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夜尿症、夜间尿失禁患病率以及对抗胆碱能药物和行为疗法的反应。

Nocturia, nocturnal incontinence prevalence, and response to anticholinergic and behavioral therapy.

作者信息

Fitzgerald M P, Lemack G, Wheeler T, Litman H J

机构信息

Loyola University Medical Center, Maywood, IL 60153, USA.

出版信息

Int Urogynecol J Pelvic Floor Dysfunct. 2008 Nov;19(11):1545-50. doi: 10.1007/s00192-008-0687-7. Epub 2008 Aug 14.

Abstract

To determine whether participants in the behavior enhances drug reduction of incontinence (BE-DRI) trial experienced reduction in the frequency of nocturia and/or nocturnal leakage during treatment with antimuscarinic phamacotherapy with or without additional behavioral therapy. We analyzed urinary diary data relating to nocturia and nocturnal incontinence before and after 8 weeks of study treatment in the BE-DRI trial, in which patients were randomly assigned to receive drug therapy with tolterodine tartrate extended-release capsules 4 mg alone or in combination with behavioral training. Chi-square tests assessed whether nocturia and nocturnal incontinence prevalence varied by treatment arm and paired t tests assessed the change in mean frequency of nocturia and nocturnal leakage. Among 305 women, 210 (69%) had an average of at least one nocturia episode at baseline. There were small but statistically significant differences (p < 0.001) in mean nocturia frequency and nocturnal incontinence frequency with both treatments after 8 weeks, but no significant difference between study treatment groups. Among these urge incontinent women, tolterodine with or without supervised behavioral therapy had little impact on either nocturic frequency or nocturnal incontinence.

摘要

为了确定参与膀胱过度活动症行为改善药物治疗(BE-DRI)试验的受试者在接受抗毒蕈碱药物治疗(无论是否联合额外行为疗法)期间夜尿症和/或夜间漏尿频率是否降低。我们分析了BE-DRI试验中研究治疗8周前后与夜尿症和夜间尿失禁相关的尿日记数据,该试验中患者被随机分配接受单独使用4mg酒石酸托特罗定缓释胶囊的药物治疗或联合行为训练。卡方检验评估夜尿症和夜间尿失禁患病率是否因治疗组而异,配对t检验评估夜尿症和夜间漏尿平均频率的变化。在305名女性中,210名(69%)在基线时平均每晚至少有一次夜尿发作。8周后,两种治疗的平均夜尿频率和夜间尿失禁频率均有微小但具有统计学意义的差异(p<0.001),但研究治疗组之间无显著差异。在这些急迫性尿失禁女性中,无论是否有监督行为疗法,托特罗定对夜尿频率或夜间尿失禁几乎没有影响。

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