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A systematic review and meta-analysis of randomized controlled trials of adjunctive ketamine in electroconvulsive therapy: Efficacy and tolerability

期刊

JOURNAL OF PSYCHIATRIC RESEARCH
卷 62, 期 -, 页码 23-30

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.jpsychires.2015.01.003

关键词

Ketamine; Ketofol; Electroconvulsive therapy; ECT; Major depression

资金

  1. Canadian Network for Mood and Anxiety Treatments (CANMAT)
  2. Canadian Psychiatric Association
  3. Pfizer
  4. Sunovion
  5. BMS
  6. Otsuka
  7. Astra-Zeneca
  8. Janssen-Ortho
  9. Myriad
  10. Canadian Institutes of Health Research (CIHR)
  11. UBC Institute of Mental Health/Coast Capital Depression Research Fund
  12. AstraZeneca
  13. Bristol-Myers Squibb
  14. Canadian Institutes of Health Research
  15. Canadian Network for Mood and Anxiety Treatments
  16. Eli Lilly Co.
  17. GlaxoSmithKline
  18. Janssen
  19. Michael Smith Foundation for Health Research
  20. Novartis
  21. Ranbaxy
  22. Servier
  23. Stanley Foundation
  24. Biovail
  25. Canadian Psychiatric Association Foundation
  26. Eli Lilly
  27. Litebook Company
  28. Lundbeck
  29. Lundbeck Institute
  30. Mochida
  31. St. Jude Medical
  32. Takeda
  33. UBC Institute of Mental Health/Coast Capital Savings

向作者/读者索取更多资源

Background: Electroconvulsive therapy (ECT) remains one of the most effective tools in the psychiatric treatment armamentarium, particularly for refractory depression. Yet, there remains a subset of patients who do not respond to ECT or for whom clinically adequate seizures cannot be elicited, for whom ketamine has emerged as a putative augmentation agent. Methods: We searched EMBASE, PsycINFO, CENTRAL and MEDLINE from 1962 to April 2014 to identify randomized controlled trials evaluating ketamine in ECT (PROSPERO #CRD42014009035). Clinical remission, response, and change in depressive symptom scores were extracted by two independent raters. Adverse events were recorded. Drop-outs were assessed as a proxy for acceptability. Meta-analyses employed a random effects model. Results: Data were synthesized from 5 RCTs, representing a total of 182 patients with major depressive episodes (n = 165 Major Depressive Disorder, n = 17 Bipolar Disorder). ECT with ketamine augmentation was not associated with higher rates of clinical remission (Risk Difference (RD) = 0.00; 95%CI = -0.08 to 0.10), response (RD = -0.01; 95%CI = -0.11 to 0.08), or improvements in depressive symptoms (SMD = 0.38; 95%CI = 0.41 to 1.17). Ketamine augmentation was associated with higher rates of confusion/disorientation/prolonged delirium (OR = 6.59, 95%CI: 1.28-33.82, NNH = 3), but not agitation, hypertension or affective switches. Conclusion: Our meta-analysis of randomized controlled trials of ketamine augmentation in the ECT setting suggests a lack of clinical efficacy, and an increased likelihood of confusion. Individuals for whom adequate seizures or therapeutic response cannot be obtained have not been studied using randomized controlled designs. Additional research is required to address the role of ketamine in this population. (C) 2015 Elsevier Ltd. All rights reserved.

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