Medications for treating alcohol use disorder: A narrative review

被引:20
作者
Kranzler, Henry R. [1 ,2 ,3 ]
Hartwell, Emily E. [1 ,2 ]
机构
[1] Univ Penn, Dept Psychiat, Perelman Sch Med, Philadelphia, PA USA
[2] Crescenz VAMC, Mental Illness Res Educ & Clin Ctr, Vet Integrated Serv Network 4, Philadelphia, PA USA
[3] Univ Penn, Ctr Studies Addict, Perelman Sch Med, 3535 Market St, Philadelphia, PA 19104 USA
来源
ALCOHOL-CLINICAL AND EXPERIMENTAL RESEARCH | 2023年 / 47卷 / 07期
关键词
alcohol use disorder; medication-assisted treatment; medications; pharmacotherapy; PLACEBO-CONTROLLED TRIAL; OPIOID RECEPTOR GENE; EXTENDED-RELEASE NALTREXONE; DOUBLE-BLIND; TARGETED NALTREXONE; DEPENDENT PATIENTS; DISULFIRAM TREATMENT; RELAPSE PREVENTION; HEAVY DRINKERS; ORAL NALMEFENE;
D O I
10.1111/acer.15118
中图分类号
R194 [卫生标准、卫生检查、医药管理];
学科分类号
摘要
Chronic heavy alcohol use impacts all major neurotransmitter systems and is associated with multiple medical, psychiatric, and social problems. Available evidence-based medications to treat alcohol use disorder (AUD) are underutilized in clinical practice. These medications promote abstinence or reduce alcohol consumption, though there are questions regarding their optimal dosage, length of treatment, and utility in combination with one another. Pharmacogenetic approaches, which use a patient's genetic make-up to inform medication selection, have garnered great interest but have yet to yield results robust enough to incorporate them in routine clinical care. This narrative review summarizes the evidence both for medications approved by the Food and Drug Administration (disulfiram, oral naltrexone, acamprosate, and extended-release naltrexone) and those commonly used off-label (e.g., gabapentin, baclofen, and topiramate) for AUD treatment. We discuss these drugs' mechanisms of action, clinical use, pharmacogenetic findings, and treatment recommendations. We conclude that the most consistent evidence supporting the pharmacotherapy of AUD is for the opioid antagonists, naltrexone and nalmefene (which is not approved in the United States), and topiramate. These medications demonstrate consistent small or moderate effects in reducing the frequency of drinking and/or heavy drinking. Lastly, we make suggestions for research needed to refine and expand the current literature on effective pharmacotherapy for AUD.
引用
收藏
页码:1224 / 1237
页数:14
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