期刊论文详细信息
PSYCHIATRY RESEARCH 卷:253
Initial Steps to inform selection of continuation cognitive therapy or fluoxetine for higher risk responders to cognitive therapy for recurrent major depressive disorder
Article
Vittengl, Jeffrey R.1  Clark, Lee Anna2  Thase, Michael E.3  Jarrett, Robin B.4 
[1] Truman State Univ, Dept Psychol, 100 East Normal St, Kirksville, MO 63501 USA
[2] Univ Notre Dame, Dept Psychol, Notre Dame, IN 46556 USA
[3] Univ Penn, Dept Psychiat, Perelman Sch Med, Philadelphia, PA 19104 USA
[4] Univ Texas Southwestern Med Ctr Dallas, Dept Psychiat, 5323 Harry Hines Blvd, Dallas, TX USA
关键词: Major depressive disorder;    Cognitive therapy;    Fluoxetine;    Relapse;    Recurrence;    Personalized advantage index;    Personalized medicine;   
DOI  :  10.1016/j.psychres.2017.03.032
来源: Elsevier
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【 摘 要 】

Responders to acute-phase cognitive therapy (A-CT) for major depressive disorder (MDD) often relapse or recur, but continuation-phase cognitive therapy (C-CT) or fluoxetine reduces risks for some patients. We tested composite moderators of C-CT versus fluoxetine's preventive effects to inform continuation treatment selection. Responders to A-CT for MDD judged to be at higher risk for relapse due to unstable or partial remission (N=172) were randomized to 8 months of C-CT or fluoxetine with clinical management and assessed, free from protocol treatment, for 24 additional months. Pre-continuation-treatment characteristics that in survival analyses moderated treatments' effects on relapse over 8 months of continuation-phase treatment (residual symptoms and negative temperament) and on relapse/recurrence over the full observation period's 32 months (residual symptoms and age) were combined to estimate the potential advantage of C-CT versus fluoxetine for individual patients. Assigning patients to optimal continuation treatment (i.e., to C-CT or fluoxetine, depending on patients' pre-continuation-treatment characteristics) resulted in absolute reduction of relapse or recurrence risk by 16-21% compared to the other non-optimal treatment. Although these novel results require replication before clinical application, selecting optimal continuation treatment (i.e., personalizing treatment) for higher risk A-CT responders may decrease risks of MDD relapse and recurrence substantively.

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