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根治性前列腺切除术后尿失禁外科治疗的利弊评估:一项系统评价和荟萃分析

Evaluation of Benefits and Harms of Surgical Treatments for Post-radical Prostatectomy Urinary Incontinence: A Systematic Review and Meta-analysis.

作者信息

Choinière Roselyne, Violette Philippe D, Morin Mélanie, Tu Le Mai, Guyatt Gordon H, Reed Christine, Philie Camille-Ariane, Legault Benjamin, Beaudry Marie-Michèle, Ahmed Muhammad Muneeb, Richard Patrick O

机构信息

Centre Hospitalier Universitaire de Sherbrooke, University of Sherbrooke, Sherbrooke, QC, Canada.

Department of Health Research Methods Evidence and Impact (HEI), McMaster University, Hamilton, ON, Canada; Department of Surgery, McMaster University, Hamilton, ON, Canada.

出版信息

Eur Urol Focus. 2022 Jul;8(4):1042-1052. doi: 10.1016/j.euf.2021.09.007. Epub 2021 Sep 22.

Abstract

CONTEXT

No meta-analysis has comprehensively addressed both benefits and harms, or the certainty of evidence of the implantable continence devices used in men to treat postprostatectomy urinary incontinence (PPI).

OBJECTIVE

To evaluate the benefits and harms of surgical treatments for patients suffering from PPI and assess the certainty of evidence. The primary benefit was cure (one or fewer pad per day), and the primary harm was reoperations defined by surgical procedures following implantation.

EVIDENCE ACQUISITION

We perform a search of Medline, PubMed, Embase, Cochrane Library, and gray literature. We included observational studies addressing PPI surgical interventions if they involved cohorts of ≥50 participants. The Grading of Recommendations, Assessment, Development and Evaluations (GRADE) approach provided the framework for certainty of evidence assessment informed by value and preference judgments provided by patients, and an advocacy group member (Canadian Cancer Society).

EVIDENCE SYNTHESIS

Of 85 observational studies involving 13 100 patients, three addressed bulking agents, 35 male synthetic slings, ten adjustable continence therapies (ACTs), and 37 artificial urinary sphincters (AUSs). Cure was 26.1% (95% confidence interval [CI]: 10.6-51.4, I = 92.8%, very-low-quality evidence) for bulking agents, 58.6% (95% CI: 51.3-65.5, I = 89.1%, low-quality evidence) for slings, 63.2% (95% CI: 57.6-68.5, I = 22.5%, very-low-quality evidence) for ACT, and 74.0% (95% CI:61.2-83.7, I = 92.1%, very-low-quality evidence) for AUS. Estimated rates of reoperation were 5.8% (95% CI: 1.9-11.6, I = 94.1%, moderate-quality evidence) for slings, 23.8% (95% CI: 5.9-61.0, I = 95.5%, low-quality evidence) for ACT, and 22.2% (95% CI: 15.2-31.3, I = 92.3%, high-quality evidence) for AUS.

CONCLUSIONS

Available evidence regarding the benefits of surgical interventions for PPI remains mainly uncertain while suggesting important harms. These results should guide consent procedures for PPI surgery in the context of shared decision-making, with disclosure of the uncertainty of evidence.

PATIENT SUMMARY

Despite being used worldwide, available evidence regarding the benefits of surgeries to treat postprostatectomy urinary incontinence remains mainly uncertain while suggesting important harms. This highlights the need for a more rigorous evaluation process for commercially available surgical devices.

摘要

背景

尚无荟萃分析全面探讨用于治疗前列腺切除术后尿失禁(PPI)的男性可植入控尿装置的益处和危害,或证据的确定性。

目的

评估PPI患者手术治疗的益处和危害,并评估证据的确定性。主要益处为治愈(每天使用一个或更少尿垫),主要危害为植入后根据手术操作定义的再次手术。

证据获取

我们检索了Medline、PubMed、Embase、Cochrane图书馆和灰色文献。如果观察性研究涉及≥50名参与者的队列,我们将其纳入有关PPI手术干预的研究。推荐分级、评估、制定与评价(GRADE)方法提供了证据确定性评估的框架,该评估由患者和一名倡导小组成员(加拿大癌症协会)提供的价值和偏好判断提供信息。

证据综合

在涉及13100名患者的85项观察性研究中,三项涉及填充剂,35项涉及男性合成吊带,十项涉及可调节控尿疗法(ACT),37项涉及人工尿道括约肌(AUS)。填充剂的治愈率为26.1%(95%置信区间[CI]:10.6 - 51.4,I² = 92.8%,极低质量证据),吊带为58.6%(95% CI:51.3 - 65.5,I² = 89.1%,低质量证据),ACT为63.2%(95% CI:57.6 - 68.5,I² = 22.5%,极低质量证据),AUS为74.0%(95% CI:61.2 - 83.7,I² = 92.1%,极低质量证据)。吊带的再次手术估计率为5.8%(95% CI:1.9 - 11.6),I² = 94.1%,中等质量证据),ACT为23.8%(95% CI:5.9 - 61.0,I² = 95.%,低质量证据),AUS为22.2%(95% CI:15.2 - 31.3,I² = 92.3%,高质量证据)。

结论

关于PPI手术干预益处的现有证据仍然主要不确定,同时提示存在重要危害。这些结果应在共同决策的背景下指导PPI手术的知情程序,并披露证据的不确定性。

患者总结

尽管在全球范围内使用,但关于治疗前列腺切除术后尿失禁手术益处的现有证据仍然主要不确定,同时提示存在重要危害。这凸显了对市售手术器械进行更严格评估过程的必要性。

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