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女性尿失禁的尿道注射治疗

Urethral injection therapy for urinary incontinence in women.

作者信息

Kirchin Vivienne, Page Tobias, Keegan Phil E, Atiemo Kofi, Cody June D, McClinton Samuel

机构信息

Department of Urology, Sunderland Royal Hospital, Sunderland,

出版信息

Cochrane Database Syst Rev. 2012 Feb 15(2):CD003881. doi: 10.1002/14651858.CD003881.pub3.

Abstract

BACKGROUND

Periurethral or transurethral injection of bulking agents is a minimally invasive surgical procedure used for the treatment of stress urinary incontinence in adult women.

OBJECTIVES

To assess the effects of periurethral or transurethral injection therapy on the cure or improvement of urinary incontinence in women.

SEARCH METHODS

We searched the Cochrane Incontinence Group Specialised Trials Register (searched 8 November 2010) and the reference lists of relevant articles.

SELECTION CRITERIA

All randomised or quasi-randomised controlled trials of treatment for urinary incontinence in which at least one management arm involved periurethral or transurethral injection therapy.

DATA COLLECTION AND ANALYSIS

Two review authors independently assessed methodological quality of each study using explicit criteria. Data extraction was undertaken independently and clarification concerning possible unreported data sought directly from the investigators.

MAIN RESULTS

Excluding duplicate reports, we identified 14 trials (excluding one that was subsequently withdrawn from publication and not included in this analysis) including 2004 women that met the inclusion criteria. The limited data available were not suitable for meta-analysis because they all came from separate trials. Trials were small and generally of moderate quality.One trial of 45 women that compared injection therapy with conservative treatment showed early benefit for the injectable with respect to continence grade (risk ratio (RR) 0.7, 95% confidence interval (CI) 0.52 to 0.94) and quality of life (RR 0.54, 95% CI 0.16 to 0.92). Another, comparing Injection of autologous fat with placebo, terminated early because of safety concerns. Two trials that compared injection with surgical management found significantly better objective cure in the surgical group (RR 4.77, 95% CI 1.96 to 11.64; and RR 1.69, 95% CI 1.02 to 2.79), although the latter trial data did not reach statistical significance if an intention-to-treat analysis was used.Eight trials compared different agents and all results had wide confidence intervals. Silicone particles, calcium hydroxylapatite, ethylene vinyl alcohol, carbon spheres and dextranomer hyaluronic acid combination gave improvements which were not shown to be more or less efficacious than collagen. Dextranomer hyaluronic acid compound treated patients appeared to have significantly higher rates of injection site complications (16% with the hyaluronic acid compound versus none with collagen; RR 37.78, 95% CI 2.34 to 610) and this product has now been withdrawn from the market.A comparison of periurethral and transurethral methods of injection found similar outcomes but a higher (though not statistically significant) rate of early complications in the periurethral group. One trial of 30 women showed a weak (but not clinically significant) advantage for patient satisfaction (data not suitable for analysis in Revman) after mid-urethral injection in comparison to bladder neck injection but with no demonstrable difference in continence levels.

AUTHORS' CONCLUSIONS: The available evidence base remains insufficient to guide practice. In addition, the finding that placebo saline injection was followed by a similar symptomatic improvement to bulking agent injection raises questions about the mechanism of any beneficial effects. One small trial comparing silicone particles with pelvic floor muscle training was suggestive of benefit at three months but it is not known if this was sustained, and the treatment was associated with high levels of postoperative retention and dysuria. Greater symptomatic improvement was observed with surgical treatments, though the advantages need to be set against likely higher risks. No clear-cut conclusions could be drawn from trials comparing alternative agents, although dextranomer hyaluronic acid was associated with more local side effects and is no longer commercially available for this indication. There is insufficient evidence to show superiority of mid-urethral or bladder neck injection. The single trial of autologous fat provides a reminder that periurethral injections can occasionally cause serious side effects.

摘要

背景

尿道周围或经尿道注射填充剂是一种用于治疗成年女性压力性尿失禁的微创手术。

目的

评估尿道周围或经尿道注射疗法对女性尿失禁治愈或改善的效果。

检索方法

我们检索了Cochrane尿失禁组专业试验注册库(检索时间为2010年11月8日)以及相关文章的参考文献列表。

选择标准

所有治疗尿失禁的随机或半随机对照试验,其中至少有一个治疗组涉及尿道周围或经尿道注射疗法。

数据收集与分析

两位综述作者使用明确的标准独立评估每项研究的方法学质量。数据提取独立进行,并直接向研究者寻求有关可能未报告数据的澄清。

主要结果

排除重复报告后,我们确定了14项试验(排除一项随后撤回发表且未纳入本分析的试验),包括2004名符合纳入标准的女性。现有数据有限,不适合进行荟萃分析,因为它们均来自不同的试验。试验规模较小,质量一般中等。一项纳入45名女性的试验比较了注射疗法与保守治疗,结果显示注射治疗在尿失禁分级(风险比(RR)0.7,95%置信区间(CI)0.52至0.94)和生活质量(RR 0.54,95%CI 0.16至0.92)方面早期有优势。另一项比较自体脂肪注射与安慰剂的试验,由于安全问题提前终止。两项比较注射与手术治疗的试验发现手术组的客观治愈率显著更高(RR 4.77,95%CI 1.96至11.64;以及RR 1.69,95%CI 1.02至2.79),尽管如果采用意向性分析,后一项试验数据未达到统计学显著性。八项试验比较了不同的药物,所有结果的置信区间都很宽。硅颗粒、羟基磷灰石钙、乙烯-乙烯醇、碳球和葡聚糖-透明质酸组合均有改善,但未显示出比胶原蛋白更有效或更无效。接受葡聚糖-透明质酸复合物治疗的患者似乎注射部位并发症发生率显著更高(透明质酸复合物组为16%,胶原蛋白组无;RR 37.78,95%CI 2.34至610),该产品现已退出市场。一项比较尿道周围和经尿道注射方法的试验发现结果相似,但尿道周围组早期并发症发生率更高(虽无统计学显著性)。一项纳入30名女性的试验显示,与膀胱颈注射相比,尿道中段注射后患者满意度有微弱(但无临床意义)优势(数据不适合在Revman中分析),但在尿失禁水平上无明显差异。

作者结论

现有证据不足以指导实践。此外,安慰剂盐水注射后症状改善与填充剂注射相似这一发现,引发了对任何有益效果机制的质疑。一项比较硅颗粒与盆底肌肉训练的小型试验提示在三个月时有获益,但不知是否持续,且该治疗与术后高保留率和排尿困难相关。手术治疗观察到有更大的症状改善,尽管其优势需与可能更高的风险相权衡。比较替代药物的试验无法得出明确结论,尽管葡聚糖-透明质酸与更多局部副作用相关,且不再用于该适应证的商业销售。没有足够证据表明尿道中段或膀胱颈注射更具优势。一项自体脂肪试验提醒我们,尿道周围注射偶尔会引起严重副作用。

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