The Warrell Unit, St Mary's Hospital, Manchester University NHS Foundation Trust, Manchester, UK.
Population Health Sciences Institute, Newcastle University, Newcastle upon Tyne, UK.
Cochrane Database Syst Rev. 2023 Oct 27;10(10):CD008709. doi: 10.1002/14651858.CD008709.pub4.
Stress urinary incontinence imposes a significant health and economic burden on individuals and society. Single-incision slings are a minimally-invasive treatment option for stress urinary incontinence. They involve passing a short synthetic device through the anterior vaginal wall to support the mid-urethra. The use of polypropylene mesh in urogynaecology, including mid-urethral slings, is restricted in many countries. This is a review update (previous search date 2012).
To assess the effects of single-incision sling operations for treating urinary incontinence in women, and to summarise the principal findings of relevant economic evaluations.
We searched the Cochrane Incontinence Specialised Register, which contains trials identified from: CENTRAL, MEDLINE, MEDLINE In-Process, MEDLINE Epub Ahead of Print, and two trials registers. We handsearched journals, conference proceedings, and reference lists of relevant articles to 20 September 2022.
We included randomised or quasi-randomised controlled trials in women with stress (or stress-predominant mixed) urinary incontinence in which at least one, but not all, trial arms included a single-incision sling.
We used standard Cochrane methodological procedures. The primary outcome was subjective cure or improvement of urinary incontinence.
We included 62 studies with a total of 8051 women in this review. We did not identify any studies comparing single-incision slings to no treatment, conservative treatment, colposuspension, or laparoscopic procedures. We assessed most studies as being at low or unclear risk of bias, with five studies at high risk of bias for outcome assessment. Sixteen trials used TVT-Secur, a single-incision sling withdrawn from the market in 2013. The primary analysis in this review excludes trials using TVT-Secur. We report separate analyses for these trials, which did not substantially alter the effect estimates. We identified two cost-effectiveness analyses and one cost-minimisation analysis. Single-incision sling versus autologous fascial sling One study (70 women) compared single-incision slings to autologous fascial slings. It is uncertain if single-incision slings have any effect on risk of dyspareunia (painful sex) or mesh exposure, extrusion or erosion compared with autologous fascial slings. Subjective cure or improvement of urinary incontinence at 12 months, patient-reported pain at 24 months or longer, number of women with urinary retention, quality of life at 12 months and the number of women requiring repeat continence surgery or sling revision were not reported for this comparison. Single-incision sling versus retropubic sling Ten studies compared single-incision slings to retropubic slings. There may be little to no difference between single-incision slings and