and Meta-Analysis Protocols (INPLASY) 202320098; https://inplasy.com/inplasy-2023-2-0098/.

International registered report identifier (irrid): DERR1-10.2196/55870.

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电针治疗轻度至中度女性压力性尿失禁的疗效:系统回顾与网络元分析协议》。
背景:压力性尿失禁(SUI)是最常见的尿失禁形式,影响着许多女性。根据国际尿失禁协会(International Continence Society)的说法,压力性尿失禁的特点是在打喷嚏、咳嗽或体力消耗等增加腹压的活动中出现不自主漏尿。SUI 会影响患者的生活质量,导致抑郁和情绪紊乱,从而对身心健康造成负面影响。由于女性患者多于男性患者,且大多数重度 SUI 患者都接受了手术治疗,因此本综述研究的参与者包括患有轻度至中度 SUI 的女性患者。此外,经检索,没有关于电针(EA)等保守疗法治疗轻中度 SUI 女性的系统综述或网络荟萃分析(NMA):本研究旨在通过网络荟萃分析(NMA)研究电针对轻中度 SUI 女性的疗效:将在 5 个英文文献数据库和 3 个中文文献数据库中检索与 SUI 保守治疗相关的随机临床试验:EMBASE、PubMed、Cochrane、Web of Science、ClinicalTrials.gov、中国国家知识基础设施(CNKI)、万方数据库和中国生物医学文献数据库。这 8 个电子数据库的检索期为 2002 年至 2022 年。此外,还将检索 PROSPERO 数据库和国际注册系统综述和元分析协议平台(INPLASY)数据库。两名审稿人将独立完成研究筛选。筛选后,另外两名研究人员将提取数据,并根据 Cochrane 协作工具(第 2 版)规定的质量标准对纳入研究的质量进行评估。主要研究结果为基线和随访结束时通过 1 小时尿垫测试确定的漏尿变化以及尿失禁国际咨询问卷简表(ICIQ-SF)得分。次要结果为 72 小时尿失禁次数、残余膀胱容量、有效率、尿动力学指数以及其他报告的测量值。将使用Stata(14.0版;StataCorp)和Review Manager(RevMan 5.3版;Cochrane)进行数据综合和荟萃分析:由于这是一项系统综述和荟萃分析协议,因此目前还无法获得结果。该方案于 2023 年 2 月 22 日在 INPLASY 上注册。截至 2023 年 4 月 6 日,我们已完成 8 个数据库的文献检索,并完成了文章的筛选和数据提取:本系统综述的结果将证明 EA 对轻度至中度 SUI 妇女的疗效。该结果将为临床医生和指南制定者选择合适的 SUI 治疗方法提供证据:国际注册系统综述和元分析协议平台(INPLASY)202320098;https://inplasy.com/inplasy-2023-2-0098/.International 注册报告标识符(irrid):DERR1-10.2196/55870。
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CiteScore
2.40
自引率
5.90%
发文量
414
审稿时长
12 weeks
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