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Midlife mortality in White non-Hispanic male veterans enrolled in Department of Veterans Affairs primary care, 2003–2014

BACKGROUND: After years of decline in mortality rates in the United States, there have been increases in mortality rates in White non-Hispanic Americans ages 45–54, due to increases in deaths from suicide, poisoning, and alcoholic liver disease. OBJECTIVES: To determine whether White non-Hispanic mi...

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Autores principales: Liu, Chuan-Fen, Hebert, Paul, Wong, Edwin S., Nelson, Karin, Maynard, Charles
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7002889/
https://www.ncbi.nlm.nih.gov/pubmed/32051882
http://dx.doi.org/10.1016/j.heliyon.2020.e03328
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author Liu, Chuan-Fen
Hebert, Paul
Wong, Edwin S.
Nelson, Karin
Maynard, Charles
author_facet Liu, Chuan-Fen
Hebert, Paul
Wong, Edwin S.
Nelson, Karin
Maynard, Charles
author_sort Liu, Chuan-Fen
collection PubMed
description BACKGROUND: After years of decline in mortality rates in the United States, there have been increases in mortality rates in White non-Hispanic Americans ages 45–54, due to increases in deaths from suicide, poisoning, and alcoholic liver disease. OBJECTIVES: To determine whether White non-Hispanic middle age male Veterans enrolled in Department of Veterans Affairs (VA) primary care had increased mortality, as found in the general population. RESEARCH DESIGN: Repeated cross-sectional analysis over 12 years to describe trends in death rates for men across 3 race/ethnicity groups (White non-Hispanic, Black non-Hispanic, Hispanic) and 2 age groups (45–54, 55–64) for the Veteran and general US male populations. SUBJECTS: 60 million patient-years for Veterans enrolled in VA primary care from 2003 to 2014 and 1.8 million who died during the study period. MEASURES: All-cause and cause specific death rates for alcoholic liver disease, poisoning, and suicide. RESULTS: For White non-Hispanic male Veterans ages 55–64, the increase in all-cause mortality from 2003 to 2014 (+309 deaths/100,000) was accompanied by significant changes in deaths due to poisoning (+30/100,000), alcoholic liver disease (+23/100,000), and suicide (+17/100,000). For US men ages 55–64, all-cause mortality decreased slightly from 2003-2014 (-22 deaths/100,000). However, there were increases in death rates due to poisoning (+17/100,000), alcoholic liver disease (+14/100,000) and suicide (+11/100,000). CONCLUSIONS: These disturbing findings for White non-Hispanic Veteran men ages 55–64 suggest the critical importance of suicide prevention programs as well as the importance of high quality integrated health care for both Veteran and non-Veteran men.
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spelling pubmed-70028892020-02-12 Midlife mortality in White non-Hispanic male veterans enrolled in Department of Veterans Affairs primary care, 2003–2014 Liu, Chuan-Fen Hebert, Paul Wong, Edwin S. Nelson, Karin Maynard, Charles Heliyon Article BACKGROUND: After years of decline in mortality rates in the United States, there have been increases in mortality rates in White non-Hispanic Americans ages 45–54, due to increases in deaths from suicide, poisoning, and alcoholic liver disease. OBJECTIVES: To determine whether White non-Hispanic middle age male Veterans enrolled in Department of Veterans Affairs (VA) primary care had increased mortality, as found in the general population. RESEARCH DESIGN: Repeated cross-sectional analysis over 12 years to describe trends in death rates for men across 3 race/ethnicity groups (White non-Hispanic, Black non-Hispanic, Hispanic) and 2 age groups (45–54, 55–64) for the Veteran and general US male populations. SUBJECTS: 60 million patient-years for Veterans enrolled in VA primary care from 2003 to 2014 and 1.8 million who died during the study period. MEASURES: All-cause and cause specific death rates for alcoholic liver disease, poisoning, and suicide. RESULTS: For White non-Hispanic male Veterans ages 55–64, the increase in all-cause mortality from 2003 to 2014 (+309 deaths/100,000) was accompanied by significant changes in deaths due to poisoning (+30/100,000), alcoholic liver disease (+23/100,000), and suicide (+17/100,000). For US men ages 55–64, all-cause mortality decreased slightly from 2003-2014 (-22 deaths/100,000). However, there were increases in death rates due to poisoning (+17/100,000), alcoholic liver disease (+14/100,000) and suicide (+11/100,000). CONCLUSIONS: These disturbing findings for White non-Hispanic Veteran men ages 55–64 suggest the critical importance of suicide prevention programs as well as the importance of high quality integrated health care for both Veteran and non-Veteran men. Elsevier 2020-01-31 /pmc/articles/PMC7002889/ /pubmed/32051882 http://dx.doi.org/10.1016/j.heliyon.2020.e03328 Text en © 2020 Published by Elsevier Ltd. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Liu, Chuan-Fen
Hebert, Paul
Wong, Edwin S.
Nelson, Karin
Maynard, Charles
Midlife mortality in White non-Hispanic male veterans enrolled in Department of Veterans Affairs primary care, 2003–2014
title Midlife mortality in White non-Hispanic male veterans enrolled in Department of Veterans Affairs primary care, 2003–2014
title_full Midlife mortality in White non-Hispanic male veterans enrolled in Department of Veterans Affairs primary care, 2003–2014
title_fullStr Midlife mortality in White non-Hispanic male veterans enrolled in Department of Veterans Affairs primary care, 2003–2014
title_full_unstemmed Midlife mortality in White non-Hispanic male veterans enrolled in Department of Veterans Affairs primary care, 2003–2014
title_short Midlife mortality in White non-Hispanic male veterans enrolled in Department of Veterans Affairs primary care, 2003–2014
title_sort midlife mortality in white non-hispanic male veterans enrolled in department of veterans affairs primary care, 2003–2014
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7002889/
https://www.ncbi.nlm.nih.gov/pubmed/32051882
http://dx.doi.org/10.1016/j.heliyon.2020.e03328
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