retropubic slings in subjective cure or improvement of incontinence at 12 months (risk ratio (RR) 0.99, 95% confidence interval (CI) 0.91 to 1.07; 2 trials, 297 women; low-certainty evidence). It is uncertain whether single-incision slings increase the risk of mesh exposure, extrusion or erosion compared with retropubic minimally-invasive slings; the wide confidence interval is consistent with both benefit and harm (RR 1.55, 95% CI 0.24 to 9.82; 3 trials, 267 women; low-certainty evidence). It is uncertain whether single-incision slings lead to fewer women having postoperative urinary retention compared with retropubic slings; the wide confidence interval is consistent with possible benefit and harm (RR 0.47, 95% CI 0.12 to 1.84; 2 trials, 209 women; low-certainty evidence). The effect of single-incision slings on the risk of repeat continence surgery or mesh revision compared with retropubic slings is uncertain (RR 4.19, 95% CI 0.31 to 57.28; 2 trials, 182 women; very low-certainty evidence). One study reported quality of life, but not in a suitable format for analysis. Patient-reported pain at more than 24 months and the number of women with dyspareunia were not reported for this comparison. We downgraded the evidence due to concerns about risks of bias, imprecision and inconsistency. Single-incision sling versus transobturator sling Fifty-one studies compared single-incision slings to transobturator slings. The evidence ranged from high to low certainty. There is no evidence of a difference in subjective cure or improvement of incontinence at 12 months when comparing single-incision slings with transobturator slings (RR 1.00, 95% CI 0.97 to 1.03; 17 trials, 2359 women; high-certainty evidence). Single-incision slings probably have a reduced risk of patient-reported pain at 24 months post-surgery compared with transobturator slings (RR 0.12, 95% CI 0.02 to 0.68; 2 trials, 250 women; moderate-certainty evidence). The effect of single-incision slings on the risk of dyspareunia is uncertain compared with transobturator slings, as the wide confidence interval is consistent with possible benefit and possible harm (RR 0.78, 95% CI 0.41 to 1.48; 8 trials, 810 women; moderate-certainty evidence). There are a similar number of mesh exposures, extrusions or erosions with single-incision slings compared with transobturator slings (RR 0.61, 95% CI 0.39 to 0.96; 16 trials, 2378 women; high-certainty evidence). Single-incision slings probably result in similar or reduced cases of postoperative urinary retention compared with transobturator slings (RR 0.68, 95% CI 0.47 to 0.97; 23 trials, 2891 women; moderate-certainty evidence). Women with single-incision slings may have lower quality of life at 12 months compared to transobturator slings (standardised mean difference (SMD) 0.24, 95% CI 0.09 to 0.39; 8 trials, 698 women; low-certainty evidence). It is unclear whether single-incision slings lead to slightly more women requiring repeat continence surgery or mesh revision compared with transobturator slings (95% CI consistent with possible benefit and harm; RR 1.42, 95% CI 0.94 to 2.16; 13 trials, 1460 women; low-certainty evidence). We downgraded the evidence due to indirectness, imprecision and risks of bias.
