Smoking is a dangerous lifestyle choice that results in increased risk of premature death or serious morbidities, such as cancer and coronary heart disease for the smoker and adverse health outcomes for the unborn children of pregnant women who smoke.1 Passive smoking also has serious health implications for both children and adults. The corollary of this situation is that smoking cessation is one of the most important, effective, and efficient health care interventions that can be undertaken. Within a year of quitting smoking, a former smoker’s chance of developing heart disease drops to half that of a continuing smoker.2 Between 5 and 15 years after quitting, the chance of lung cancer decreases by almost half, and the risk of dying from cancer becomes similar to that of a nonsmoker.3 However, smoking is a particularly addictive behaviour, and stopping is not easy. While it is possible to stop smoking with just a behavioural intervention, the introduction of complementary pharmacological treatments, such as nicotine replacement therapy and varenicline, has increased rates of smoking cessation. The pharmacy profession has played its part by providing behavioural support and supplying therapies. Societal recognition of the dangers of smoking and support for a smoke-free environment have also contributed to the overall reduction of smoking prevalence in the Western world. For example, in Canada the prevalence of smoking has declined from about 26% in 2001 to 20% in 20114 and to 13% in 2015.5
Despite these developments, quitting is still not possible for many current smokers, and alternative approaches are required. The introduction of e-cigarettes is one such alternative approach. The e-cigarette was first developed by a pharmacist in China in the early 2000s. It is a device that produces a nicotine aerosol by using a battery to heat a solution (typically based on propylene glycol or glycerol) of nicotine and flavouring agents. The device is cylindrical and has a mouthpiece for inhaling the vapour. In contrast to other forms of nicotine replacement, e-cigarettes allow the user to mimic the hand-to-mouth ritual of smoking a cigarette but deliver the vapourized nicotine to the lungs without the toxic by-products that accompany the smoking of tobacco. Thus, they intuitively feel more natural and acceptable to the habituated smoker.
A recent Cochrane review of the evidence for the effectiveness of e-cigarettes6 has suggested that e-cigarettes may increase the chance of a long-term quit. The review included 24 completed studies: 21 cohort studies; 2 RCTs comparing e-cigarettes with placebo e-cigarettes (i.e., without nicotine), with a combined sample of 662 participants, in which the 6-month quit rates were 9% with e-cigarettes and 5% with the placebo device; and a third RCT, which compared e-cigarettes with a nicotine patch and found no difference in quit rates at 6 months. None of the included studies reported serious adverse effects from e-cigarettes, although it was acknowledged that the quality of the evidence was weak because of the small number of trials, the low event rates, and the wide confidence intervals around the estimates; furthermore, there is limited evidence of the long-term safety of e-cigarettes for either the user or those exposed passively to the vapours.7 Concerns have been expressed repeatedly that e-cigarettes represent a gateway to smoking cigarettes for young people, that they have toxic effects, and that they produce carcinogens. It is unclear the extent to which e-cigarettes are being used as aids to smoking cessation, for smoking reduction, or just as a new nicotine-related habit. It is generally acknowledged that all of this deserves thorough exploration.
Internationally, there is great variation in the extent to which countries support or restrict the use of e-cigarettes. A survey of different countries’ regulatory approaches reported that 26 countries have banned all use of e-cigarettes and 21 have imposed restrictions on their sale.8 In Canada, e-cigarettes containing nicotine cannot be legally manufactured, sold, or imported, yet despite these prohibitions, the devices are available online and in some retail outlets. In the United States, an increasing number of states are banning indoor use of e-cigarettes.9 Among countries of the Western world, England has adopted a more liberal approach to e-cigarettes, prioritizing the importance of helping people to quit smoking over any safety concerns. Public Health England has claimed that e-cigarettes are 95% safer than smoked tobacco and has expressed concern that increasing numbers of people think e-cigarettes are more harmful than smoking.10 In a recent commissioned report, the same agency presented data confirming that the vast majority of e-cigarette users are current or ex-smokers and that the number of people using e-cigarettes who have never smoked is very small.11 The report also suggested that nicotine release into the environment is negligible and that there is no indication that e-cigarette users are exposed to dangerous levels of toxic chemicals, such as aldehydes. A recently published cross-sectional survey involving 5863 adults who smoked concluded that continued abstinence was more likely for those using e-cigarettes than for those who bought over-the-counter nicotine replacement therapy.12 In a later analysis, the same authors estimated that in 2015 e-cigarettes helped about 18 000 people to give up smoking in England, and suggested that these data justify use of these devices.13 There are also indications that the UK National Institute for Health and Care Excellence will soon endorse use of e-cigarettes as a smoking cessation aid.
No medicine is completely safe, and the decision on whether or not to use a medicine must balance the risks and the benefits. Although e-cigarettes are not classified as a medicine, similar principles should arguably be adopted when deciding on whether to support their use. This is the basis upon which Public Health England strongly supports the use of e-cigarettes, justifying this stance by highlighting the known negative health implications of smoked tobacco relative to the lesser risks of e-cigarettes. At present, e-cigarettes are largely unregulated, and there is little quality control over different components of e-cigarettes (the solvent, the additives such as flavour enhancers, or even the concentration of active ingredient). This lack of quality control is a valid cause for concern that needs to be addressed if e-cigarettes are to become an established part of the health care professional’s armamentarium. However, recent European guidance, effective from 2017, has introduced rules to ensure minimum safety standards for the safety and quality of e-cigarettes,14 thus removing some of the potential for harm. Guidance on the product information leaflet and restrictions on advertising are also included in the European document. Supporting the wider adoption of such standards and recommending only licensed products for smoking cessation should allow patients to experience the benefits of e-cigarettes while minimizing the risks.
In summary, a quality-controlled e-cigarette, used as part of a structured smoking cessation program, could provide an effective additional option for smokers for whom other approaches have failed.
Footnotes
Competing interests: None declared.
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