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A comparison of alternative strategies for choosing control populations in observational studies

Various approaches have been used to select control groups in observational studies: (1) from within the intervention area; (2) from a convenience sample, or randomly chosen areas; (3) from areas matched on area-level characteristics; and (4) nationally. The consequences of the decision are rarely a...

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Autores principales: Steventon, Adam, Grieve, Richard, Sekhon, Jasjeet S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4565881/
https://www.ncbi.nlm.nih.gov/pubmed/26380564
http://dx.doi.org/10.1007/s10742-014-0135-8
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author Steventon, Adam
Grieve, Richard
Sekhon, Jasjeet S.
author_facet Steventon, Adam
Grieve, Richard
Sekhon, Jasjeet S.
author_sort Steventon, Adam
collection PubMed
description Various approaches have been used to select control groups in observational studies: (1) from within the intervention area; (2) from a convenience sample, or randomly chosen areas; (3) from areas matched on area-level characteristics; and (4) nationally. The consequences of the decision are rarely assessed but, as we show, it can have complex impacts on confounding at both the area and individual levels. We began by reanalyzing data collected for an evaluation of a rapid response service on rates of unplanned hospital admission. Balance on observed individual-level variables was better with external than local controls, after matching. Further, when important prognostic variables were omitted from the matching algorithm, imbalances on those variables were also minimized using external controls. Treatment effects varied markedly depending on the choice of control area, but in the case study the variation was minimal after adjusting for the characteristics of areas. We used simulations to assess relative bias and means-squared error, as this could not be done in the case study. A particular feature of the simulations was unexplained variation in the outcome between areas. We found that the likely impact of unexplained variation for hospital admissions dwarfed the benefits of better balance on individual-level variables, leading us to prefer local controls in this instance. In other scenarios, in which there was less unexplained variation in the outcome between areas, bias and mean-squared error were optimized using external controls. We identify some general considerations relevant to the choice of control population in observational studies. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s10742-014-0135-8) contains supplementary material, which is available to authorized users.
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spelling pubmed-45658812015-09-15 A comparison of alternative strategies for choosing control populations in observational studies Steventon, Adam Grieve, Richard Sekhon, Jasjeet S. Health Serv Outcomes Res Methodol Article Various approaches have been used to select control groups in observational studies: (1) from within the intervention area; (2) from a convenience sample, or randomly chosen areas; (3) from areas matched on area-level characteristics; and (4) nationally. The consequences of the decision are rarely assessed but, as we show, it can have complex impacts on confounding at both the area and individual levels. We began by reanalyzing data collected for an evaluation of a rapid response service on rates of unplanned hospital admission. Balance on observed individual-level variables was better with external than local controls, after matching. Further, when important prognostic variables were omitted from the matching algorithm, imbalances on those variables were also minimized using external controls. Treatment effects varied markedly depending on the choice of control area, but in the case study the variation was minimal after adjusting for the characteristics of areas. We used simulations to assess relative bias and means-squared error, as this could not be done in the case study. A particular feature of the simulations was unexplained variation in the outcome between areas. We found that the likely impact of unexplained variation for hospital admissions dwarfed the benefits of better balance on individual-level variables, leading us to prefer local controls in this instance. In other scenarios, in which there was less unexplained variation in the outcome between areas, bias and mean-squared error were optimized using external controls. We identify some general considerations relevant to the choice of control population in observational studies. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s10742-014-0135-8) contains supplementary material, which is available to authorized users. Springer US 2015-01-30 2015 /pmc/articles/PMC4565881/ /pubmed/26380564 http://dx.doi.org/10.1007/s10742-014-0135-8 Text en © The Author(s) 2015 https://creativecommons.org/licenses/by/4.0/ Open AccessThis article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited.
spellingShingle Article
Steventon, Adam
Grieve, Richard
Sekhon, Jasjeet S.
A comparison of alternative strategies for choosing control populations in observational studies
title A comparison of alternative strategies for choosing control populations in observational studies
title_full A comparison of alternative strategies for choosing control populations in observational studies
title_fullStr A comparison of alternative strategies for choosing control populations in observational studies
title_full_unstemmed A comparison of alternative strategies for choosing control populations in observational studies
title_short A comparison of alternative strategies for choosing control populations in observational studies
title_sort comparison of alternative strategies for choosing control populations in observational studies
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4565881/
https://www.ncbi.nlm.nih.gov/pubmed/26380564
http://dx.doi.org/10.1007/s10742-014-0135-8
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