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Assessing the effect of blood type on death and a novel scoring system to assess clinical course in patients with COVID-19
BACKGROUND: Coronavirus disease (COVID-19) continues to lead to worldwide morbidity and mortality. This study examined the association between blood type and clinical outcomes in patients with COVID-19 measured by a calculated morbidity score and mortality rates. The secondary aim was to investigate...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Southern Society for Clinical Investigation. Published by Elsevier Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8720494/ https://www.ncbi.nlm.nih.gov/pubmed/34986364 http://dx.doi.org/10.1016/j.amjms.2021.12.006 |
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author | Thomas, Katharine E. Karamanis, Amber Dauchy, Erin Chapple, Andrew G. Loch, Michelle M. |
author_facet | Thomas, Katharine E. Karamanis, Amber Dauchy, Erin Chapple, Andrew G. Loch, Michelle M. |
author_sort | Thomas, Katharine E. |
collection | PubMed |
description | BACKGROUND: Coronavirus disease (COVID-19) continues to lead to worldwide morbidity and mortality. This study examined the association between blood type and clinical outcomes in patients with COVID-19 measured by a calculated morbidity score and mortality rates. The secondary aim was to investigate the relationship between patient characteristics and COVID-19 associated clinical outcomes and mortality. METHODS: Logistic regression was used to determine what factors were associated with death. A total morbidity score was constructed based on overall patient's COVID-19 clinical course. This score was modeled using Quasi-Poisson regression. Bayesian variable selection was used for the logistic regression to obtain a posterior probability that blood type is important in predicting worsened clinical outcomes and death. RESULTS: Neither blood type nor Rh+ status was a significant moderator of death or morbidity score in regression analyses. Increased age (adjusted Odds Ratio=3.37, 95% CI=2.44–4.67), male gender (aOR=1.35, 95% CI=1.08-1.69), and number of comorbid conditions (aOR=1.28, 95% CI=1.01-1.63) were significantly associated with death. Significant factors in predicting total morbidity score were age (adjusted Multiplicative Effect=1.45; 95% CI=1.349-1.555) and gender (aME=1.17; 95% CI=1.109-1.243). The posterior probability that blood type influenced death was only 10%. CONCLUSIONS: There is strong evidence that blood type was not a significant predictor of clinical course or death in patients hospitalized with COVID-19. Older age and male gender led to worse clinical outcomes and higher rates of death; older age, male gender, and comorbidities predicted a worse clinical course and higher morbidity score. Race was not a significant predictor of death in our population and was associated with an increased, albeit not significant, morbidity score. |
format | Online Article Text |
id | pubmed-8720494 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Southern Society for Clinical Investigation. Published by Elsevier Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-87204942022-01-03 Assessing the effect of blood type on death and a novel scoring system to assess clinical course in patients with COVID-19 Thomas, Katharine E. Karamanis, Amber Dauchy, Erin Chapple, Andrew G. Loch, Michelle M. Am J Med Sci Clinical Investigation BACKGROUND: Coronavirus disease (COVID-19) continues to lead to worldwide morbidity and mortality. This study examined the association between blood type and clinical outcomes in patients with COVID-19 measured by a calculated morbidity score and mortality rates. The secondary aim was to investigate the relationship between patient characteristics and COVID-19 associated clinical outcomes and mortality. METHODS: Logistic regression was used to determine what factors were associated with death. A total morbidity score was constructed based on overall patient's COVID-19 clinical course. This score was modeled using Quasi-Poisson regression. Bayesian variable selection was used for the logistic regression to obtain a posterior probability that blood type is important in predicting worsened clinical outcomes and death. RESULTS: Neither blood type nor Rh+ status was a significant moderator of death or morbidity score in regression analyses. Increased age (adjusted Odds Ratio=3.37, 95% CI=2.44–4.67), male gender (aOR=1.35, 95% CI=1.08-1.69), and number of comorbid conditions (aOR=1.28, 95% CI=1.01-1.63) were significantly associated with death. Significant factors in predicting total morbidity score were age (adjusted Multiplicative Effect=1.45; 95% CI=1.349-1.555) and gender (aME=1.17; 95% CI=1.109-1.243). The posterior probability that blood type influenced death was only 10%. CONCLUSIONS: There is strong evidence that blood type was not a significant predictor of clinical course or death in patients hospitalized with COVID-19. Older age and male gender led to worse clinical outcomes and higher rates of death; older age, male gender, and comorbidities predicted a worse clinical course and higher morbidity score. Race was not a significant predictor of death in our population and was associated with an increased, albeit not significant, morbidity score. Southern Society for Clinical Investigation. Published by Elsevier Inc. 2022-07 2022-01-02 /pmc/articles/PMC8720494/ /pubmed/34986364 http://dx.doi.org/10.1016/j.amjms.2021.12.006 Text en © 2022 Southern Society for Clinical Investigation. Published by Elsevier Inc. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active. |
spellingShingle | Clinical Investigation Thomas, Katharine E. Karamanis, Amber Dauchy, Erin Chapple, Andrew G. Loch, Michelle M. Assessing the effect of blood type on death and a novel scoring system to assess clinical course in patients with COVID-19 |
title | Assessing the effect of blood type on death and a novel scoring system to assess clinical course in patients with COVID-19 |
title_full | Assessing the effect of blood type on death and a novel scoring system to assess clinical course in patients with COVID-19 |
title_fullStr | Assessing the effect of blood type on death and a novel scoring system to assess clinical course in patients with COVID-19 |
title_full_unstemmed | Assessing the effect of blood type on death and a novel scoring system to assess clinical course in patients with COVID-19 |
title_short | Assessing the effect of blood type on death and a novel scoring system to assess clinical course in patients with COVID-19 |
title_sort | assessing the effect of blood type on death and a novel scoring system to assess clinical course in patients with covid-19 |
topic | Clinical Investigation |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8720494/ https://www.ncbi.nlm.nih.gov/pubmed/34986364 http://dx.doi.org/10.1016/j.amjms.2021.12.006 |
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