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Alcohol and Alcoholism Advance Access published online on August 10, 2004

Alcohol and Alcoholism, doi:10.1093/alcalc/agh088
© 2004 by Medical Council on Alcohol
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Received May 12, 2004
Revised July 15, 2004
Accepted July 15, 2004


Article

A PRAGMATIC TRIAL OF ACAMPROSATE IN THE TREATMENT OF ALCOHOL DEPENDENCE IN PRIMARY CARE

PAUL KIRITZÉ-TOPOR 1*, DOMINIQUE HUAS 2, CLAUDE ROSENZWEIG 3, SYLVIE COMTE 4, FRANÇOIS PAILLE 5, PHILIPPE LEHERT 6

1 11 avenue du Grain d'Or, 49600 Beaupreau, France
2 Department of General Practice, Xavier Bichat University, 75018 Paris, France
3 Le Clos Macé, 35850 Geveze, France
4 Merck Santé, 37 rue Saint-Romain, 69379 Lyon cedex 08, France
5 Hôpital Villemin, 17 rue de Nabecor, 54000 Nancy, France
6 Statistics Department, University of Mons, FuCam, Mons, Belgium and Faculty of Medicine, University of Melbourne, Melbourne, Australia

* To whom correspondence should be addressed. E-mail: pkiritze001{at}cegetel.rss.fr.


   Abstract

Aims: To assess the effectiveness of pharmacotherapy with acamprosate in alcohol-dependent patients treated in a naturalistic setting in primary care in France. Methods: The ARES (Acamprosate et Répercussions Économiques et Sociales; Acamprosate and Economic and Social Repercussions) study was performed by 149 general practitioners interested in treating alcohol use disorders in France who included patients fulfilling DSM-IV criteria for alcohol dependence. The only exclusion criteria concerned contra-indications to acamprosate, co-medication with naltrexone and multiple substance abuse. Eligible patients were randomized to one of two treatment arms, either standard care alone or standard care with acamprosate, using an open-label design and followed up quarterly for a period of 1 year. The primary outcome variable was the change from baseline on the Alcohol-Related Problems Questionnaire. Secondary efficacy variables were abstinence, Clinical Global Impression, quality of life measured with the SF-36 and incidence of adverse events. An intent-to-treat population was used for outcome analysis. Results: 422 patients were included, of whom 348 (82%) completed the protocol as planned. At the end of the study, patients randomized to the acamprosate group had significantly better outcomes in terms of total ARPQ score, change from baseline (-2.61 vs -3.44) and number of subjects with no alcohol-related problem. On average, patients treated with acamprosate had one less alcohol-related problem than did the controls. The number needed to treat in order to save one additional patient from alcohol-related problems compared to standard care was 7.14. Statistically significant differences in favour of the acamprosate group were observed for all secondary efficacy outcome measures including quality of life. Conclusions: Adjunctive therapy with acamprosate in primary care is associated with significantly better functional outcome. Pragmatic trials in alcohol dependence are both feasible and informative.


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[Abstract] [Full Text] [PDF]



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