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在有膀胱过度活动症的老年和年轻受试者中,非索罗定与托特罗定的疗效和耐受性:两项安慰剂对照试验的事后汇总分析。

Efficacy and tolerability of fesoterodine versus tolterodine in older and younger subjects with overactive bladder: a post hoc, pooled analysis from two placebo-controlled trials.

机构信息

University of Massachusetts Medical School and UMassMemorial Medical Center, Worcester, Massachusetts 01605, USA.

出版信息

Neurourol Urodyn. 2012 Nov;31(8):1258-65. doi: 10.1002/nau.22252. Epub 2012 Aug 20.

Abstract

AIMS

To assess the efficacy and tolerability of fesoterodine 8 mg versus tolterodine extended release (ER) 4 mg in subjects with overactive bladder (OAB) stratified by age (<65, 65-74, and ≥75 years).

METHODS

This was a post hoc analysis of data from two double-blind trials. Subjects reporting ≥1 urgency urinary incontinence (UUI) episode and ≥8 micturitions/24 hr at baseline were randomized to fesoterodine (4 mg for 1 week, 8 mg for 11 weeks), tolterodine ER 4 mg, or placebo. Subjects completed 3-day bladder diaries, Urgency Perception Scale (UPS), Patient Perception of Bladder Condition (PPBC), and OAB questionnaire (OAB-q) at baseline and week 12. The primary endpoint in both studies was change from baseline to week 12 in UUI episodes.

RESULTS

Among subjects <65 years (n = 2,670), improvements in UUI episodes, micturitions, urgency episodes, severe urgency episodes, frequency-urgency sum, UPS, PPBC, and all OAB-q scales and domains were significantly greater with fesoterodine versus tolterodine ER, and diary-dry rates were significantly higher. Among subjects 65-74 years (n = 990), improvements in mean voided volume per void, PPBC, and OAB-q Symptom Bother and Coping were significantly greater with fesoterodine versus tolterodine ER. Among subjects aged ≥75 years (n = 448), improvements in urgency episodes, severe urgency episodes, frequency-urgency sum, UPS, and OAB-q Symptom Bother were significantly greater with fesoterodine versus tolterodine ER. Both active treatments produced significant improvements in most outcomes versus placebo across age groups. Adverse event rates were similar among age groups.

CONCLUSIONS

Fesoterodine 8 mg consistently improved several OAB-related variables versus tolterodine ER 4 mg in subjects aged <65, 65-74, and ≥75 years, with some differences reaching statistical significance, and was generally well tolerated.

摘要

目的

评估非索罗定 8mg 与托特罗定延长释放(ER)4mg 在伴有膀胱过度活动症(OAB)的患者中的疗效和耐受性,这些患者根据年龄(<65 岁、65-74 岁和≥75 岁)进行分层。

方法

这是两项双盲试验的事后分析。报告≥1 次急迫性尿失禁(UUI)发作和≥8 次/24 小时排尿的患者随机分为非索罗定(第 1 周 4mg,第 11 周 8mg)、托特罗定 ER 4mg 或安慰剂组。患者在基线时和第 12 周完成 3 天膀胱日记、急迫感感知量表(UPS)、患者对膀胱状况的感知(PPBC)和膀胱过度活动症问卷(OAB-q)。两项研究的主要终点均为从基线到第 12 周 UUI 发作的变化。

结果

在<65 岁的患者中(n=2670),与托特罗定 ER 相比,非索罗定在 UUI 发作、排尿次数、急迫感发作、严重急迫感发作、频数-急迫感总和、UPS、PPBC 以及所有 OAB-q 量表和维度的改善均更为显著,且日记干燥率显著更高。在 65-74 岁的患者中(n=990),与托特罗定 ER 相比,非索罗定在平均每次排尿量、PPBC 和 OAB-q 症状困扰和应对方面的改善更为显著。在≥75 岁的患者中(n=448),与托特罗定 ER 相比,非索罗定在急迫感发作、严重急迫感发作、频数-急迫感总和、UPS 和 OAB-q 症状困扰方面的改善更为显著。在所有年龄组中,两种活性治疗均显著改善了大多数结局。在不同年龄组中,不良事件发生率相似。

结论

非索罗定 8mg 与托特罗定 ER 4mg 相比,可持续改善各年龄组患者的 OAB 相关变量,其中一些差异具有统计学意义,且总体耐受性良好。

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