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Risk factors and electrocardiogram characteristics for mortality in critical inpatients with COVID‐19

BACKGROUND: The novel severe acute respiratory syndrome coronavirus 2 (SARS‐CoV‐2) has spread worldwide. HYPOTHESIS: The possible risk factors that lead to death in critical inpatients with coronavirus disease 2019 (COVID‐19) are not yet fully understood. METHODS: In this single‐center, retrospectiv...

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Autores principales: Li, Lingzhi, Zhang, Shudi, He, Bing, Chen, Xiaobei, Wang, Shihong, Zhao, Qingyan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wiley Periodicals, Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7724237/
https://www.ncbi.nlm.nih.gov/pubmed/33094522
http://dx.doi.org/10.1002/clc.23492
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author Li, Lingzhi
Zhang, Shudi
He, Bing
Chen, Xiaobei
Wang, Shihong
Zhao, Qingyan
author_facet Li, Lingzhi
Zhang, Shudi
He, Bing
Chen, Xiaobei
Wang, Shihong
Zhao, Qingyan
author_sort Li, Lingzhi
collection PubMed
description BACKGROUND: The novel severe acute respiratory syndrome coronavirus 2 (SARS‐CoV‐2) has spread worldwide. HYPOTHESIS: The possible risk factors that lead to death in critical inpatients with coronavirus disease 2019 (COVID‐19) are not yet fully understood. METHODS: In this single‐center, retrospective study, we enrolled 113 critical patients with COVID‐19 from Renmin Hospital of Wuhan University between February 1, 2020 and March 15, 2020. Patients who survived or died were compared. RESULTS: A total of 113 critical patients with COVID‐19 were recruited; 50 (44.3%) died, and 63 (55.7%) recovered. The proportion of patients with ventricular arrhythmia was higher in the death group than in the recovery group (P = .021) and was higher among patients with myocardial damage than patients without myocardial damage (P = .013). Multivariate analysis confirmed independent predictors of mortality from COVID‐19: age > 70 years (HR 1.84, 95% CI 1.03‐3.28), initial neutrophil count over 6.5 × 10(9)/L (HR 3.43, 95% CI 1.84‐6.40), C‐reactive protein greater than 100 mg/L (HR 1.93, 95% CI 1.04‐3.59), and lactate dehydrogenase over 300 U/L (HR 2.90, 95% CI 1.26‐6.67). Immunoglobulin treatment (HR 0.39, 95% CI 0.21‐0.73) can reduce the risk of death. Sinus tachycardia (HR 2.94, 95% CI 1.16‐7.46) and ventricular arrhythmia (HR 2.79, 95% CI 1.11‐7.04) were independent ECG risk factors for mortality from COVID‐19. CONCLUSIONS: Old age (>70 years), neutrophilia, C‐reactive protein greater than 100 mg/L and lactate dehydrogenase over 300 U/L are high‐risk factors for mortality in critical patients with COVID‐19. Sinus tachycardia and ventricular arrhythmia are independent ECG risk factors for mortality from COVID‐19.
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spelling pubmed-77242372020-12-11 Risk factors and electrocardiogram characteristics for mortality in critical inpatients with COVID‐19 Li, Lingzhi Zhang, Shudi He, Bing Chen, Xiaobei Wang, Shihong Zhao, Qingyan Clin Cardiol Clinical Investigations BACKGROUND: The novel severe acute respiratory syndrome coronavirus 2 (SARS‐CoV‐2) has spread worldwide. HYPOTHESIS: The possible risk factors that lead to death in critical inpatients with coronavirus disease 2019 (COVID‐19) are not yet fully understood. METHODS: In this single‐center, retrospective study, we enrolled 113 critical patients with COVID‐19 from Renmin Hospital of Wuhan University between February 1, 2020 and March 15, 2020. Patients who survived or died were compared. RESULTS: A total of 113 critical patients with COVID‐19 were recruited; 50 (44.3%) died, and 63 (55.7%) recovered. The proportion of patients with ventricular arrhythmia was higher in the death group than in the recovery group (P = .021) and was higher among patients with myocardial damage than patients without myocardial damage (P = .013). Multivariate analysis confirmed independent predictors of mortality from COVID‐19: age > 70 years (HR 1.84, 95% CI 1.03‐3.28), initial neutrophil count over 6.5 × 10(9)/L (HR 3.43, 95% CI 1.84‐6.40), C‐reactive protein greater than 100 mg/L (HR 1.93, 95% CI 1.04‐3.59), and lactate dehydrogenase over 300 U/L (HR 2.90, 95% CI 1.26‐6.67). Immunoglobulin treatment (HR 0.39, 95% CI 0.21‐0.73) can reduce the risk of death. Sinus tachycardia (HR 2.94, 95% CI 1.16‐7.46) and ventricular arrhythmia (HR 2.79, 95% CI 1.11‐7.04) were independent ECG risk factors for mortality from COVID‐19. CONCLUSIONS: Old age (>70 years), neutrophilia, C‐reactive protein greater than 100 mg/L and lactate dehydrogenase over 300 U/L are high‐risk factors for mortality in critical patients with COVID‐19. Sinus tachycardia and ventricular arrhythmia are independent ECG risk factors for mortality from COVID‐19. Wiley Periodicals, Inc. 2020-10-22 /pmc/articles/PMC7724237/ /pubmed/33094522 http://dx.doi.org/10.1002/clc.23492 Text en © 2020 The Authors. Clinical Cardiology published by Wiley Periodicals LLC. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Clinical Investigations
Li, Lingzhi
Zhang, Shudi
He, Bing
Chen, Xiaobei
Wang, Shihong
Zhao, Qingyan
Risk factors and electrocardiogram characteristics for mortality in critical inpatients with COVID‐19
title Risk factors and electrocardiogram characteristics for mortality in critical inpatients with COVID‐19
title_full Risk factors and electrocardiogram characteristics for mortality in critical inpatients with COVID‐19
title_fullStr Risk factors and electrocardiogram characteristics for mortality in critical inpatients with COVID‐19
title_full_unstemmed Risk factors and electrocardiogram characteristics for mortality in critical inpatients with COVID‐19
title_short Risk factors and electrocardiogram characteristics for mortality in critical inpatients with COVID‐19
title_sort risk factors and electrocardiogram characteristics for mortality in critical inpatients with covid‐19
topic Clinical Investigations
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7724237/
https://www.ncbi.nlm.nih.gov/pubmed/33094522
http://dx.doi.org/10.1002/clc.23492
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