Patnode Carrie D, Henderson Jillian T, Coppola Erin L, Melnikow Joy, Durbin Shauna, Thomas Rachel G
Kaiser Permanente Evidence-based Practice Center, Center for Health Research, Kaiser Permanente, Portland, Oregon.
Center for Healthcare Policy and Research, University of California, Davis, Sacramento.
JAMA. 2021 Jan 19;325(3):280-298. doi: 10.1001/jama.2020.23541.
It has been estimated that in 2018 nearly 20% of adults in the US were currently using a tobacco product.
To systematically review the effectiveness and safety of pharmacotherapy, behavioral interventions, and electronic cigarettes for tobacco cessation among adults, including pregnant persons, to inform the US Preventive Services Task Force.
PubMed, PsycInfo, Database of Abstracts of Reviews of Effects, Cochrane Database of Systematic Reviews, Centre for Reviews and Dissemination of Health Technology Assessment; surveillance through September 25, 2020.
Systematic reviews of tobacco cessation interventions and randomized clinical trials that evaluated the effects of electronic cigarettes (e-cigarettes) or pharmacotherapy among pregnant persons.
Independent critical appraisal and data abstraction; qualitative synthesis and random-effects meta-analyses.
Health outcomes, tobacco cessation at 6 months or more, and adverse events.
Sixty-seven reviews addressing pharmacotherapy and behavioral interventions were included as well as 9 trials (N = 3942) addressing e-cigarettes for smoking cessation and 7 trials (N = 2285) of nicotine replacement therapy (NRT) use in pregnancy. Combined pharmacotherapy and behavioral interventions (pooled risk ratio [RR], 1.83 [95% CI, 1.68-1.98]), NRT (RR, 1.55 [95% CI, 1.49-1.61]), bupropion (RR, 1.64 [95% CI, 1.52-1.77]), varenicline (RR, 2.24 [95% CI, 2.06-2.43]), and behavioral interventions such as advice from clinicians (RR, 1.76 [95% CI, 1.58-1.96]) were all associated with increased quit rates compared with minimal support or placebo at 6 months or longer. None of the drugs were associated with serious adverse events. Five trials (n = 3117) reported inconsistent findings on the effectiveness of electronic cigarettes on smoking cessation at 6 to 12 months among smokers when compared with placebo or NRT, and none suggested higher rates of serious adverse events. Among pregnant persons, behavioral interventions were associated with greater smoking cessation during late pregnancy (RR, 1.35 [95% CI, 1.23-1.48]), compared with no intervention. Rates of validated cessation among pregnant women allocated to NRT compared with placebo were not significantly different (pooled RR, 1.11 [95% CI, 0.79-1.56], n = 2033).
There is strong evidence that a range of pharmacologic and behavioral interventions, both individually and in combination, are effective in increasing smoking cessation in nonpregnant adults. In pregnancy, behavioral interventions are effective for smoking cessation, but data are limited on the use of pharmacotherapy for smoking cessation. Data on the effectiveness and safety of electronic cigarettes for smoking cessation among adults are also limited and results are inconsistent.
据估计,2018年美国近20%的成年人目前正在使用烟草制品。
系统评价药物治疗、行为干预和电子烟对成年人(包括孕妇)戒烟的有效性和安全性,为美国预防服务工作组提供信息。
PubMed、PsycInfo、效果评价摘要数据库、Cochrane系统评价数据库、卫生技术评估综述与传播中心;截至2020年9月25日的监测数据。
对戒烟干预措施的系统评价以及评估电子烟或药物治疗对孕妇影响的随机临床试验。
独立的严格评价和数据提取;定性合成和随机效应荟萃分析。
健康结局、6个月或更长时间的戒烟情况以及不良事件。
纳入了67篇关于药物治疗和行为干预的综述,以及9项针对电子烟戒烟的试验(N = 3942)和7项关于孕期使用尼古丁替代疗法(NRT)的试验(N = 2285)。联合药物治疗和行为干预(合并风险比[RR],1.83[95%CI,1.68 - 1.98])、NRT(RR,1.55[95%CI,1.49 - 1.61])、安非他酮(RR,1.64[95%CI,1.52 - 1.77])、伐尼克兰(RR,2.24[95%CI,2.06 - 2.43])以及诸如临床医生建议等行为干预(RR,1.76[95%CI,1.58 - 1.96])与6个月或更长时间时与极少支持或安慰剂相比戒烟率增加均相关。没有一种药物与严重不良事件相关。5项试验(n = 3117)报告,与安慰剂或NRT相比,电子烟在6至12个月对吸烟者戒烟有效性的结果不一致,且没有试验提示严重不良事件发生率更高。在孕妇中,与未干预相比,行为干预与妊娠晚期更高的戒烟率相关(RR,1.35[95%CI,1.23 - 1.48])。与安慰剂相比,分配接受NRT的孕妇中经证实的戒烟率无显著差异(合并RR,1.11[95%CI,0.79 - 1.56],n = 2033)。
有强有力的证据表明,一系列药物和行为干预措施,单独或联合使用,对增加非孕妇成年人的戒烟率有效。在孕期,行为干预对戒烟有效,但关于药物治疗用于戒烟的数据有限。关于电子烟对成年人戒烟有效性和安全性的数据也有限且结果不一致。