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女性压力性尿失禁的微创合成尿道下吊带手术

Minimally invasive synthetic suburethral sling operations for stress urinary incontinence in women.

作者信息

Ogah Joseph, Cody June D, Rogerson Lynne

机构信息

Department of Gynaecology, Leeds University Teaching Hospital, Gledwhow wing Level 6, Beckett Street, Leeds, UK, LS9 7TF.

出版信息

Cochrane Database Syst Rev. 2009 Oct 7(4):CD006375. doi: 10.1002/14651858.CD006375.pub2.

DOI:10.1002/14651858.CD006375.pub2
PMID:19821363
Abstract

BACKGROUND

Stress urinary incontinence (SUI) is a common condition affecting up to 30% of women. Minimally invasive synthetic suburethral sling operations are among the latest forms of procedures introduced to treat SUI.

OBJECTIVES

To assess the effects of minimally invasive synthetic suburethral sling operations for treatment of SUI, urodynamic stress incontinence (USI) or mixed urinary incontinence (MUI) in women.

SEARCH STRATEGY

We searched the Cochrane Incontinence Group Specialised Register (searched 20 March 2008), MEDLINE (January 1950 to April 2008), EMBASE (January 1988 to April 2008), CINAHL (January 1982 to April 2008), AMED (January 1985 to April 2008), the UK National Research Register, ClinicalTrials.gov, and reference lists of relevant articles.

SELECTION CRITERIA

Randomised or quasi-randomised controlled trials amongst women with SUI, USI or symptoms of stress or mixed urinary incontinence, in which at least one trial arm involved a minimally invasive synthetic suburethral sling operations.

DATA COLLECTION AND ANALYSIS

Two review authors assessed the methodological quality of potentially eligible studies and independently extracted data from the included trials.

MAIN RESULTS

Sixty two trials involving 7101 women were included. The quality of evidence was moderate for most trials. Minimally invasive synthetic suburethral sling operations appeared to be as effective as traditional suburethral slings ( trials, n = 599, Risk Ratio (RR) 1.03, 95% Confidence Interval (CI) 0.94 to 1.13) but with shorter operating time and less post-operative voiding dysfunction and de novo urgency symptoms.Minimally invasive synthetic suburethral sling operations appeared to be as effective as open retropubic colposuspension (subjective cure rate at 12 months RR 0.96, 95% CI 0.90 to 1.03; at 5 years RR 0.91, 95% CI 0.74 to 1.12) with fewer perioperative complications, less postoperative voiding dysfunction, shorter operative time and hospital stay but significantly more bladder perforations (6% versus 1%, RR 4.24, 95% CI 1.71 to 10.52).There was conflicting evidence about the effectiveness of minimally invasive synthetic suburethral sling operations compared to laparoscopic colposuspension in the short term (objective cure, RR 1.15, 95% CI 1.06 to 1.24; subjective cure RR 1.11, 95% CI 0.99 to 1.24). Minimally invasive synthetic suburethral sling operations had significantly less de novo urgency and urgency incontinence, shorter operating time, hospital stay and time to return to daily activities.A retropubic bottom-to-top route was more effective than top-to-bottom route (RR 1.10, 95% CI 1.01 to 1.20; RR 1.06, 95% CI 1.01 to 1.11) and incurred significantly less voiding dysfunction, bladder perforations and tape erosions.Monofilament tapes had significantly higher objective cure rates (RR 1.15, 95% CI 1.02 to 1.30) compared to multifilament tapes and fewer tape erosions (1.3% versus 6% RR 0.25, 95% CI 0.06 to 1.00).The obturator route was less favourable than the retropubic route in objective cure (84% versus 88%; RR 0.96, 95% CI 0.93 to 0.99; 17 trials, n = 2434), although there was no difference in subjective cure rates. However, there was less voiding dysfunction, blood loss, bladder perforation (0.3% versus 5.5%, RR 0.14, 95% CI 0.07 to 0.26) and shorter operating time with the obturator route.

