Information Services Division, National Health Service National Services Scotland, Edinburgh, UK; Division of Epidemiology and Public Health, University of Nottingham, Nottingham, UK.
Information Services Division, National Health Service National Services Scotland, Edinburgh, UK; Institute of Health and Wellbeing, University of Glasgow, Glasgow, UK.
Lancet. 2017 Feb 11;389(10069):629-640. doi: 10.1016/S0140-6736(16)32572-7. Epub 2016 Dec 21.
Concerns have been raised about the safety of surgery for stress urinary incontinence and pelvic organ prolapse using transvaginal mesh. We assessed adverse outcomes after first, single mesh procedures and comparable non-mesh procedures.
We did a cohort study of women in Scotland aged 20 years or older undergoing a first, single incontinence procedure or prolapse procedure during 1997-98 to 2015-16 identified from a national hospital admission database. Primary outcomes were immediate postoperative complications and subsequent (within 5 years) readmissions for later postoperative complications, further incontinence surgery, or further prolapse surgery. Poisson regression models were used to compare outcomes after procedures carried out with and without mesh.
Between April 1, 1997, and March 31, 2016, 16 660 women underwent a first, single incontinence procedure, 13 133 (79%) of which used mesh. Compared with non-mesh open surgery (colposuspension), mesh procedures had a lower risk of immediate complications (adjusted relative risk [aRR] 0·44 [95% CI 0·36-0·55]) and subsequent prolapse surgery (adjusted incidence rate ratio [aIRR] 0·30 [0·24-0·39]), and a similar risk of further incontinence surgery (0·90 [0·73-1·11]) and later complications (1·12 [0·98-1·27]); all ratios are for retropubic mesh. During the same time period, 18 986 women underwent a first, single prolapse procedure, 1279 (7%) of which used mesh. Compared with non-mesh repair, mesh repair of anterior compartment prolapse was associated with a similar risk of immediate complications (aRR 0·93 [95% CI 0·49-1·79]); an increased risk of further incontinence (aIRR 3·20 [2·06-4·96]) and prolapse surgery (1·69 [1·29-2·20]); and a substantially increased risk of later complications (3·15 [2·46-4·04]). Compared with non-mesh repair, mesh repair of posterior compartment prolapse was associated with a similarly increased risk of repeat prolapse surgery and later complications. No difference in any outcome was observed between vaginal and, separately, abdominal mesh repair of vaginal vault prolapse compared with vaginal non-mesh repair.
Our results support the use of mesh procedures for incontinence, although further research on longer term outcomes would be beneficial. Mesh procedures for anterior and posterior compartment prolapse cannot be recommended for primary prolapse repair. Both vaginal and abdominal mesh procedures for vaginal vault prolapse repair are associated with similar effectiveness and complication rates to non-mesh vaginal repair. These results therefore do not clearly favour any particular vault repair procedure.
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人们对经阴道网片治疗压力性尿失禁和盆腔器官脱垂手术的安全性表示担忧。我们评估了初次单一切口手术和可比非网片手术的不良结局。
我们对 1997 年 9 月 1 日至 2015 年 3 月 31 日期间在苏格兰接受初次单一切口手术治疗压力性尿失禁或脱垂的 20 岁及以上女性进行了队列研究,这些患者的信息来自国家住院数据库。主要结局为术后即刻并发症,以及 5 年内因术后晚期并发症、进一步尿失禁手术或进一步脱垂手术而再次入院的情况。采用泊松回归模型比较有无网片的手术结果。
在 1997 年 4 月 1 日至 2016 年 3 月 31 日期间,有 16660 名女性接受了初次单一切口尿失禁手术,其中 13133 例(79%)采用了网片。与非网片开放式手术(耻骨后悬吊术)相比,网片手术的即刻并发症风险较低(校正相对风险[ARR]0.44[95%CI 0.36-0.55]),且后续发生脱垂手术的风险较低(校正发病率比[aIRR]0.30[0.24-0.39]),进一步发生尿失禁手术的风险相似(0.90[0.73-1.11]),以及晚期并发症风险相似(1.12[0.98-1.27]);所有比值均为经耻骨后网片。在同一时期,有 18986 名女性接受了初次单一切口脱垂手术,其中 1279 例(7%)采用了网片。与非网片修复相比,网片修复前盆腔脱垂的即刻并发症风险相似(ARR 0.93[95%CI 0.49-1.79]);进一步发生尿失禁(aIRR 3.20[2.06-4.96])和脱垂手术(1.69[1.29-2.20])的风险增加;晚期并发症的风险显著增加(3.15[2.46-4.04])。与非网片修复相比,网片修复后盆腔脱垂的再次脱垂手术和晚期并发症风险也同样增加。与阴道非网片修复相比,阴道穹窿脱垂阴道网片和单独的经腹网片修复在任何结局方面均无差异。
我们的研究结果支持使用网片手术治疗尿失禁,但进一步的长期结局研究将是有益的。网片手术不能作为原发性脱垂修复的首选方法。阴道前、后盆腔网片手术不能推荐用于原发性脱垂修复。阴道穹窿脱垂的阴道网片和经腹网片修复与阴道非网片修复的有效性和并发症发生率相似。因此,这些结果并没有明显支持任何特定的穹窿修复方法。
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