An Update on the Efficacy of Single and Serial Intravenous Ketamine Infusions and Esketamine for Bipolar Depression: A Systematic Review and Meta-Analysis

Author:

Nunez Nicolas A.12,Joseph Boney3ORCID,Kumar Rakesh1ORCID,Douka Ioanna2,Miola Alessandro14,Prokop Larry J.5,Mickey Brian J.2,Singh Balwinder1ORCID

Affiliation:

1. Department of Psychiatry & Psychology, Mayo Clinic, 200 First Street SW, Rochester, MN 55905, USA

2. Department of Psychiatry, University of Utah, Salt Lake City, UT 84112, USA

3. Department of Neurology, Mayo Clinic, Rochester, MN 55905, USA

4. Department of Neuroscience (DNS), University of Padova, 35122 Padua, Italy

5. Mayo Medical Libraries, Mayo Clinic College of Medicine, Rochester, MN 55905, USA

Abstract

Ketamine has shown rapid antidepressant and anti-suicidal effects in treatment-resistant depression (TRD) with single and serial intravenous (IV) infusions, but the effectiveness for depressive episodes of bipolar disorder is less clear. We conducted an updated systematic review and meta-analysis to appraise the current evidence on the efficacy and tolerability of ketamine/esketamine in bipolar depression. A search was conducted to identify randomized controlled trials (RCTs) and non-randomized studies examining single or multiple infusions of ketamine or esketamine treatments. A total of 2657 articles were screened; 11 studies were included in the systematic review of which 7 studies were included in the meta-analysis (five non-randomized, N = 159; two RCTs, N = 33) with a mean age of 42.58 ± 13.1 years and 54.5% females. Pooled analysis from two RCTs showed a significant improvement in depression symptoms measured with MADRS after receiving a single infusion of ketamine (1-day WMD = −11.07; and 2 days WMD = −12.03). Non-randomized studies showed significant response (53%, p < 0.001) and remission rates (38%, p < 0.001) at the study endpoint. The response (54% vs. 55%) and remission (30% vs. 40%) rates for single versus serial ketamine infusion studies were similar. The affective switch rate in the included studies approximated 2.4%. Esketamine data for bipolar depression are limited, based on non-randomized, small sample-sized studies. Further studies with larger sample sizes are required to strengthen the evidence.

Publisher

MDPI AG

Subject

General Neuroscience

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