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Predictive Model of Severity in SARS CoV-2 Patients at Hospital Admission Using Blood-Related Parameters

INTRODUCTION: Blood test alterations are crucial in SARS CoV-2 (COVID-19) patients. Blood parameters, such as lymphocytes, C reactive protein (CRP), creatinine, lactate dehydrogenase, or D-dimer, are associated with severity and prognosis of SARS CoV-2 patients. This study aims to identify blood-rel...

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Autores principales: Gómez, Laura Criado, Curto, Santiago Villanueva, Sebastian, Maria Belén Pérez, Jiménez, Begoña Fernández, Duniol, Melisa Duque
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Communications and Publications Division (CPD) of the IFCC 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8343039/
https://www.ncbi.nlm.nih.gov/pubmed/34421494
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author Gómez, Laura Criado
Curto, Santiago Villanueva
Sebastian, Maria Belén Pérez
Jiménez, Begoña Fernández
Duniol, Melisa Duque
author_facet Gómez, Laura Criado
Curto, Santiago Villanueva
Sebastian, Maria Belén Pérez
Jiménez, Begoña Fernández
Duniol, Melisa Duque
author_sort Gómez, Laura Criado
collection PubMed
description INTRODUCTION: Blood test alterations are crucial in SARS CoV-2 (COVID-19) patients. Blood parameters, such as lymphocytes, C reactive protein (CRP), creatinine, lactate dehydrogenase, or D-dimer, are associated with severity and prognosis of SARS CoV-2 patients. This study aims to identify blood-related predictors of severe hospitalization in patients diagnosed with SARS CoV-2. METHODS: Observational retrospective study of all rt-PCR and blood-test positive (at 48 hours of hospitalization) SARS CoV-2 diagnosed inpatients between March-May 2020. Deceased and/or ICU inpatients were considered as severe cases, whereas those patients after hospital discharge were considered as non-severe. Multivariate logistic regression was used to identify predictors of severity, based on bivariate contrast between severe and mild inpatients. RESULTS: The overall sample comprised 540 patients, with 374 mild cases (69.26%), and 166 severe cases (30.75%). The multivariate logistic regression model for predicting SARS CoV-2 severity included lymphocytes, C reactive protein (CRP), creatinine, total protein levels, glucose and aspartate aminotransferase as predictors, showing an area under the curve (AUC) of 0.895 at a threshold of 0.29, with 81.5% of sensitivity and 81% of specificity. DISCUSSION: Our results suggest that our predictive model allows identifying and stratifying SARS CoV-2 patients in risk of developing severe medical complications based on blood-test parameters easily measured at hospital admission, improving health-care resources management and distribution.
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spelling pubmed-83430392021-08-20 Predictive Model of Severity in SARS CoV-2 Patients at Hospital Admission Using Blood-Related Parameters Gómez, Laura Criado Curto, Santiago Villanueva Sebastian, Maria Belén Pérez Jiménez, Begoña Fernández Duniol, Melisa Duque EJIFCC Research Article INTRODUCTION: Blood test alterations are crucial in SARS CoV-2 (COVID-19) patients. Blood parameters, such as lymphocytes, C reactive protein (CRP), creatinine, lactate dehydrogenase, or D-dimer, are associated with severity and prognosis of SARS CoV-2 patients. This study aims to identify blood-related predictors of severe hospitalization in patients diagnosed with SARS CoV-2. METHODS: Observational retrospective study of all rt-PCR and blood-test positive (at 48 hours of hospitalization) SARS CoV-2 diagnosed inpatients between March-May 2020. Deceased and/or ICU inpatients were considered as severe cases, whereas those patients after hospital discharge were considered as non-severe. Multivariate logistic regression was used to identify predictors of severity, based on bivariate contrast between severe and mild inpatients. RESULTS: The overall sample comprised 540 patients, with 374 mild cases (69.26%), and 166 severe cases (30.75%). The multivariate logistic regression model for predicting SARS CoV-2 severity included lymphocytes, C reactive protein (CRP), creatinine, total protein levels, glucose and aspartate aminotransferase as predictors, showing an area under the curve (AUC) of 0.895 at a threshold of 0.29, with 81.5% of sensitivity and 81% of specificity. DISCUSSION: Our results suggest that our predictive model allows identifying and stratifying SARS CoV-2 patients in risk of developing severe medical complications based on blood-test parameters easily measured at hospital admission, improving health-care resources management and distribution. The Communications and Publications Division (CPD) of the IFCC 2021-06-29 /pmc/articles/PMC8343039/ /pubmed/34421494 Text en Copyright © 2021 International Federation of Clinical Chemistry and Laboratory Medicine (IFCC). All rights reserved. https://creativecommons.org/licenses/by-nc/4.0/This is a Platinum Open Access Journal distributed under the terms of the Creative Commons Attribution Non-Commercial License which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Gómez, Laura Criado
Curto, Santiago Villanueva
Sebastian, Maria Belén Pérez
Jiménez, Begoña Fernández
Duniol, Melisa Duque
Predictive Model of Severity in SARS CoV-2 Patients at Hospital Admission Using Blood-Related Parameters
title Predictive Model of Severity in SARS CoV-2 Patients at Hospital Admission Using Blood-Related Parameters
title_full Predictive Model of Severity in SARS CoV-2 Patients at Hospital Admission Using Blood-Related Parameters
title_fullStr Predictive Model of Severity in SARS CoV-2 Patients at Hospital Admission Using Blood-Related Parameters
title_full_unstemmed Predictive Model of Severity in SARS CoV-2 Patients at Hospital Admission Using Blood-Related Parameters
title_short Predictive Model of Severity in SARS CoV-2 Patients at Hospital Admission Using Blood-Related Parameters
title_sort predictive model of severity in sars cov-2 patients at hospital admission using blood-related parameters
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8343039/
https://www.ncbi.nlm.nih.gov/pubmed/34421494
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