Document Detail

Revealing and addressing length bias and heterogeneous effects in frequency case-crossover studies.
MedLine Citation:
PMID:  15003964     Owner:  NLM     Status:  MEDLINE    
The case-crossover design is useful for assessing whether a recurrent exposure (e.g., drug) triggers an event (e.g., myocardial infarction), using only cases, when finding good controls is impractical. In the basic frequency design, the observed exposure odds among cases, during a period immediately before the event, are compared with the expected exposure odds, based on their usual frequency of past exposures. This is equivalent to comparing observed gap times between the event and the last exposure with the expected gap times based on the subjects' exposure experience under the null hypothesis of no exposure-event relation. Such a comparison reveals two problems in the usual-frequency analyses: 1) length bias that exists even under the null hypothesis; and 2) loss of efficiency when exposure effects do exist. The first problem arises because the event will more likely fall on a longer-than-average period between exposures, even under the null hypothesis, resulting in a systematic downward bias of risk ratios. The second problem arises from categorizing cases as exposed or unexposed and from not fully using the data on gap times between events and preceding exposures. A new method of analysis is presented that is free from length bias and that efficiently uses gap time data.
Ravi Varadhan; Constantine E Frangakis
Related Documents :
17092494 - Exposure and risk assessment of 1,3-butadiene in japan.
15895244 - Neurobehavioral science in hazard identification and risk assessment of neurotoxic agen...
12075684 - Absorption of strontium from the gastrointestinal tract into plasma in healthy human ad...
3329094 - Effects of time-variant exposure on toxic substance response.
14713054 - Statistical analysis of honeybee survival after chronic exposure to insecticides.
18365124 - Detection limit estimator for multivariate calibration by an extension of the iupac rec...
Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.    
Journal Detail:
Title:  American journal of epidemiology     Volume:  159     ISSN:  0002-9262     ISO Abbreviation:  Am. J. Epidemiol.     Publication Date:  2004 Mar 
Date Detail:
Created Date:  2004-03-08     Completed Date:  2004-04-09     Revised Date:  2007-11-14    
Medline Journal Info:
Nlm Unique ID:  7910653     Medline TA:  Am J Epidemiol     Country:  United States    
Other Details:
Languages:  eng     Pagination:  596-602     Citation Subset:  IM    
Department of Biostatistics, Johns Hopkins Bloomberg School of Public Health, 615 North Wolfe Street, Baltimore, MD 21205, USA.
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Bias (Epidemiology)*
Cross-Over Studies*
Epidemiologic Methods
Likelihood Functions
Models, Statistical
Stochastic Processes
Grant Support
EY 014314-01/EY/NEI NIH HHS

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine

Previous Document:  Metacarpal cortical area and risk of coronary heart disease: the Framingham Study.
Next Document:  Comparison of the missing-indicator method and conditional logistic regression in 1:m matched case-c...