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. 2017 Jul 13;7(3):144–150. doi: 10.1080/20009666.2017.1343076

Table 4.

Practitioners’ responses to questions regarding concerns and regulations regarding e-cigarettes.

Participant responses N (%)
What should the FDA do with regard to e-cigarettes?  
Regulate them like other NRT products: gums/inhalers/patches. 62 (53)
Have warning labels like other tobacco products 61 (52.5)
Regulate them like other tobacco products. 60 (51.7)
Restrictions on advertising, promotion and sponsorship 42 (36.2)
A ban on sales to minors only. 39 (33.6)
Ban e-cigarette use in public places 28 (24.1)
Ban flavors that appeal to kids 27 (23.2)
Ban them altogether from the marketplace. 5 (4.3)
Not sure 11 (9.5)
Maintain status quo until further research is available. 9 (7.8)
What are your concerns regarding e-cigarettes?  
Lack of evidence regarding the long-term safety of the product 88 (76.5)
Virtual absence of regulatory controls by the FDA 59 (51.3)
Function as attractive starter products for young non-smokers and a gateway to smoking for adolescents 57 (49.5)
The long-term impact of repeated propylene glycol (major component of some e-cigarettes) inhalation is unknown 52 (45.2)
Marketing and advertising of e-cigarettes, especially to children and youth 48 (41.7)
Become ‘bridge product’ for use in places where smoking is prohibited: schools/offices/airports 41 (35.65)
E-cigarette advertising and photos of celebrities vaping will make cigarette smoking glamorous again and ‘renormalize’ smoking 40 (34.7)
Their use may instead perpetuate smokers’ addiction 37 (32.1)
FDA may ban or restrict them from the marketplace, resulting in lack of less-harmful alternatives to smoking 6 (5.2)