Control sampling strategies for case-crossover studies : an assessment of relative efficiency.

Author(s)
Mittleman, M.A. Maclure, M. & Robins, J.M.
Year
Abstract

The case-crossover study design is a method to assess the effect of transient exposures on the risk of onset of acute events. Control information for each case is based on his/her past exposure experience, and a self-matched analysis is conducted. Empiric evaluation of five approaches to the analysis of case-crossover data from a study of heavy physical exertion and acute myocardial infarction onset is shown. The data presented are from the Onset Study, a case-crossover study of the determinants of myocardial infarction onset conducted in 45 centres from August 1989 to October 1992. In model 1, exactly one control period (matched on clock-time) was sampled per case. in models 2-4, up to 25 control periods were sampled, and the effect of clock-time on the baseline hazard of infarction was modelled. In model 5, a census of the person-time experienced by each subject over the year preceding the infarction was sampled. The 95% confidence interval for model 1 was 2.7 times wider, and the relative efficiency, defined as P-1v" where v, represents the asymptotic variance estimate of the estimated log relative risk with M control periods sampled per case, was only about 14% of model 5. In models 2-4, the efficiency increased with the number of control periods, regardless of the modelling assumptions. Even with many control periods sampled, models 2-4 achieved only half the efficiency of model 5. The control sampling strategy in any given case-crossover study should be selected with the trade-offs between precision and potential biases of the estimates in mind. (A)

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Publication

Library number
972466 ST [electronic version only]
Source

American Journal of Epidemiology, Vol. 142 (1995), No. 1, p. 91-98, 14 ref.

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