Eszopiclone co-administered with fluoxetine in patients with insomnia coexisting with major depressive disorder

被引:323
|
作者
Fava, M
McCall, WV
Krystal, A
Wessel, T
Rubens, R
Caron, J
Amato, D
Roth, T
机构
[1] Massachusetts Gen Hosp, Dept Psychiat, Depress Clin & Res Program, Boston, MA 02114 USA
[2] Sepracor, Marlborough, MA USA
[3] Wake Forest Univ, Dept Psychiat & Behav Sci, Winston Salem, NC 27109 USA
[4] Duke Univ, Med Ctr, Dept Psychiat & Behav Sci, Durham, NC USA
[5] Henry Ford Hosp, Sleep Ctr, Detroit, MI 48202 USA
关键词
insomnia; major depressive disorder; comorbidity; adjunctive antidepressant therapy; antidepressant remission rates; eszopiclone;
D O I
10.1016/j.biopsych.2006.01.016
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Background. Insomnia and major depressive disorder (MDD) can coexist. This study evaluated the effect of adding eszopiclone to fluoxetine. Methods: Patients who met DSM-IV criteria for both MDD and insomnia (n = 545) received morning fluoxetine and were randomized to nightly eszopiclone 3 mg (ESZ+FLX) or placebo (PBO+FLX)for 8 weeks. Subjective sleep and daytime function were assessed weekly. Depression was assessed with the 17-item Hamilton Rating Scale for Depression (HAM-D-17) and the Clinical Global Impression Improvement (CGI-I) and Severity items (CGI-S). Results: Patients in the ESZ+FLX group bad significantly decreased sleep latency, wake time after sleep onset (WASO), increased total sleep time (TST), sleep quality, and depth of sleep at all double-blind time points (all p < .05). Eszopiclone co-therapy also resulted in: significantly greater changes in HAM-D-17 scores at Week 4 (p = .01) with progressive improvement at Week 8 (p = .002); significantly improved CGI-I and CGI-S scores at all time points beyond Week 1 (p < .05); and significantly more responders (59% vs. 48%'; p = .009) and remitters (42% vs. 33%; p = .03) at Week 8. Treatment was well tolerated, with similar adverse event and dropout rates. Conclusions: In this study, eszopiclone/fluoxetine co-therapy was relatively well tolerated and associated with rapid, substantial, and sustained sleep improvement, a faster onset of antidepressant response on the basis of CGI, and a greater magnitude of the antidepressant effect.
引用
收藏
页码:1052 / 1060
页数:9
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