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Tobacco and Public Health - TCSC Indonesia

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it seems likely that some of this variation may have arisen from including in the control<br />

series patients hospitalized for diseases that later proved to be smoking-attributable.<br />

In any case, epidemiologists agreed that sound evidence was essential, given the high<br />

prevalence of smoking <strong>and</strong> the social <strong>and</strong> economic implications of the results.<br />

The need for cohort studies<br />

Doll <strong>and</strong> Hill realized that the simplest way to attempt to replicate the findings of the<br />

case-control studies, using a different methodology, was to obtain information on the<br />

individual smoking habits of a large number of people, <strong>and</strong> to follow them to determine<br />

whether an individual’s smoking habits predicted the risk of developing disease<br />

(Doll 1998b). Such cohort studies would need to be large so that they could provide a<br />

sufficient number of events to be informative within a reasonable time period. They<br />

would need to collect questionnaire information on smoking behavior, since such<br />

information was not then (<strong>and</strong> is not now) routinely collected on vital statistics<br />

records. In turn, the cohort studies would provide several important advantages over<br />

case-control studies. They could examine the relationship between smoking <strong>and</strong> many<br />

different end points, not just a single disease. This was important, because more than<br />

70 per cent of deaths caused by smoking result from diseases other than lung cancer<br />

(CDC 2002). The comparison group in cohort studies could be defined as lifelong<br />

non-smokers, thus avoiding the problem of including patients with other smokingattributable<br />

diseases in the control group. Finally, cohort studies are intuitively more<br />

underst<strong>and</strong>able than case-control studies, because they reflect the desired temporal<br />

sequence in which exposure precedes disease.<br />

The earliest cohort studies<br />

MICHAEL J. THUN AND JANE HENLEY 21<br />

The two earliest cohort studies of tobacco use <strong>and</strong> mortality were the British Doctors<br />

Study, which began in the United Kingdom in 1951 (Doll <strong>and</strong> Hill 1954, 1956), <strong>and</strong> the<br />

Hammond Horn or Nine-State study, initiated by the American Cancer Society (ACS)<br />

in 1952 (Hammond 1953, 1954). Both of these were designed to facilitate enrollment<br />

<strong>and</strong> follow-up of large populations. For instance, the physicians who participated in<br />

the British Doctors Study were identified from the Medical Register of the United<br />

Kingdom <strong>and</strong> followed through the Registrars General, the British Medical Association,<br />

<strong>and</strong> the General Medical Council (Doll <strong>and</strong> Hill 1956). The information on clinical<br />

diagnoses <strong>and</strong> cause of death was thought to be more accurate for doctors than for the<br />

general population. Similarly, the extensive network of local volunteers for ACS provided<br />

an extraordinary human resource to enroll, <strong>and</strong> help to follow, large prospective<br />

epidemiological studies in the United States (Thun et al. 2000). Both the ACS cohorts<br />

<strong>and</strong> the British Doctors Study provided effective conduits for disseminating information<br />

about the adverse effects of tobacco use. <strong>Public</strong>ity about the studies caused many<br />

doctors in the United Kingdom <strong>and</strong> United States to stop smoking, well ahead of the<br />

general public.

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