新型聚己内酯类生物可吸收尿道膨松剂治疗轻度至中度压力性尿失禁

E. Koldewijn, D. Oerlemans, A. Beulens, M. D. De Wildt, V. Vandoninck, S. de Wachter
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引用次数: 1

摘要

对一种完全生物可吸收的聚己内酯基生物可吸收填充剂在轻度至中度压力性尿失禁女性患者中的安全性和有效性进行了评估,这些女性患者曾尝试过盆底肌肉训练,但未能成功。50名女性受试者接受经尿道黏膜下注射治疗。在24个月的随访期内对安全性进行了评估。在12个月的访视中,进行膀胱镜检查,对注射区域进行目视检查。使用Stamey分级系统(SGS)等以相同的间隔评估疗效。只有6/50的受试者报告了短暂的轻度不良事件。结果显示,对于SGS等级,超过55%的参与者的SGS等级有所改善,其中40%在治疗后的前12个月内治愈。在第二年的随访中,效果似乎有所减弱,50%的受试者得到了改善,其中25%得到了治愈。研究结果表明,使用生物可吸收的PCL基填充剂治疗轻度或中度压力性尿失禁是一种安全有效的替代永久性填充剂的方法,也是在使用永久性中尿道吊带之前的中间治疗选择。
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Treatment of mild to moderate stress urinary incontinence with a novel polycaprolactonebased bioresorbable urethral bulking agent
A fully bioresorbable polycaprolactonebased bioresorbable bulking agent was evaluated for safety and efficacy in female patients with mild to moderate stress urinary incontinence who attempted and failed prior pelvic floor muscle training. Fifty female subjects were treated by transurethral sub-mucosal injection. Safety was evaluated over a 24-monts follow-up period. At the 12-months visit, a cystoscopy was performed for visual inspection of the injected area. Efficacy was assessed with the same intervals with the Stamey Grading System (SGS) among others. Only 6/50 subjects reported transient mild adverse events. The results show for the SGS grade more than 55% of the participants had an improvement in SGS grade, 40% of whom were cured within the first 12 months after treatment. During the second year of follow- up the effect seems to falter with an improvement of 50% of the subjects of whom 25% were cured. The results of the study suggest that treatment of mild-tomoderate stress urinary incontinence with a bioresorbable PCL-based bulking agent is a safe and effective alternative to permanent bulking agents and intermediate treatment option before the use of the permanent midurethral sling.
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来源期刊
Urogynaecologia International Journal
Urogynaecologia International Journal Medicine-Obstetrics and Gynecology
CiteScore
0.20
自引率
0.00%
发文量
10
期刊最新文献
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