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J Clin Epidemiol. 2012 Apr;65(4):384-93. doi: 10.1016/j.jclinepi.2011.09.004. Epub 2011 Dec 23.

Within-person study designs had lower precision and greater susceptibility to bias because of trends in exposure than cohort and nested case-control designs.

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  • 1Department of Primary Care and Public Health Sciences, King's College London, 42 Weston Street, London, United Kingdom. jennifer.nicholas@kcl.ac.uk

Abstract

OBJECTIVE:

To compare precision and apparent bias between cohort, nested case-control, self-controlled case series, case-crossover, and case-time-control study designs.

STUDY DESIGN AND SETTING:

Study designs were implemented to evaluate the association between thiazolidinediones (TZDs) and heart failure, TZDs and fracture, and liver enzyme-inducing anticonvulsants and fracture.

RESULTS:

Effect estimates were similar for the cohort and case-control study; for the association between TZDs and fracture in women, the hazard ratio was 1.36 (1.18, 1.56) and odds ratio (OR) was 1.44 (1.21, 1.70). For this clinical example, the self-controlled case series gave upward bias when follow-up was censored at the outcome (incidence rate ratio [IRR], 7.08; 4.96, 10.09) but was otherwise unbiased (IRR, 1.41; 1.14, 1.75). The retrospective case-crossover OR was 3.24 (2.18, 4.80), which was reduced by either bidirectional sampling (OR, 1.20; 0.98, 1.46) or with the case-time-control design (OR, 1.40; 1.09, 1.81). Findings on apparent bias were similar for the other two clinical examples. In each clinical example, within-person designs had considerably lower precision than the cohort or case-control study designs.

CONCLUSION:

When long-term exposures are analyzed, within-person study designs may have lower precision and greater susceptibility to bias. Bias may be reduced by sampling follow-up both before and after the outcome or with the case-time-control study design.

Copyright © 2012 Elsevier Inc. All rights reserved.

PMID:
22197519
[PubMed - indexed for MEDLINE]
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