Efficacy of adjunctive aripiprazole in patients with major depressive disorder whose symptoms worsened with antidepressant monotherapy

被引:12
作者
Nelson, J. Craig [1 ]
Rahman, Zia [2 ]
Laubmeier, Kimberly K. [3 ]
Eudicone, James M. [4 ]
McQuade, Robert D. [5 ]
Berman, Robert M. [6 ]
Marcus, Ronald N. [7 ]
Baker, Ross A. [8 ]
Sheehan, John J. [2 ]
机构
[1] Univ Calif San Francisco, Dept Psychiat, San Francisco, CA 94143 USA
[2] Bristol Myers Squibb Co, Med Affairs Neurosci Dept, Plainsboro, NJ USA
[3] Otsuka Amer Pharmaceut Inc, Field Med Affairs Dept, Princeton, NJ USA
[4] Bristol Myers Squibb Co, Global Biometr Sci Dept, Plainsboro, NJ USA
[5] Otsuka Pharmaceut Dev & Commercializat Inc, Global Med Regulatory Affairs & Alliances, Princeton, NJ USA
[6] Bristol Myers Squibb Co, Global Clin Res Neurosci, Wallingford, CT USA
[7] Bristol Myers Squibb Co, NS Global Clin Res, Wallingford, CT USA
[8] Otsuka Pharmaceut Dev & Commercializat Inc, CNS Global Med Affairs, Princeton, NJ USA
关键词
Adjunctive treatment; antidepressant; inadequate response; major depressive disorder; symptom worsening; TREATMENT-RESISTANT DEPRESSION; DOUBLE-BLIND; AUGMENTATION; THERAPY; COMBINATION; MULTICENTER; STRATEGIES; MANAGEMENT; TRIALS; SAFETY;
D O I
10.1017/S109285291300103X
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Introduction. Efficacy of depression treatments, including adjunctive antipsychotic treatment, has not been explored for patients with worsening symptoms after antidepressant therapy (ADT). Methods. This post-hoc analysis utilized pooled data from 3 similarly designed, randomized, double-blind, placebo-controlled trials that assessed the efficacy, safety, and tolerability of adjunctive aripiprazole in patients with major depressive disorder with inadequate response to ADT. The studies had 2 phases: an 8-week prospective ADT phase and 6-week adjunctive (aripiprazole or placebo) treatment phase. This analysis focused on patients whose symptoms worsened during the prospective 8-week ADT phase (worsening defined as > 0% increase in Montgomery-Asberg Depressive Rating Scale [MADRS] Total score). During the 6-week, double-blind, adjunctive phase, response was defined as >= 50% reduction in MADRS Total score and remission as >= 50% reduction in MADRS Total score and MADRS score <= 10. Results. Of 1065 patients who failed to achieve a response during the prospective phase, 160 exhibited worsening of symptoms (ADT-Worseners), and 905 exhibited no change/reduction in MADRS scores (ADT-Non-worseners). Response rates for ADT-Worseners at endpoint were 36.6% (adjunctive aripiprazole) and 22.5% (placebo). Similarly, response rates at endpoint for ADT-Non-worseners were 37.5% (adjunctive aripiprazole) and 22.5% (placebo). Remission rates at endpoint for ADT-Worseners were 25.4% (adjunctive aripiprazole) and 12.4% (placebo). For ADT-Non-worseners, remission rates were 29.9% (adjunctive aripiprazole) and 17.4% (placebo). Conclusion. These results suggest that adjunctive aripiprazole is an effective intervention for patients whose symptoms worsen during antidepressant monotherapy. The results challenge the view that benefits of adjunctive therapy with aripiprazole are limited to partial responders to ADT.
引用
收藏
页码:528 / 534
页数:7
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