4.5 Article

Cognitive Behavior Therapy May Sustain Antidepressant Effects of Intravenous Ketamine in Treatment-Resistant Depression

Journal

PSYCHOTHERAPY AND PSYCHOSOMATICS
Volume 86, Issue 3, Pages 162-167

Publisher

KARGER
DOI: 10.1159/000457960

Keywords

Cognitive behavior therapy; Major depressive disorder; Relapse; Treatment-resistant depression; Cognition; Ketamine

Funding

  1. National Institutes of Health [T32MH062994-15, 5R25MH071584-09]
  2. Thomas Detre Fellowship
  3. Brain and Behavior Research Foundation
  4. American Psychiatric Institute for Research and Education/Janssen Resident Psychiatric Research Scholars Program
  5. Robert E. Leet and Clara Guthrie Patterson Trust
  6. National Institute of Mental Health
  7. Allergan
  8. Alkermes
  9. AstraZeneca
  10. BioHaven Pharmaceuticals
  11. Bristol-Myers Squibb
  12. Connecticut Department of Mental Health and Addiction Services
  13. Hoffman La-Roche
  14. Eli Lilly and Co.
  15. Janssen Pharmaceuticals
  16. Merck and Co.
  17. Naurex
  18. Servier Pharmaceuticals
  19. Taisho Pharmaceuticals
  20. Teva
  21. Valeant Pharmaceuticals North America
  22. Vistagen
  23. West Haven VA Hospital CAP award

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Introduction: Ketamine has shown rapid though short-lived antidepressant effects. The possibility of concerning neurobiological changes following repeated exposure to the drug motivates the development of strategies that obviate or minimize the need for longer-term treatment with ketamine. In this open-label trial, we investigated whether cognitive behavioral therapy (CBT) can sustain or extend ketamine's antidepressant effects. Methods: Patients who were pursuing ketamine infusion therapy for treatment-resistant depression were invited to participate in the study. If enrolled, the subjects initiated a 12-session, 10-week course of CBT concurrently with a short 4-treatment, 2-week course of intravenous ketamine (0.5 mg/kg infused over 40 min) provided under a standardized clinical protocol. Results: Sixteen participants initiated the protocol, with 8 (50%) attaining a response to the ketamine and 7 (43.8%) achieving remission during the first 2 weeks of protocol. Among ketamine responders, the relapse rate at the end of the CBT course (8 weeks following the last ketamine exposure) was 25% (2/8). On longer-term follow-up, 5 of 8 subjects eventually relapsed, the median time to relapse being 12 weeks following ketamine exposure. Among ketamine remitters, 3 of 7 retained remission until at least 4 weeks following the last ketamine exposure, with 2 retaining remission through 8 weeks following ketamine exposure. Ketamine nonresponders did not appear to benefit from CBT. Conclusions: CBT may sustain the antidepressant effects of ketamine in treatment-resistant depression. Well-powered randomized controlled trials are warranted to further investigate this treatment combination as a way to sustain ketamine's antidepressant effects. (C) 2017 S. Karger AG, Basel

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