Department of Respiratory, Central Hospital, Shenyang Medical College, Shenyang, China.
Department of Geriatric Cardiology, First Affiliated Hospital, China Medical University, Shenyang, China.
Compr Psychiatry. 2019 Nov;95:152125. doi: 10.1016/j.comppsych.2019.152125. Epub 2019 Sep 5.
The effects of the combination therapy of varenicline and bupropion in smoking cessation are still controversial.
Databases including PubMed, EMBASE, Cochrane Library and Web of Science were scanned without time and language limitation. Subgroup analysis was performed to assess the effect of combination therapy in smokers with different level of nicotine dependence and cigarette consumption.
Four randomized controlled trials involving a total of 1230 smokers were included. Compared with varenicline monotherapy, combination treatment with varenicline and bupropion could significantly improve the abstinence rate at the end of treatment (RR 1.153, 95% CI 1.019 to 1.305, P=0.024). The benefit existed at 6months follow-up (RR 1.231, 95% CI 1.017 to 1.490, P=0.033), disappeared at 12months follow-up (RR 1.130, 95% CI 0.894 to 1.428, P=0.305), and mainly concentrated in highly dependent smokers (RR 1.631, 95% CI 1.290 to 2.061, P<0.001) and heavy smokers (RR 1.515, 95% CI 1.226 to 1.873, P<0.001) rather than individuals with low nicotine dependence (RR 0.989, 95% CI 0.815 to 1.199, P=0.907) or low cigarette consumption (RR 0.985, 95% CI 0.800 to 1.212, P=0.252). For safety outcomes, the combination treatment was associated with more anxiety (RR 1.717, 95% CI 1.176 to 2.505, P=0.005) and insomnia (RR 1.268, 95% CI 1.076 to 1.494, P=0.005) symptoms compared with varenicline monotherapy.
Compared with varenicline monotherapy, combination treatment with varenicline and bupropion can significantly improve the abstinence rate at the end of treatment and 6months follow-up, mainly in highly dependent smokers and heavy smokers.
伐尼克兰与安非他酮联合治疗戒烟的效果仍存在争议。
无时间和语言限制地扫描PubMed、EMBASE、Cochrane 图书馆和 Web of Science 等数据库。进行亚组分析以评估联合治疗对不同尼古丁依赖程度和吸烟量的吸烟者的疗效。
纳入了四项随机对照试验,共涉及 1230 名吸烟者。与伐尼克兰单药治疗相比,伐尼克兰联合安非他酮治疗可显著提高治疗结束时的戒烟率(RR 1.153,95%CI 1.019 至 1.305,P=0.024)。这种获益在 6 个月随访时仍然存在(RR 1.231,95%CI 1.017 至 1.490,P=0.033),但在 12 个月随访时消失(RR 1.130,95%CI 0.894 至 1.428,P=0.305),且主要集中在高度依赖者(RR 1.631,95%CI 1.290 至 2.061,P<0.001)和重度吸烟者(RR 1.515,95%CI 1.226 至 1.873,P<0.001)中,而不是在低尼古丁依赖者(RR 0.989,95%CI 0.815 至 1.199,P=0.907)或低吸烟量者(RR 0.985,95%CI 0.800 至 1.212,P=0.252)中。安全性结局方面,与伐尼克兰单药治疗相比,联合治疗与更多的焦虑(RR 1.717,95%CI 1.176 至 2.505,P=0.005)和失眠(RR 1.268,95%CI 1.076 至 1.494,P=0.005)症状相关。
与伐尼克兰单药治疗相比,伐尼克兰联合安非他酮治疗可显著提高治疗结束时和 6 个月随访时的戒烟率,主要在高度依赖者和重度吸烟者中。