Section of Digestive Diseases, Yale School of Medicine, New Haven, Connecticut, USA.
Division of Gastroenterology and Hepatology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, USA.
Hepatol Commun. 2023 Mar 24;7(4). doi: 10.1097/HC9.0000000000000093. eCollection 2023 Apr 1.
Medications for alcohol use disorder (MAUD) are highly effective in achieving and maintaining abstinence in patients with alcohol use disorder (AUD). Our aim was to evaluate the effect of MAUD on all-cause mortality in patients with alcohol-associated cirrhosis and active alcohol use.
This was a retrospective cohort study of patients with alcohol-associated cirrhosis and high-risk alcohol use disorder in the Veterans Outcomes and Costs Associated with Liver Disease (VOCAL) database. Propensity score matching for exposure to MAUD (acamprosate or naltrexone) within a year after cirrhosis diagnosis was performed to account for potential confounders, and the association between MAUD and all-cause mortality was subsequently evaluated using Cox regression analysis.
A total of 9131 patients were included, of whom 886 (9.7%) were exposed to MAUD (naltrexone: 520, acamprosate: 307, both medications: 59). The duration of MAUD exposure was >3 months in 345 patients (39%). The strongest positive predictor of MAUD prescription was an inpatient diagnosis code for AUD, followed by a concurrent diagnosis of depression; the strongest negative predictor was a history of cirrhosis decompensation. After propensity score matching (866 patients in each group) with excellent covariate balance (absolute standardized mean differences <0.1), MAUD exposure was associated with improved survival, with an HR of 0.80 relative to no MAUD exposure (95% CI: 0.67-0.97, p = 0.024).
MAUD are underutilized in patients with alcohol-associated cirrhosis with high-risk alcohol use behavior but are associated with improved survival after adjustment for confounders such as the severity of liver disease, age, and engagement in the healthcare system.
对于酒精使用障碍(AUD)患者,酒精使用障碍(MAUD)药物在实现和维持戒断方面非常有效。我们的目的是评估 MAUD 对伴有酒精性肝硬化和活跃饮酒的 AUD 患者全因死亡率的影响。
这是退伍军人结局和肝病相关成本(VOCAL)数据库中伴有酒精性肝硬化和高危酒精使用障碍患者的回顾性队列研究。对 MAUD(安非他酮或纳曲酮)暴露进行倾向评分匹配(在肝硬化诊断后一年内),以解释潜在的混杂因素,随后使用 Cox 回归分析评估 MAUD 与全因死亡率之间的关联。
共纳入 9131 例患者,其中 886 例(9.7%)接受 MAUD 治疗(纳曲酮:520 例,安非他酮:307 例,两种药物:59 例)。345 例(39%)患者的 MAUD 暴露持续时间>3 个月。MAUD 处方的最强预测因子是 AUD 的住院诊断代码,其次是并发的抑郁症诊断;最强的负预测因子是肝硬化失代偿病史。在进行倾向评分匹配(每组 866 例患者)后,协变量平衡极佳(绝对标准化均值差异<0.1),MAUD 暴露与生存率提高相关,相对于无 MAUD 暴露,风险比为 0.80(95%CI:0.67-0.97,p=0.024)。
尽管 MAUD 在具有高危酒精使用行为的伴有酒精性肝硬化患者中未得到充分利用,但在调整了肝脏疾病严重程度、年龄和参与医疗保健系统等混杂因素后,与生存率提高相关。