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[INVANCE假体治疗男性术后尿失禁:初步结果]

[Treatment of postoperative male urinary incontinence by INVANCE prosthesis: preliminary results].

作者信息

Fassi-Fehri Hakim, Cherasse Arnaud, Badet Lionel, Pasticier Gilles, Landry Jean Luc, Martin Xavier, Gelet Albert

机构信息

Service d'Urologie et de la Transplantation, Hôpital Edouard Herriot, Lyon, France.

出版信息

Prog Urol. 2004 Dec;14(6):1171-6.

Abstract

PURPOSE

To evaluate the preliminary results of treatment of postoperative male stress urinary incontinence (SUI) by the INVANCE (AMS) suburethral sling.

MATERIAL AND METHODS

From June 2003 to May 2004, 22 patients with stress urinary incontinence secondary to prostatic surgery (13 radical prostatectomies, 7 Ablatherm, 2 transurethral resections of the prostate) were treated by INVANCE sling. The patients presented either grade 1 incontinence (1 to 2 pads per day), or grade 2 incontinence (3 to 4 pads per day), or grade 3 incontinence (5 or more pads per day). The INVANCE process uses a rectangular polyester sling positioned under the bulbar urethra via a perineal incision. It is attached to the 2 ischiopubic rami by 3 titanium screws using a disposable electric screwdriver. Patients were reviewed every 3 months to evaluate the results (continence, Qmax, post-voiding residual volume, IPSS score, quality of life)

RESULTS

The mean duration of the procedure was 79 minutes (range: 60-120). No intraoperative incidents were observed. The bladder catheter was removed on D1 (n=20) or D2 (n=2). The mean length of stay was 3.3 days (range: 2-8). Complications consisted of perineal haematoma (n=1), acute urinary retention after catheter removal (n=4), sling infection requiring removal (n=1), and prolonged perineal pain (n=5). No de novo irritative or obstructive urinary tract disorders were observed. With a median follow-up of 12 weeks (range: 3-44), 11 patients were completely continent (50%), 5 patients were significantly improved (22.7%) and 6 patients were considered to be failures (27.3%), 3 of whom had previously received external beam radiotherapy.

CONCLUSION

The INVANCE process appears to be a simple and effective option for the treatment of grade 1 and 2 postoperative male stress urinary incontinence.

摘要

目的

评估INVANCE(美国美敦力公司)尿道下悬吊带治疗男性术后压力性尿失禁(SUI)的初步结果。

材料与方法

2003年6月至2004年5月,22例前列腺手术后出现压力性尿失禁的患者(13例行根治性前列腺切除术,7例行Ablatherm治疗,2例行经尿道前列腺切除术)接受了INVANCE悬吊带治疗。这些患者表现为1级尿失禁(每天使用1至2片尿垫)、2级尿失禁(每天使用3至4片尿垫)或3级尿失禁(每天使用5片或更多尿垫)。INVANCE手术过程是通过会阴切口将一个矩形聚酯悬吊带置于球部尿道下方。使用一次性电动螺丝刀通过3枚钛螺钉将其固定在双侧耻骨支上。每3个月对患者进行复查以评估结果(控尿情况、最大尿流率、排尿后残余尿量、国际前列腺症状评分、生活质量)。

结果

手术平均时长为79分钟(范围:60 - 120分钟)。未观察到术中不良事件。20例患者在术后第1天拔除膀胱导尿管,2例在术后第2天拔除。平均住院时间为3.3天(范围:2 - 8天)。并发症包括会阴血肿(1例)、拔除导尿管后急性尿潴留(4例)、因吊带感染需取出(1例)以及会阴疼痛持续时间延长(5例)。未观察到新发的刺激性或梗阻性尿路疾病。中位随访时间为12周(范围:3 - 44周),11例患者完全控尿(50%),5例患者有显著改善(22.7%),6例患者被视为治疗失败(27.3%),其中3例之前接受过体外照射放疗。

结论

对于治疗1级和2级男性术后压力性尿失禁,INVANCE手术似乎是一种简单有效的选择。

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