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Ketamine and depression: a narrative review

Alexandrine Corriger, G. Pickering

Drug Design, Development and Therapy August 1, 2019 DOI: 10.2147/dddt.s221437 via Semantic Scholar

Summary

AI-generated from the abstract

Ketamine, an NMDA receptor antagonist, produces a rapid antidepressant effect within 24 hours that lasts one to two weeks after a single low-dose infusion, though longer-term effects are not well documented. It does not appear to improve depressive symptoms when used as an anesthetic adjuvant before electroconvulsive therapy. Safety and tolerability at low single doses are generally good, but data on repeated or higher doses are lacking. Intranasal (S)-ketamine has been approved for depression. The overall level of evidence for efficacy remains low, and more randomized controlled trials are needed.

Study at a glance

Characteristics Review Randomized Peer reviewed
Population Patients with major depressive disorder and/or bipolar disorder
Intervention Ketamine
Keywords Medicine
Citations 197
Key finding Ketamine provides a rapid antidepressant effect with maximum efficacy at 24 hours, lasting one to two weeks after infusion, but the level of proof of efficacy remains low.

Abstract

Abstract Depression is the third leading cause of disability in the world. Depressive symptoms may be reduced within several weeks after the start of conventional antidepressants, but treatment resistance concerns one-third of patients who fail to achieve recovery. Over the last 20 years, ketamine, an antagonist of the N-methyl-D-aspartate receptor, has been described to have antidepressant properties. A literature review was conducted through an exhaustive electronic search. It was restricted to Cochrane reviews, meta-analyses, and randomized controlled trials (RCTs) of ketamine for major depressive disorder and/or bipolar disorder. This review included two Cochrane reviews, 14 meta-analyses and 15 trials. Ketamine was studied versus placebo, versus other comparators and as an anesthetic adjuvant before electroconvulsive therapy. In 14 publications, ketamine provided a rapid antidepressant effect with a maximum efficacy reached at 24 hrs. Its effect lasted for 1–2 weeks after infusion, but a longer-term effect is little reported. Ketamine does not seem to improve depressive symptoms at the end of electroconvulsive sessions. Safety and tolerability profiles with ketamine at low single dose are generally good in depressed patients. However, there is a lack of data concerning ketamine with repeated administration at higher doses. The clinical use of ketamine is increasing. Intranasal (S)-ketamine has recently been approved for depression by the Food and Drug Administration. It could be a promising treatment in depressed patients with suicidal ideation. Collectively, the level of proof of efficacy remains low and more RCTs are needed to explore efficacy and safety issues of ketamine in depression.

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