Division of General Internal Medicine, Mayo Clinic, Rochester, MN, United States.
Division of Primary Care Internal Medicine, Mayo Clinic, Rochester, MN, United States; Nicotine Dependence Center, Mayo Clinic, Rochester, MN, United States.
Drug Alcohol Depend. 2018 Mar 1;184:12-17. doi: 10.1016/j.drugalcdep.2017.11.017. Epub 2018 Jan 2.
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.
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.
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.
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.
烟草使用在酒精滥用和依赖人群中很普遍。维拉唑尼已被证明是最有效的戒烟药物治疗方法,并且可能会减少酒精的摄入量。本研究的目的是评估 12 周维拉唑尼治疗对有酒精滥用或依赖的吸烟者增加戒烟成功率的效果。
如果参与者年龄在 18 岁或以上,每天吸烟 10 支或更多,且至少持续 6 个月,目前有酒精滥用或依赖,并且有戒烟的意愿,则有资格入组。参与者被随机分配接受 12 周的维拉唑尼 1mg,每日两次,或匹配的安慰剂。主要终点是 12 周时 7 天点患病率的戒烟率。
在 12 周时,维拉唑尼组(n=16)的 7 天点患病率戒烟率显著高于安慰剂组(n=17)(43.8% vs. 5.9%;P=0.01)。在 24 周时,维拉唑尼组的 7 天点患病率戒烟率仍显著高于安慰剂组(31.3% vs. 0%;P=0.02)。在 12 周时,维拉唑尼组的平均(SD)每日饮酒量显著低于安慰剂组(5.7 [3.9] 与 9.0 [5.3] 杯;治疗效果估计值,-2.8 [90%CI,-6.6 至-1.0])。不良事件轻微,与维拉唑尼临床试验相当。
维拉唑尼对有酒精滥用或依赖的吸烟者增加戒烟成功率是安全且有效的。维拉唑尼可能会减少该人群中吸烟者的酒精摄入量。