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首页> 外文期刊>Urology >Complications of ethylene vinyl alcohol copolymer as an intraurethral bulking agent in men with stress urinary incontinence.
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Complications of ethylene vinyl alcohol copolymer as an intraurethral bulking agent in men with stress urinary incontinence.

机译:乙烯-乙烯醇共聚物作为压力性尿失禁男性尿道内填充剂的并发症。

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OBJECTIVES: To report the short-term safety and efficacy of ethylene vinyl alcohol (EVA) copolymer (Tegress; C.R. Bard, Inc., Covington, GA) in the off-label treatment of male stress urinary incontinence. METHODS: We reviewed the charts of all adult male patients who received EVA copolymer between 2005 and 2006 for demographics, physical examination findings, urodynamic findings, outcomes, and complications. RESULTS: A total of 17 of 18 men completed follow-up after receiving EVA during this time period. With an average of 1.4 injection sessions, 58.8% of patients experienced a complication related to the procedure, with 41.1% of these complications being urethral erosion of the material and 22% experiencing severe pain on injection. Subjective improvement of at least 50% was reported by 41.1% of patients. The mean follow-up period was 4.2 months. CONCLUSIONS: Intraurethral bulking agents are meant to be a minimally invasive procedure with lower complication rates than alternatives such as the artificial urinary sphincter and male sling. The off-label use of EVA in men in this case series resulted in a significant complication rate. Urethral erosion was the most common complication causing dysuria, precluding further bulking in others, and resulting in loss of benefit with passage of material. In addition, EVA used in men may be less efficacious than the Food and Drug Administration data reported in women, especially with prior injectable therapy. In December 2006, EVA was voluntarily taken off the marketplace by CR Bard owing to reports from clinicians.
机译:目的:报告乙烯-乙烯醇(EVA)共聚物(Tegress; C.R。Bard,Inc.,科文顿,乔治亚州)在男性压力性尿失禁的标签外治疗中的短期安全性和有效性。方法:我们回顾了2005年至2006年期间接受EVA共聚物的所有成年男性患者的人口统计,体格检查结果,尿动力学检查结果,结局和并发症的图表。结果:18名男性中有17名在此期间接受EVA治疗后完成了随访。平均进行1.4次注射后,有58.8%的患者经历了与手术相关的并发症,其中41.1%的并发症为尿道对材料的侵蚀,而22%的患者在注射时感到剧烈疼痛。据报告,41.1%的患者主观改善至少50%。平均随访期为4.2个月。结论:尿道内填充剂是一种微创手术,其并发症发生率低于人工尿道括约肌和男性吊带等替代品。在该病例系列中男性不按标准使用EVA导致显着的并发症发生率。尿道糜烂是引起排尿困难的最常见并发症,排除了其他尿道的进一步肿大,并导致物质流失。此外,男性使用的EVA可能不如女性报道的美国食品药品监督管理局的数据有效,尤其是在使用先前的可注射疗法的情况下。 2006年12月,由于临床医生的报道,CR Bard自愿将EVA撤出市场。

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