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Laboratory abnormalities and risk factors associated with in‐hospital death in patients with severe COVID‐19

BACKGROUND: In the context of the COVID‐19 outbreak of worldwide, we aim to analyze the laboratory risk factors of in‐hospital death in patients with severe COVID‐19. METHODS: All ≥18‐year‐old patients with confirmed severe COVID‐19 admitted to Tongji Hospital (Wuhan, China) from February 3 to Febru...

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Autores principales: Chen, Xing, Yan, Li, Fei, Yang, Zhang, Chi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7595920/
https://www.ncbi.nlm.nih.gov/pubmed/32656888
http://dx.doi.org/10.1002/jcla.23467
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author Chen, Xing
Yan, Li
Fei, Yang
Zhang, Chi
author_facet Chen, Xing
Yan, Li
Fei, Yang
Zhang, Chi
author_sort Chen, Xing
collection PubMed
description BACKGROUND: In the context of the COVID‐19 outbreak of worldwide, we aim to analyze the laboratory risk factors of in‐hospital death in patients with severe COVID‐19. METHODS: All ≥18‐year‐old patients with confirmed severe COVID‐19 admitted to Tongji Hospital (Wuhan, China) from February 3 to February 20, 2020, were retrospectively enrolled and followed up until March 20, 2020. Epidemiological, clinical, laboratory, and treatment data were collected and explored the risk factors associated with in‐hospital death. RESULTS: A total of 73 severe patients were enrolled in the study, of whom 20 (27%) patients died in hospital during the average 28 days of follow‐up period. The median age of non‐survivors was significantly older than survivors (69 [64‐76.5] years vs 64 [56‐71.3] years, P = .033) and 15 (75%) patients were males. The laboratory abnormalities of non‐survivors mainly presented in serious inflammation response and multiple organ failure, with high levels of cytokines and deranged coagulation parameters. Multivariable regression showed that neutrophil count greater than 4.47 × 10(9)/L (OR, 58.35; 95%CI: 2.16‐1571.69; P = .016), hypersensitivity C‐reactive protein greater than 86.7 mg/L (OR, 14.90; 95%CI: 1.29‐171.10; P = .030), creatine kinase greater than 101 U/L (OR, 161.62; 95%CI: 6.45‐4045.20; P = .002), and blood urea nitrogen greater than 6.7 mmol/L (OR, 11.18; 95%CI: 1.36‐91.62; P = .024) were risk factors for in‐hospital death. CONCLUSION: The risk factors of neutrophil count, hypersensitivity C‐reactive protein, creatine kinase, and blood urea nitrogen could help clinicians to early identify COVID‐19 severe patients with poor outcomes on admission. Virus direct attack and cytokine storm play a major role in the death of COVID‐19.
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spelling pubmed-75959202020-11-02 Laboratory abnormalities and risk factors associated with in‐hospital death in patients with severe COVID‐19 Chen, Xing Yan, Li Fei, Yang Zhang, Chi J Clin Lab Anal Research Articles BACKGROUND: In the context of the COVID‐19 outbreak of worldwide, we aim to analyze the laboratory risk factors of in‐hospital death in patients with severe COVID‐19. METHODS: All ≥18‐year‐old patients with confirmed severe COVID‐19 admitted to Tongji Hospital (Wuhan, China) from February 3 to February 20, 2020, were retrospectively enrolled and followed up until March 20, 2020. Epidemiological, clinical, laboratory, and treatment data were collected and explored the risk factors associated with in‐hospital death. RESULTS: A total of 73 severe patients were enrolled in the study, of whom 20 (27%) patients died in hospital during the average 28 days of follow‐up period. The median age of non‐survivors was significantly older than survivors (69 [64‐76.5] years vs 64 [56‐71.3] years, P = .033) and 15 (75%) patients were males. The laboratory abnormalities of non‐survivors mainly presented in serious inflammation response and multiple organ failure, with high levels of cytokines and deranged coagulation parameters. Multivariable regression showed that neutrophil count greater than 4.47 × 10(9)/L (OR, 58.35; 95%CI: 2.16‐1571.69; P = .016), hypersensitivity C‐reactive protein greater than 86.7 mg/L (OR, 14.90; 95%CI: 1.29‐171.10; P = .030), creatine kinase greater than 101 U/L (OR, 161.62; 95%CI: 6.45‐4045.20; P = .002), and blood urea nitrogen greater than 6.7 mmol/L (OR, 11.18; 95%CI: 1.36‐91.62; P = .024) were risk factors for in‐hospital death. CONCLUSION: The risk factors of neutrophil count, hypersensitivity C‐reactive protein, creatine kinase, and blood urea nitrogen could help clinicians to early identify COVID‐19 severe patients with poor outcomes on admission. Virus direct attack and cytokine storm play a major role in the death of COVID‐19. John Wiley and Sons Inc. 2020-07-12 /pmc/articles/PMC7595920/ /pubmed/32656888 http://dx.doi.org/10.1002/jcla.23467 Text en © 2020 The Authors. Journal of Clinical Laboratory Analysis 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 Research Articles
Chen, Xing
Yan, Li
Fei, Yang
Zhang, Chi
Laboratory abnormalities and risk factors associated with in‐hospital death in patients with severe COVID‐19
title Laboratory abnormalities and risk factors associated with in‐hospital death in patients with severe COVID‐19
title_full Laboratory abnormalities and risk factors associated with in‐hospital death in patients with severe COVID‐19
title_fullStr Laboratory abnormalities and risk factors associated with in‐hospital death in patients with severe COVID‐19
title_full_unstemmed Laboratory abnormalities and risk factors associated with in‐hospital death in patients with severe COVID‐19
title_short Laboratory abnormalities and risk factors associated with in‐hospital death in patients with severe COVID‐19
title_sort laboratory abnormalities and risk factors associated with in‐hospital death in patients with severe covid‐19
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7595920/
https://www.ncbi.nlm.nih.gov/pubmed/32656888
http://dx.doi.org/10.1002/jcla.23467
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