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18例经尿道中段吊带术穿透尿道或膀胱患者的管理与随访回顾性研究

Retrospective study on the management and follow-up of 18 patients with a mid-urethral sling penetrating the urethra or bladder.

作者信息

Goujon Edouard, Jarniat Adélaide, Bardet Florian, Bergogne Lise, Delorme Emmanuel

机构信息

Department of Gynecology, Private Hospital Sainte Thérèse, 6 quai du mas Coulet, 34200 Sète, France.

Department of Gynecology, Hospital of Auxerre, France.

出版信息

J Gynecol Obstet Hum Reprod. 2018 Sep;47(7):289-297. doi: 10.1016/j.jogoh.2018.05.007. Epub 2018 May 18.

Abstract

INTRODUCTION

The mid-urethral sling (MUS) procedure is the gold-standard for the surgical treatment of stress urinary incontinence (SUI). Urethro-vesical sling exposure is one of the most serious complications of this procedure. We describe the treatment and follow-up of 18 patients with bladder or urethral sling exposure.

PATIENTS AND METHODS

This single-center, retrospective study assessed the diagnosis and management of MUS penetrating the lower urinary tract in 18 women. The lesions included were classed as 4B, T3-4, S3 according to the international classification of complications related to the insertion of prostheses. Diagnosis was confirmed by flexible urethro-cystoscopy. The patients were treated surgically. In all cases, the aim was to remove all synthetic materials eroding the bladder or urethra. The patients were reassessed 6 weeks after the procedure, and functional urologic sequelae were treated. Urologic symptoms were evaluated using the USP questionnaire and urologic comfort was assessed using the Contilife questionnaire.

RESULTS

Seven MUSs were retro-pubic and 11 were trans-obturators. The material was 11 polypropylene macroporous monofilament, four polypropylene silicone coated and three non-available. There were six cases of urethral sling exposure, nine cases of bladder sling exposure, and three cases of urethral and bladder sling exposure, including five complicated cases of lithiasis and one urethra-vaginal fistula. Thirteen patients underwent one surgical procedure, four underwent two, and one underwent five procedures. Seven patients received a Martius flap. Three surgical approaches were necessary: (i) vaginal approach; (ii) urologic (urethral and suprapubic) cystoscopy approach; and (iii) laparoscopy approach. Median follow-up time was 34.5 months. At the end of follow-up, 17/18 patients had no sling exposure from the MUS, and 12/13 patients were considered comfortable from a functional urologic viewpoint.

CONCLUSION

Our study showed that surgery could treat urethro-vesical sling exposure. Three surgical approaches may be necessary. Controlled cystoscopy is vital to confirm healing due to the recurrences of sling exposure in our study.

摘要

引言

中段尿道吊带术(MUS)是压力性尿失禁(SUI)手术治疗的金标准。尿道膀胱吊带暴露是该手术最严重的并发症之一。我们描述了18例膀胱或尿道吊带暴露患者的治疗及随访情况。

患者与方法

这项单中心回顾性研究评估了18名女性中MUS穿透下尿路的诊断与处理。根据与假体植入相关并发症的国际分类,所纳入的病变被归类为4B、T3 - 4、S3。通过软性尿道膀胱镜检查确诊。患者接受手术治疗。在所有病例中,目标是清除所有侵蚀膀胱或尿道的合成材料。术后6周对患者进行重新评估,并对功能性泌尿系统后遗症进行治疗。使用美国药典问卷评估泌尿系统症状,使用Contilife问卷评估泌尿系统舒适度。

结果

7例MUS为耻骨后位,11例为经闭孔位。材料为11根聚丙烯大孔单丝、4根聚丙烯涂硅和3根不明材料。有6例尿道吊带暴露、9例膀胱吊带暴露以及3例尿道和膀胱吊带暴露,包括5例合并结石的复杂病例和1例尿道阴道瘘。13例患者接受了1次手术,4例接受了2次手术,1例接受了5次手术。7例患者接受了Martius皮瓣移植。需要三种手术入路:(i)经阴道入路;(ii)泌尿外科(尿道和耻骨上)膀胱镜入路;(iii)腹腔镜入路。中位随访时间为34.5个月。随访结束时,18例患者中有17例无MUS吊带暴露,从功能性泌尿系统角度来看,13例患者中有12例感觉舒适。

结论

我们的研究表明手术可治疗尿道膀胱吊带暴露。可能需要三种手术入路。由于本研究中吊带暴露有复发情况,因此控制膀胱镜检查对于确认愈合至关重要。

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