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Position statement on electronic cigarettes or electronic nicotine delivery systems [Official statement]
47
Citations
62
References
2013
Year
Tobacco CessationWorld Health OrganizationEc CartridgesHarm ReductionTobacco ControlPreventive MedicineNicotineEnvironmental HealthClinical EpidemiologyDigital HealthRegulatory ConsiderationPublic HealthPosition StatementSmoking Related Lung DiseaseHealth PolicyTobacco UseClinical SafetyPublic Health PolicyElectronic CigarettesMedical Device RegulationGlobal HealthPatient SafetyInternational HealthTobacco PolicyTechnologyMedicineVaping
Few studies have evaluated ECs/ENDS for harm reduction, yet their use is rapidly increasing and several countries have banned them. The Union advocates regulating ECs/ENDS as medicines to control their manufacture, marketing, and sale. The Union recommends a comprehensive regulatory package covering advertising bans, retail restrictions, age limits, flavour controls, ingredient disclosure, nicotine limits, public use prohibitions, and cartridge safety standards. Evidence shows that ECs/ENDS lack proven safety or benefits, pose potential third‑party health risks, and could undermine WHO tobacco control efforts.
• The International Union Against Tuberculosis and Lung Disease (The Union) has issued this position statement based on a careful review of the scientifi c evidence; the position statement will be reviewed by mid-2015. • The safety of electronic cigarettes (ECs) or electronic nicotine delivery systems (ENDS) has not been scientifi cally demonstrated. • Adverse health effects for third parties exposed (second-hand exposure) cannot be excluded because the use of electronic cigarettes leads to emission of fi ne and ultrafi ne inhalable liquid particles, nicotine and cancer-causing substances into indoor air. • The benefi ts of e-cigarettes have not been scientifi cally proven. To date, very few studies have assessed ECs/ENDS as a harm reduction and cessation aid, with confl icting fi ndings. • The Union is concerned that the marketing, awareness and use of ECs or ENDS is growing rapidly. • A range of current and proposed legislative and regulatory options exists; some countries (such as Brazil, Norway, and Singapore) have banned ECs/ ENDS completely. • ENDS could undermine the implementation of the World Health Organization (WHO) Framework Convention on Tobacco Control (FCTC) Article 12 (denormalisation of tobacco use); use of ENDS could also hamper the implementation of Article 8 (protection from exposure to tobacco smoke), as ENDS users in public places may claim that their electronic cigarette does not contain tobacco and/ or does not produce second-hand tobacco smoke. • The Union strongly supports the regulation of the manufacture, marketing and sale of electronic cigarettes or ENDS; the preferred option is to regulate ECs or ENDS as medicines. • If regulation as medicines is not feasible, the following measures should be considered, pending the availability of reliable evidence: — a comprehensive ban on all advertising, promotion and sponsorship; — promotion of ECs/ENDS for tobacco cessation to be prohibited; — display of ECs/ENDS in retail stores to be prohibited; — sale to minors (persons under the age of full legal responsibility) to be prohibited; — ECs/ENDS and their refi lls should not be sold in fl avours that are appealing to children; — packaging and labelling of EC/ENDS cartridges and disposable ECs/ENDS should include a list of all ingredients, stipulate the quantity of nicotine and include appropriate warning labels; — ECs/ENDS should not be used in public places, workplaces or on public transportation; — consumer safety standards for EC cartridges should be established, including ensuring manufacturing consistency and regulating the maximum quantity/dosage of nicotine they may contain.
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