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Long-term PM(2.5) exposure and sepsis mortality in a US medicare cohort

BACKGROUND: Risk factors contributing to sepsis-related mortality include clinical conditions such as cardiovascular disease, chronic lung disease, and diabetes, all of which have also been shown to be associated with air pollution exposure. However, the impact of chronic exposure to air pollution o...

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Autores principales: Honda, Trenton J., Kazemiparkouhi, Fatemeh, Henry, Trenton D., Suh, Helen H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9206363/
https://www.ncbi.nlm.nih.gov/pubmed/35717154
http://dx.doi.org/10.1186/s12889-022-13628-5
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author Honda, Trenton J.
Kazemiparkouhi, Fatemeh
Henry, Trenton D.
Suh, Helen H.
author_facet Honda, Trenton J.
Kazemiparkouhi, Fatemeh
Henry, Trenton D.
Suh, Helen H.
author_sort Honda, Trenton J.
collection PubMed
description BACKGROUND: Risk factors contributing to sepsis-related mortality include clinical conditions such as cardiovascular disease, chronic lung disease, and diabetes, all of which have also been shown to be associated with air pollution exposure. However, the impact of chronic exposure to air pollution on sepsis-related mortality has been little studied.  METHODS: In a cohort of 53 million Medicare beneficiaries (228,439 sepsis-related deaths) living across the conterminous United States between 2000 and 2008, we examined the association of long-term PM(2.5) exposure and sepsis-related mortality. For each Medicare beneficiary (ages 65–120), we estimated the 12-month moving average PM(2.5) concentration for the 12 month before death, for their ZIP code of residence using well validated GIS-based spatio-temporal models. Deaths were categorized as sepsis-related if they have ICD-10 codes for bacterial or other sepsis. We used Cox proportional hazard models to assess the association of long-term PM(2.5) exposure on sepsis-related mortality. Models included strata for age, sex, race, and ZIP code and controlled for neighborhood socio-economic status (SES). We also evaluated confounding through adjustment of neighborhood behavioral covariates. RESULTS: A 10 μg/m(3) increase in 12-month moving average PM(2.5) was associated with a 9.1% increased risk of sepsis mortality (95% CI: 3.6–14.9) in models adjusted for age, sex, race, ZIP code, and SES. HRs for PM(2.5) were higher and statistically significant for older (> 75), Black, and urban beneficiaries. In stratified analyses, null associations were found for younger beneficiaries (65–75), beneficiaries who lived in non-urban ZIP codes, and those residing in low-SES urban ZIP codes. CONCLUSIONS: Long-term PM(2.5) exposure is associated with elevated risks of sepsis-related mortality.
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spelling pubmed-92063632022-06-19 Long-term PM(2.5) exposure and sepsis mortality in a US medicare cohort Honda, Trenton J. Kazemiparkouhi, Fatemeh Henry, Trenton D. Suh, Helen H. BMC Public Health Research BACKGROUND: Risk factors contributing to sepsis-related mortality include clinical conditions such as cardiovascular disease, chronic lung disease, and diabetes, all of which have also been shown to be associated with air pollution exposure. However, the impact of chronic exposure to air pollution on sepsis-related mortality has been little studied.  METHODS: In a cohort of 53 million Medicare beneficiaries (228,439 sepsis-related deaths) living across the conterminous United States between 2000 and 2008, we examined the association of long-term PM(2.5) exposure and sepsis-related mortality. For each Medicare beneficiary (ages 65–120), we estimated the 12-month moving average PM(2.5) concentration for the 12 month before death, for their ZIP code of residence using well validated GIS-based spatio-temporal models. Deaths were categorized as sepsis-related if they have ICD-10 codes for bacterial or other sepsis. We used Cox proportional hazard models to assess the association of long-term PM(2.5) exposure on sepsis-related mortality. Models included strata for age, sex, race, and ZIP code and controlled for neighborhood socio-economic status (SES). We also evaluated confounding through adjustment of neighborhood behavioral covariates. RESULTS: A 10 μg/m(3) increase in 12-month moving average PM(2.5) was associated with a 9.1% increased risk of sepsis mortality (95% CI: 3.6–14.9) in models adjusted for age, sex, race, ZIP code, and SES. HRs for PM(2.5) were higher and statistically significant for older (> 75), Black, and urban beneficiaries. In stratified analyses, null associations were found for younger beneficiaries (65–75), beneficiaries who lived in non-urban ZIP codes, and those residing in low-SES urban ZIP codes. CONCLUSIONS: Long-term PM(2.5) exposure is associated with elevated risks of sepsis-related mortality. BioMed Central 2022-06-18 /pmc/articles/PMC9206363/ /pubmed/35717154 http://dx.doi.org/10.1186/s12889-022-13628-5 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://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
Honda, Trenton J.
Kazemiparkouhi, Fatemeh
Henry, Trenton D.
Suh, Helen H.
Long-term PM(2.5) exposure and sepsis mortality in a US medicare cohort
title Long-term PM(2.5) exposure and sepsis mortality in a US medicare cohort
title_full Long-term PM(2.5) exposure and sepsis mortality in a US medicare cohort
title_fullStr Long-term PM(2.5) exposure and sepsis mortality in a US medicare cohort
title_full_unstemmed Long-term PM(2.5) exposure and sepsis mortality in a US medicare cohort
title_short Long-term PM(2.5) exposure and sepsis mortality in a US medicare cohort
title_sort long-term pm(2.5) exposure and sepsis mortality in a us medicare cohort
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9206363/
https://www.ncbi.nlm.nih.gov/pubmed/35717154
http://dx.doi.org/10.1186/s12889-022-13628-5
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