Varenicline for tobacco-dependence treatment in alcohol-dependent smokers: A randomized controlled trial

被引:26
|
作者
Hurt, Ryan T. [1 ]
Ebbert, Jon O. [2 ,3 ]
Croghan, Ivana T. [2 ,3 ]
Schroeder, Darrell R. [4 ]
Hurt, Richard D. [2 ,3 ]
Hays, J. Taylor [1 ,3 ]
机构
[1] Mayo Clin, Div Gen Internal Med, 200 First St SW, Rochester, MN 55905 USA
[2] Mayo Clin, Div Primary Care Internal Med, Rochester, MN 55905 USA
[3] Mayo Clin, Nicotine Dependence Ctr, Rochester, MN 55905 USA
[4] Mayo Clin, Div Biomed Stat & Informat, Rochester, MN 55905 USA
关键词
Alcohol use disorder; Nicotine; Pharmacotherapy; Smoking cessation; RECEPTOR PARTIAL AGONIST; SUSTAINED-RELEASE BUPROPION; SMOKING-CESSATION; NICOTINE DEPENDENCE; ACETYLCHOLINE-RECEPTORS; COOCCURRING ALCOHOL; CONCURRENT ALCOHOL; ETHANOL; PLACEBO; CONSUMPTION;
D O I
10.1016/j.drugalcdep.2017.11.017
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: Tobacco use is prevalent among persons with alcohol abuse and dependence. Varenicline has been shown to be the most effective pharmacotherapy for smoking cessation and may decrease alcohol consumption. The purpose of this study was to evaluate the efficacy of 12 weeks of varenicline for increasing smoking abstinence rates in smokers with alcohol abuse or dependence. Methods: Participants were eligible for enrollment if they were 18 years or older, smoked 10 or more cigarettes per day for at least 6 months, had current alcohol abuse or dependence, and were interested in quitting smoking. Participants were randomly assigned to receive 12 weeks of varenicline 1 mg twice daily or matching placebo. The primary end point was 7-day point prevalence smoking abstinence at week 12. Results: The 7-day point prevalence smoking abstinence rate at 12 weeks was significantly higher with varenicline (n = 16) than placebo (n = 17) (43.8% vs 5.9%; P = .01). At 24 weeks, the 7-day point prevalence smoking abstinence rate was still significantly higher with varenicline than placebo (31.3% vs 0%; P = .02). At 12 weeks, mean (SD) drinks per drinking day was significantly lower with varenicline than placebo (5.7 [3.9] vs 9.0 [5.3] drinks; treatment effect estimate, -2.8 [90% CI, -6.6 to -1.0]). Adverse events were minor and comparable to varenicline clinical trials. Conclusions: Varenicline is safe and efficacious for increasing smoking abstinence rates in smokers with alcohol abuse or dependence. Varenicline may decrease alcohol consumption in this population of smokers.
引用
收藏
页码:12 / 17
页数:6
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