Academic Journal
Low-dose ketamine does not improve the speed of recovery from depression in electroconvulsive therapy: a randomized controlled trial
| العنوان: | Low-dose ketamine does not improve the speed of recovery from depression in electroconvulsive therapy: a randomized controlled trial |
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| المؤلفون: | Adrianna J. Woolsey, Jalal A. Nanji, Chantal Moreau, Sudhakar Sivapalan, Stephane L. Bourque, Alfonso Ceccherini-Nelli, Ferrante S. Gragasin |
| المصدر: | Brazilian Journal of Psychiatry (2021) |
| بيانات النشر: | Associação Brasileira de Psiquiatria (ABP), 2021. |
| سنة النشر: | 2021 |
| المجموعة: | LCC:Psychiatry |
| مصطلحات موضوعية: | Depressive disorder, major/drug therapy, depressive disorder, major/therapy, ketamine/therapeutic use, anesthesia/therapeutic use, electroconvulsive therapy/therapeutic use, ketamine/adverse effects, Psychiatry, RC435-571 |
| الوصف: | Objective: Electroconvulsive therapy (ECT) is a well-established therapeutic intervention for major depressive disorder. Recent literature has shown that the anesthetic agent ketamine has some antidepressant properties at low doses and may be an alternative therapy for treatment-resistant major depressive disorder. We hypothesized that the use of low-dose ketamine as an anesthetic adjunct in ECT would more rapidly improve depression while maintaining hemodynamic stability than ECT with propofol alone. Methods: Institutional ethics approval was obtained, and the use of ketamine in this study was approved by Health Canada. This is a randomized, double-blinded, placebo-controlled trial that involved ketamine administration at 0.5 mg/kg IV in addition to propofol anesthesia for ECT. The primary outcome was the number of ECT treatments required to achieve a 50% reduction in the Montgomery-Asberg Depression Rating Scale (MADRS). Secondary outcomes included the number of ECT treatments required to achieve a 25% reduction in MADRS score, as well as any differences in the Clinical Global Impression Scale for Severity, hemodynamic variables, and seizure duration. Adverse events were recorded for safety assessment. Results: A total of 45 patients completed the study. No difference was found between groups with respect to the primary or secondary outcomes. The ketamine group showed a trend towards a decreased dose of propofol required to achieve adequate anesthesia. No adverse events were reported. Conclusion: Low-dose ketamine does not improve psychiatric outcomes in the setting of propofol-based anesthesia for ECT. Specifically, ketamine did not reduce the number of ECT sessions necessary to achieve a 50 or 25% reduction in MADRS scores. Reassuringly, the fact that no differences in hemodynamic variables or unexpected adverse events occurred suggests that low-dose ketamine may be safely used in this setting should clinical indications warrant its use. Clinical trial registration: ClinicalTrials.gov, NCT02579642 |
| نوع الوثيقة: | article |
| وصف الملف: | electronic resource |
| اللغة: | English Portuguese |
| تدمد: | 1809-452X 1516-4446 |
| Relation: | http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1516-44462021005017202&tlng=en; https://doaj.org/toc/1809-452X |
| DOI: | 10.1590/1516-4446-2020-1705 |
| URL الوصول: | https://doaj.org/article/ba04001be1064cb688531a25390af727 |
| رقم الانضمام: | edsdoj.ba04001be1064cb688531a25390af727 |
| قاعدة البيانات: | Directory of Open Access Journals |
Full Text Finder | تدمد: | 1809452X 15164446 |
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| DOI: | 10.1590/1516-4446-2020-1705 |