Alcohol does not impact chronic hepatitis C treatment outcomes but increases risk for progressive liver disease: Findings from a prospective multicentre Australian study (OPERA-C)

IF 3 3区 医学 Q2 SUBSTANCE ABUSE Drug and alcohol review Pub Date : 2024-08-02 DOI:10.1111/dar.13914
Paul J. Clark, Patricia C. Valery, Simone I. Strasser, Martin Weltman, Alex Thompson, Miriam T. Levy, Barbara Leggett, Amany Zekry, Julian Rong, Marie Sinclair, Jacob George, William Sievert, Gerry MacQuillan, Edmund Tse, Amanda Nicoll, Amanda Wade, Wendy Cheng, Stuart K. Roberts
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Abstract

Introduction

Alcohol use is common in patients with chronic hepatitis C virus (HCV) infection. We examined the impact of alcohol use on direct-acting antiviral (DAA) therapy outcome and the clinical course of liver disease and 2-year survival for patients receiving HCV DAA therapy.

Methods

Adults (n = 2624) recruited from 26 Australian hospital liver clinics during 2016–2021 were followed up for 2 years. Risky alcohol use was defined by a combination of self-report (≥40 g/day of ethanol), physician-reported history of problematic alcohol use, and anti-craving medication prescription via population-based database linkage. We examined factors associated with advanced liver fibrosis and survival using multivariable logistic and Cox regression.

Results

Among 1634 patients (62.3%) with risky alcohol use, 24.6% reported consuming ≥40 g/day of alcohol, 98.3% physician-reported problematic alcohol use; only 4.1% were dispensed naltrexone/acamprosate. One hundred and forty-three patients with cirrhosis reported ≥40 g/day of alcohol, 6 (4.3%) were prescribed naltrexone/acamprosate. Risky alcohol use was associated with advanced fibrosis (adjusted-odds ratio 1.69, 95% confidence interval 1.32–2.17) and patients were over-represented for cirrhosis (45.1% vs. 25.6% in no-risky alcohol use [p < 0.001]) and hepatocellular carcinoma (5.7% vs. 2.5% [p < 0.001]). Sustained viral response (p = 0.319) and 2-year survival (adjusted-hazard ratio 1.98, 95% confidence interval 0.84–4.63) after DAA therapy were not associated with risky alcohol use.

Discussion and Conclusions

Risky alcohol use in HCV patients was prevalent, but did not reduce HCV cure. Treatment for alcohol dependence was low. Risky alcohol use may be under-recognised in liver clinics. Better integration of addiction medicine into liver services and increased resourcing and addiction medicine training opportunities for hepatologists may help address this.

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酒精不会影响慢性丙型肝炎的治疗效果,但会增加进展性肝病的风险:澳大利亚前瞻性多中心研究(OPERA-C)的结果。
导言:酗酒在慢性丙型肝炎病毒(HCV)感染患者中很常见。我们研究了饮酒对直接作用抗病毒疗法(DAA)疗效的影响,以及接受HCV DAA疗法患者的肝病临床过程和2年生存率:2016-2021年间从澳大利亚26家医院肝病门诊招募的成年人(n = 2624)接受了为期2年的随访。风险性饮酒由自我报告(乙醇摄入量≥40克/天)、医生报告的问题性饮酒史以及通过基于人群的数据库链接开具的抗嗜酒药物处方共同定义。我们使用多变量逻辑回归和 Cox 回归研究了与晚期肝纤维化和存活率相关的因素:在1634名有饮酒风险的患者(62.3%)中,24.6%的患者报告每天饮酒量≥40克,98.3%的患者由医生报告有饮酒问题;只有4.1%的患者获得了纳曲酮/阿坎酸的处方。143名肝硬化患者报告每天饮酒量≥40克,其中6人(4.3%)获得了纳曲酮/阿坎酸处方。危险饮酒与晚期纤维化有关(调整后的比率为 1.69,95% 置信区间为 1.32-2.17),而且肝硬化患者的比例过高(45.1% 对比起无危险饮酒的 25.6% [p 讨论和结论:危险饮酒在 HCV 患者中很普遍,但不会降低 HCV 的治愈率。酒精依赖治疗率较低。肝病诊所可能对酗酒风险认识不足。将成瘾医学更好地融入肝病服务、增加资源配置以及为肝病医生提供成瘾医学培训机会可能有助于解决这一问题。
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来源期刊
Drug and alcohol review
Drug and alcohol review SUBSTANCE ABUSE-
CiteScore
4.80
自引率
10.50%
发文量
151
期刊介绍: Drug and Alcohol Review is an international meeting ground for the views, expertise and experience of all those involved in studying alcohol, tobacco and drug problems. Contributors to the Journal examine and report on alcohol and drug use from a wide range of clinical, biomedical, epidemiological, psychological and sociological perspectives. Drug and Alcohol Review particularly encourages the submission of papers which have a harm reduction perspective. However, all philosophies will find a place in the Journal: the principal criterion for publication of papers is their quality.
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