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Randomized Controlled Trial
. 2018 Feb;131(2):204-211.
doi: 10.1097/AOG.0000000000002443.

Association of Pharmacologic Treatment of Urgency Urinary Incontinence With Sleep Quality and Daytime Sleepiness

Affiliations
Randomized Controlled Trial

Association of Pharmacologic Treatment of Urgency Urinary Incontinence With Sleep Quality and Daytime Sleepiness

Qurratul A Warsi et al. Obstet Gynecol. 2018 Feb.

Abstract

Objective: To evaluate the association between pharmacologic therapy for urgency urinary incontinence (UUI) and sleep quality.

Methods: We conducted a planned secondary data analysis of sleep outcomes in a previously conducted multicenter, double-blind, 12-week randomized trial of pharmacologic therapy for urgency-predominant incontinence among community-dwelling women self-diagnosed using the 3-Incontinence Questions questionnaire. Participants (N=645) were assigned randomly to 4-8 mg antimuscarinic therapy daily or placebo. At baseline and 12 weeks, participants completed a validated voiding diary to evaluate incontinence and voiding symptoms, the Pittsburgh Sleep Quality Index to evaluate sleep quality, and the Epworth Sleepiness Scale to evaluate daytime sleepiness.

Results: Mean (SD) age was 56 (±14) years, 68% were white, and 57% had poor sleep quality (Pittsburgh Sleep Quality Index score greater than 5). Mean frequency of any urinary incontinence and UUI was 4.6 and 3.9 episodes/d, respectively. After 12 weeks, women randomized to the antimuscarinic group reported greater decrease compared with the placebo group in UUI frequency (0.9 episodes/d; P<.001) and diurnal and nocturnal voiding frequency (P<.05). As compared with the placebo group, women in the antimuscarinic group also reported greater improvement in sleep quality (total Pittsburgh Sleep Quality Index score 0.48; P=.02) with greater improvement in sleep duration and sleep efficiency subscales (P<.05). The intervention did not affect daytime sleepiness.

Conclusion: Pharmacologic treatment of UUI is associated with decreased incontinence frequency and nocturia and improvement in overall sleep quality, sleep duration, and sleep efficiency.

Clinical trial registration: ClinicalTrials.gov, NCT00862745.

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Conflict of interest statement

Financial Disclosure: The other authors did not report any potential conflicts of interest.

Figures

Figure 1
Figure 1. Recruitment, randomization, and retention in the BRIDGES trial
Recruitment, randomization, and retention in the Bringing Simple Urge Incontinence Diagnosis and Treatment to Providers (BRIDGES) trial. 3-IQ-3, 3-Incontinence Questions. *Not mutually exclusive.

Comment in

  • In Search of More Sleep.
    Amundsen CL, Preud'Homme XA. Amundsen CL, et al. Obstet Gynecol. 2018 Feb;131(2):201-203. doi: 10.1097/AOG.0000000000002470. Obstet Gynecol. 2018. PMID: 29324616 No abstract available.

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