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Delineating COVID-19 subgroups using routine clinical data identifies distinct in-hospital outcomes
The COVID-19 pandemic has been a great challenge to healthcare systems worldwide. It highlighted the need for robust predictive models which can be readily deployed to uncover heterogeneities in disease course, aid decision-making and prioritise treatment. We adapted an unsupervised data-driven mode...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10282086/ https://www.ncbi.nlm.nih.gov/pubmed/37339958 http://dx.doi.org/10.1038/s41598-023-32469-9 |
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author | Rangelov, Bojidar Young, Alexandra Lilaonitkul, Watjana Aslani, Shahab Taylor, Paul Guðmundsson, Eyjólfur Yang, Qianye Hu, Yipeng Hurst, John R. Hawkes, David J. Jacob, Joseph |
author_facet | Rangelov, Bojidar Young, Alexandra Lilaonitkul, Watjana Aslani, Shahab Taylor, Paul Guðmundsson, Eyjólfur Yang, Qianye Hu, Yipeng Hurst, John R. Hawkes, David J. Jacob, Joseph |
author_sort | Rangelov, Bojidar |
collection | PubMed |
description | The COVID-19 pandemic has been a great challenge to healthcare systems worldwide. It highlighted the need for robust predictive models which can be readily deployed to uncover heterogeneities in disease course, aid decision-making and prioritise treatment. We adapted an unsupervised data-driven model—SuStaIn, to be utilised for short-term infectious disease like COVID-19, based on 11 commonly recorded clinical measures. We used 1344 patients from the National COVID-19 Chest Imaging Database (NCCID), hospitalised for RT-PCR confirmed COVID-19 disease, splitting them equally into a training and an independent validation cohort. We discovered three COVID-19 subtypes (General Haemodynamic, Renal and Immunological) and introduced disease severity stages, both of which were predictive of distinct risks of in-hospital mortality or escalation of treatment, when analysed using Cox Proportional Hazards models. A low-risk Normal-appearing subtype was also discovered. The model and our full pipeline are available online and can be adapted for future outbreaks of COVID-19 or other infectious disease. |
format | Online Article Text |
id | pubmed-10282086 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-102820862023-06-22 Delineating COVID-19 subgroups using routine clinical data identifies distinct in-hospital outcomes Rangelov, Bojidar Young, Alexandra Lilaonitkul, Watjana Aslani, Shahab Taylor, Paul Guðmundsson, Eyjólfur Yang, Qianye Hu, Yipeng Hurst, John R. Hawkes, David J. Jacob, Joseph Sci Rep Article The COVID-19 pandemic has been a great challenge to healthcare systems worldwide. It highlighted the need for robust predictive models which can be readily deployed to uncover heterogeneities in disease course, aid decision-making and prioritise treatment. We adapted an unsupervised data-driven model—SuStaIn, to be utilised for short-term infectious disease like COVID-19, based on 11 commonly recorded clinical measures. We used 1344 patients from the National COVID-19 Chest Imaging Database (NCCID), hospitalised for RT-PCR confirmed COVID-19 disease, splitting them equally into a training and an independent validation cohort. We discovered three COVID-19 subtypes (General Haemodynamic, Renal and Immunological) and introduced disease severity stages, both of which were predictive of distinct risks of in-hospital mortality or escalation of treatment, when analysed using Cox Proportional Hazards models. A low-risk Normal-appearing subtype was also discovered. The model and our full pipeline are available online and can be adapted for future outbreaks of COVID-19 or other infectious disease. Nature Publishing Group UK 2023-06-20 /pmc/articles/PMC10282086/ /pubmed/37339958 http://dx.doi.org/10.1038/s41598-023-32469-9 Text en © The Author(s) 2023, corrected publication 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Rangelov, Bojidar Young, Alexandra Lilaonitkul, Watjana Aslani, Shahab Taylor, Paul Guðmundsson, Eyjólfur Yang, Qianye Hu, Yipeng Hurst, John R. Hawkes, David J. Jacob, Joseph Delineating COVID-19 subgroups using routine clinical data identifies distinct in-hospital outcomes |
title | Delineating COVID-19 subgroups using routine clinical data identifies distinct in-hospital outcomes |
title_full | Delineating COVID-19 subgroups using routine clinical data identifies distinct in-hospital outcomes |
title_fullStr | Delineating COVID-19 subgroups using routine clinical data identifies distinct in-hospital outcomes |
title_full_unstemmed | Delineating COVID-19 subgroups using routine clinical data identifies distinct in-hospital outcomes |
title_short | Delineating COVID-19 subgroups using routine clinical data identifies distinct in-hospital outcomes |
title_sort | delineating covid-19 subgroups using routine clinical data identifies distinct in-hospital outcomes |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10282086/ https://www.ncbi.nlm.nih.gov/pubmed/37339958 http://dx.doi.org/10.1038/s41598-023-32469-9 |
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