慢性丙型肝炎患者的心理过程与减少饮酒:HepART 试验的结果。

IF 3 Q2 SUBSTANCE ABUSE
Donna M. Evon, Jia Yao, Catherine Zimmer, Andrew J. Muir, Christian S. Hendershot, Rae Jean Proeschold-Bell
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引用次数: 0

摘要

背景:目前缺乏与慢性肝病(如丙型肝炎病毒(HCV)感染)患者减酒相关的行为干预随机对照试验和过程层面的研究。我们对丙型肝炎-酒精减少治疗(HepART)试验进行了过程层面的二次分析,以研究综合行为模型(IBM)假设的心理过程变化与世界卫生组织(WHO)饮酒风险水平变化之间的关联:方法:从肝病诊所招募饮酒的 HCV 患者,让他们接受由医疗服务提供者提供的 SBIRT(筛查、简单干预、转介治疗)或 SBIRT+ 6 个月的同地酒精咨询。由于未发现组间差异,因此本分析合并了治疗组。在基线和 6 个月时,根据 2000 年世界卫生组织的风险类别(基于每天平均饮酒克数),采用时间轴回溯法确定酒精风险水平。从基线到 6 个月期间,酒精消耗量和世卫组织风险水平的变化被量化,并与个人心理过程(如准备程度、自我效能、动机、态度和策略)的变化进行回归:在基线评估中,162 名参与者被划分为禁欲(5%)、低度(47%)、中度(16%)、高度(19%)或极高度(13%)世卫组织风险水平。6 个月后,38% 的参与者风险水平保持不变,48% 的参与者风险水平至少降低了一个等级。在单变量分析中,12 个心理过程中有 7 个过程的变化与风险水平的变化有关。调整后的多变量分析表明,四个过程的变化与风险水平的变化有显著相关性,包括 SOCRATES 采取步骤、矛盾心理和认识评分以及减少饮酒策略:这些研究结果表明,在对丙型肝炎病毒感染者进行机会性酒精干预后,酒精消耗量的定量指标明显降低。然而,结果对 IBM 心理过程的变化与饮酒量之间的关联提供了不同的支持。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Psychological processes and alcohol reduction in patients with chronic hepatitis C: Results from the HepART trial

Psychological processes and alcohol reduction in patients with chronic hepatitis C: Results from the HepART trial

Psychological processes and alcohol reduction in patients with chronic hepatitis C: Results from the HepART trial

Background

There is a lack of randomized controlled trials of behavioral interventions and process-level research related to alcohol reduction among patients with chronic liver disease (e.g., hepatitis C viral (HCV) infection). We conducted a process-level, secondary analysis of the Hepatitis C-Alcohol Reduction Treatment (HepART) trial to investigate the association between change in psychological processes posited by the Integrated Behavioral Model (IBM) and change in World Health Organization (WHO) drinking risk levels.

Methods

Patients with HCV who consume alcohol were recruited from hepatology clinics and received provider-delivered SBIRT (Screening, Brief Intervention, Referral to Treatment) or SBIRT+ 6 months of co-located alcohol counseling. Treatment arms were combined for this analysis because no between-group differences were found. At baseline and 6 months, the timeline followback method was used to determine alcohol risk levels according to the 2000 WHO risk categories (based on average grams of alcohol per day). Changes in alcohol consumption and WHO risk levels were quantified and regressed on change in individual psychological processes (e.g., readiness, self-efficacy, motives, attitudes, and strategies) from baseline to 6 months.

Results

At the baseline assessment, 162 participants were classified as abstinent (5%), low (47%), moderate (16%), high (19%), or very high (13%) WHO risk levels. At 6 months, 38% remained at the same risk level and 48% decreased by at least one level. In univariate analyses, changes in 7 of 12 psychological processes were associated with change in risk levels. Adjusted multivariate analyses demonstrated that change in four processes were significantly associated with change in risk levels, including SOCRATES Taking Steps, Ambivalence, and Recognition scores and alcohol reduction strategies.

Conclusions

These findings demonstrate significant reductions in quantitative indices of alcohol consumption following opportunistic alcohol interventions in patients with HCV. However, results provided mixed support for associations between change in IBM psychological processes and alcohol consumption.

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