Department of Surgery, Faculty of Medical and Health Sciences, The University of Auckland, Auckland, New Zealand.
Colorectal Dis. 2010 Apr;12(4):296-303. doi: 10.1111/j.1463-1318.2009.01828.x. Epub 2009 Mar 6.
The aim of this study was to systematically review all published evidence to determine the efficacy and safety of injectable bulking agents for passive faecal incontinence (FI) in adults.
Electronic searches were performed for MEDLINE, EMBASE, ISI Web of Knowledge and other relevant databases. Hand searching of relevant conference proceedings was undertaken. Studies were considered if they met the predefined inclusion criteria of more than ten adult patients and receiving an injectable bulking agent for passive FI with a validated means of assessing preoperative and postoperative incontinence.
Thirteen case series studies and one randomized placebo-controlled trial (RCT) were included with a total of 420 patients. Two completed RCTs with placebo control were identified but results were unobtainable. Coaptite, Contigen, Durasphere, EVOH and PTQ injections were assessed with 24, 73, 83, 21 and 208 patients respectively. Most studies reported a statistically significant improvement in incontinence scores and quality of life. No statistically significant difference was found between the treatment and placebo arms in the RCT. No serious adverse events were reported.
Currently there is little evidence for the effectiveness of injectable bulking agents in managing passive FI. The inability to obtain results from two further RCTs concerned the reviewers and hindered their ability to make strong recommendations. The identified injectable bulking agents appear to be safe with only minor complications reported.
本研究旨在系统回顾所有已发表的证据,以确定用于治疗成人被动性粪便失禁(FI)的注射性填充剂的疗效和安全性。
对 MEDLINE、EMBASE、ISI Web of Knowledge 和其他相关数据库进行电子检索。并进行了相关会议论文集的手工检索。如果研究符合以下预先设定的纳入标准,即超过 10 名成年患者接受注射性填充剂治疗被动性 FI,并使用经过验证的方法评估术前和术后失禁情况,则将其纳入研究。
共纳入了 13 项病例系列研究和 1 项随机安慰剂对照试验(RCT),共有 420 名患者。虽然确定了两项完成的 RCT 且有安慰剂对照,但结果无法获取。Coaptite、Contigen、Durasphere、EVOH 和 PTQ 注射剂分别评估了 24、73、83、21 和 208 名患者。大多数研究报告了失禁评分和生活质量的统计学显著改善。RCT 中治疗组和安慰剂组之间未发现统计学显著差异。未报告严重不良事件。
目前,注射性填充剂治疗被动性 FI 的有效性证据有限。未能从另外两项 RCT 中获得结果令审查员感到担忧,并阻碍了他们做出强烈推荐的能力。已确定的注射性填充剂似乎是安全的,仅报告了一些轻微的并发症。