Abstract
The benefits of preventing smoking onset are well known, and even just delaying smoking onset conveys benefits. Tobacco control policies are of critical importance to low-income countries with high smoking rates such as Vietnam where smoking prevalence is greater than 55 % in young men between the ages of 25 and 45. Using a survey of teens and young adults, I conducted duration analyses to explore the impact of tobacco price on smoking onset. The results suggest that tobacco prices in Vietnam have a statistically significant and fairly substantial effect on the onset of smoking. Increases in average tobacco prices, measured by an index of tobacco prices and by the prices of two popular brands, are found to delay smoking onset. Of particular interest is the finding that Vietnamese youth are more sensitive to changes in prices of a popular international brand that has had favourable tax treatment since the late 1990s.
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Notes
Such an assumption is reasonable when mortality is the outcome under study but is problematic when smoking onset is the outcome being modelled because large proportion of individuals never start smoking. López Nicolás [19] and Kidd and Hopkins [20] compare models that relax the assumption that each individual will eventually fail with standard duration models (i.e. split and non-split population models) and find vastly different effects. Split population duration models are also known as mixture models or cure models and have a long history in the biostatistical literature. See for example, Boag [21] and Berkson and Gage [22].
Several studies include price as a time-invariant covariate. Treating price as a time-variant variable is conceptually more intuitive as the decision whether or not to start smoking is an on-going decision, made on the basis of current information [24].
Until the late 2000s, Vietnam was categorised as a low-income economy by the World Bank. It is now categorised as a lower-middle-income economy.
In 2003, Vietnam had 61 provinces; in 2012, Vietnam had 63 provinces.
I use Stata’s pgmhaz8 and spsurv routine developed by Stephen Jenkins. spsurv does not allow the inclusion of covariates in the participation component of the model.
I also attempt to estimate province-FE continuous-time split population log-logistic duration models with cloglog, logit and probit links. These models, however, do not converge.
Duration models presented in accelerated time format can be interpreted as regression equations for ln(failure time) [18]. Note that elasticities are likely not comparable across studies as different ‘time origins are used. For example, Forster and Jones [18] and López Nicolás [19] assume individuals are first exposed to the risk of starting at age 0, Etilé and Jones [38], Kidd and Hopkins [20] and Madden [26] at age 10 and Douglas [24] at age 11.
As the data utilised do not allow one to disentangle peer influence from peer selection, these results should be interpreted with caution; peer selection may be more important than peer influence [70]. Moreover, the measure of peer influence is time invariant and reflects peer behaviour in 2003/2004.
One disadvantage of this approach is that it is not possible include covariates in the participation component of the model.
It is worth noting that examining plots based on the Cox-Snell residuals to assess model fit has limitations. Collett [71] argues that in practice a straight line plot is often obtained even when the model fitted is known to be incorrect.
Waterpipe tobacco is not subject to taxation in Vietnam. Much of the tobacco consumed in this form is home-produced, which renders tax collection difficult.
See Peng and Zhang [77] for a more detailed discussion of the identifiability of the split population model.
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Acknowledgments
Financial support from the Social Sciences and Humanities Research Council of Canada, the McMaster University Centre for Health Economics and Policy Analysis and the Bloomberg Philanthropies is acknowledged. I thank Jeremiah Hurley, Michael Boyle, Michel Grignon, Joy de Beyer, Jinhu Li, Noori Akhtar-Danesh, Myra Yazbeck and Willard Manning for helpful comments and/or discussions. I am indebted to Martin Forster and Andrew Jones for providing public access to their Stata codes.
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Appendix: The split population duration model
Appendix: The split population duration model
Following the notation of Schmidt and Witte [79, 80], let F be an unobservable variable indicating whether an individual i would or would not eventually start smoking (i.e. fail). Formally:
Let g(t\F = 1) and G(t\F = 1) be the conditional density of survival times and its corresponding cumulative distribution function for individuals who eventually fail. Let T be the length of the follow-up period (i.e. T i indicates censoring time). Let R be an observable indicator so that Ri = 1 if there is failure by time T and Ri = 0 if not. For the starters (R i = 1), the unconditional density is:
For the nonstarters (R i = 0), the unconditional density is:
Combining the two unconditional densities yields the following likelihood function:
The contribution of individual i to the log-likelihood function is:
The probability δ i is typically modelled as a logit or a probit but can also be modelled as a complementary log–log (cloglog). Unlike probit or logit for which the response curve is symmetric about δ i = 0.5, the cloglog model has a response curve that is asymmetric [23]. Formally [23]:
where z i is a vector of time invariant covariates, \( \Upphi \) is the cumulative density function for the standard normal distribution, and α is a parameter vector. When δi = 1 for all individuals, the split population duration model reduces to a standard duration model.
Both theory and data indicate that the hazard rate first increases and then decreases, which rules out exponential and Weibull duration models. Log-logistic and lognormal models are typically used. Formally, the probability density function g(t/F = 1) and the survival function G(t/F = 1) for the log-logistic distributions are [23]:
where ρ is a shape parameter, \( \lambda = e^{ - \beta 'X} \), Xi is a vector of time invariant and time variant covariates, and β is a parameter vector.
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Guindon, G.E. The impact of tobacco prices on smoking onset in Vietnam: duration analyses of retrospective data. Eur J Health Econ 15, 19–39 (2014). https://doi.org/10.1007/s10198-012-0444-1
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DOI: https://doi.org/10.1007/s10198-012-0444-1