dc.contributor.author |
Berenguer, Juan |
dc.contributor.author |
Borobia, Alberto M. |
dc.contributor.author |
Ryan, Pablo |
dc.contributor.author |
Rodríguez Baño, Jesús |
dc.contributor.author |
Bellón, José M. |
dc.contributor.author |
Jarrín, Inmaculada |
dc.contributor.author |
Carratalà, Jordi |
dc.contributor.author |
Pachón, Jerónimo |
dc.contributor.author |
Carcas, Antonio J. |
dc.contributor.author |
Yllescas, María |
dc.contributor.author |
Arribas, José Ramón |
dc.date.accessioned |
2022-09-28T07:15:47Z |
dc.date.available |
2022-09-28T07:15:47Z |
dc.date.issued |
2021 |
dc.identifier.citation |
Berenguer J, Borobia AM, Ryan P, Rodríguez-Baño J, Bellón JM, Jarrín I, et al. Development and validation of a prediction model for 30-day mortality in hospitalised patients with COVID-19: the COVID-19 SEIMC score. Thorax. 2021 Sep; 76(9): 920-9. DOI: 10.1136/thoraxjnl-2020-216001 |
dc.identifier.issn |
0040-6376 |
dc.identifier.uri |
http://hdl.handle.net/10230/54190 |
dc.description.abstract |
Objective: to develop and validate a prediction model of mortality in patients with COVID-19 attending hospital emergency rooms. Design: Multivariable prognostic prediction model. Setting: 127 Spanish hospitals. Participants: derivation (DC) and external validation (VC) cohorts were obtained from multicentre and single-centre databases, including 4035 and 2126 patients with confirmed COVID-19, respectively. Interventions: prognostic variables were identified using multivariable logistic regression. Main outcome measures: 30-day mortality. Results: patients' characteristics in the DC and VC were median age 70 and 61 years, male sex 61.0% and 47.9%, median time from onset of symptoms to admission 5 and 8 days, and 30-day mortality 26.6% and 15.5%, respectively. Age, low age-adjusted saturation of oxygen, neutrophil-to-lymphocyte ratio, estimated glomerular filtration rate by the Chronic Kidney Disease Epidemiology Collaboration (CKD-EPI) equation, dyspnoea and sex were the strongest predictors of mortality. Calibration and discrimination were satisfactory with an area under the receiver operating characteristic curve with a 95% CI for prediction of 30-day mortality of 0.822 (0.806-0.837) in the DC and 0.845 (0.819-0.870) in the VC. A simplified score system ranging from 0 to 30 to predict 30-day mortality was also developed. The risk was considered to be low with 0-2 points (0%-2.1%), moderate with 3-5 (4.7%-6.3%), high with 6-8 (10.6%-19.5%) and very high with 9-30 (27.7%-100%). Conclusions: a simple prediction score, based on readily available clinical and laboratory data, provides a useful tool to predict 30-day mortality probability with a high degree of accuracy among hospitalised patients with COVID-19. |
dc.format.mimetype |
application/pdf |
dc.language.iso |
eng |
dc.publisher |
BMJ Publishing Group |
dc.rights |
Copyright © Author(s) (or their employer(s)) 2021. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/. |
dc.rights.uri |
http://creativecommons.org/licenses/by-nc/4.0 |
dc.title |
Development and validation of a prediction model for 30-day mortality in hospitalised patients with COVID-19: the COVID-19 SEIMC score |
dc.type |
info:eu-repo/semantics/article |
dc.identifier.doi |
http://dx.doi.org/10.1136/thoraxjnl-2020-216001 |
dc.subject.keyword |
Clinical epidemiology |
dc.subject.keyword |
Critical care |
dc.subject.keyword |
Emergency medicine |
dc.subject.keyword |
Pneumonia |
dc.subject.keyword |
Respiratory infection |
dc.subject.keyword |
Viral infection |
dc.rights.accessRights |
info:eu-repo/semantics/openAccess |
dc.type.version |
info:eu-repo/semantics/publishedVersion |