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dc.contributor.authorWickstrøm, Kristin E.
dc.contributor.authorVitelli, Valeria
dc.contributor.authorCarr, Ewan
dc.contributor.authorHolten, Aleksander R.
dc.contributor.authorBendayan, Rebecca
dc.contributor.authorReiner, Andrew H.
dc.contributor.authorBean, Daniel
dc.contributor.authorSearle, Tom
dc.contributor.authorShek, Anthony
dc.contributor.authorKraljevic, Zeljko
dc.contributor.authorTeo, James
dc.contributor.authorDobson, Richard
dc.contributor.authorTonby, Kristian
dc.contributor.authorKöhn-Luque, Alvaro
dc.contributor.authorAmundsen, Erik K.
dc.date.accessioned2021-10-15T19:05:06Z
dc.date.available2021-10-15T19:05:06Z
dc.date.created2021-09-15T16:13:53Z
dc.date.issued2021-08-25
dc.identifier.citationPLOS ONE. 2021, 16 (8), 1-13.en_US
dc.identifier.issn1932-6203
dc.identifier.urihttps://hdl.handle.net/11250/2823466
dc.description.abstractBackground: Prediction models should be externally validated to assess their performance before implementation. Several prediction models for coronavirus disease-19 (COVID-19) have been published. This observational cohort study aimed to validate published models of severity for hospitalized patients with COVID-19 using clinical and laboratory predictors. Methods: Prediction models fitting relevant inclusion criteria were chosen for validation. The outcome was either mortality or a composite outcome of mortality and ICU admission (severe disease). 1295 patients admitted with symptoms of COVID-19 at Kings Cross Hospital (KCH) in London, United Kingdom, and 307 patients at Oslo University Hospital (OUH) in Oslo, Norway were included. The performance of the models was assessed in terms of discrimination and calibration. Results: We identified two models for prediction of mortality (referred to as Xie and Zhang1) and two models for prediction of severe disease (Allenbach and Zhang2). The performance of the models was variable. For prediction of mortality Xie had good discrimination at OUH with an area under the receiver-operating characteristic (AUROC) 0.87 [95% confidence interval (CI) 0.79–0.95] and acceptable discrimination at KCH, AUROC 0.79 [0.76–0.82]. In prediction of severe disease, Allenbach had acceptable discrimination (OUH AUROC 0.81 [0.74–0.88] and KCH AUROC 0.72 [0.68–0.75]). The Zhang models had moderate to poor discrimination. Initial calibration was poor for all models but improved with recalibration. Conclusions: The performance of the four prediction models was variable. The Xie model had the best discrimination for mortality, while the Allenbach model had acceptable results for prediction of severe disease.en_US
dc.description.sponsorshipOne of the authors (JTHT) have previously received research support and funding from InnovateUL, Bristol-Myers-Squibb, iRhytm Technologies, and hold shares under £5000 in Glaxo SmithKline and Biogen.en_US
dc.language.isoengen_US
dc.publisherPublic Library of Scienceen_US
dc.relation.ispartofseriesPLOS ONE;16 (8): e0255748
dc.rightsNavngivelse 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/deed.no*
dc.subjectForecastingen_US
dc.subjectCOVID-19en_US
dc.subjectIntensive care unitsen_US
dc.subjectVirus testingen_US
dc.subjectLymphocytesen_US
dc.subjectOxygenen_US
dc.subjectClinical laboratoriesen_US
dc.titleRegional performance variation in external validation of four prediction models for severity of COVID-19 at hospital admission: An observational multi-centre cohort studyen_US
dc.typePeer revieweden_US
dc.typeJournal articleen_US
dc.description.versionpublishedVersionen_US
dc.rights.holder© 2021 Wickstrøm et al.en_US
dc.source.articlenumbere0255748en_US
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1
dc.identifier.doihttps://doi.org/10.1371/journal.pone.0255748
dc.identifier.cristin1934650
dc.source.journalPLOS ONEen_US
dc.source.volume16en_US
dc.source.issue8en_US
dc.source.pagenumber1-13en_US


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