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Treatment of urge-predominant mixed urinary incontinence with tolterodine extended release: a randomized, placebo-controlled trial.

机译:托特罗定缓释治疗急症为主的混合性尿失禁:一项随机,安慰剂对照的试验。

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OBJECTIVES: To examine the efficacy and tolerability of antimuscarinic therapy in women with urge-predominant mixed incontinence. METHODS: This was a double-blind, randomized, placebo-controlled trial comprising 854 women with urge-predominant mixed incontinence, including urge incontinence (five or more episodes per week), urinary frequency (eight or more micturitions on average in 24 hours), and urgency in combination with stress incontinence. Women received 8 weeks of treatment with tolterodine tartrate extended-release (ER) 4 mg or placebo once daily. The outcome measures included urge incontinence episodes per week, stress incontinence episodes per week, micturition frequency per 24 hours, urgency episodes per 24 hours, volume voided per micturition, patient perception of bladder condition, and assessment of treatment benefit. RESULTS: After 8 weeks, tolterodine ER produced a statistically significant decrease in the weekly urge incontinence episodes compared with placebo (-12.3 versus -8.0; P <0.0001). Other micturition variables improved significantly more with tolterodine ER. No difference was found between treatment groups regarding the change in the number of stress incontinence episodes. A significantly greater proportion of patients receiving tolterodine ER than those receiving placebo reported improvement in bladder condition (61% versus 46%; P <0.001) and treatment benefit (76% versus 55%; P <0.001). After 8 weeks, the tolterodine ER group had experienced statistically significant improvements compared with the placebo group in 9 of 10 quality-of-life domains. The frequency of adverse events was similar between treatment groups. CONCLUSIONS: Tolterodine ER is an effective treatment of urge urinary incontinence, frequency, and urgency in women with concomitant stress urinary incontinence. The efficacy of tolterodine ER in reducing urge incontinence episodes was unaffected by the presence of stress incontinence. The results of this study support the first-line use of antimuscarinic therapy to treat the urge incontinence component of urge-predominant mixed incontinence.
机译:目的:探讨抗毒蕈碱疗法对急症为主的混合性失禁妇女的疗效和耐受性。方法:这是一项双盲,随机,安慰剂对照试验,包括854名急躁为主的混合性尿失禁的女性,包括急迫性尿失禁(每周5次或以上),尿频(24小时平均排尿8次或以上)和紧迫性与压力性尿失禁相结合。女性每天接受一次酒石酸托特罗定缓释(ER)4毫克或安慰剂治疗8周。结果指标包括每周急迫性尿失禁发作,每周压力性尿失禁发作,每24小时排尿次数,每24小时尿急发作,每排尿排尿量,患者对膀胱状况的感知以及对治疗益处的评估。结果:与安慰剂相比,托特罗定ER在8周后的每周急迫性尿失禁发作有统计学意义的降低(-12.3对-8.0; P <0.0001)。使用托特罗定ER可以明显改善其他排尿变量。治疗组之间在压力性尿失禁发作次数的变化上没有发现差异。据报告,接受托特罗定ER的患者比接受安慰剂的患者比例要高得多(61%比46%; P <0.001)和治疗获益(76%比55%; P <0.001)。 8周后,在10个生活质量域中的9个域中,托特罗定ER组与安慰剂组相比在统计学上有显着改善。治疗组之间不良事件的发生频率相似。结论:托特罗定ER是伴有压力性尿失禁的女性的急迫性尿失禁,尿频和尿急的有效治疗方法。托特罗定ER减少急迫性尿失禁发作的疗效不受压力性尿失禁的影响。这项研究的结果支持一线使用抗毒蕈碱疗法来治疗以冲动为主的混合性尿失禁的冲动性尿失禁。

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