Baseline Trajectories of Drinking Moderate Acamprosate and Naltrexone Effects in the COMBINE Study

被引:17
作者
Gueorguieva, Ralitza [1 ]
Wu, Ran [2 ]
Donovan, Dennis [3 ]
Rounsaville, Bruce J. [2 ]
Couper, David [4 ]
Krystal, John H. [2 ,5 ]
O'Malley, Stephanie S. [2 ]
机构
[1] Yale Univ, Sch Publ Hlth, New Haven, CT USA
[2] Yale Univ, Sch Med, Dept Psychiat, New Haven, CT USA
[3] Univ Washington, Sch Med, Dept Psychiat & Behav Sci, Seattle, WA 98195 USA
[4] Univ N Carolina, Dept Biostat, Chapel Hill, NC USA
[5] VA Connecticut Healthcare Syst, West Haven, CT USA
来源
ALCOHOLISM-CLINICAL AND EXPERIMENTAL RESEARCH | 2011年 / 35卷 / 03期
关键词
Naltrexone; Acamprosate; Clinical Trial; Latent Class; Trajectory-Based Analysis; ANALYZING DEVELOPMENTAL TRAJECTORIES; ALCOHOL DEPENDENCE; INSTRUMENT; WITHDRAWAL; EFFICACY; SCALE;
D O I
10.1111/j.1530-0277.2010.01369.x
中图分类号
R194 [卫生标准、卫生检查、医药管理];
学科分类号
摘要
Background: The COMBINE study evaluated the effects of acamprosate, naltrexone, and the Combined Behavioral Intervention (CBI). In secondary analyses, our goals were to identify trajectories of any drinking prior to randomization, to characterize subjects in these trajectories, and to assess whether prerandomization trajectories predict drinking outcomes and moderate treatment response. Methods: We analyzed daily indicators of any drinking in 90 days prior to randomization using a trajectory-based approach. General linear models and generalized logistic regression assessed main and interactive effects of prerandomization drinking trajectories and treatment on summary drinking measures during active treatment. Results: We identified five trajectories of any drinking prior to randomization: "T1: frequent drinkers", "T2: very frequent drinkers", "T3: nearly daily drinkers", "T4: consistent daily drinkers", and "T5: daily drinkers stopping early". During treatment, "T3: nearly daily drinkers" and "T4: consistent daily drinkers" had significantly worse drinking outcomes than "T1: frequent drinkers", while "T5: daily drinkers stopping early" had comparable drinking outcomes to "T1: frequent drinkers". Acamprosate significantly increased the chance of abstinence from heavy drinking for the "T2: very frequent drinking" trajectory but decreased the chance of abstinence from heavy drinking for "T5: daily drinkers stopping early". Naltrexone differentially improved rates of continuous abstinence for very frequent drinkers. Conclusions: Acamprosate benefited very frequent drinkers and contrary to expectations was associated with poorer response compared to placebo for consistent daily drinkers who had longer durations of pretreatment abstinence (e.g., >= 14 days). Baseline drinking trajectories also moderated naltrexone effects. These findings may help clinicians identify patients for whom acamprosate and naltrexone may be most beneficial.
引用
收藏
页码:523 / 531
页数:9
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