AUTHORS' CONCLUSIONS: The current evidence base suggests that minimally invasive synthetic suburethral sling operations are as effective as traditional suburethral slings, open retropubic colposuspension and laparoscopic colposuspension in the short term but with less postoperative complications. Women were less likely to be continent after operations performed via the obturator (rather than retropubic) route, but they had fewer complications. Most of the trials had short term follow up and the quality of the evidence was variable.

摘要

背景

压力性尿失禁(SUI)是一种常见病症,影响着高达30%的女性。微创合成尿道下吊带手术是治疗SUI的最新手术方式之一。

目的

评估微创合成尿道下吊带手术治疗女性压力性尿失禁(SUI)、尿动力学压力性尿失禁(USI)或混合性尿失禁(MUI)的效果。

检索策略

我们检索了Cochrane尿失禁组专业注册库(检索时间为2008年3月20日)、MEDLINE(1950年1月至2008年4月)、EMBASE(1988年1月至2008年4月)、CINAHL(1982年1月至2008年4月)、AMED(1985年1月至2008年4月)、英国国家研究注册库、ClinicalTrials.gov以及相关文章的参考文献列表。

入选标准

针对患有SUI、USI或压力性或混合性尿失禁症状的女性进行的随机或半随机对照试验,其中至少有一个试验组涉及微创合成尿道下吊带手术。

数据收集与分析

两名综述作者评估了潜在合格研究的方法学质量,并独立从纳入试验中提取数据。

主要结果

纳入了62项涉及7101名女性的试验。大多数试验的证据质量为中等。微创合成尿道下吊带手术似乎与传统尿道下吊带手术效果相当(试验,n = 599,风险比(RR)1.03,95%置信区间(CI)0.94至1.13),但手术时间更短,术后排尿功能障碍和新发尿急症状更少。微创合成尿道下吊带手术似乎与耻骨后开放式阴道悬吊术效果相当(12个月时主观治愈率RR 0.96,95% CI 0.90至1.03;5年时RR 0.91,95% CI 0.74至1.12)且围手术期并发症更少,术后排尿功能障碍更少,手术时间和住院时间更短,但膀胱穿孔明显更多(6%对1%,RR 4.24,95% CI 1.71至10.52)。与腹腔镜阴道悬吊术相比,微创合成尿道下吊带手术在短期内的有效性存在相互矛盾的证据(客观治愈率,RR 1.15,95% CI 1.06至1.24;主观治愈率RR 1.11,95% CI 0.99至1.24)。微创合成尿道下吊带手术的新发尿急和急迫性尿失禁明显更少,手术时间、住院时间和恢复日常活动的时间更短。耻骨后自下而上途径比自上而下途径更有效(RR 1.10,95% CI 1.01至1.20;RR 1.06,95% CI 1.01至1.11),且排尿功能障碍、膀胱穿孔和吊带侵蚀明显更少。与多丝吊带相比,单丝吊带的客观治愈率明显更高(RR 1.15,95% CI 1.02至1.30),吊带侵蚀更少(1.3%对6%,RR 0.25,95% CI 0.06至1.00)。在客观治愈率方面,闭孔途径不如耻骨后途径(84%对88%;RR 0.96,95% CI 0.93至0.99;17项试验,n = 2434),尽管主观治愈率没有差异。然而,闭孔途径的排尿功能障碍、失血、膀胱穿孔更少(0.3%对%,RR至0.26),手术时间更短。

作者结论

目前的证据表明,微创合成尿道下吊带手术在短期内与传统尿道下吊带手术、耻骨后开放式阴道悬吊术和腹腔镜阴道悬吊术效果相当,但术后并发症更少。通过闭孔(而非耻骨后)途径进行手术的女性术后尿失禁的可能性较小,但并发症较少。大多数试验的随访时间较短,证据质量参差不齐。

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