Hide metadata

dc.date.accessioned2024-02-11T17:47:33Z
dc.date.available2024-02-11T17:47:33Z
dc.date.created2024-01-08T17:23:22Z
dc.date.issued2023
dc.identifier.citationShakibfar, Saeed Zhao, Jing Li, Huiqi Nordeng, Hedvig Marie Egeland Lupattelli, Angela Pavlović, Milena Sandve, Geir Kjetil Ferkingstad Nyberg, Fredrik Wettermark, Björn Hajiebrahimi, Mohammadhossein Andersen, Morten Sessa, Maurizio . Machine learning-driven development of a disease risk score for COVID-19 hospitalization and mortality: a Swedish and Norwegian register-based study. Frontiers in Public Health. 2023, 11
dc.identifier.urihttp://hdl.handle.net/10852/107878
dc.description.abstractAims To develop a disease risk score for COVID-19-related hospitalization and mortality in Sweden and externally validate it in Norway. Method We employed linked data from the national health registries of Sweden and Norway to conduct our study. We focused on individuals in Sweden with confirmed SARS-CoV-2 infection through RT-PCR testing up to August 2022 as our study cohort. Within this group, we identified hospitalized cases as those who were admitted to the hospital within 14 days of testing positive for SARS-CoV-2 and matched them with five controls from the same cohort who were not hospitalized due to SARS-CoV-2. Additionally, we identified individuals who died within 30 days after being hospitalized for COVID-19. To develop our disease risk scores, we considered various factors, including demographics, infectious, somatic, and mental health conditions, recorded diagnoses, and pharmacological treatments. We also conducted age-specific analyses and assessed model performance through 5-fold cross-validation. Finally, we performed external validation using data from the Norwegian population with COVID-19 up to December 2021. Results During the study period, a total of 124,560 individuals in Sweden were hospitalized, and 15,877 individuals died within 30 days following COVID-19 hospitalization. Disease risk scores for both hospitalization and mortality demonstrated predictive capabilities with ROC-AUC values of 0.70 and 0.72, respectively, across the entire study period. Notably, these scores exhibited a positive correlation with the likelihood of hospitalization or death. In the external validation using data from the Norwegian COVID-19 population (consisting of 53,744 individuals), the disease risk score predicted hospitalization with an AUC of 0.47 and death with an AUC of 0.74. Conclusion The disease risk score showed moderately good performance to predict COVID-19-related mortality but performed poorly in predicting hospitalization when externally validated.
dc.languageEN
dc.rightsAttribution 4.0 International
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.titleMachine learning-driven development of a disease risk score for COVID-19 hospitalization and mortality: a Swedish and Norwegian register-based study
dc.title.alternativeENEngelskEnglishMachine learning-driven development of a disease risk score for COVID-19 hospitalization and mortality: a Swedish and Norwegian register-based study
dc.typeJournal article
dc.creator.authorShakibfar, Saeed
dc.creator.authorZhao, Jing
dc.creator.authorLi, Huiqi
dc.creator.authorNordeng, Hedvig Marie Egeland
dc.creator.authorLupattelli, Angela
dc.creator.authorPavlović, Milena
dc.creator.authorSandve, Geir Kjetil Ferkingstad
dc.creator.authorNyberg, Fredrik
dc.creator.authorWettermark, Björn
dc.creator.authorHajiebrahimi, Mohammadhossein
dc.creator.authorAndersen, Morten
dc.creator.authorSessa, Maurizio
cristin.unitcode185,15,23,10
cristin.unitnameSeksjon for galenisk farmasi og samfunns
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1
dc.identifier.cristin2222641
dc.identifier.bibliographiccitationinfo:ofi/fmt:kev:mtx:ctx&ctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=Frontiers in Public Health&rft.volume=11&rft.spage=&rft.date=2023
dc.identifier.jtitleFrontiers in Public Health
dc.identifier.volume11
dc.identifier.pagecount0
dc.identifier.doihttps://doi.org/10.3389/fpubh.2023.1258840
dc.type.documentTidsskriftartikkel
dc.type.peerreviewedPeer reviewed
dc.source.issn2296-2565
dc.type.versionPublishedVersion
cristin.articleid125884
dc.relation.projectNORDFORSK/105670
dc.relation.projectNFR/312707


Files in this item

Appears in the following Collection

Hide metadata

Attribution 4.0 International
This item's license is: Attribution 4.0 International