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Clinical and laboratory predictors for disease progression in patients with COVID-19: A multi-center cohort study

BACKGROUND: Reliable clinical and laboratory predictors of coronavirus disease 2019 (COVID-19) disease progression could help to identify the subset of patients who are susceptible to severe symptoms. This study sought to identify the predictors for disease progression in patients with COVID-19. MET...

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Autores principales: Lin, Shu-Min, Huang, Allen Chung-Cheng, Chiu, Tzu-Hsuan, Chang, Ko-Wei, Huang, Tse-Hung, Yang, Tsung-Hsien, Shiao, Yi-Hsien, Lee, Chung-Shu, Chung, Fu-Tsai, Chen, Chyi-Liang, Chiu, Cheng-Hsun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Chang Gung University 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9674567/
https://www.ncbi.nlm.nih.gov/pubmed/36414180
http://dx.doi.org/10.1016/j.bj.2022.11.002
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author Lin, Shu-Min
Huang, Allen Chung-Cheng
Chiu, Tzu-Hsuan
Chang, Ko-Wei
Huang, Tse-Hung
Yang, Tsung-Hsien
Shiao, Yi-Hsien
Lee, Chung-Shu
Chung, Fu-Tsai
Chen, Chyi-Liang
Chiu, Cheng-Hsun
author_facet Lin, Shu-Min
Huang, Allen Chung-Cheng
Chiu, Tzu-Hsuan
Chang, Ko-Wei
Huang, Tse-Hung
Yang, Tsung-Hsien
Shiao, Yi-Hsien
Lee, Chung-Shu
Chung, Fu-Tsai
Chen, Chyi-Liang
Chiu, Cheng-Hsun
author_sort Lin, Shu-Min
collection PubMed
description BACKGROUND: Reliable clinical and laboratory predictors of coronavirus disease 2019 (COVID-19) disease progression could help to identify the subset of patients who are susceptible to severe symptoms. This study sought to identify the predictors for disease progression in patients with COVID-19. METHODS: This study recruited consecutive patients from four hospitals between March 1, 2020, and July 31, 2021. Demographic characteristics, laboratory results, and clinical outcomes were collected. RESULTS: Among the 239 enrolled patients, 39.3% (94/239) experienced in-hospital disease progression. Multivariate logistic regression revealed that coronary arterial disease (CAD) (OR, 4.15; 95% C.I., 1.47–11.66), cerebrovascular attack (CVA) (OR, 12.98; 95% C.I., 1.30–129.51), platelet count < median value (OR, 3.23; 95% C.I., 1.65–6.32), and C-reactive protein (CRP) levels > median value of (OR, 2.25; 95% C.I., 1.02–4.99) were independent factors associated with COVID-19 progression. Patients who underwent disease progression at days 1, 4, and 7 presented lower lymphocyte counts and higher CRP levels, compared to patients without disease progression. CONCLUSIONS: The study revealed that in hospitalized COVID-19 patients, comorbidity with CAD and CVA, low platelet count, and elevated CRP levels were independently associated with disease progression. Compared with patients without disease progression, those with disease progression presented persistently low lymphocyte counts and elevated CRP levels.
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spelling pubmed-96745672022-11-21 Clinical and laboratory predictors for disease progression in patients with COVID-19: A multi-center cohort study Lin, Shu-Min Huang, Allen Chung-Cheng Chiu, Tzu-Hsuan Chang, Ko-Wei Huang, Tse-Hung Yang, Tsung-Hsien Shiao, Yi-Hsien Lee, Chung-Shu Chung, Fu-Tsai Chen, Chyi-Liang Chiu, Cheng-Hsun Biomed J Original Article BACKGROUND: Reliable clinical and laboratory predictors of coronavirus disease 2019 (COVID-19) disease progression could help to identify the subset of patients who are susceptible to severe symptoms. This study sought to identify the predictors for disease progression in patients with COVID-19. METHODS: This study recruited consecutive patients from four hospitals between March 1, 2020, and July 31, 2021. Demographic characteristics, laboratory results, and clinical outcomes were collected. RESULTS: Among the 239 enrolled patients, 39.3% (94/239) experienced in-hospital disease progression. Multivariate logistic regression revealed that coronary arterial disease (CAD) (OR, 4.15; 95% C.I., 1.47–11.66), cerebrovascular attack (CVA) (OR, 12.98; 95% C.I., 1.30–129.51), platelet count < median value (OR, 3.23; 95% C.I., 1.65–6.32), and C-reactive protein (CRP) levels > median value of (OR, 2.25; 95% C.I., 1.02–4.99) were independent factors associated with COVID-19 progression. Patients who underwent disease progression at days 1, 4, and 7 presented lower lymphocyte counts and higher CRP levels, compared to patients without disease progression. CONCLUSIONS: The study revealed that in hospitalized COVID-19 patients, comorbidity with CAD and CVA, low platelet count, and elevated CRP levels were independently associated with disease progression. Compared with patients without disease progression, those with disease progression presented persistently low lymphocyte counts and elevated CRP levels. Chang Gung University 2023-02 2022-11-19 /pmc/articles/PMC9674567/ /pubmed/36414180 http://dx.doi.org/10.1016/j.bj.2022.11.002 Text en © 2022 Chang Gung University. Publishing services by Elsevier B.V.
spellingShingle Original Article
Lin, Shu-Min
Huang, Allen Chung-Cheng
Chiu, Tzu-Hsuan
Chang, Ko-Wei
Huang, Tse-Hung
Yang, Tsung-Hsien
Shiao, Yi-Hsien
Lee, Chung-Shu
Chung, Fu-Tsai
Chen, Chyi-Liang
Chiu, Cheng-Hsun
Clinical and laboratory predictors for disease progression in patients with COVID-19: A multi-center cohort study
title Clinical and laboratory predictors for disease progression in patients with COVID-19: A multi-center cohort study
title_full Clinical and laboratory predictors for disease progression in patients with COVID-19: A multi-center cohort study
title_fullStr Clinical and laboratory predictors for disease progression in patients with COVID-19: A multi-center cohort study
title_full_unstemmed Clinical and laboratory predictors for disease progression in patients with COVID-19: A multi-center cohort study
title_short Clinical and laboratory predictors for disease progression in patients with COVID-19: A multi-center cohort study
title_sort clinical and laboratory predictors for disease progression in patients with covid-19: a multi-center cohort study
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9674567/
https://www.ncbi.nlm.nih.gov/pubmed/36414180
http://dx.doi.org/10.1016/j.bj.2022.11.002
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