BMJ Health & Care Informatics (Mar 2021)

Validation of parsimonious prognostic models for patients infected with COVID-19

  • Nicole M Adler,
  • Leora I Horwitz,
  • Yindalon Aphinyanaphongs,
  • Ben Zhang,
  • Keerthi Harish,
  • Peter Stella,
  • Kevin Hauck,
  • Marwa M Moussa

DOI
https://doi.org/10.1136/bmjhci-2020-100267
Journal volume & issue
Vol. 28, no. 1

Abstract

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Objectives Predictive studies play important roles in the development of models informing care for patients with COVID-19. Our concern is that studies producing ill-performing models may lead to inappropriate clinical decision-making. Thus, our objective is to summarise and characterise performance of prognostic models for COVID-19 on external data.Methods We performed a validation of parsimonious prognostic models for patients with COVID-19 from a literature search for published and preprint articles. Ten models meeting inclusion criteria were either (a) externally validated with our data against the model variables and weights or (b) rebuilt using original features if no weights were provided. Nine studies had internally or externally validated models on cohorts of between 18 and 320 inpatients with COVID-19. One model used cross-validation. Our external validation cohort consisted of 4444 patients with COVID-19 hospitalised between 1 March and 27 May 2020.Results Most models failed validation when applied to our institution’s data. Included studies reported an average validation area under the receiver–operator curve (AUROC) of 0.828. Models applied with reported features averaged an AUROC of 0.66 when validated on our data. Models rebuilt with the same features averaged an AUROC of 0.755 when validated on our data. In both cases, models did not validate against their studies’ reported AUROC values.Discussion Published and preprint prognostic models for patients infected with COVID-19 performed substantially worse when applied to external data. Further inquiry is required to elucidate mechanisms underlying performance deviations.Conclusions Clinicians should employ caution when applying models for clinical prediction without careful validation on local data.