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可调节性中段尿道吊带术(Remeex系统)治疗复发性或固有括约肌功能不全的女性压力性尿失禁的中期疗效及并发症

Midterm efficacy and complications of readjustable midurethral sling (Remeex system) in female stress urinary incontinence with recurrence or intrinsic sphincter deficiency.

作者信息

Park Bong Hee, Kim Joon Chul, Kim Hyun Woo, Kim Young Ho, Choi Jong Bo, Lee Dong Hwan

机构信息

Department of Urology, Uijeongbu St. Mary's Hospital, College of Medicine, The Catholic University of Korea, Uijeongbu, Korea.

Department of Urology, Bucheon St. Mary's Hospital, College of Medicine, The Catholic University of Korea, Bucheon, Korea.

出版信息

Urology. 2015 Jan;85(1):79-84. doi: 10.1016/j.urology.2014.10.003.

Abstract

OBJECTIVE

To evaluate the efficacy, complications, and managements of the readjustable midurethral sling (Remeex system) for the treatment of recurrent stress urinary incontinence (SUI) after previous anti-incontinence surgeries or intrinsic sphincter deficiency (ISD).

METHODS

Between March 2008 and February 2012, 102 women, who presented with previous failed surgery or ISD, were treated with the Remeex system at 4 different institutions. We retrospectively reviewed medical history, physical examination, urodynamic study, postvoiding residual volume, and/or 1-hour pad test of the patients. Surgical outcomes were evaluated using the Severity Index for Urinary Incontinence. The degree of patient satisfaction was assessed, and all complications were classified according to the modified Clavien classification system.

RESULTS

After a mean follow-up of 27.6 months (range, 14-56 months), 91 patients (89.2%) were cured and 6 patients (5.9%) were improved. The patient's satisfaction rate was 87.2% (89 of 102 patients). Overall, 41 patients (40.2%) experienced 53 complications; 15 patients (14.7%) presented de novo urgency, which was properly managed with anticholinergics, and 14 patients (13.7%) underwent delayed sling readjustment for recurrent SUI (n = 13) and urinary retention (n = 1) during follow-up. Among 6 patients (5.9%) with wound infection, 4 patients were successfully treated by daily dressing with antibiotics, and 2 patients underwent removal of the Remeex system owing to intractable infection. Most complications were classified as grade 1 (54.8%) or 2 (15.1%) and were successfully treated with minimal conservative measures.

CONCLUSION

The Remeex system is a valuable adjunct for recurrent SUI after previous anti-incontinence surgeries or ISD, considering most complications are Clavien grade I or II.

摘要

目的

评估可调节性中段尿道吊带术(Remeex系统)治疗既往抗尿失禁手术失败或存在固有括约肌缺陷(ISD)的复发性压力性尿失禁(SUI)的疗效、并发症及处理方法。

方法

2008年3月至2012年2月期间,102例既往手术失败或存在ISD的女性患者在4家不同机构接受了Remeex系统治疗。我们回顾性分析了患者的病史、体格检查、尿动力学检查、排尿后残余尿量和/或1小时尿垫试验。使用尿失禁严重程度指数评估手术效果。评估患者的满意度,并根据改良的Clavien分类系统对所有并发症进行分类。

结果

平均随访27.6个月(范围14 - 56个月)后,91例患者(89.2%)治愈,6例患者(5.9%)症状改善。患者满意度为87.2%(102例患者中的89例)。总体而言,41例患者(40.2%)出现了53种并发症;15例患者(14.7%)出现新发尿急,使用抗胆碱能药物妥善处理;14例患者(13.7%)在随访期间因复发性SUI(n = 13)和尿潴留(n = 1)接受了吊带延迟调整。在6例伤口感染患者(5.9%)中,4例患者通过每日使用抗生素换药成功治疗,2例患者因顽固性感染接受了Remeex系统取出术。大多数并发症分类为1级(54.8%)或2级(15.1%),通过最小限度的保守措施成功治疗。

结论

考虑到大多数并发症为Clavien I级或II级,Remeex系统是既往抗尿失禁手术失败或存在ISD的复发性SUI的一种有价值的辅助治疗方法。

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