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Fine Particulate Matter and Respiratory Healthcare Encounters among Survivors of Childhood Cancers

Some chemotherapies that treat childhood cancers have pulmonary-toxic properties that increase risk for adverse respiratory-health outcomes. PM(2.5) causes similar outcomes but its effect among pulmonary compromised cancer survivors is unknown. This case-crossover study identified the PM(2.5)-associ...

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Autores principales: Ou, Judy Y., Hanson, Heidi A., Ramsay, Joemy M., Leiser, Claire L., Zhang, Yue, VanDerslice, James A., Pope, C. Arden, Kirchhoff, Anne C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6466161/
https://www.ncbi.nlm.nih.gov/pubmed/30917578
http://dx.doi.org/10.3390/ijerph16061081
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author Ou, Judy Y.
Hanson, Heidi A.
Ramsay, Joemy M.
Leiser, Claire L.
Zhang, Yue
VanDerslice, James A.
Pope, C. Arden
Kirchhoff, Anne C.
author_facet Ou, Judy Y.
Hanson, Heidi A.
Ramsay, Joemy M.
Leiser, Claire L.
Zhang, Yue
VanDerslice, James A.
Pope, C. Arden
Kirchhoff, Anne C.
author_sort Ou, Judy Y.
collection PubMed
description Some chemotherapies that treat childhood cancers have pulmonary-toxic properties that increase risk for adverse respiratory-health outcomes. PM(2.5) causes similar outcomes but its effect among pulmonary compromised cancer survivors is unknown. This case-crossover study identified the PM(2.5)-associated odds for primary-respiratory hospitalizations and emergency department visits among childhood cancer survivors in Utah. We compared risk among chemotherapy-treated survivors to a cancer-free sample. We calculated 3-day-average PM(2.5) by ZIP code and county for event and control days. Conditional logistic regression estimated odds ratios. Models were stratified by cause of admission (infection, respiratory disease, asthma), previous chemotherapy, National Ambient Air Quality Standard (NAAQS), and other variables. Results are presented per 10 µg/m(3) of PM(2.5). 90% of events occurred at 3-day PM(2.5) averages <35.4 µg/m(3), the NAAQS 24-h standard. For survivors, PM(2.5) was associated with respiratory hospitalizations (OR = 1.84, 95% CI = 1.13–3.00) and hospitalizations from respiratory infection (OR = 2.09, 95% CI = 1.06–4.14). Among chemotherapy-treated survivors, the PM(2.5)-associated odds of respiratory hospitalization (OR = 2.03, 95% CI = 1.14–3.61) were significantly higher than the cancer-free sample (OR = 0.84, 95% CI = 0.57–1.25). This is the first study to report significant associations between PM(2.5) and respiratory healthcare encounters in childhood cancer survivors. Chemotherapy-treated survivors displayed the highest odds of hospitalization due to PM(2.5) exposure and their risk is significantly higher than a cancer-free sample.
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spelling pubmed-64661612019-04-22 Fine Particulate Matter and Respiratory Healthcare Encounters among Survivors of Childhood Cancers Ou, Judy Y. Hanson, Heidi A. Ramsay, Joemy M. Leiser, Claire L. Zhang, Yue VanDerslice, James A. Pope, C. Arden Kirchhoff, Anne C. Int J Environ Res Public Health Article Some chemotherapies that treat childhood cancers have pulmonary-toxic properties that increase risk for adverse respiratory-health outcomes. PM(2.5) causes similar outcomes but its effect among pulmonary compromised cancer survivors is unknown. This case-crossover study identified the PM(2.5)-associated odds for primary-respiratory hospitalizations and emergency department visits among childhood cancer survivors in Utah. We compared risk among chemotherapy-treated survivors to a cancer-free sample. We calculated 3-day-average PM(2.5) by ZIP code and county for event and control days. Conditional logistic regression estimated odds ratios. Models were stratified by cause of admission (infection, respiratory disease, asthma), previous chemotherapy, National Ambient Air Quality Standard (NAAQS), and other variables. Results are presented per 10 µg/m(3) of PM(2.5). 90% of events occurred at 3-day PM(2.5) averages <35.4 µg/m(3), the NAAQS 24-h standard. For survivors, PM(2.5) was associated with respiratory hospitalizations (OR = 1.84, 95% CI = 1.13–3.00) and hospitalizations from respiratory infection (OR = 2.09, 95% CI = 1.06–4.14). Among chemotherapy-treated survivors, the PM(2.5)-associated odds of respiratory hospitalization (OR = 2.03, 95% CI = 1.14–3.61) were significantly higher than the cancer-free sample (OR = 0.84, 95% CI = 0.57–1.25). This is the first study to report significant associations between PM(2.5) and respiratory healthcare encounters in childhood cancer survivors. Chemotherapy-treated survivors displayed the highest odds of hospitalization due to PM(2.5) exposure and their risk is significantly higher than a cancer-free sample. MDPI 2019-03-26 2019-03 /pmc/articles/PMC6466161/ /pubmed/30917578 http://dx.doi.org/10.3390/ijerph16061081 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Ou, Judy Y.
Hanson, Heidi A.
Ramsay, Joemy M.
Leiser, Claire L.
Zhang, Yue
VanDerslice, James A.
Pope, C. Arden
Kirchhoff, Anne C.
Fine Particulate Matter and Respiratory Healthcare Encounters among Survivors of Childhood Cancers
title Fine Particulate Matter and Respiratory Healthcare Encounters among Survivors of Childhood Cancers
title_full Fine Particulate Matter and Respiratory Healthcare Encounters among Survivors of Childhood Cancers
title_fullStr Fine Particulate Matter and Respiratory Healthcare Encounters among Survivors of Childhood Cancers
title_full_unstemmed Fine Particulate Matter and Respiratory Healthcare Encounters among Survivors of Childhood Cancers
title_short Fine Particulate Matter and Respiratory Healthcare Encounters among Survivors of Childhood Cancers
title_sort fine particulate matter and respiratory healthcare encounters among survivors of childhood cancers
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6466161/
https://www.ncbi.nlm.nih.gov/pubmed/30917578
http://dx.doi.org/10.3390/ijerph16061081
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