Response to Letter to the Editors regarding ‘Efficacy of psychosocial interventions to reduce alcohol use in comorbid alcohol use disorder and alcohol-related liver disease: a systematic review of randomized controlled trials’
Sofia Hemrage, Eileen Brobbin, Paolo Deluca, Colin Drummond

Abstract
Genes, proteins, chemicals, diseases, species, mutations and cell lines named across the full text — each resolved to its canonical identifier and authoritative record.
- —National Institute for Health Research Applied Research Collaboration South London10.13039/501100023232
- —Department of Health and Social Care10.13039/501100000276
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Taxonomy
TopicsAlcohol Consumption and Health Effects · Substance Abuse Treatment and Outcomes · Liver Disease Diagnosis and Treatment
Dear Editors,
We thank Dr Wei for reading, considering, and taking the time to provide feedback on our findings published under ‘Efficacy of psychosocial interventions to reduce alcohol use in comorbid alcohol use disorder and alcohol-related liver disease: a systematic review of randomized controlled trials’ (Hemrage et al. 2023). We also wish to thank you for the opportunity to further clarify the points raised in Dr Wei’s letter. We appreciate the occasion to engage in constructive discussions that further the scientific method.
Dr Wei requested further context to the risk of bias assessment for the included randomized controlled trials. We conducted an assessment of the risk of bias using the Cochrane’s Risk-of-Bias 2 tool, as the gold standard to determine the risk of bias in randomized controlled trials (Sterne et al. 2019). The tool includes criteria such as random sequence generation and allocation concealment (selection bias) and incomplete outcome data (attrition bias). Similar to Kelly and colleagues (Kelly et al. 2020), blinding of participants and personnel delivering the intervention is not always possible given the nature of psychosocial interventions. Despite being of moderate certainty, the findings of our systematic review grant further evidence to the scope of psychosocial interventions to reduce harm in alcohol-related liver disease. Given the methodological limitations of some of the published research on this topic, this points to the need for more high-quality studies on psychosocial interventions in alcohol-related liver disease in the future to enrich the evidence base.
We agree with Dr Wei, that given the physical and mental comorbidities inherent to alcohol-use disorder and alcohol-related liver disease, treatment approaches should consider and tailor interventions to the unique therapeutic needs of this clinical population. Despite the effectiveness of pharmacotherapy for the management of alcohol-use disorder, patients with comorbid alcohol-use disorder and alcohol-related liver disease often present different responses to medication given the heterogeneity in their hepatic profiles and respective pharmacodynamic processes. There are also several contraindications for various pharmacotherapies in alcohol-related liver disease due to abnormalities in liver function, especially for disulfiram and naltrexone (Thursz and Lingford-Hughes 2023). Hence, there is an important role in the use of psychosocial interventions to improve patient outcomes and reduce alcohol-related harm in comorbid alcohol-use disorder and alcohol-related liver disease, which was the focus of our systematic review. Where clinically possible, these psychosocial interventions should be used in conjunction with effective pharmacotherapies to maximize clinical effectiveness, although there is currently a lack of research on combined therapies specifically in alcohol-related liver disease (Thursz and Lingford-Hughes 2023).
Motivational enhancement therapy was consistently found to be effective in the included randomized controlled trials in addressing comorbid alcohol-use disorder and alcohol-related liver disease by improving both reduction and abstinence outcomes. While a study trialling cognitive behavioural therapy saw a significant increase in abstinence, their implications should be noted with caution given age baseline differences and protocol deviations (Willenbring and Olson 1999).
Ultimately, we concur with Dr Wei’s call for future research to build upon evidence-based interventions that address this unmet need, to improve patient outcomes among this clinical population, particularly the need for care which effectively integrates psychosocial, pharmacological and hepatology interventions.
The reference list from the paper itself. Each links out to its DOI / PubMed record.
- 1Hemrage S , Brobbin E, Deluca P. et al. Efficacy of psychosocial interventions to reduce alcohol use in comorbid alcohol use disorder and alcohol-related liver disease: a systematic review of randomized controlled trials. Alcohol Alcohol 2023;58:478–84. 10.1093/alcalc/agad 051.37530582 PMC 10493519 · doi ↗ · pubmed ↗
- 2Kelly JF , Humphreys K, Ferri M. Alcoholics Anonymous and other 12-step programs for alcohol use disorder. Cochrane Database Syst Rev 2020;3:CD 012880. 10.1002/14651858.CD 012880.pub 2.32159228 PMC 7065341 · doi ↗ · pubmed ↗
- 3Sterne JAC , SavovićJ, Page MJ. et al. Ro B 2: A revised tool for assessing risk of bias in randomised trials. BMJ 2019;366:l 4898. 10.1136/bmj.l 4898.31462531 · doi ↗ · pubmed ↗
- 4Thursz M , Lingford-Hughes A. Advances in the understanding and management of alcohol-related liver disease. BMJ 2023;383:e 077090. 10.1136/bmj-2023-077090.37984967 · doi ↗ · pubmed ↗
- 5Willenbring ML , Olson DH. A randomized trial of integrated outpatient treatment for medically ill alcoholic men. Arch Intern Med 1999;159:1946–52. 10.1001/archinte.159.16.1946.10493326 · doi ↗ · pubmed ↗
