Providence Veterans Affairs Medical Center, Providence, RI, USA.
Center for Alcohol and Addiction Studies, Brown University School of Public Health, Providence, RI, USA.
Addiction. 2017 Oct;112(10):1808-1820. doi: 10.1111/add.13861. Epub 2017 Jul 4.
Varenicline was compared with transdermal nicotine (NRT) for smokers with current substance use disorders (SUD) for effects on 3-month smoking abstinence (primary outcome) and, secondarily, on 3- and 6 month abstinence while adjusting for medication adherence, and on additional smoking and substance use outcomes. Moderation by major depressive disorder history (MDD) and adherence were investigated.
Double-blind double-placebo-controlled randomized design, stratifying by MDD, gender and nicotine dependence, with 3 and 6 months follow-up.
University offices in Rhode Island, USA.
Adult smokers (n = 137), in SUD treatment, substance abstinent <12 months (n = 77 varenicline, 60 NRT).
Twelve weeks of varenicline (2 mg/day, after 1-week dose run-up) or NRT (21 mg/day decreasing to 7 mg/day).
Primary: point-prevalence smoking abstinence (7-day, confirmed) at 3 months. Secondary: point-prevalence abstinence at 6 months, quantity and frequency of smoking and substance use at 3 and 6 months, and within-treatment abstinence, medication adherence and depressive symptoms. Smoking outcome analyses were repeated controlling for adherence and investigating adherence as a moderator.
Effects on 3-month abstinence were P < 0.065 without a covariate (Bayes factor 3.35, supporting the effect strongly) and differed significantly when controlling for baseline smoking [varenicline: 13%, NRT: 3%; odds ratio (OR) = 4.81, 95% confidence interval (CI) 1.00, 23.13, P < 0.05]. The threefold difference at 6 months was not significant. Medication effect on abstinence across time was significant (P < 0.05) covarying adherence and baseline smoking (OR = 6.40, 95% CI = 1.00, 40.93). Medication differences in 3-month abstinence occurred among participants with ≥ 77% adherence (P < 0.02). No significant medication effects on heavy drinking, drug use or depressive symptoms were found.
Varenicline appears to improve the chances of achieving at least 3 months of smoking abstinence in smokers with substance use disorders trying to stop, compared with transdermal nicotine patches, the effect being independent of history of depressive disorder.
比较伐伦克林与透皮尼古丁(NRT)治疗有当前物质使用障碍(SUD)的吸烟者在 3 个月的吸烟戒断(主要结局)方面的效果,其次,调整药物依从性后,在 3 个月和 6 个月的戒断方面,以及在其他吸烟和物质使用结果方面。还研究了主要抑郁障碍史(MDD)和依从性的调节作用。
双盲双安慰剂对照随机设计,按 MDD、性别和尼古丁依赖分层,随访 3 个月和 6 个月。
美国罗德岛州的大学办公室。
成年吸烟者(n=137),在 SUD 治疗中,物质戒断<12 个月(n=77 例伐伦克林,60 例 NRT)。
12 周的伐伦克林(2mg/天,1 周剂量上调后)或 NRT(21mg/天,逐渐减少至 7mg/天)。
主要:3 个月时的点流行吸烟戒断(7 天,确认)。次要:6 个月时的点流行戒断,3 个月和 6 个月时的吸烟和物质使用量和频率,以及治疗内戒断、药物依从性和抑郁症状。在控制依从性的情况下重复吸烟结果分析,并将依从性作为一个调节因素进行调查。
在不考虑协变量的情况下,3 个月的戒烟效果为 P<0.065(贝叶斯因子 3.35,强烈支持该效果),当控制基线吸烟时,差异显著[伐伦克林:13%,NRT:3%;比值比(OR)=4.81,95%置信区间(CI)1.00,23.13,P<0.05]。6 个月时的三倍差异无统计学意义。在考虑依从性和基线吸烟的情况下,药物对戒烟的影响随时间显著(P<0.05)(OR=6.40,95%CI=1.00,40.93)。在依从性≥77%的参与者中,3 个月的药物戒断差异有统计学意义(P<0.02)。未发现药物对重度饮酒、药物使用或抑郁症状有显著影响。
与透皮尼古丁贴片相比,伐伦克林似乎可以提高有物质使用障碍的吸烟者至少 3 个月的吸烟戒断机会,试图戒烟,而这种效果独立于抑郁障碍史。