Value of dynamic clinical and biomarker data for mortality risk prediction in COVID-19: a multicentre retrospective cohort study.


Journal

BMJ open
ISSN: 2044-6055
Titre abrégé: BMJ Open
Pays: England
ID NLM: 101552874

Informations de publication

Date de publication:
23 09 2020
Historique:
entrez: 24 9 2020
pubmed: 25 9 2020
medline: 6 10 2020
Statut: epublish

Résumé

Being able to predict which patients with COVID-19 are going to deteriorate is important to help identify patients for clinical and research practice. Clinical prediction models play a critical role in this process, but current models are of limited value because they are typically restricted to baseline predictors and do not always use contemporary statistical methods. We sought to explore the benefits of incorporating dynamic changes in routinely measured biomarkers, non-linear effects and applying 'state-of-the-art' statistical methods in the development of a prognostic model to predict death in hospitalised patients with COVID-19. The data were analysed from admissions with COVID-19 to three hospital sites. Exploratory data analysis included a graphical approach to partial correlations. Dynamic biomarkers were considered up to 5 days following admission rather than depending solely on baseline or single time-point data. Marked departures from linear effects of covariates were identified by employing smoothing splines within a generalised additive modelling framework. 3 secondary and tertiary level centres in Greater Manchester, the UK. 392 hospitalised patients with a diagnosis of COVID-19. 392 patients with a COVID-19 diagnosis were identified. Area under the receiver operating characteristic curve increased from 0.73 using admission data alone to 0.75 when also considering results of baseline blood samples and to 0.83 when considering dynamic values of routinely collected markers. There was clear non-linearity in the association of age with patient outcome. This study shows that clinical prediction models to predict death in hospitalised patients with COVID-19 can be improved by taking into account both non-linear effects in covariates such as age and dynamic changes in values of biomarkers.

Identifiants

pubmed: 32967887
pii: bmjopen-2020-041983
doi: 10.1136/bmjopen-2020-041983
pmc: PMC7513423
doi:

Substances chimiques

Biomarkers 0
Urea 8W8T17847W
C-Reactive Protein 9007-41-4
Creatinine AYI8EX34EU
Bilirubin RFM9X3LJ49

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

e041983

Subventions

Organisme : Medical Research Council
ID : MR/T016515/1
Pays : United Kingdom

Informations de copyright

© Author(s) (or their employer(s)) 2020. Re-use permitted under CC BY. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: Swedish Orphan Biovitrum have provided investigational medicinal product for public-funded, peer-reviewed trials on which AK, AV, JG, HCP and SH are coinvestigators. The other authors declare no competing interests.

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Auteurs

Carlo Berzuini (C)

Centre for Biostatistics, The University of Manchester, Manchester Academic Health Sciences Centre, Manchester, UK.

Cathal Hannan (C)

Manchester Centre for Clinical Neurosciences, Salford Royal Hospitals NHS Trust, Salford, UK.

Andrew King (A)

Manchester Centre for Clinical Neurosciences, Salford Royal Hospitals NHS Trust, Salford, UK.

Andy Vail (A)

Centre for Biostatistics, The University of Manchester, Manchester Academic Health Sciences Centre, Manchester, UK.

Claire O'Leary (C)

Division of Neuroscience and Experimental Psychology, The University of Manchester, Manchester, UK.

David Brough (D)

Division of Neuroscience and Experimental Psychology, The University of Manchester, Manchester, UK.

James Galea (J)

Cardiff and Vale University Health Board, Cardiff, UK.

Kayode Ogungbenro (K)

Department of Pharmacy and Optometry, The University of Manchester, Manchester, UK.

Megan Wright (M)

Manchester Centre for Clinical Neurosciences, Salford Royal Hospitals NHS Trust, Salford, UK.

Omar Pathmanaban (O)

Manchester Centre for Clinical Neurosciences, Salford Royal Hospitals NHS Trust, Salford, UK.

Sharon Hulme (S)

Division of Neuroscience and Experimental Psychology, The University of Manchester, Manchester, UK.

Stuart Allan (S)

Division of Neuroscience and Experimental Psychology, The University of Manchester, Manchester, UK.

Luisa Bernardinelli (L)

Department of Brain and Behavioural Sciences, The University of Pavia, Pavia, Italy.

Hiren C Patel (HC)

Manchester Centre for Clinical Neurosciences, Salford Royal Hospitals NHS Trust, Salford, UK hiren.Patel@srft.nhs.uk.

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Classifications MeSH