TY - JOUR
T1 - Implementation of the COVID-19 vulnerability index across an international network of health care data sets
T2 - Collaborative external validation study
AU - Reps, Jenna M.
AU - Kim, Chungsoo
AU - Williams, Ross D.
AU - Markus, Aniek F.
AU - Yang, Cynthia
AU - Salles, Talita Duarte
AU - Falconer, Thomas
AU - Jonnagaddala, Jitendra
AU - Williams, Andrew
AU - Fernández-Bertolín, Sergio
AU - DuVall, Scott L.
AU - Kostka, Kristin
AU - Rao, Gowtham
AU - Shoaibi, Azza
AU - Ostropolets, Anna
AU - Spotnitz, Matthew E.
AU - Zhang, Lin
AU - Casajust, Paula
AU - Steyerberg, Ewout W.
AU - Nyberg, Fredrik
AU - Kaas-Hansen, Benjamin Skov
AU - Choi, Young Hwa
AU - Morales, Daniel
AU - Liaw, Siaw-Teng
AU - Abrahão, Maria Tereza Fernandes
AU - Areia, Carlos
AU - Matheny, Michael E.
AU - Aragón, María
AU - Park, Rae Woong
AU - Hripcsak, George
AU - Reich, Christian G.
AU - Suchard, Marc A.
AU - You, Seng Chan
AU - Ryan, Patrick B.
AU - Prieto-Alhambra, Daniel
AU - Rijnbeek, Peter R.
N1 - We would like to acknowledge the patients who have contracted or died of this devastating disease, as well as their families and caregivers. We would also like to thank the health care professionals involved in the management of COVID-19 during these challenging times, from primary care to intensive care units. The authors appreciate the health care professionals dedicated to treating patients with COVID-19 in Korea and the Ministry of Health and Welfare and the Health Insurance Review & Assessment Service of Korea for sharing invaluable national health insurance claims data in a prompt manner. This project has received support from the European Health Data and Evidence Network (EHDEN) project. EHDEN received funding from the Innovative Medicines Initiative 2 Joint Undertaking (JU) under grant agreement No 806968. The JU receives support from the European Union’s Horizon 2020 research and innovation programme and EFPIA. This work was also supported by the Bio Industrial Strategic Technology Development Program (20001234, 20003883) funded by the Ministry of Trade, Industry & Energy (Korea) and a grant from the Korea Health Technology R&D Project through the Korea Health Industry Development Institute (KHIDI), funded by the Ministry of Health & Welfare, Republic of Korea [grant number: HI16C0992]. This project is funded by the Health Department from the Generalitat de Catalunya with a grant for research projects on SARS-CoV-2 and COVID-19 disease organized by the Direcció General de Recerca i Innovació en Salut. The University of Oxford received a grant related to this work from the Bill & Melinda Gates Foundation (Investment ID INV-016201) and partial support from the UK National Institute for Health Research (NIHR) Oxford Biomedical Research Centre. DPA is funded through a NIHR Senior Research Fellowship (Grant number SRF-2018-11-ST2-004). The views expressed in this publication are those of the author(s) and not necessarily those of the National Health Service, the National Institute for Health Research, the Department of Health, the Department of Veterans Affairs, or the United States Government. BSKH is funded through Innovation Fund Denmark (5153-00002B) and the Novo Nordisk Foundation (NNF14CC0001). This project is part funded by the University of New South Wales Research Infrastructure Scheme grant. SLD and MEM report funding from NIH NHBLI R-01, NIH NIDDK R-01 grant, and VA HSR&D. This work was supported using resources and facilities of the Department of Veterans Affairs (VA) Informatics and Computing Infrastructure (VINCI), VA HSR RES 13-457.
Publisher Copyright:
© 2021 JMIR Publications Inc.. All right reserved.
