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Propensity score matching for multilevel spatial data: accounting for geographic confounding in health disparity studies

BACKGROUND: Diabetes is a public health burden that disproportionately affects military veterans and racial minorities. Studies of racial disparities are inherently observational, and thus may require the use of methods such as Propensity Score Analysis (PSA). While traditional PSA accounts for pati...

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Autores principales: Davis, Melanie L., Neelon, Brian, Nietert, Paul J., Burgette, Lane F., Hunt, Kelly J., Lawson, Andrew B., Egede, Leonard E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7913404/
https://www.ncbi.nlm.nih.gov/pubmed/33639940
http://dx.doi.org/10.1186/s12942-021-00265-1
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author Davis, Melanie L.
Neelon, Brian
Nietert, Paul J.
Burgette, Lane F.
Hunt, Kelly J.
Lawson, Andrew B.
Egede, Leonard E.
author_facet Davis, Melanie L.
Neelon, Brian
Nietert, Paul J.
Burgette, Lane F.
Hunt, Kelly J.
Lawson, Andrew B.
Egede, Leonard E.
author_sort Davis, Melanie L.
collection PubMed
description BACKGROUND: Diabetes is a public health burden that disproportionately affects military veterans and racial minorities. Studies of racial disparities are inherently observational, and thus may require the use of methods such as Propensity Score Analysis (PSA). While traditional PSA accounts for patient-level factors, this may not be sufficient when patients are clustered at the geographic level and thus important confounders, whether observed or unobserved, vary by geographic location. METHODS: We employ a spatial propensity score matching method to account for “geographic confounding”, which occurs when the confounding factors, whether observed or unobserved, vary by geographic region. We augment the propensity score and outcome models with spatial random effects, which are assigned scaled Besag-York-Mollié priors to address spatial clustering and improve inferences by borrowing information across neighboring geographic regions. We apply this approach to a study exploring racial disparities in diabetes specialty care between non-Hispanic black and non-Hispanic white veterans. We construct multiple global estimates of the risk difference in diabetes care: a crude unadjusted estimate, an estimate based solely on patient-level matching, and an estimate that incorporates both patient and spatial information. RESULTS: In simulation we show that in the presence of an unmeasured geographic confounder, ignoring spatial heterogeneity results in increased relative bias and mean squared error, whereas incorporating spatial random effects improves inferences. In our study of racial disparities in diabetes specialty care, the crude unadjusted estimate suggests that specialty care is more prevalent among non-Hispanic blacks, while patient-level matching indicates that it is less prevalent. Hierarchical spatial matching supports the latter conclusion, with a further increase in the magnitude of the disparity. CONCLUSIONS: These results highlight the importance of accounting for spatial heterogeneity in propensity score analysis, and suggest the need for clinical care and management strategies that are culturally sensitive and racially inclusive.
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spelling pubmed-79134042021-03-02 Propensity score matching for multilevel spatial data: accounting for geographic confounding in health disparity studies Davis, Melanie L. Neelon, Brian Nietert, Paul J. Burgette, Lane F. Hunt, Kelly J. Lawson, Andrew B. Egede, Leonard E. Int J Health Geogr Research BACKGROUND: Diabetes is a public health burden that disproportionately affects military veterans and racial minorities. Studies of racial disparities are inherently observational, and thus may require the use of methods such as Propensity Score Analysis (PSA). While traditional PSA accounts for patient-level factors, this may not be sufficient when patients are clustered at the geographic level and thus important confounders, whether observed or unobserved, vary by geographic location. METHODS: We employ a spatial propensity score matching method to account for “geographic confounding”, which occurs when the confounding factors, whether observed or unobserved, vary by geographic region. We augment the propensity score and outcome models with spatial random effects, which are assigned scaled Besag-York-Mollié priors to address spatial clustering and improve inferences by borrowing information across neighboring geographic regions. We apply this approach to a study exploring racial disparities in diabetes specialty care between non-Hispanic black and non-Hispanic white veterans. We construct multiple global estimates of the risk difference in diabetes care: a crude unadjusted estimate, an estimate based solely on patient-level matching, and an estimate that incorporates both patient and spatial information. RESULTS: In simulation we show that in the presence of an unmeasured geographic confounder, ignoring spatial heterogeneity results in increased relative bias and mean squared error, whereas incorporating spatial random effects improves inferences. In our study of racial disparities in diabetes specialty care, the crude unadjusted estimate suggests that specialty care is more prevalent among non-Hispanic blacks, while patient-level matching indicates that it is less prevalent. Hierarchical spatial matching supports the latter conclusion, with a further increase in the magnitude of the disparity. CONCLUSIONS: These results highlight the importance of accounting for spatial heterogeneity in propensity score analysis, and suggest the need for clinical care and management strategies that are culturally sensitive and racially inclusive. BioMed Central 2021-02-27 /pmc/articles/PMC7913404/ /pubmed/33639940 http://dx.doi.org/10.1186/s12942-021-00265-1 Text en © The Author(s) 2021 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Davis, Melanie L.
Neelon, Brian
Nietert, Paul J.
Burgette, Lane F.
Hunt, Kelly J.
Lawson, Andrew B.
Egede, Leonard E.
Propensity score matching for multilevel spatial data: accounting for geographic confounding in health disparity studies
title Propensity score matching for multilevel spatial data: accounting for geographic confounding in health disparity studies
title_full Propensity score matching for multilevel spatial data: accounting for geographic confounding in health disparity studies
title_fullStr Propensity score matching for multilevel spatial data: accounting for geographic confounding in health disparity studies
title_full_unstemmed Propensity score matching for multilevel spatial data: accounting for geographic confounding in health disparity studies
title_short Propensity score matching for multilevel spatial data: accounting for geographic confounding in health disparity studies
title_sort propensity score matching for multilevel spatial data: accounting for geographic confounding in health disparity studies
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7913404/
https://www.ncbi.nlm.nih.gov/pubmed/33639940
http://dx.doi.org/10.1186/s12942-021-00265-1
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