Covid-19: contribution of clinical characteristics and laboratory features for early detection of patients with high risk of severe evolution.


Journal

Acta clinica Belgica
ISSN: 2295-3337
Titre abrégé: Acta Clin Belg
Pays: England
ID NLM: 0370306

Informations de publication

Date de publication:
Apr 2022
Historique:
pubmed: 17 9 2020
medline: 9 3 2022
entrez: 16 9 2020
Statut: ppublish

Résumé

The aim of this study was to identify early clinical and laboratory predictive factors of a severe coronavirus disease 2019 (COVID-19). A retrospective study was conducted on adult patients hospitalized for COVID-19 in our hospital. Diagnosis was based on a positive real-time reverse transcription-polymerase chain reaction (RT-PCR) on nasopharyngeal samples. The cohort was divided into two groups, i.e. a favorable evolution (FE) group and an unfavorable evolution (UFE) group, including intensive care unit (ICU) and deceased patients.Results: A total of 198 patients were enrolled in the study, with 138 FE (70%) and 60 UFE (30%). Older age, male gender, comorbidities and dyspnea at admission constituted significantly worse prognosis factors. Among laboratory features, lymphocyte and platelet counts as well as corrected glomerular filtration rate were significantly lower in UFE patients, while neutrophil to lymphocyte ratio, inflammation biomarkers, creatinine, aspartate aminotransferase, lactate dehydrogenase (LDH), glycemia and D-dimer were significantly higher. Procalcitonin and LDH appeared as the most accurate variables according to receiver operating characteristic curves. This Belgian study revealed clinical and laboratory features able to predict high risk of ICU requirement, or even death, at admission time. These results provide a potential tool for patient's triage in a context of pandemic.

Sections du résumé

BACKGROUND BACKGROUND
The aim of this study was to identify early clinical and laboratory predictive factors of a severe coronavirus disease 2019 (COVID-19).
METHODS METHODS
A retrospective study was conducted on adult patients hospitalized for COVID-19 in our hospital. Diagnosis was based on a positive real-time reverse transcription-polymerase chain reaction (RT-PCR) on nasopharyngeal samples. The cohort was divided into two groups, i.e. a favorable evolution (FE) group and an unfavorable evolution (UFE) group, including intensive care unit (ICU) and deceased patients.Results: A total of 198 patients were enrolled in the study, with 138 FE (70%) and 60 UFE (30%). Older age, male gender, comorbidities and dyspnea at admission constituted significantly worse prognosis factors. Among laboratory features, lymphocyte and platelet counts as well as corrected glomerular filtration rate were significantly lower in UFE patients, while neutrophil to lymphocyte ratio, inflammation biomarkers, creatinine, aspartate aminotransferase, lactate dehydrogenase (LDH), glycemia and D-dimer were significantly higher. Procalcitonin and LDH appeared as the most accurate variables according to receiver operating characteristic curves.
CONCLUSIONS CONCLUSIONS
This Belgian study revealed clinical and laboratory features able to predict high risk of ICU requirement, or even death, at admission time. These results provide a potential tool for patient's triage in a context of pandemic.

Identifiants

pubmed: 32935644
doi: 10.1080/17843286.2020.1822078
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

261-267

Auteurs

Edith Sepulchre (E)

Department of Laboratory Medicine, CHR Citadelle, Liège, Belgium.

Guillaume Pittie (G)

Department of Laboratory Medicine, CHR Citadelle, Liège, Belgium.

Violeta Stojkovic (V)

Department of Laboratory Medicine, CHR Citadelle, Liège, Belgium.

Gentiane Haesbroek (G)

Department of Mathematics, University of Liège, Liège, Belgium.

Yves Crama (Y)

HEC Liège, Management School of the University of Liège, Liège, Belgium.

Michaël Schyns (M)

HEC Liège, Management School of the University of Liège, Liège, Belgium.

Henry Paridaens (H)

Department of Laboratory Medicine, CHR Citadelle, Liège, Belgium.

Jerôme de Marchin (J)

Department of Laboratory Medicine, CHR Citadelle, Liège, Belgium.

Stéphane Degesves (S)

Department of Emergencies, CHR Citadelle, Liège, Belgium.

Christian Biemar (C)

Department of Emergencies, CHR Citadelle, Liège, Belgium.

Sandrine Boccar (S)

Department of Intensive Care, CHR Citadelle, Liège, Belgium.

Jean-Marc Senterre (JM)

Department of Laboratory Medicine, CHR Citadelle, Liège, Belgium.

Jean-Marc Minon (JM)

Department of Laboratory Medicine, CHR Citadelle, Liège, Belgium.

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Classifications MeSH