PY - 2021/4
Y1 - 2021/4
N2 - Background: SARS-CoV-2 is straining health care systems globally. The burden on hospitals during the pandemic could be reduced by implementing prediction models that can discriminate patients who require hospitalization from those who do not. The COVID-19 vulnerability (C-19) index, a model that predicts which patients will be admitted to hospital for treatment of pneumonia or pneumonia proxies, has been developed and proposed as a valuable tool for decision-making during the pandemic. However, the model is at high risk of bias according to the "prediction model risk of bias assessment" criteria, and it has not been externally validated.Objective: The aim of this study was to externally validate the C-19 index across a range of health care settings to determine how well it broadly predicts hospitalization due to pneumonia in COVID-19 cases.Methods: We followed the Observational Health Data Sciences and Informatics (OHDSI) framework for external validation to assess the reliability of the C-19 index. We evaluated the model on two different target populations, 41,381 patients who presented with SARS-CoV-2 at an outpatient or emergency department visit and 9,429,285 patients who presented with influenza or related symptoms during an outpatient or emergency department visit, to predict their risk of hospitalization with pneumonia during the following 0-30 days. In total, we validated the model across a network of 14 databases spanning the United States, Europe, Australia, and Asia.Results: The internal validation performance of the C-19 index had a C statistic of 0.73, and the calibration was not reported by the authors. When we externally validated it by transporting it to SARS-CoV-2 data, the model obtained C statistics of 0.36, 0.53 (0.473-0.584) and 0.56 (0.488-0.636) on Spanish, US, and South Korean data sets, respectively. The calibration was poor, with the model underestimating risk. When validated on 12 data sets containing influenza patients across the OHDSI network, the C statistics ranged between 0.40 and 0.68.Conclusions: Our results show that the discriminative performance of the C-19 index model is low for influenza cohorts and even worse among patients with COVID-19 in the United States, Spain, and South Korea. These results suggest that C-19 should not be used to aid decision-making during the COVID-19 pandemic. Our findings highlight the importance of performing external validation across a range of settings, especially when a prediction model is being extrapolated to a different population. In the field of prediction, extensive validation is required to create appropriate trust in a model.
AB - Background: SARS-CoV-2 is straining health care systems globally. The burden on hospitals during the pandemic could be reduced by implementing prediction models that can discriminate patients who require hospitalization from those who do not. The COVID-19 vulnerability (C-19) index, a model that predicts which patients will be admitted to hospital for treatment of pneumonia or pneumonia proxies, has been developed and proposed as a valuable tool for decision-making during the pandemic. However, the model is at high risk of bias according to the "prediction model risk of bias assessment" criteria, and it has not been externally validated.Objective: The aim of this study was to externally validate the C-19 index across a range of health care settings to determine how well it broadly predicts hospitalization due to pneumonia in COVID-19 cases.Methods: We followed the Observational Health Data Sciences and Informatics (OHDSI) framework for external validation to assess the reliability of the C-19 index. We evaluated the model on two different target populations, 41,381 patients who presented with SARS-CoV-2 at an outpatient or emergency department visit and 9,429,285 patients who presented with influenza or related symptoms during an outpatient or emergency department visit, to predict their risk of hospitalization with pneumonia during the following 0-30 days. In total, we validated the model across a network of 14 databases spanning the United States, Europe, Australia, and Asia.Results: The internal validation performance of the C-19 index had a C statistic of 0.73, and the calibration was not reported by the authors. When we externally validated it by transporting it to SARS-CoV-2 data, the model obtained C statistics of 0.36, 0.53 (0.473-0.584) and 0.56 (0.488-0.636) on Spanish, US, and South Korean data sets, respectively. The calibration was poor, with the model underestimating risk. When validated on 12 data sets containing influenza patients across the OHDSI network, the C statistics ranged between 0.40 and 0.68.Conclusions: Our results show that the discriminative performance of the C-19 index model is low for influenza cohorts and even worse among patients with COVID-19 in the United States, Spain, and South Korea. These results suggest that C-19 should not be used to aid decision-making during the COVID-19 pandemic. Our findings highlight the importance of performing external validation across a range of settings, especially when a prediction model is being extrapolated to a different population. In the field of prediction, extensive validation is required to create appropriate trust in a model.
KW - Bias
KW - C-19
KW - COVID-19
KW - Datasets
KW - Decision-making
KW - External validation
KW - Hospitalization
KW - Modeling
KW - Observation
KW - Prediction
KW - Prognostic model
KW - Risk
KW - Transportability
UR - http://www.scopus.com/inward/record.url?scp=85104129882&partnerID=8YFLogxK
U2 - 10.2196/21547
DO - 10.2196/21547
M3 - Article
C2 - 33661754
SN - 2291-9694
VL - 9
JO - JMIR Medical Informatics
JF - JMIR Medical Informatics
IS - 4
M1 - e21547
ER -