AUTHORS' CONCLUSIONS: Single-incision sling operations have been extensively researched in randomised controlled trials. They may be as effective as retropubic slings and are as effective as transobturator slings for subjective cure or improvement of stress urinary incontinence at 12 months. It is uncertain if single-incision slings lead to better or worse rates of subjective cure or improvement compared with autologous fascial slings. There are still uncertainties regarding adverse events and longer-term outcomes. Therefore, longer-term data are needed to clarify the safety and long-term effectiveness of single-incision slings compared to other mid-urethral slings.
压力性尿失禁给个人和社会带来了重大的健康和经济负担。单切口吊带是治疗压力性尿失禁的一种微创治疗选择。它们通过阴道前壁将一个短的合成装置穿过,以支撑中尿道。在妇科领域,包括中尿道吊带在内,聚丙烯网的使用受到许多国家的限制。这是一项(先前的搜索日期为 2012 年)更新的综述。
评估单切口吊带手术治疗女性尿失禁的效果,并总结相关经济评估的主要发现。
我们检索了 Cochrane 尿失禁专门登记册,其中包含从以下来源确定的试验:CENTRAL、MEDLINE、MEDLINE 正在进行的检索、MEDLINE 提前在线出版和两个试验登记册。我们还手检了期刊、会议记录和相关文章的参考文献,检索截止日期为 2022 年 9 月 20 日。
我们纳入了在患有压力性(或压力主导的混合性)尿失禁的女性中进行的至少有一个但不是所有试验臂均包括单切口吊带的随机或准随机对照试验。
我们使用了标准的 Cochrane 方法学程序。主要结局是尿失禁的主观治愈或改善。
我们共纳入了 62 项研究,涉及 8051 名女性。我们没有发现任何将单切口吊带与不治疗、保守治疗、耻骨后悬吊或腹腔镜手术进行比较的研究。我们评估了大多数研究为低或不确定偏倚风险,有五项研究为高偏倚风险的结局评估。16 项试验使用了 TVT-Secur,这是一种已退出市场的单切口吊带。本综述中的主要分析排除了使用 TVT-Secur 的试验。我们对这些试验进行了单独分析,这些分析并没有实质性地改变效应估计值。我们确定了两项成本效益分析和一项成本最小化分析。单切口吊带与自体筋膜吊带:一项研究(70 名女性)比较了单切口吊带与自体筋膜吊带。与自体筋膜吊带相比,单切口吊带对性交疼痛(疼痛性性行为)或网片暴露、脱出或侵蚀的风险是否有任何影响尚不确定。12 个月时尿失禁的主观治愈或改善、24 个月或更长时间时的患者报告疼痛、需要留置导尿的女性人数、12 个月时的生活质量以及需要再次进行控尿手术或吊带修正的女性人数,这些比较都没有报告。单切口吊带与耻骨后吊带:10 项研究比较了单切口吊带与耻骨后吊带。单切口吊带与耻骨后吊带在 12 个月时尿失禁的主观治愈或改善方面可能没有差异(风险比(RR)0.99,95%置信区间(CI)0.91 至 1.07;2 项试验,297 名女性;低质量证据)。与耻骨后微创吊带相比,单切口吊带增加网片暴露、脱出或侵蚀的风险尚不确定;宽置信区间与获益和危害一致(RR 1.55,95%CI 0.24 至 9.82;3 项试验,267 名女性;低质量证据)。与耻骨后吊带相比,单切口吊带导致术后需要留置导尿的女性人数减少尚不确定;宽置信区间与获益和危害一致(RR 0.47,95%CI 0.12 至 1.84;2 项试验,209 名女性;低质量证据)。与耻骨后吊带相比,单切口吊带对再次进行控尿手术或网片修正的风险的影响尚不确定(RR 4.19,95%CI 0.31 至 57.28;2 项试验,182 名女性;极低质量证据)。一项研究报告了生活质量,但不适于进行分析。12 个月时的患者报告疼痛和性交疼痛的人数都没有报告。我们由于对偏倚、不精确性和不一致性的担忧,降低了证据的等级。单切口吊带与经闭孔吊带:51 项研究比较了单切口吊带与经闭孔吊带。证据的确定性从高到低不等。在 12 个月时,与经闭孔吊带相比,单切口吊带在尿失禁的主观治愈或改善方面没有差异(RR 1.00,95%CI 0.97 至 1.03;17 项试验,2359 名女性;高质量证据)。与经闭孔吊带相比,单切口吊带可能在术后 24 个月时患者报告的疼痛风险降低(RR 0.12,95%CI 0.02 至 0.68;2 项试验,250 名女性;中等质量证据)。与经闭孔吊带相比,单切口吊带对性交疼痛的风险的影响尚不确定,因为宽置信区间与可能的获益和可能的危害一致(RR 0.78,95%CI 0.41 至 1.48;8 项试验,810 名女性;中等质量证据)。与经闭孔吊带相比,单切口吊带的网片暴露、脱出或侵蚀的数量相似(RR 0.61,95%CI 0.39 至 0.96;16 项试验,2378 名女性;高质量证据)。与经闭孔吊带相比,单切口吊带可能导致术后需要留置导尿的人数减少(RR 0.68,95%CI 0.47 至 0.97;23 项试验,2891 名女性;中等质量证据)。与经闭孔吊带相比,使用单切口吊带的女性在 12 个月时的生活质量可能较低(标准化均数差(SMD)0.24,95%CI 0.09 至 0.39;8 项试验,698 名女性;低质量证据)。与经闭孔吊带相比,单切口吊带可能导致需要再次进行控尿手术或网片修正的女性人数略有增加(95%CI 一致,可能受益和危害;RR 1.42,95%CI 0.94 至 2.16;13 项试验,1460 名女性;低质量证据)。我们由于间接性、不精确性和偏倚风险而降低了证据的等级。
单切口吊带手术在随机对照试验中得到了广泛研究。它们可能与耻骨后吊带一样有效,并且在 12 个月时与经闭孔吊带一样有效,用于治疗压力性尿失禁的主观治愈或改善。与自体筋膜吊带相比,单切口吊带是否能更好或更差地改善主观治愈或改善尚不确定。因此,需要更长时间的数据来阐明单切口吊带与其他中尿道吊带相比的安全性和长期有效性。