» Articles » PMID: 20824837

Acamprosate for Alcohol Dependence

Overview
Publisher Wiley
Date 2010 Sep 9
PMID 20824837
Citations 154
Authors
Affiliations
Soon will be listed here.
Abstract

Background: Alcohol dependence is among the main leading health risk factors in most developed and developing countries. Therapeutic success of psychosocial programs for relapse prevention is moderate, but could potentially be increased by an adjuvant treatment with the glutamate antagonist acamprosate.

Objectives: To determine the effectiveness and tolerability of acamprosate in comparison to placebo and other pharmacological agents.

Search Strategy: We searched the Cochrane Drugs and Alcohol Group (CDAG) Specialized Register, PubMed, EMBASE and CINAHL in January 2009 and inquired manufacturers and researchers for unpublished trials.

Selection Criteria: All double-blind randomised controlled trials (RCTs) which compare the effects of acamprosate with placebo or active control on drinking-related outcomes.

Data Collection And Analysis: Two authors independently extracted data. Trial quality was assessed by one author and cross-checked by a second author. Individual patient data (IPD) meta-analyses were used to verify the primary effectiveness outcomes.

Main Results: 24 RCTs with 6915 participants fulfilled the criteria of inclusion and were included in the review. Compared to placebo, acamprosate was shown to significantly reduce the risk of any drinking RR 0.86 (95% CI 0.81 to 0.91); NNT 9.09 (95% CI 6.66 to 14.28) and to significantly increase the cumulative abstinence duration MD 10.94 (95% CI 5.08 to 16.81), while secondary outcomes (gamma-glutamyltransferase, heavy drinking) did not reach statistical significance. Diarrhea was the only side effect that was more frequently reported under acamprosate than placebo RD 0.11 (95% 0.09 to 0.13); NNTB 9.09 (95% CI 7.69 to 11.11). Effects of industry-sponsored trials RR 0.88 (95% 0.80 to 0.97) did not significantly differ from those of non-profit funded trials RR 0.88 (95% CI 0.81 to 0.96). In addition, the linear regression test did not indicate a significant risk of publication bias (p = 0.861).

Authors' Conclusions: Acamprosate appears to be an effective and safe treatment strategy for supporting continuous abstinence after detoxification in alcohol dependent patients. Even though the sizes of treatment effects appear to be rather moderate in their magnitude, they should be valued against the background of the relapsing nature of alcoholism and the limited therapeutic options currently available for its treatment.

Citing Articles

Alcohol-Associated Hepatitis: Short- and Long-Term Management.

De La Torre Jr S, Morcos M, Saab S, Shetty A Dig Dis Sci. 2024; 70(1):74-84.

PMID: 39576428 PMC: 11761462. DOI: 10.1007/s10620-024-08705-1.


Exploring the Role of DARPP-32 in Addiction: A Review of the Current Limitations of Addiction Treatment Pathways and the Role of DARPP-32 to Improve Them.

Greener M, Storr S NeuroSci. 2024; 3(3):494-509.

PMID: 39483434 PMC: 11523713. DOI: 10.3390/neurosci3030035.


Treatment of Alcohol Use Disorder: Behavioral and Pharmacologic Therapies.

Tareen K, Clifton E, Perumalswami P, Mellinger J, Winder G Clin Liver Dis. 2024; 28(4):761-778.

PMID: 39362720 PMC: 11450263. DOI: 10.1016/j.cld.2024.06.011.


Alcohol pharmacotherapy dispensing trends in Australia between 2006 and 2023.

Quintrell E, Page A, Wyrwoll C, Larcombe A, Preen D, Almeida O Alcohol Alcohol. 2024; 59(5).

PMID: 39242103 PMC: 11379491. DOI: 10.1093/alcalc/agae063.


A Narrative Review of Current and Emerging Trends in the Treatment of Alcohol Use Disorder.

Celik M, Gold M, Fuehrlein B Brain Sci. 2024; 14(3).

PMID: 38539681 PMC: 10969323. DOI: 10.3390/brainsci14030294.