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      Management of alcohol use disorder in patients with cirrhosis in the setting of liver transplantation

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          Abstract

          The prevalence of alcohol use disorder (AUD) has been steadily increasing over the past decade. In parallel, alcohol-associated liver disease (ALD) has been increasing at an alarming rate, especially among young patients. Data suggest that most patients with ALD do not receive AUD therapy. Although liver transplantation is the only curative therapy for end-stage ALD, transplant candidacy is often a matter of debate given concerns about patients being under-treated for AUD and fears of post-transplantation relapse affecting the allograft. In this Review, we discuss diagnosis, predictors and effects of relapse, behavioural therapies and pharmacotherapies, and we also propose an integrative, multidisciplinary and multimodality approach for treating AUD in patients with cirrhosis, especially in the setting of liver transplantation. Notably, this approach takes into account the utility of AUD pharmacotherapy in patients on immunosuppressive medications and those with renal impairment after liver transplantation. We also propose a comprehensive and objective definition of relapse utilizing contemporary biomarkers to guide future clinical trials. Future research using the proposed approach and definition is warranted with the goal of optimizing AUD treatment in patients with cirrhosis, the transplant selection process and post-transplantation care of patients with AUD.

          Abstract

          In this Review, Arab and colleagues discuss management of alcohol use disorder in patients with alcohol-associated liver disease, particularly in the setting of liver transplantation. An integrative, multidisciplinary approach is proposed.

          Key points

          • The prevalence of alcohol use disorder (AUD) and alcohol-associated liver disease has increased over the past few decades globally.

          • Definitions of relapse after liver transplantation vary widely.

          • Currently, our understanding of the predictors and effects of relapse after liver transplantation is growing and together with a multidisciplinary approach might improve patient outcomes.

          • The use of pharmacotherapies for AUD is feasible in patients with cirrhosis after tailoring the regimen to account for comorbid illnesses such as renal dysfunction.

          • Relapse-prevention medications do not have notable interactions with immunosuppressants commonly used after liver transplantation.

          • Combining medications and behavioural treatments with medical care at the transplant centre might maximize relapse prevention potential.

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          Most cited references137

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          Development of the Alcohol Use Disorders Identification Test (AUDIT): WHO Collaborative Project on Early Detection of Persons with Harmful Alcohol Consumption-II

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            The AUDIT alcohol consumption questions (AUDIT-C): an effective brief screening test for problem drinking. Ambulatory Care Quality Improvement Project (ACQUIP). Alcohol Use Disorders Identification Test.

            To evaluate the 3 alcohol consumption questions from the Alcohol Use Disorders Identification Test (AUDIT-C) as a brief screening test for heavy drinking and/or active alcohol abuse or dependence. Patients from 3 Veterans Affairs general medical clinics were mailed questionnaires. A random, weighted sample of Health History Questionnaire respondents, who had 5 or more drinks over the past year, were eligible for telephone interviews (N = 447). Heavy drinkers were oversampled 2:1. Patients were excluded if they could not be contacted by telephone, were too ill for interviews, or were female (n = 54). Areas under receiver operating characteristic curves (AUROCs) were used to compare mailed alcohol screening questionnaires (AUDIT-C and full AUDIT) with 3 comparison standards based on telephone interviews: (1) past year heavy drinking (>14 drinks/week or > or =5 drinks/ occasion); (2) active alcohol abuse or dependence according to the Diagnostic and Statistical Manual of Mental Disorders, Revised Third Edition, criteria; and (3) either. Of 393 eligible patients, 243 (62%) completed AUDIT-C and interviews. For detecting heavy drinking, AUDIT-C had a higher AUROC than the full AUDIT (0.891 vs 0.881; P = .03). Although the full AUDIT performed better than AUDIT-C for detecting active alcohol abuse or dependence (0.811 vs 0.786; P<.001), the 2 questionnaires performed similarly for detecting heavy drinking and/or active abuse or dependence (0.880 vs 0.881). Three questions about alcohol consumption (AUDIT-C) appear to be a practical, valid primary care screening test for heavy drinking and/or active alcohol abuse or dependence.
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              Prevalence of 12-Month Alcohol Use, High-Risk Drinking, and DSM-IV Alcohol Use Disorder in the United States, 2001-2002 to 2012-2013

              Lack of current and comprehensive trend data derived from a uniform, reliable, and valid source on alcohol use, high-risk drinking, and DSM-IV alcohol use disorder (AUD) represents a major gap in public health information.

