Development and validation of a simplified risk score for the prediction of critical COVID-19 illness in newly diagnosed patients.


Journal

Journal of medical virology
ISSN: 1096-9071
Titre abrégé: J Med Virol
Pays: United States
ID NLM: 7705876

Informations de publication

Date de publication:
12 2021
Historique:
revised: 13 05 2021
received: 19 03 2021
accepted: 29 07 2021
pubmed: 1 8 2021
medline: 28 10 2021
entrez: 31 7 2021
Statut: ppublish

Résumé

Scores to identify patients at high risk of progression of coronavirus disease (COVID-19), caused by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), may become instrumental for clinical decision-making and patient management. We used patient data from the multicentre Lean European Open Survey on SARS-CoV-2-Infected Patients (LEOSS) and applied variable selection to develop a simplified scoring system to identify patients at increased risk of critical illness or death. A total of 1946 patients who tested positive for SARS-CoV-2 were included in the initial analysis and assigned to derivation and validation cohorts (n = 1297 and n = 649, respectively). Stability selection from over 100 baseline predictors for the combined endpoint of progression to the critical phase or COVID-19-related death enabled the development of a simplified score consisting of five predictors: C-reactive protein (CRP), age, clinical disease phase (uncomplicated vs. complicated), serum urea, and D-dimer (abbreviated as CAPS-D score). This score yielded an area under the curve (AUC) of 0.81 (95% confidence interval [CI]: 0.77-0.85) in the validation cohort for predicting the combined endpoint within 7 days of diagnosis and 0.81 (95% CI: 0.77-0.85) during full follow-up. We used an additional prospective cohort of 682 patients, diagnosed largely after the "first wave" of the pandemic to validate the predictive accuracy of the score and observed similar results (AUC for the event within 7 days: 0.83 [95% CI: 0.78-0.87]; for full follow-up: 0.82 [95% CI: 0.78-0.86]). An easily applicable score to calculate the risk of COVID-19 progression to critical illness or death was thus established and validated.

Identifiants

pubmed: 34331717
doi: 10.1002/jmv.27252
pmc: PMC8426905
doi:

Substances chimiques

Fibrin Fibrinogen Degradation Products 0
fibrin fragment D 0
Urea 8W8T17847W
C-Reactive Protein 9007-41-4

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

6703-6713

Subventions

Organisme : German Centre for Infection Research
Organisme : Willy Robert Pitzer Foundation

Commentaires et corrections

Type : ErratumIn

Informations de copyright

© 2021 The Authors. Journal of Medical Virology Published by Wiley Periodicals LLC.

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Auteurs

Stanislas Werfel (S)

Department of Nephrology, School of Medicine, Technical University of Munich, Klinikum rechts der Isar, Munich, Germany.

Carolin E M Jakob (CEM)

Department I for Internal Medicine, University Hospital of Cologne, University of Cologne, Cologne, Germany.
German Centre for Infection Research (DZIF), Partner Site Bonn-Cologne, Cologne, Germany.

Stefan Borgmann (S)

Department of Infectious Diseases and Infection Control, Ingolstadt Hospital, Ingolstadt, Germany.

Jochen Schneider (J)

Department of Internal Medicine II, School of Medicine, Technical University of Munich, University Hospital rechts der Isar, Munich, Germany.
German Centre for Infection Research (DZIF), Partner Site Munich, Munich, Germany.

Christoph Spinner (C)

Department of Internal Medicine II, School of Medicine, Technical University of Munich, University Hospital rechts der Isar, Munich, Germany.
German Centre for Infection Research (DZIF), Partner Site Munich, Munich, Germany.

Maximilian Schons (M)

Department I for Internal Medicine, University Hospital of Cologne, University of Cologne, Cologne, Germany.

Martin Hower (M)

Department of Pneumology, Infectious Diseases and Internal Medicine, Klinikum Dortmund gGmbH, Dortmund, Germany.

Kai Wille (K)

University Clinic for Haematology, Oncology, Haemostaseology and Palliative Care, Johannes Wesling Medical Centre Minden UKRUB, University of Bochum, Minden, Germany.

Martina Haselberger (M)

Department of Internal Medicine I, Klinikum Passau, Passau, Germany.

Hanno Heuzeroth (H)

Department of Emergency and Intensive Care Medicine, Klinikum Ernst von Bergmann, Potsdam, Germany.

Maria M Rüthrich (MM)

Department of Internal Medicine II, Hematology and Medical Oncology, University Hospital Jena, Jena, Germany.

Sebastian Dolff (S)

Department of Infectious Diseases, University Hospital Essen, University Duisburg-Essen, Essen, Germany.

Johanna Kessel (J)

Department of Internal Medicine, Hematology and Oncology, Goethe University Frankfurt, Frankfurt, Germany.

Uwe Heemann (U)

Department of Nephrology, School of Medicine, Technical University of Munich, Klinikum rechts der Isar, Munich, Germany.

Jörg J Vehreschild (JJ)

Department I for Internal Medicine, University Hospital of Cologne, University of Cologne, Cologne, Germany.
German Centre for Infection Research (DZIF), Partner Site Bonn-Cologne, Cologne, Germany.
Department of Internal Medicine, Hematology and Oncology, Goethe University Frankfurt, Frankfurt, Germany.

Siegbert Rieg (S)

Department of Medicine II, University of Freiburg, Freiburg, Germany.

Christoph Schmaderer (C)

Department of Nephrology, School of Medicine, Technical University of Munich, Klinikum rechts der Isar, Munich, Germany.

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Classifications MeSH