Effects of liquid nicotine concentration and flavour on the acceptability of electronic nicotine delivery systems (ENDS) among people who smoke participating in a randomised controlled trial to reduce cigarette consumption.

IF 4.7 2区 医学 Q1 PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH
Jessica Yingst, Vishal Midya, Augustus White, Jonathan Foulds, Caroline O Cobb, Susan Veldheer, Miao-Shan Yen, Thomas Eissenberg
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Abstract

Background: Research is needed to understand the acceptability of electronic nicotine delivery systems (ENDS) as a smoking reduction aid. This study examines the acceptability of ENDS by liquid nicotine concentration and flavour among people who smoke using ENDS to reduce their smoking.

Methods: People who smoke cigarettes but were naïve to ENDS participated in a double-blind randomised controlled trial to reduce conventional cigarette smoking. Participants were randomised to either a control cigarette substitute (CS) or one of three ENDS groups; 0 mg/mL, 8 mg/mL or 36 mg/mL nicotine concentration. ENDS flavour was chosen by the participant (tobacco or menthol). Participants reported their CS, ENDS and cigarettes per day (CPD) from the past 7 days at 1-month, 3-month and 6-month follow-up visits. Participants also reported side effects and measures of satisfaction, psychological reward, aversion and craving relief. Outcome variables were modelled using linear mixed effects by the following groups: liquid nicotine concentration, flavour and a flavour-nicotine concentration interaction.

Results: Participants (n=520) were 41.2% male, 67.3% white, had a mean age of 46.2 years and smoked a mean of 18.6 CPD (SD=7.74) at baseline. All flavour and concentration groups decreased CPD from baseline to all follow-up visits with the 36 mg/mL experiencing the greatest reduction, compared with the 0 mg/mL and 8 mg/mL groups. All groups except the 36 mg/mL group decreased their product use over time. The use of menthol flavour was associated with fewer side effects at 3 months (p=0.02) and lesser aversion at 1 month (p=0.03) compared with tobacco-flavoured ENDS. The 36 mg/mL group experienced the greatest craving relief and greatest aversion compared with other groups.

Conclusions: Both nicotine concentration and flavour appear to have independent, as well as interactive, effects that influence ENDS acceptability among people who use cigarettes.

液体尼古丁浓度和口味对参与减少香烟消费随机对照试验的吸烟者接受电子尼古丁释放系统(ENDS)的影响。
背景:需要开展研究以了解电子尼古丁输送系统(ENDS)作为减烟辅助工具的可接受性。本研究通过液体尼古丁浓度和口味来考察吸烟者对ENDS的接受程度:吸烟但对ENDS不了解的人参加了一项双盲随机对照试验,以减少传统香烟的吸烟量。参与者被随机分配到香烟替代品(CS)对照组或三个ENDS组中的一组;尼古丁浓度分别为0毫克/毫升、8毫克/毫升或36毫克/毫升。ENDS口味由参与者自行选择(烟草或薄荷)。在 1 个月、3 个月和 6 个月的随访中,参与者报告了他们的 CS、ENDS 和过去 7 天的日吸烟量(CPD)。参与者还报告了副作用以及满意度、心理奖励、厌恶感和渴求缓解度的测量结果。结果变量采用线性混合效应模型,按以下分组:尼古丁液体浓度、口味以及口味与尼古丁浓度的交互作用:参与者(n=520)中男性占 41.2%,白人占 67.3%,平均年龄 46.2 岁,基线吸烟量平均为 18.6 CPD(SD=7.74)。与 0 毫克/毫升和 8 毫克/毫升组相比,36 毫克/毫升组的 CPD 降低幅度最大。除 36 毫克/毫升组外,其他各组的产品使用量均随时间推移而减少。与烟草味ENDS相比,使用薄荷味的ENDS在3个月时副作用较少(p=0.02),在1个月时厌恶感较低(p=0.03)。与其他组相比,36 毫克/毫升组的渴求感和厌恶感得到最大缓解:尼古丁浓度和口味似乎既有独立影响,也有交互影响,影响着使用香烟者对ENDS的接受度。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Tobacco Control
Tobacco Control 医学-公共卫生、环境卫生与职业卫生
CiteScore
9.10
自引率
26.90%
发文量
223
审稿时长
6-12 weeks
期刊介绍: Tobacco Control is an international peer-reviewed journal covering the nature and consequences of tobacco use worldwide; tobacco''s effects on population health, the economy, the environment, and society; efforts to prevent and control the global tobacco epidemic through population-level education and policy changes; the ethical dimensions of tobacco control policies; and the activities of the tobacco industry and its allies.
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