TY - JOUR
T1 - COVID-19 in patients with autoimmune diseases
T2 - characteristics and outcomes in a multinational network of cohorts across three countries
AU - Tan, Eng Hooi
AU - Sena, Anthony G.
AU - Prats-Uribe, Albert
AU - You, Seng Chan
AU - Ahmed, Waheed-Ul-Rahman
AU - Kostka, Kristin
AU - Reich, Christian
AU - Duvall, Scott L.
AU - Lynch, Kristine E.
AU - Matheny, Michael E.
AU - Duarte-Salles, Talita
AU - Bertolin, Sergio Fernandez
AU - Hripcsak, George
AU - Natarajan, Karthik
AU - Falconer, Thomas
AU - Spotnitz, Matthew
AU - Ostropolets, Anna
AU - Blacketer, Clair
AU - Alshammari, Thamir M.
AU - Alghoul, Heba
AU - Alser, Osaid
AU - Lane, Jennifer C. E.
AU - Dawoud, Dalia M.
AU - Shah, Karishma
AU - Yang, Yue
AU - Zhang, Lin
AU - Areia, Carlos
AU - Golozar, Asieh
AU - Recalde, Martina
AU - Casajust, Paula
AU - Jonnagaddala, Jitendra
AU - Subbian, Vignesh
AU - Vizcaya, David
AU - Lai, Lana Y. H.
AU - Nyberg, Fredrik
AU - Morales, Daniel R.
AU - Posada, Jose D.
AU - Shah, Nigam H.
AU - Gong, Mengchun
AU - Vivekanantham, Arani
AU - Abend, Aaron
AU - Minty, Evan P.
AU - Suchard, Marc
AU - Rijnbeek, Peter
AU - Ryan, Patrick B.
AU - Prieto-Alhambra, Daniel
N1 - The European Health Data & Evidence Network (EHDEN) has received funding from the Innovative Medicines Initiative (IMI) 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 European Federation of Pharmaceutical Industries and Associations (EFPIA). The University of Oxford received a grant related to this work from the Bill & Melinda Gates Foundation (Investment ID INV-016201). This research received partial support from the National Institute for Health Research (NIHR) Oxford Biomedical Research Centre (BRC), US National Institutes of Health, US Department of Veterans Affairs, Janssen Research & Development, and IQVIA. This work was also supported by the Bio Industrial Strategic Technology Development Program (20001234) funded by the Ministry of Trade, Industry & Energy (MOTIE, 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), and the Health Department from the Generalitat de Catalunya with a grant for research projects on SARSCoV-2 and COVID-19 disease organized by the Direcció General de Recerca i Innovació en Salut. DPA is funded through a National Institute for Health Research (NIHR) Senior Research Fellowship (Grant number SRF-2018-11-ST2-004). APU is supported by MRC-DTP [MR/K501256/1, MR/N013468/1] and Fundación Alfonso Martín Escudero (FAME). GHsupported by the US National Library of Medicine (LM006910)
PY - 2021/10/6
Y1 - 2021/10/6
N2 - Objective: Patients with autoimmune diseases were advised to shield to avoid coronavirus disease 2019 (COVID-19), but information on their prognosis is lacking. We characterized 30-day outcomes and mortality after hospitalization with COVID-19 among patients with prevalent autoimmune diseases, and compared outcomes after hospital admissions among similar patients with seasonal influenza.Methods: A multinational network cohort study was conducted using electronic health records data from Columbia University Irving Medical Center [USA, Optum (USA), Department of Veterans Affairs (USA), Information System for Research in Primary Care-Hospitalization Linked Data (Spain) and claims data from IQVIA Open Claims (USA) and Health Insurance and Review Assessment (South Korea). All patients with prevalent autoimmune diseases, diagnosed and/or hospitalized between January and June 2020 with COVID-19, and similar patients hospitalized with influenza in 2017-18 were included. Outcomes were death and complications within 30 days of hospitalization.Results: We studied 133 589 patients diagnosed and 48 418 hospitalized with COVID-19 with prevalent autoimmune diseases. Most patients were female, aged ≥50 years with previous comorbidities. The prevalence of hypertension (45.5-93.2%), chronic kidney disease (14.0-52.7%) and heart disease (29.0-83.8%) was higher in hospitalized vs diagnosed patients with COVID-19. Compared with 70 660 hospitalized with influenza, those admitted with COVID-19 had more respiratory complications including pneumonia and acute respiratory distress syndrome, and higher 30-day mortality (2.2-4.3% vs 6.32-24.6%).Conclusion: Compared with influenza, COVID-19 is a more severe disease, leading to more complications and higher mortality.
AB - Objective: Patients with autoimmune diseases were advised to shield to avoid coronavirus disease 2019 (COVID-19), but information on their prognosis is lacking. We characterized 30-day outcomes and mortality after hospitalization with COVID-19 among patients with prevalent autoimmune diseases, and compared outcomes after hospital admissions among similar patients with seasonal influenza.Methods: A multinational network cohort study was conducted using electronic health records data from Columbia University Irving Medical Center [USA, Optum (USA), Department of Veterans Affairs (USA), Information System for Research in Primary Care-Hospitalization Linked Data (Spain) and claims data from IQVIA Open Claims (USA) and Health Insurance and Review Assessment (South Korea). All patients with prevalent autoimmune diseases, diagnosed and/or hospitalized between January and June 2020 with COVID-19, and similar patients hospitalized with influenza in 2017-18 were included. Outcomes were death and complications within 30 days of hospitalization.Results: We studied 133 589 patients diagnosed and 48 418 hospitalized with COVID-19 with prevalent autoimmune diseases. Most patients were female, aged ≥50 years with previous comorbidities. The prevalence of hypertension (45.5-93.2%), chronic kidney disease (14.0-52.7%) and heart disease (29.0-83.8%) was higher in hospitalized vs diagnosed patients with COVID-19. Compared with 70 660 hospitalized with influenza, those admitted with COVID-19 had more respiratory complications including pneumonia and acute respiratory distress syndrome, and higher 30-day mortality (2.2-4.3% vs 6.32-24.6%).Conclusion: Compared with influenza, COVID-19 is a more severe disease, leading to more complications and higher mortality.
KW - COVID-19
KW - