基于生物可吸收聚己内酯的注射剂对女性压力性尿失禁的长期疗效和安全性

Anđelo Mojsović, A. Beulens, Evert L. Koldewijn
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引用次数: 0

摘要

我们对一种基于全生物可吸收聚己内酯(PCL)的膨大剂的安全性和有效性进行了评估,该膨大剂适用于患有轻度至中度压力性尿失禁(SUI)并尝试过盆底肌肉训练但失败的女性患者。共有 44 名患有轻度或中度 SUI 的成年女性受试者(中位年龄分别为 60 岁和 57 岁)接受了经尿道粘膜下注射治疗。在 6 个月、12 个月和 24 个月的随访中对安全性进行了评估。在相同的时间间隔内,采用斯塔米分级系统(SGS)对疗效进行了评估。轻度和中度 SUI 组的 SGS 均有改善。在 24 个月时,大多数参与者都能继续排尿:轻度 SUI 组为 78.1%,中度 SUI 组为 66.7%。中度 SUI 组的所有参与者的 SGS 分级都有所改善,大多数参与者都能保持大便通畅。研究结果表明,基于 PCL 的生物可吸收膨润剂疗法似乎是一种安全有效的治疗方案,适用于患有轻度至中度 SUI 并尝试过盆底锻炼但失败的妇女。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Long-term efficacy and safety of a bioresorbable polycaprolactone-based injectable in female stress incontinence
A fully bioresorbable polycaprolactone (PCL)-based bulking agent was evaluated for safety and efficacy in female patients with mild to moderate stress urinary incontinence (SUI) who attempted and failed prior pelvic floor muscle training. A total of 44 adult female subjects with mild or moderate SUI (median age 60 and 57, respectively) were treated by transurethral sub-mucosal injection. Safety was evaluated at 6-, 12-, and 24-month follow-up visits. Efficacy was assessed at the same intervals with the Stamey grading system (SGS). SGS improvement was shown in both the mild and moderate SUI groups. At 24 months, most participants were continent: 78.1% in the mild SUI group and 66.7% in the moderate SUI group. All participants in the moderate SUI group showed an improvement in the SGS grade, and most participants were continent. The study shows that the PCL-based bioresorbable bulking agent treatment seems to be a safe and effective treatment option for women with mild to moderate SUI who attempted and failed prior pelvic floor exercises.
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