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A Single Ketamine Infusion Combined With Motivational Enhancement Therapy for Alcohol Use Disorder: A Randomized Midazolam-Controlled Pilot Trial.

E. Dakwar, F. Levin, C. Hart, Cale N. Basaraba, Jean C Choi, M. Pavlicova, E. Nunes

American Journal of Psychiatry December 2, 2019 DOI: 10.1176/appi.ajp.2019.19070684 via Semantic Scholar

Summary

A single low-dose ketamine infusion, combined with motivational enhancement therapy, increased the likelihood of abstinence and reduced heavy drinking days in adults with alcohol dependence. In a pilot study, 40 participants received either ketamine or the active control midazolam. Ketamine delayed relapse and was well tolerated, with no dropouts due to adverse events. The results suggest a potential new approach integrating pharmacotherapy with behavioral treatment, though larger studies are needed to confirm these findings.

Study at a glance

Characteristics Randomized controlled trial Longitudinal Pilot study Peer reviewed
Sample size 40
Population Adults with alcohol dependence engaged in motivational enhancement therapy
Keywords Medicine Psychology
Citations 179
Key finding Ketamine significantly increased the likelihood of abstinence, delayed time to relapse, and reduced heavy drinking days compared with midazolam.

Abstract

OBJECTIVE Pharmacotherapy and behavioral treatments for alcohol use disorder are limited in their effectiveness, and new treatments with innovative mechanisms would be valuable. In this pilot study, the authors tested whether a single subanesthetic infusion of ketamine administered to adults with alcohol dependence and engaged in motivational enhancement therapy affects drinking outcomes. METHODS Participants were randomly assigned to a 52-minute intravenous administration of ketamine (0.71 mg/kg, N=17) or the active control midazolam (0.025 mg/kg, N=23), provided during the second week of a 5-week outpatient regimen of motivational enhancement therapy. Alcohol use following the infusion was assessed with timeline followback method, with abstinence confirmed by urine ethyl glucuronide testing. A longitudinal logistic mixed-effects model was used to model daily abstinence from alcohol over the 21 days after ketamine infusion. RESULTS Participants (N=40) were mostly middle-aged (mean age=53 years [SD=9.8]), predominantly white (70.3%), and largely employed (71.8%) and consumed an average of five drinks per day prior to entering the study. Ketamine significantly increased the likelihood of abstinence, delayed the time to relapse, and reduced the likelihood of heavy drinking days compared with midazolam. Infusions were well tolerated, with no participants removed from the study as a result of adverse events. CONCLUSIONS A single ketamine infusion was found to improve measures of drinking in persons with alcohol dependence engaged in motivational enhancement therapy. These preliminary data suggest new directions in integrated pharmacotherapy-behavioral treatments for alcohol use disorder. Further research is needed to replicate these promising results in a larger sample.

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