Efficacy of Ketamine in Bipolar Depression: Systematic Review and Meta-analysis.
Ajay K Parsaik, Balwinder Singh, Darrow Khosh-chashm, Soniya S Mascarenhas
Journal of psychiatric practice November 1, 2015 Peer reviewed DOI: 10.1097/pra.0000000000000106 via PubMed
Summary
Ketamine is effective in treating bipolar depression, showing significant improvement compared to placebo after a single intravenous dose. In a meta-analysis of 3 randomized controlled trials involving 69 subjects, the standardized mean difference was -1.01, indicating a notable reduction in depression symptoms. Improvement peaked 40 minutes post-infusion. No serious side effects were reported, and both ketamine and placebo groups experienced similar side effects.
Study at a glance
| Design | meta-analysis |
|---|---|
| Sample size | 125 |
| Population | subjects with bipolar depression |
| Key finding | The meta-analysis showed significant improvement in depression among patients receiving a single dose of intravenous ketamine compared with those who received placebo. |
Abstract
To consolidate the evidence from the literature to evaluate the role of ketamine in the treatment of bipolar depression. Major databases, including MEDLINE, EMBASE, Cochrane, and Scopus, were searched through October 2014, for studies reporting the role of ketamine in the treatment of bipolar depression. Only randomized controlled trials were included in the meta-analysis. We calculated standardized mean differences (SMDs) with SE for each study included in the meta-analysis. A random effect model was used to calculate the pooled SMDs. Heterogeneity was assessed using the Cochran Q test and I statistic. Of the 721 articles that were screened, 5 studies that enrolled a total of 125 subjects with bipolar depression (mean age, 44.6±4.3 y and 65.6% females) were included in the systematic review; 3 randomized controlled trials (69 subjects) were included in the meta-analysis. The meta-analysis showed significant improvement in depression among patients receiving a single dose of intravenous ketamine compared with those who received placebo (SMD=-1.01; 95% confidence interval, -1.37, -0.66; P<0.0001). The maximum improvement was observed 40 minutes after the ketamine infusion. No heterogeneity was observed between the studies (Cochran Q test P=0.38, I=0%). The 2 studies that were excluded from the meta-analysis also showed significant improvement in depression after ketamine therapy. Individual studies also reported improvement in anhedonia and suicidal ideation after ketamine therapy. None of the subjects had serious side effects, and the side effects were similar between the ketamine and placebo groups. This study suggests that ketamine is effective in treatment-resistant bipolar depression and may reduce suicidal ideation and anhedonia.