4.5 Review

Remifentanil in electroconvulsive therapy: a systematic review and meta-analysis of randomized controlled trials

Journal

Publisher

SPRINGER HEIDELBERG
DOI: 10.1007/s00406-016-0670-0

Keywords

Remifentanil; Electroconvulsive therapy; Seizure duration; Systolic blood pressure; Meta-analysis

Funding

  1. Japan Society for the Promotion of Science (JSPS)
  2. Eli Lilly
  3. Tanabe-Mitsubishi
  4. Dainippon-Sumitomo Pharma
  5. Otsuka
  6. Meiji-Seika Pharma
  7. Janssen Pharmaceutical
  8. Daiichi-Sankyo company
  9. Takeda Pharmaceutical
  10. MSD K.K. Shionogi
  11. Astellas Pharma
  12. Eisai
  13. GlaxoSmithkline
  14. Ono Pharmaceutical
  15. Meiji
  16. Mochida
  17. MSD
  18. Sekisui Chemicals
  19. Takeda Science Foundation
  20. Japanese Ministry of Education, Science, and Technology
  21. Japanese Ministry of Health, Labour and Welfare
  22. Japan Society for the Promotion of Science
  23. Japan Foundation for Neuroscience and Mental Health

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In electroconvulsive therapy (ECT), remifentanil is often used concurrently with anesthetics. The objective of this study was to provide an up-to-date and comprehensive review on how the addition of remifentanil to anesthetics affects seizure duration and circulatory dynamics in mECT. We performed a meta-analysis of RCTs that investigated seizure duration and circulatory dynamics in patients treated with ECT using anesthetics alone (non-remifentanil group) and with anesthetics plus remifentanil (remifentanil group). A total of 13 RCTs (380 patients and 1024 ECT sessions) were included. The remifentanil group showed a significantly prolonged seizure duration during ECT compared to the non-remifentanil group [motor: 9 studies, SMD = 1.25, 95 % CI (0.21, 2.29), p = 0.02; electroencephalogram: 8 studies, SMD = 0.98, 95 % CI (0.14, 1.82), p = 0.02]. The maximum systolic blood pressure (SBP) was significantly reduced in the remifentanil group compared to the non-remifentanil group [7 studies, SMD = -0.36, 95 % CI (-0.65, 0.07), p = 0.02]. Substantial heterogeneity was observed for meta-analyses for seizure durations, but a pre-planned subgroup analysis revealed that seizure duration was prolonged only when the use of the anesthetic dose was reduced in the remifentanil group. The results of our study suggest that addition of remifentanil to anesthesia in ECT may lead to prolonged seizure duration when it allows the use of reduced anesthetic doses. Further, the addition of remifentanil was associated with reduced maximum SBP.

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