4.6 Review

Effect of extended-release naltrexone on alcohol consumption: a systematic review and meta-analysis

期刊

ADDICTION
卷 117, 期 2, 页码 271-281

出版社

WILEY
DOI: 10.1111/add.15572

关键词

Alcohol; extended-release naltrexone; meta-analysis

资金

  1. CARESTAR foundation

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The study showed that extended-release naltrexone can reduce the number of drinking days and heavy drinking days per month in patients with AUD, with larger reductions seen with longer duration of treatment.
Aims The aims of this study were to (1) estimate the effect of extended-release naltrexone compared with placebo on alcohol consumption in patients with alcohol use disorder (AUD) and (2) conduct pre-planned subgroup analyses to test whether being abstinent when initiating treatment (lead-in abstinence) or the duration of treatment improves treatment efficacy. Design Systematic review and random-effects meta-analysis of blinded randomized placebo-controlled trials reporting the effect extended-release naltrexone on alcohol consumption. Setting Outpatient clinics. Participants Seven trials evaluating a total of 1500 adults with AUD receiving monthly injections of either placebo or extended-release naltrexone at doses of 150-400 mg for 2-6 months and some form of behavioral therapy. Measurements Pooled weighted mean difference (WMD) in drinking days per month and heavy drinking days per month. Findings The WMD was -2.0 [95% confidence interval (CI) = -3.4, -0.6; P = 0.03] in favor of extended-release naltrexone for drinking days per month and -1.2 (95% CI = -0.2, -2.1; P = 0.02) for heavy drinking days per month, indicating that treatment resulted in two fewer drinking days per month and 1.2 fewer heavy drinking days per month compared with placebo. Trials not requiring lead-in abstinence and those lasting longer than 3 months reported larger reductions in heavy drinking days per month; WMD -2.0 (95% CI = -3.52, -0.48; P = 0.01) and -1.9 (95% CI = -3.2, -0.5; P = 0.01), respectively. In all cases, the I-2 statistics (0-7.2%) did not suggest substantial heterogeneity. Conclusions Extended-release naltrexone reduces drinking days and heavy drinking days per month compared with placebo. Reductions are larger with a longer duration of treatment.

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