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Methods for Observed-Cluster Inference When Cluster Size Is Informative: A Review and Clarifications
Clustered data commonly arise in epidemiology. We assume each cluster member has an outcome Y and covariates [Image: see text]. When there are missing data in Y, the distribution of Y given [Image: see text] in all cluster members (“complete clusters”) may be different from the distribution just in...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Blackwell Publishing Ltd
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4312901/ https://www.ncbi.nlm.nih.gov/pubmed/24479899 http://dx.doi.org/10.1111/biom.12151 |
Sumario: | Clustered data commonly arise in epidemiology. We assume each cluster member has an outcome Y and covariates [Image: see text]. When there are missing data in Y, the distribution of Y given [Image: see text] in all cluster members (“complete clusters”) may be different from the distribution just in members with observed Y (“observed clusters”). Often the former is of interest, but when data are missing because in a fundamental sense Y does not exist (e.g., quality of life for a person who has died), the latter may be more meaningful (quality of life conditional on being alive). Weighted and doubly weighted generalized estimating equations and shared random-effects models have been proposed for observed-cluster inference when cluster size is informative, that is, the distribution of Y given [Image: see text] in observed clusters depends on observed cluster size. We show these methods can be seen as actually giving inference for complete clusters and may not also give observed-cluster inference. This is true even if observed clusters are complete in themselves rather than being the observed part of larger complete clusters: here methods may describe imaginary complete clusters rather than the observed clusters. We show under which conditions shared random-effects models proposed for observed-cluster inference do actually describe members with observed Y. A psoriatic arthritis dataset is used to illustrate the danger of misinterpreting estimates from shared random-effects models. |
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