Department of Urology and Andrology, Clinic Korneuburg, Austria.
BJU Int. 2011 Mar;107(5):777-782. doi: 10.1111/j.1464-410X.2010.09619.x. Epub 2010 Oct 21.
• To report our experience using an adjustable bulbourethral sling since April 2005 for male stress urinary incontinence (SUI) after prostatic surgery. • To evaluate the safety, efficacy and health-related quality of life in recipients of the Argus® (Promedon SA; Cordoba, Argentina) adjustable bulbourethral sling.
• Between April 2005 and April 2009, 101 men with moderate-to-severe SUI after prostatic surgery were implanted with the Argus sling. • The radio-opaque Argus system comprises a thick silicone-foam pad for soft bulbar urethral support. The pad is attached to silicone columns that, after being passed with needles from the perineum to the abdominal wall, are adjusted with silicone washers to maintain the desired position. • Between prostatic surgery and Argus sling placement, most patients (74.3%) had undergone various procedures for SUI or bladder neck pathologies: 22 had undergone secondary irradiation therapy after surgery (19 after retropubic radical prostatectomy [RP], one after perineal RP and two after transurethral resection of the prostate). • All patients were evaluated before and after sling placement with 20-min pad tests, the Urinary Incontinence Quality of Life Scale (I-QoL), cystoscopy and uroflowmetry. The study was designed in a retrospective longitudinal fashion.
• The mean (range) follow-up was 2.1 (0.1-4.5) years. The mean (range) sling surgery duration was 49 (28-105) min. • Adjustment was necessary in 39 cases (38.6%), either loosening (10/101; 9.9%) or tightening (29/101; 28.7%) at a mean of 104.3 (14-910) days after the initial implantation. • The sling had to be removed in 16/101 patients (15.8%) at a mean of 371.1 (20-1260) days after implantation due to urethral erosion or infection. However, six of the 16 patients were within the first 22 placements and probably represent the 'learning curve'. In all, 13 of these patients received later successful treatment (seven with an artificial urinary sphincter, five with re-implantation of the sling). Four of these patients were lost for follow-up. • After a median (mean) follow-up of 2.2 (2.1) years, 80/101 (79.2%) patients were considered as dry, with a pad test of 0-1 g (70 patients, 0 g; 10 patients, 1 g). The I-QoL score improved from a mean of 28.8 (14.5-61.8) to 63.2 (16.4-115) points after sling placement. • Both the 20-min pad-weight tests and I-QoL responses improved significantly compared with baseline (P < 0.001).
• We think that the Argus male bulbourethral sling system is an excellent first- or second-line treatment for moderate-to-severe male SUI, even after external beam radiation treatment.
• 报告自 2005 年 4 月以来,我们使用可调节球部尿道吊带治疗前列腺手术后男性压力性尿失禁(SUI)的经验。• 评估 Argus®(Promedon SA;科尔多瓦,阿根廷)可调节球部尿道吊带的安全性、疗效和与健康相关的生活质量。
• 2005 年 4 月至 2009 年 4 月期间,101 例前列腺手术后出现中度至重度 SUI 的男性患者植入 Argus 吊带。• 可透射线的 Argus 系统由一个用于柔软球部尿道支撑的厚硅胶泡沫垫组成。该垫附着在硅胶柱上,硅胶柱通过从会阴到腹壁的针穿过,然后用硅胶垫圈进行调整,以保持所需的位置。• 在前列腺手术和 Argus 吊带放置之前,大多数患者(74.3%)已经接受了各种 SUI 或膀胱颈部病变的治疗:22 例在手术后接受了辅助放疗(19 例经耻骨后前列腺切除术 [RP],1 例经会阴 RP,2 例经尿道前列腺切除术)。• 所有患者在吊带放置前后均进行了 20 分钟的垫测试、尿失禁生活质量量表(I-QoL)、膀胱镜检查和尿流率检查。该研究采用回顾性纵向设计。
• 平均(范围)随访时间为 2.1(0.1-4.5)年。平均(范围)吊带手术时间为 49(28-105)分钟。• 在初始植入后平均 104.3(14-910)天,需要调整 39 例(38.6%),包括松动(10/101;9.9%)或收紧(29/101;28.7%)。• 在植入后平均 371.1(20-1260)天,16/101(15.8%)患者因尿道侵蚀或感染需要取出吊带。然而,这 16 例患者中有 6 例是在前 22 例中,可能代表“学习曲线”。在所有这些患者中,有 13 例后来接受了成功的治疗(7 例接受人工尿道括约肌治疗,5 例接受吊带重新植入)。其中 4 例患者失访。• 在中位数(平均)随访 2.2(2.1)年后,80/101(79.2%)名患者被认为是干燥的,垫测试为 0-1 g(70 名患者,0 g;10 名患者,1 g)。I-QoL 评分从植入吊带前的平均 28.8(14.5-61.8)分提高到 63.2(16.4-115)分。• 20 分钟垫重测试和 I-QoL 反应均与基线相比显著改善(P < 0.001)。
• 我们认为 Argus 男性球部尿道吊带系统是治疗中重度男性 SUI 的极好的一线或二线治疗方法,甚至在接受外照射治疗后也是如此。