Effectiveness of Existing Insomnia Therapies for Patients Undergoing Hemodialysis: A Randomized Clinical Trial

被引:3
|
作者
Mehrotra, Rajnish [1 ,6 ]
Cukor, Daniel [2 ]
McCurry, Susan M. [3 ]
Rue, Tessa [4 ]
Roumelioti, Maria-Eleni [5 ]
Heagerty, Patrick J. [4 ]
Unruh, Mark [5 ]
机构
[1] Univ Washington, Kidney Res Inst, Dept Med, Div Nephrol,Sch Med, Seattle, WA USA
[2] Rogosin Inst, New York, NY USA
[3] Univ Washington, Sch Nursing, Seattle, WA USA
[4] Univ Washington, Ctr Biomed Stat, Sch Publ Hlth, Seattle, WA USA
[5] Univ New Mexico, Dept Med, Div Nephrol, Albuquerque, NM USA
[6] Univ Washington, Kidney Res Inst, Dept Med, Div Nephrol,Sch Med, 1919 NE Pacific St, Box 356521, Seattle, WA 98195 USA
基金
美国国家卫生研究院;
关键词
COGNITIVE-BEHAVIORAL THERAPY; QUALITY-OF-LIFE; CHRONIC KIDNEY-DISEASE; HEALTH-RELATED QUALITY; SLEEP QUALITY; DAYTIME SLEEPINESS; PRACTICE GUIDELINE; PHYSICAL-ACTIVITY; SEVERITY INDEX; DIALYSIS;
D O I
10.7326/M23-1794
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Chronic insomnia is common in patients undergoing in-center hemodialysis, yet there is limited evidence on effective treatments for this population.Objective: To compare the effectiveness of cognitive behavioral therapy for insomnia (CBT-I), trazodone, and placebo for insomnia in patients undergoing long-term hemodialysis.Design: Randomized, multicenter, double-blinded, placebo-controlled trial. (ClinicalTrials.gov: NCT03534284)Setting: 26 dialysis units in Albuquerque, New Mexico, and Seattle, Washington.Participants: Patients with Insomnia Severity Index (ISI) score of 10 or greater, with sleep disturbances on 3 or more nights per week for 3 or more months.Intervention: Participants were randomly assigned to 6 weeks of CBT-I, trazodone, or placebo.Measurements: The primary outcome was the ISI score at 7 and 25 weeks from randomization.Results: A total of 923 patients were prescreened, and of the 411 patients with chronic insomnia, 126 were randomly assigned to CBT-I (n = 43), trazodone (n = 42), or placebo (n = 41). The change in ISI scores from baseline to 7 weeks with CBT-I or trazodone was no different from placebo: CBT-I, -3.7 (95% CI, -5.5 to -1.9); trazodone, -4.2 (CI, -5.9 to -2.4); and placebo, -3.1 (CI, -4.9 to -1.3). There was no meaningful change in ISI scores from baseline to 25 weeks: CBT-I, -4.8 (CI, -7.0 to -2.7); trazodone, -4.0 (CI, -6.0 to -1.9); and placebo, -4.3 (CI, -6.4 to -2.2). Serious adverse events (SAEs), particularly serious cardiovascular events, were more frequent with trazodone (annualized cardiovascular SAE incidence rates: CBT-I, 0.05 [CI, 0.00 to 0.29]; trazodone, 0.64 [CI, 0.34 to 1.10]; and placebo, 0.21 [CI, 0.06 to 0.53]).Limitation: Modest sample size and most participants had mild or moderate insomnia.Conclusion: In patients undergoing hemodialysis with mild or moderate chronic insomnia, there was no difference in the effectiveness of 6 weeks of CBT-I or trazodone compared with placebo. The incidence of SAEs was higher with trazodone.
引用
收藏
页码:177 / 188
页数:13
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