Intravenous Ketamine for Treatment-Resistant Major Depressive Disorder

Author:

Covvey Jordan R1,Crawford Alexis Noble2,Lowe Denise K3

Affiliation:

1. Jordan R Covvey PharmD BCPS, at time of writing, PGY1 Pharmacy Practice Resident, Virginia Commonwealth University Health System, Richmond, VA; now, PhD candidate and Fulbright-Strathclyde Postgraduate Scholar, Strathclyde Institute of Pharmacy and Biomedical Sciences, University of Strathclyde, Glasgow, Scotland

2. Alexis Noble Crawford PharmD BCPS, at time of writing, PGY1 Pharmacy Practice Resident, Virginia Commonwealth University Health System: now, PGY2 Critical Care Pharmacy Resident, Virginia Commonwealth University Health System

3. Denise K Lowe PharmD BCPS, Director, Drug Information Services, Virginia Commonwealth University Health System/Medical College of Virginia Hospitals; Associate Clinical Professor, School of Pharmacy, Virginia Commonwealth University

Abstract

OBJECTIVE: To evaluate the literature regarding the efficacy and safety of intravenous ketamine for treatment-resistant major depressive disorder (MDD). DATA SOURCES: A MEDLINE search (1966-September 2011) was performed using the terms treatment-resistant depression and ketamine. The search was restricted to articles published in English and reporting on use of ketamine in humans. STUDY SELECTION AND DATA EXTRACTION: All English-language articles identified from the data search were evaluated. Data were eligible for inclusion if they were primary literature and evaluated the efficacy of ketamine for depressive symptoms in treatment-resistant MDD. One case report, 3 case series, 3 open-label trials, and 1 randomized crossover trial were included. DATA SYNTHESIS: Several medications are available for treatment-resistant MDD; however, they are often limited by a slow onset of therapeutic effect and tolerability. It has been suggested that ketamine, a rapid-acting, N-methyl-D-aspartate glutamate receptor antagonist, may have antidepressant effects. Case reports, case series, and select trials evaluating ketamine use for depressive symptoms in treatment-resistant MDD have demonstrated a rapid effect for reductions of scores on a number of depression scales; however, its sustainability effect remains unknown. Several studies reported a large or moderate to large effect size for ketamine. Additionally, these studies showed that ketamine use in this patient population is associated with relatively well-tolerated adverse effects. CONCLUSIONS: Ketamine for treatment-resistant MDD requires further evaluation before it can be considered a viable treatment option.

Publisher

SAGE Publications

Subject

Pharmacology (medical)

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