La Capria Kathryn, Hamilton-Moseley Kristen R, Phan Lilianna, Jewett Bambi, Hacker Kiana, Choi Kelvin, Chen-Sankey Julia
Rutgers Institute for Nicotine and Tobacco Studies, New Brunswick, New Jersey, United States.
National Institute of Minority Health and Health Disparities, Bethesda, Maryland, United States.
Tob Prev Cessat. 2024 Jul 29;10. doi: 10.18332/tpc/190582. eCollection 2024.
It is unclear how young adults who do not use tobacco perceive FDA-authorized e-cigarettes for market entry. This study explored the perceptions and use interests of FDA-authorized e-cigarettes among this population to inform policy decision-making.
We conducted in-depth interviews with young adults in the US, aged 18-29 years, who do not use tobacco (n=25). Participants viewed images of FDA-authorized e-cigarettes and discussed their perceptions and interest in using these products. We used reflexive thematic analysis to analyze interview data.
Many participants stated that they were not interested in using FDA-authorized e-cigarettes because they had little interest in using e-cigarettes in general. Additionally, almost all participants found the tobacco flavor and product design of these products unappealing, which further added to their disinterest. Most reported high trust in the FDA and its authorization process for e-cigarette market entry and considered FDA-authorized e-cigarettes safe to use. Most considered FDA-authorized products less harmful than other (unauthorized) e-cigarettes they saw in daily life but were not more interested in using the authorized products. When given the hypothetical scenario where FDA-authorized products come with a variety of fruit and candy flavors, most participants still expressed little interest in using them, mainly due to the high perceived harm from using any e-cigarette products.
Although non-tobacco-using young adults in our study reported low interest in using FDA-authorized e-cigarettes for market entry and e-cigarettes in general, the FDA is recommended to continue to evaluate the impact of flavorings and packages on e-cigarette product appeal to reduce e-cigarette use among young people. The FDA should also examine strategies to effectively communicate the purpose of FDA authorization to the public and emphasize that it does not mean these products are 'approved' or safer than unauthorized products.
尚不清楚不使用烟草的年轻成年人如何看待美国食品药品监督管理局(FDA)批准进入市场的电子烟。本研究探讨了这一人群对FDA批准的电子烟的看法和使用兴趣,以为政策决策提供参考。
我们对美国18至29岁不使用烟草的年轻成年人(n = 25)进行了深入访谈。参与者观看了FDA批准的电子烟图片,并讨论了他们对使用这些产品的看法和兴趣。我们采用反思性主题分析法对访谈数据进行分析。
许多参与者表示,他们对使用FDA批准的电子烟不感兴趣,因为他们总体上对使用电子烟兴趣不大。此外,几乎所有参与者都认为这些产品的烟草口味和产品设计缺乏吸引力,这进一步增加了他们的反感。大多数人表示对FDA及其电子烟市场准入授权程序高度信任,并认为FDA批准的电子烟使用安全。大多数人认为FDA批准的产品比他们在日常生活中看到的其他(未经批准的)电子烟危害小,但对使用这些批准产品并没有更浓厚的兴趣。当给出FDA批准的产品有各种水果和糖果口味的假设情景时,大多数参与者仍然表示对使用它们兴趣不大,主要是因为他们认为使用任何电子烟产品的危害都很大。
尽管我们研究中的不使用烟草的年轻成年人对FDA批准进入市场的电子烟以及总体上对电子烟的使用兴趣较低,但建议FDA继续评估调味剂和包装对电子烟产品吸引力的影响,以减少年轻人对电子烟的使用。FDA还应研究如何有效地向公众传达FDA授权的目的,并强调这并不意味着这些产品是“被批准的”或比未经批准的产品更安全。