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Antibacterial mesh sling: a prospective outcome analysis.

机译:抗菌网状吊索:前瞻性结果分析。

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OBJECTIVES: To prospectively assess the outcome results of the Gore-Tex antibacterial mesh sling in women with pelvic prolapse and stress incontinence. METHODS: Between July 1997 and November 1998, 30 women with stress incontinence and vaginal prolapse underwent vaginal reconstruction with the antibacterial mesh sling. All patients had documented stress incontinence by preoperative urodynamic evaluation. Postoperatively, we conducted an outcome analysis on the basis of the results from a self-reported satisfaction questionnaire, a detailed pelvic examination, a cough stress test, and the Q-tip test. Urodynamic studies were performed on patients with persistent stress incontinence or urge symptoms. Cystoscopy was performed on patients suspected of having urethral erosion. RESULTS: Complete follow-up was available for all 30 patients. Of the group, 12 (40.0%) of 30 underwent implantation of the antibacterial mesh sling alone and 18 (60.0%) underwent additional prolapse repair. The mean follow-up was 18 months (range 9 to 24); mean age was 58 years (range 29 to 87). Stress incontinence was cured in 28 (93.3%) of 30 patients. De novo urge incontinence developed in 1 (5.2%) of 18 patients; urge symptoms persisted in 5 (41.7%) of 12 patients. The postoperative mean Valsalva Q-tip angle was 15 degrees (range 0 degrees to 25 degrees ). The incidence of urethral obstruction and erosion was zero. The mean postoperative pain score was 3 of 10 (range 0 to 6), and the mean satisfaction score was 9 of 10 (range 7 to 10). The mean time to discharge was 21 hours (range 6 to 29). All 30 women (100%) were willing to undergo surgery again. CONCLUSIONS: The safety profile of the Gore-Tex antibacterial mesh is better than that of the conventional Gore-Tex sling. When meticulous surgical technique is used, excellent short-term results can be achieved in the correction of female stress incontinence.
机译:目的:前瞻性评估骨盆脱垂和压力性尿失禁妇女的戈尔-特克斯(Gore-Tex)抗菌网状吊带的结局结果。方法:在1997年7月至1998年11月之间,30例压力性尿失禁和阴道脱垂的妇女使用抗菌网状吊带进行了阴道重建。通过术前尿动力学评估,所有患者均已记录到压力性尿失禁。术后,我们根据自我报告的满意度问卷,详细的骨盆检查,咳嗽压力测试和Q-tip测试的结果进行了结果分析。对持续性压力性尿失禁或冲动症状的患者进行了尿动力学研究。对怀疑患有尿道糜烂的患者进行膀胱镜检查。结果:所有30例患者均获得了完整的随访。在该组中,有30名中的12名(40.0%)仅接受了抗菌网状吊带的植入,另外18名(60.0%)接受了脱垂修复。平均随访18个月(9至24个月);平均年龄为58岁(29岁至87岁)。 30名患者中有28名(93.3%)的压力性尿失禁得到了治愈。 18例患者中有1例(5.2%)发生了新生急迫性尿失禁; 12例患者中有5例(41.7%)出现了强烈的冲动症状。术后平均Valsalva Q尖角为15度(范围为0度至25度)。尿道梗阻和糜烂的发生率为零。术后平均疼痛评分为10分之3(0至6),平均满意度评分为10分之9(7至10)。平均放电时间为21小时(范围为6到29)。所有30位女性(100%)都愿意再次接受手术。结论:Gore-Tex抗菌网的安全性优于传统的Gore-Tex吊带。当使用细致的手术技术时,在矫正女性压力性尿失禁方面可以取得极好的短期效果。

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