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Value of dynamic clinical and biomarker data for mortality risk prediction in COVID-19: a multicentre retrospective cohort study.
Berzuini, Carlo; Hannan, Cathal; King, Andrew; Vail, Andy; O'Leary, Claire; Brough, David; Galea, James; Ogungbenro, Kayode; Wright, Megan; Pathmanaban, Omar; Hulme, Sharon; Allan, Stuart; Bernardinelli, Luisa; Patel, Hiren C.
  • Berzuini C; Centre for Biostatistics, The University of Manchester, Manchester Academic Health Sciences Centre, Manchester, UK.
  • Hannan C; Manchester Centre for Clinical Neurosciences, Salford Royal Hospitals NHS Trust, Salford, UK.
  • King A; Manchester Centre for Clinical Neurosciences, Salford Royal Hospitals NHS Trust, Salford, UK.
  • Vail A; Centre for Biostatistics, The University of Manchester, Manchester Academic Health Sciences Centre, Manchester, UK.
  • O'Leary C; Division of Neuroscience and Experimental Psychology, The University of Manchester, Manchester, UK.
  • Brough D; Division of Neuroscience and Experimental Psychology, The University of Manchester, Manchester, UK.
  • Galea J; Cardiff and Vale University Health Board, Cardiff, UK.
  • Ogungbenro K; Department of Pharmacy and Optometry, The University of Manchester, Manchester, UK.
  • Wright M; Manchester Centre for Clinical Neurosciences, Salford Royal Hospitals NHS Trust, Salford, UK.
  • Pathmanaban O; Manchester Centre for Clinical Neurosciences, Salford Royal Hospitals NHS Trust, Salford, UK.
  • Hulme S; Division of Neuroscience and Experimental Psychology, The University of Manchester, Manchester, UK.
  • Allan S; Division of Neuroscience and Experimental Psychology, The University of Manchester, Manchester, UK.
  • Bernardinelli L; Department of Brain and Behavioural Sciences, The University of Pavia, Pavia, Italy.
  • Patel HC; Manchester Centre for Clinical Neurosciences, Salford Royal Hospitals NHS Trust, Salford, UK hiren.Patel@srft.nhs.uk.
BMJ Open ; 10(9): e041983, 2020 09 23.
Article in English | MEDLINE | ID: covidwho-791536
ABSTRACT

OBJECTIVES:

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.

DESIGN:

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.

SETTING:

3 secondary and tertiary level centres in Greater Manchester, the UK.

PARTICIPANTS:

392 hospitalised patients with a diagnosis of COVID-19.

RESULTS:

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.

CONCLUSIONS:

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.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Pneumonia, Viral / Urea / Bilirubin / C-Reactive Protein / Coronavirus Infections / Lymphocyte Count / Creatinine / Neutrophils Type of study: Cohort study / Diagnostic study / Experimental Studies / Observational study / Prognostic study Limits: Aged / Female / Humans / Male / Middle aged Country/Region as subject: Europa Language: English Journal: BMJ Open Year: 2020 Document Type: Article Affiliation country: Bmjopen-2020-041983

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Pneumonia, Viral / Urea / Bilirubin / C-Reactive Protein / Coronavirus Infections / Lymphocyte Count / Creatinine / Neutrophils Type of study: Cohort study / Diagnostic study / Experimental Studies / Observational study / Prognostic study Limits: Aged / Female / Humans / Male / Middle aged Country/Region as subject: Europa Language: English Journal: BMJ Open Year: 2020 Document Type: Article Affiliation country: Bmjopen-2020-041983