Naltrexone for the treatment of alcoholism: A meta-analysis of randomized controlled trials

Many trials of naltrexone have been carried out in alcohol-dependent patients. This paper is aimed to systematically review its benefits, adverse effects, and discontinuation of treatment. We assessed and extracted the data of double-blind, randomized controlled trials (RCTs) comparing naltrexone wi...

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Main Authors: Manit Srisurapanont, Ngamwong Jarusuraisin
Format: Journal
Published: 2018
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spelling th-cmuir.6653943832-623872018-09-11T09:27:49Z Naltrexone for the treatment of alcoholism: A meta-analysis of randomized controlled trials Manit Srisurapanont Ngamwong Jarusuraisin Medicine Pharmacology, Toxicology and Pharmaceutics Many trials of naltrexone have been carried out in alcohol-dependent patients. This paper is aimed to systematically review its benefits, adverse effects, and discontinuation of treatment. We assessed and extracted the data of double-blind, randomized controlled trials (RCTs) comparing naltrexone with placebo or other treatment in people with alcoholism. Two primary outcomes were subjects who relapsed (including heavy drinking) and those who returned to drinking. Secondary outcomes were time to first drink, drinking days, number of standard drinks for a defined period, and craving. All outcomes were reported for the short, medium, and long term. Five common adverse effects and dropout rates in short-term treatment were also examined. A total of 2861 subjects in 24 RCTs presented in 32 papers were included. For short-term treatment, naltrexone significantly decreased relapses [relative risk (RR) 0.64, 95% confidence interval (CI) 0.51-0.82], but not return to drinking (RR 0.91,95% CI 0.81-1.02). Short-term treatment of naltrexone significantly increased nausea, dizziness, and fatigue in comparison to placebo [RRs (95% CIs) 2.14 (1.61-2.83), 2.09 (1.28-3.39), and 1.35 (1.04-1.75)]. Naltrexone administration did not significantly diminish short-term discontinuation of treatment (RR 0.85, 95% CI 0.70-1.01). Naltrexone should be accepted as a short-term treatment for alcoholism. As yet, we do not know the appropriate duration of treatment continuation in an alcohol-dependent patient who responds to short-term naltrexone administration. To ensure that the real-world treatment is as effective as the research findings, a form of psychosocial therapy should be concomitantly given to all alcohol-dependent patients receiving naltrexone administration. Copyright © 2005 CINP. 2018-09-11T09:26:32Z 2018-09-11T09:26:32Z 2005-06-01 Journal 14611457 2-s2.0-20044378930 10.1017/S1461145704004997 https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=20044378930&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/62387
institution Chiang Mai University
building Chiang Mai University Library
country Thailand
collection CMU Intellectual Repository
topic Medicine
Pharmacology, Toxicology and Pharmaceutics
spellingShingle Medicine
Pharmacology, Toxicology and Pharmaceutics
Manit Srisurapanont
Ngamwong Jarusuraisin
Naltrexone for the treatment of alcoholism: A meta-analysis of randomized controlled trials
description Many trials of naltrexone have been carried out in alcohol-dependent patients. This paper is aimed to systematically review its benefits, adverse effects, and discontinuation of treatment. We assessed and extracted the data of double-blind, randomized controlled trials (RCTs) comparing naltrexone with placebo or other treatment in people with alcoholism. Two primary outcomes were subjects who relapsed (including heavy drinking) and those who returned to drinking. Secondary outcomes were time to first drink, drinking days, number of standard drinks for a defined period, and craving. All outcomes were reported for the short, medium, and long term. Five common adverse effects and dropout rates in short-term treatment were also examined. A total of 2861 subjects in 24 RCTs presented in 32 papers were included. For short-term treatment, naltrexone significantly decreased relapses [relative risk (RR) 0.64, 95% confidence interval (CI) 0.51-0.82], but not return to drinking (RR 0.91,95% CI 0.81-1.02). Short-term treatment of naltrexone significantly increased nausea, dizziness, and fatigue in comparison to placebo [RRs (95% CIs) 2.14 (1.61-2.83), 2.09 (1.28-3.39), and 1.35 (1.04-1.75)]. Naltrexone administration did not significantly diminish short-term discontinuation of treatment (RR 0.85, 95% CI 0.70-1.01). Naltrexone should be accepted as a short-term treatment for alcoholism. As yet, we do not know the appropriate duration of treatment continuation in an alcohol-dependent patient who responds to short-term naltrexone administration. To ensure that the real-world treatment is as effective as the research findings, a form of psychosocial therapy should be concomitantly given to all alcohol-dependent patients receiving naltrexone administration. Copyright © 2005 CINP.
format Journal
author Manit Srisurapanont
Ngamwong Jarusuraisin
author_facet Manit Srisurapanont
Ngamwong Jarusuraisin
author_sort Manit Srisurapanont
title Naltrexone for the treatment of alcoholism: A meta-analysis of randomized controlled trials
title_short Naltrexone for the treatment of alcoholism: A meta-analysis of randomized controlled trials
title_full Naltrexone for the treatment of alcoholism: A meta-analysis of randomized controlled trials
title_fullStr Naltrexone for the treatment of alcoholism: A meta-analysis of randomized controlled trials
title_full_unstemmed Naltrexone for the treatment of alcoholism: A meta-analysis of randomized controlled trials
title_sort naltrexone for the treatment of alcoholism: a meta-analysis of randomized controlled trials
publishDate 2018
url https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=20044378930&origin=inward
http://cmuir.cmu.ac.th/jspui/handle/6653943832/62387
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