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首页> 外文期刊>BJU international >Prospective multi-centre study of adjustable single-incision mini-sling (Ajust?) in the management of stress urinary incontinence in women: 1-year follow-up study
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Prospective multi-centre study of adjustable single-incision mini-sling (Ajust?) in the management of stress urinary incontinence in women: 1-year follow-up study

机译:可调式单切口迷你吊带(Ajust?)在女性应激性尿失禁管理中的前瞻性多中心研究:1年随访研究

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摘要

OBJECTIVES To determine whether an adjustable single-incision mini-sling (SIMS, Ajust?) is safe and effective in the management of female stress urinary incontinence (SUI) at 12 months follow-up. To determine whether it is feasible to be performed under local anesthesia (LA). MATERIALS AND METHODS The present study is a multicentre prospective cohort study in which 90 female patients underwent SIMS-Ajust? using a standardized insertion technique. The last 45 women were offered the procedure under LA. All patients completed their 12-month follow-up. RESULTS The patient-reported success rate, using Patient Global Impression of Improvement (PGI-I), was 80% at 12 months follow-up and a further 6% (n= 5) reported themselves to be 'improved'. In all, 32/45 (71%) patients agreed to undergo the procedure under LA while one patient required conversion to general anaesthetic. There was no organ damage or requirement for blood transfusion. Significantly lower rates of blood loss (P= 0.025) and postoperative voiding difficulties (P= 0.026) were seen in the LA group. The re-operation rate for SUI was 6% at 12 months. CONCLUSIONS SIMS (Ajust) appears to be a safe procedure, which is feasible under LA. SIMS (Ajust) have an 80% patient-reported success rate at 12 months follow-up.
机译:目的确定可调整的单切口迷你吊带(SIMS,Ajust?)在12个月的随访中是否安全有效地治疗女性压力性尿失禁(SUI)。确定在局部麻醉(LA)下进行手术是否可行。材料与方法本研究是一项多中心前瞻性队列研究,其中90例女性患者接受了SIMS-Ajust?使用标准化的插入技术。在洛杉矶,为最后45名妇女提供了程序。所有患者均完成了12个月的随访。结果使用患者总体改善印象(PGI-I),患者报告的成功率在12个月的随访中为80%,另有6%(n = 5)的患者报告自己“得到改善”。总共有32/45(71%)的患者同意接受LA手术,而一名患者需要转换为全身麻醉。没有器官损伤或输血的要求。在LA组中,失血率(P = 0.025)和术后排尿困难(P = 0.026)明显降低。 SUI的12个月再手术率为6%。结论SIMS(Ajust)似乎是一个安全的程序,在LA下可行。 SIMS(Ajust)在12个月的随访中患者报告的成功率为80%。

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