                Author and article information

                Contributors
                jparab@uc.cl
                manhal.izzy@vumc.org
                Journal
                Nat Rev Gastroenterol Hepatol
                Nat Rev Gastroenterol Hepatol
                Nature Reviews. Gastroenterology & Hepatology
                Nature Publishing Group UK (London )
                1759-5045
                1759-5053
                1 November 2021
                : 1-15
                Affiliations
                [1 ]GRID grid.7870.8, ISNI 0000 0001 2157 0406, Departamento de Gastroenterología, Escuela de Medicina, , Pontificia Universidad Católica de Chile, ; Santiago, Chile
                [2 ]GRID grid.7870.8, ISNI 0000 0001 2157 0406, Centro de Envejecimiento y Regeneración (CARE), Departamento de Biología Celular y Molecular, Facultad de Ciencias Biológicas, , Pontificia Universidad Católica de Chile, ; Santiago, Chile
                [3 ]GRID grid.412807.8, ISNI 0000 0004 1936 9916, Division of Gastroenterology, Hepatology, and Nutrition, , Vanderbilt University Medical Center, ; Nashville, TN USA
                [4 ]GRID grid.94365.3d, ISNI 0000 0001 2297 5165, Clinical Psychoneuroendocrinology and Neuropsychopharmacology Section, , National Institute on Drug Abuse Intramural Research Program and National Institute on Alcohol Abuse and Alcoholism Division of Intramural Clinical and Biological Research, National Institutes of Health, ; Baltimore and Bethesda, MD USA
                [5 ]GRID grid.94365.3d, ISNI 0000 0001 2297 5165, Medication Development Program, National Institute on Drug Abuse Intramural Research Program, , National Institutes of Health, ; Baltimore, MD USA
                [6 ]GRID grid.40263.33, ISNI 0000 0004 1936 9094, Center for Alcohol and Addiction Studies, Department of Behavioral and Social Sciences, , Brown University School of Public Health, ; Providence, RI USA
                [7 ]GRID grid.21107.35, ISNI 0000 0001 2171 9311, Division of Addiction Medicine, Department of Medicine, , School of Medicine, Johns Hopkins University, ; Baltimore, MD USA
                [8 ]GRID grid.411667.3, ISNI 0000 0001 2186 0438, Department of Neuroscience, , Georgetown University Medical Center, ; Washington, DC USA
                [9 ]GRID grid.412689.0, ISNI 0000 0001 0650 7433, Division of Gastroenterology, Hepatology and Nutrition, , University of Pittsburgh Medical Center, ; Pittsburgh, PA USA
                [10 ]GRID grid.66875.3a, ISNI 0000 0004 0459 167X, Division of Gastroenterology and Hepatology, , Mayo Clinic, ; Rochester, MN USA
                Author information
                http://orcid.org/0000-0002-8561-396X
                http://orcid.org/0000-0002-1119-7799
                http://orcid.org/0000-0001-7620-573X
                Article
                527
                10.1038/s41575-021-00527-0
                8559139
                34725498
                a4176655-81c1-4845-a2f0-6bb6c294a42f
                © This is a U.S. government work and not under copyright protection in the U.S.; foreign copyright protection may apply 2021

                This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.

                History
                : 21 September 2021
                Categories
                Review Article

                alcoholic liver disease,liver cirrhosis
                alcoholic liver disease, liver cirrhosis

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