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Pharmacotherapy for relapse prevention of alcohol use disorder in the Indian setting: A systematic review
Alcohol use disorders (AUDs) is an important public health concern as estimates of the prevalence of AUD range at 4%–6% in the Indian population. Currently, there is limited literature on the pharmacotherapeutic interventions for AUD in the Indian setting. It is imperative to identify the possible v...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Wolters Kluwer - Medknow
2018
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6592216/ https://www.ncbi.nlm.nih.gov/pubmed/31359967 http://dx.doi.org/10.4103/ipj.ipj_79_17 |
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author | Bharadwaj, Balaji Selvakumar, Nivedhitha Kuppili, Pooja Patnaik |
author_facet | Bharadwaj, Balaji Selvakumar, Nivedhitha Kuppili, Pooja Patnaik |
author_sort | Bharadwaj, Balaji |
collection | PubMed |
description | Alcohol use disorders (AUDs) is an important public health concern as estimates of the prevalence of AUD range at 4%–6% in the Indian population. Currently, there is limited literature on the pharmacotherapeutic interventions for AUD in the Indian setting. It is imperative to identify the possible variations in their effects from Western studies, and hence the current review was attempted to perform a comprehensive evaluation and critical appraisal of the methodology of the evidence on pharmacological strategies of relapse prevention of AUD in the Indian setting. A total of 18 studies were included in the review. Disulfiram was the most common pharmacological agent to be studied. The initial literature before 2000 focused primarily on disulfiram, whereas the studies in the next decade compared it to acamprosate and naltrexone and emerging interest in anticraving agents such as baclofen and topiramate had been noted over the past few years. No studies were available on newer agents such as ondansetron, selective serotonin reuptake inhibitors or formulations such as depot and implants. Deterrent agents were found to be better when compared to anticraving agents in terms of abstinence and relapse, whereas the latter were more effective for control of craving. Among the pharmacological agents studied, the greatest evidence exists for disulfiram for relapse prevention which could be due to affordability of disulfiram and social support in the Indian context. The chief methodological limitations include the lack of randomized trials and objective measures for assessing abstinence. |
format | Online Article Text |
id | pubmed-6592216 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Wolters Kluwer - Medknow |
record_format | MEDLINE/PubMed |
spelling | pubmed-65922162019-07-29 Pharmacotherapy for relapse prevention of alcohol use disorder in the Indian setting: A systematic review Bharadwaj, Balaji Selvakumar, Nivedhitha Kuppili, Pooja Patnaik Ind Psychiatry J Review Article Alcohol use disorders (AUDs) is an important public health concern as estimates of the prevalence of AUD range at 4%–6% in the Indian population. Currently, there is limited literature on the pharmacotherapeutic interventions for AUD in the Indian setting. It is imperative to identify the possible variations in their effects from Western studies, and hence the current review was attempted to perform a comprehensive evaluation and critical appraisal of the methodology of the evidence on pharmacological strategies of relapse prevention of AUD in the Indian setting. A total of 18 studies were included in the review. Disulfiram was the most common pharmacological agent to be studied. The initial literature before 2000 focused primarily on disulfiram, whereas the studies in the next decade compared it to acamprosate and naltrexone and emerging interest in anticraving agents such as baclofen and topiramate had been noted over the past few years. No studies were available on newer agents such as ondansetron, selective serotonin reuptake inhibitors or formulations such as depot and implants. Deterrent agents were found to be better when compared to anticraving agents in terms of abstinence and relapse, whereas the latter were more effective for control of craving. Among the pharmacological agents studied, the greatest evidence exists for disulfiram for relapse prevention which could be due to affordability of disulfiram and social support in the Indian context. The chief methodological limitations include the lack of randomized trials and objective measures for assessing abstinence. Wolters Kluwer - Medknow 2018 /pmc/articles/PMC6592216/ /pubmed/31359967 http://dx.doi.org/10.4103/ipj.ipj_79_17 Text en Copyright: © 2019 Industrial Psychiatry Journal http://creativecommons.org/licenses/by-nc-sa/4.0 This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms. |
spellingShingle | Review Article Bharadwaj, Balaji Selvakumar, Nivedhitha Kuppili, Pooja Patnaik Pharmacotherapy for relapse prevention of alcohol use disorder in the Indian setting: A systematic review |
title | Pharmacotherapy for relapse prevention of alcohol use disorder in the Indian setting: A systematic review |
title_full | Pharmacotherapy for relapse prevention of alcohol use disorder in the Indian setting: A systematic review |
title_fullStr | Pharmacotherapy for relapse prevention of alcohol use disorder in the Indian setting: A systematic review |
title_full_unstemmed | Pharmacotherapy for relapse prevention of alcohol use disorder in the Indian setting: A systematic review |
title_short | Pharmacotherapy for relapse prevention of alcohol use disorder in the Indian setting: A systematic review |
title_sort | pharmacotherapy for relapse prevention of alcohol use disorder in the indian setting: a systematic review |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6592216/ https://www.ncbi.nlm.nih.gov/pubmed/31359967 http://dx.doi.org/10.4103/ipj.ipj_79_17 |
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