Cognitive-behavioral therapy to prevent relapse in pediatric responders to pharmacotherapy for major depressive disorder
- PMID: 18978634
- PMCID: PMC2826176
- DOI: 10.1097/CHI.0b013e31818914a1
Cognitive-behavioral therapy to prevent relapse in pediatric responders to pharmacotherapy for major depressive disorder
Abstract
Objective: We present results of a feasibility test of a sequential treatment strategy using continuation phase cognitive-behavioral therapy (CBT) to prevent relapse in youths with major depressive disorder (MDD) who have responded to acute phase pharmacotherapy.
Method: Forty-six youths (ages 11-18 years) who had responded to 12 weeks of treatment with fluoxetine were randomized to receive either 6 months of continued antidepressant medication management (MM) or antidepressant MM plus relapse prevention CBT (MM+CBT). Primary outcome was time to relapse, defined as a Childhood Depression Rating Scale-Revised score of 40 or higher and 2 weeks of symptom worsening or clinical deterioration warranting alteration of treatment to prevent full relapse.
Results: Cox proportional hazards regression, adjusting for depression severity at randomization and for the hazard of relapsing by age across the trial, revealed that participants in the MM treatment group had a significantly greater risk for relapse than those in the MM+CBT treatment group (hazard ratio = 8.80; 95% confidence interval 1.01-76.89; chi = 3.86, p =.049) during 6 months of continuation treatment. In addition, patient satisfaction was significantly higher in the MM+CBT group. No differences were found between the two treatment groups on attrition rate, serious adverse events, and overall global functioning.
Conclusions: These preliminary results suggest that continuation phase CBT reduces the risk for relapse by eightfold compared with pharmacotherapy responders who received antidepressant medication alone during the 6-month continuation phase.
Trial registration: ClinicalTrials.gov NCT00158301.
Conflict of interest statement
Disclosure: Dr. Emslie receives research support from the National Institute of Mental Health, Eli Lilly, Organon, Shire, Somerset, Forest Laboratories, and Biobehavioral Diagnostics; is a consultant for Eli Lilly, Forest Laboratories, GlaxoSmithKline, Wyeth-Ayerst, Shire, and Biobehavioral Diagnostics; and is on the speakers’ bureau for McNeil. The other authors report no conflicts of interests.
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Comment in
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Relapse prevention in childhood depression.Curr Psychiatry Rep. 2010 Apr;12(2):85-7. doi: 10.1007/s11920-010-0095-9. Curr Psychiatry Rep. 2010. PMID: 20425291 No abstract available.
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