A Randomized Trial of E-Cigarettes versus Nicotine-Replacement Therapy

被引:974
|
作者
Hajek, Peter [1 ]
Phillips-Waller, Anna [1 ]
Przulj, Dunja [1 ]
Pesola, Francesca [2 ]
Smith, Katie Myers [1 ]
Bisal, Natalie [1 ]
Li, Jinshuo [4 ]
Parrott, Steve [4 ]
Sasieni, Peter [2 ]
Dawkins, Lynne [3 ]
Ross, Louise [5 ]
Goniewicz, Maciej [6 ]
Wu, Qi [4 ]
McRobbie, Hayden J. [1 ]
机构
[1] Queen Mary Univ London, London, England
[2] Kings Coll London, London, England
[3] London South Bank Univ, London, England
[4] Univ York, York, N Yorkshire, England
[5] Leicester City Council, Leicester, Leics, England
[6] Roswell Pk Comprehens Canc Ctr, Buffalo, NY USA
来源
NEW ENGLAND JOURNAL OF MEDICINE | 2019年 / 380卷 / 07期
关键词
SMOKING-CESSATION; WITHDRAWAL; RESOLUTION; NONSMOKER;
D O I
10.1056/NEJMoa1808779
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUND E-cigarettes are commonly used in attempts to stop smoking, but evidence is limited regarding their effectiveness as compared with that of nicotine products approved as smoking-cessation treatments. METHODS We randomly assigned adults attending U.K. National Health Service stop-smoking services to either nicotine-replacement products of their choice, including product combinations, provided for up to 3 months, or an e-cigarette starter pack (a second-generation refillable e-cigarette with one bottle of nicotine e-liquid [18 mg per milli-liter]), with a recommendation to purchase further e-liquids of the flavor and strength of their choice. Treatment included weekly behavioral support for at least 4 weeks. The primary outcome was sustained abstinence for 1 year, which was validated biochemically at the final visit. Participants who were lost to follow-up or did not provide biochemical validation were considered to not be abstinent. Secondary outcomes included participant-reported treatment usage and respiratory symptoms. RESULTS A total of 886 participants underwent randomization. The 1-year abstinence rate was 18.0% in the e-cigarette group, as compared with 9.9% in the nicotine-replacement group (relative risk, 1.83; 95% confidence interval [CI], 1.30 to 2.58; P<0.001). Among participants with 1-year abstinence, those in the e-cigarette group were more likely than those in the nicotine-replacement group to use their assigned product at 52 weeks (80% [63 of 79 participants] vs. 9% [4 of 44 participants]). Overall, throat or mouth irritation was reported more frequently in the e-cigarette group (65.3%, vs. 51.2% in the nicotine-replacement group) and nausea more frequently in the nicotine-replacement group (37.9%, vs. 31.3% in the e-cigarette group). The e-cigarette group reported greater declines in the incidence of cough and phlegm production from baseline to 52 weeks than did the nicotine-replacement group (relative risk for cough, 0.8; 95% CI, 0.6 to 0.9; relative risk for phlegm, 0.7; 95% CI, 0.6 to 0.9). There were no significant between-group differences in the incidence of wheezing or shortness of breath. CONCLUSIONS E-cigarettes were more effective for smoking cessation than nicotine-replacement therapy, when both products were accompanied by behavioral support.
引用
收藏
页码:629 / 637
页数:9
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