(Circulation. 2007;115:2340-2343.)
© 2007 American Heart Association, Inc.
Statistical Primer for Cardiovascular Research |
From the Department of Biostatistical Sciences, Wake Forest University School of Medicine, Winston-Salem, NC.
Correspondence to Dr Ralph B. DAgostino, Jr, Department of Biostatistical Sciences, Medical Center Boulevard, Wake Forest University School of Medicine, Winston-Salem, NC 27157. E-mail rdagosti@wfubmc.edu
Key Words: cardiovascular diseases epidemiology risk factors statistics
An extract of the first 250 words of the full text is provided, because this article has no abstract. |
| Introduction |
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Large-scale epidemiological cohort studies such as the Multi-Ethnic Study of Atherosclerosis (MESA)2 are designed to follow a large sample of participants over time without active administration of any interventions. Within MESA, lack of randomization can complicate potential treatment comparisons such as the impact of ß-blocker versus angiotensin-converting enzyme inhibitor usage. Nonrandomized comparisons may also arise from within a randomized clinical trial. For instance, the Clopidogrel as Adjunctive Reperfusion Therapy - Thrombolysis in Myocardial Infarction 28 (CLARITY-TIMI 28) trial3 is a randomized study that compares clopidogrel with placebo in 3491 ST-elevation myocardial infarction patients aged 18 to 75 years who have undergone fibrinolysis. In addition to the primary end points, investigators wished to compare the effects of low molecular weight heparin with unfractionated heparin on angiographic and clinical outcomes in participants.4 These treatments were not randomly assigned.
In studies such as these, the treatment groups may markedly differ with respect to the observed pretreatment covariates measured on participants. These differences could lead to biased estimates of treatment effects. The propensity score for an individual, defined as the conditional probability of being treated given the individuals covariates, can be used to balance the covariates in the 2 groups
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