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Charlson Comorbidity Index in Predicting Poor Clinical Outcomes and Mortality in Patients with COVID-19
OBJECTIVE: : As known, older age and comorbidities are associated with poor clinical outcomes in patients with coronavirus disease 19. The aim of this study was to investigate the effect of the Charlson Comorbidity Index in predicting poor clinical outcomes in coronavirus disease 19 patients. MATERI...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Turkish Thoracic Society
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9449884/ https://www.ncbi.nlm.nih.gov/pubmed/35404247 http://dx.doi.org/10.5152/TurkThoracJ.2022.21076 |
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author | Argun Barış, Serap Boyacı, Haşim Akhan, Sıla Mutlu, Birsen Deniz, Müge Başyiğit, İlknur |
author_facet | Argun Barış, Serap Boyacı, Haşim Akhan, Sıla Mutlu, Birsen Deniz, Müge Başyiğit, İlknur |
author_sort | Argun Barış, Serap |
collection | PubMed |
description | OBJECTIVE: : As known, older age and comorbidities are associated with poor clinical outcomes in patients with coronavirus disease 19. The aim of this study was to investigate the effect of the Charlson Comorbidity Index in predicting poor clinical outcomes in coronavirus disease 19 patients. MATERIAL AND METHODS: Demographic characteristics and poor clinical outcomes (presence of pneumonia, respiratory failure, intensive care unit admission, and mortality) of the patients were evaluated retrospectively. Classical and modified Charlson Comorbidity Index was calculated and adjusted according to age. RESULTS: In this study, 106 women and 107 men were included. The comorbidity rate was 50.7% and the most common comorbidities were hypertension (21.6%) and diabetes mellitus (15%). The rates of respiratory failure, intensive care unit admission, and mortality were 15%, 2.3%, and 2.8%, respectively. Older age was a high risk for poor outcomes. Pneumonia (odds ratio: 6.6; 95% CI: 3.4-12.7), respiratory failure (odds ratio: 5.2; 95% CI: 2.03-13.2), and intensive care unit admission (odds ratio: 1.1; 95% CI: 1.01-1.1) were significantly higher in patients with comorbid diseases than patients without any comorbidity (P < .05). Both median-modified and classical Charlson Comorbidity Index and their age-adjusted scores were significantly higher in patients with poor outcomes. CONCLUSIONS: It is suggested that evaluation of the Charlson Comorbidity Index might contribute to the management of the patients with coronavirus disease 19 by predicting risk group for poor clinical outcomes and mortality. |
format | Online Article Text |
id | pubmed-9449884 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Turkish Thoracic Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-94498842022-09-19 Charlson Comorbidity Index in Predicting Poor Clinical Outcomes and Mortality in Patients with COVID-19 Argun Barış, Serap Boyacı, Haşim Akhan, Sıla Mutlu, Birsen Deniz, Müge Başyiğit, İlknur Turk Thorac J Original Article OBJECTIVE: : As known, older age and comorbidities are associated with poor clinical outcomes in patients with coronavirus disease 19. The aim of this study was to investigate the effect of the Charlson Comorbidity Index in predicting poor clinical outcomes in coronavirus disease 19 patients. MATERIAL AND METHODS: Demographic characteristics and poor clinical outcomes (presence of pneumonia, respiratory failure, intensive care unit admission, and mortality) of the patients were evaluated retrospectively. Classical and modified Charlson Comorbidity Index was calculated and adjusted according to age. RESULTS: In this study, 106 women and 107 men were included. The comorbidity rate was 50.7% and the most common comorbidities were hypertension (21.6%) and diabetes mellitus (15%). The rates of respiratory failure, intensive care unit admission, and mortality were 15%, 2.3%, and 2.8%, respectively. Older age was a high risk for poor outcomes. Pneumonia (odds ratio: 6.6; 95% CI: 3.4-12.7), respiratory failure (odds ratio: 5.2; 95% CI: 2.03-13.2), and intensive care unit admission (odds ratio: 1.1; 95% CI: 1.01-1.1) were significantly higher in patients with comorbid diseases than patients without any comorbidity (P < .05). Both median-modified and classical Charlson Comorbidity Index and their age-adjusted scores were significantly higher in patients with poor outcomes. CONCLUSIONS: It is suggested that evaluation of the Charlson Comorbidity Index might contribute to the management of the patients with coronavirus disease 19 by predicting risk group for poor clinical outcomes and mortality. Turkish Thoracic Society 2022-03-01 /pmc/articles/PMC9449884/ /pubmed/35404247 http://dx.doi.org/10.5152/TurkThoracJ.2022.21076 Text en Turkish Thoracic Society https://creativecommons.org/licenses/by-nc/4.0/ Content of this journal is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License. (https://creativecommons.org/licenses/by-nc/4.0/) |
spellingShingle | Original Article Argun Barış, Serap Boyacı, Haşim Akhan, Sıla Mutlu, Birsen Deniz, Müge Başyiğit, İlknur Charlson Comorbidity Index in Predicting Poor Clinical Outcomes and Mortality in Patients with COVID-19 |
title | Charlson Comorbidity Index in Predicting Poor Clinical Outcomes and Mortality in Patients with COVID-19 |
title_full | Charlson Comorbidity Index in Predicting Poor Clinical Outcomes and Mortality in Patients with COVID-19 |
title_fullStr | Charlson Comorbidity Index in Predicting Poor Clinical Outcomes and Mortality in Patients with COVID-19 |
title_full_unstemmed | Charlson Comorbidity Index in Predicting Poor Clinical Outcomes and Mortality in Patients with COVID-19 |
title_short | Charlson Comorbidity Index in Predicting Poor Clinical Outcomes and Mortality in Patients with COVID-19 |
title_sort | charlson comorbidity index in predicting poor clinical outcomes and mortality in patients with covid-19 |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9449884/ https://www.ncbi.nlm.nih.gov/pubmed/35404247 http://dx.doi.org/10.5152/TurkThoracJ.2022.21076 |
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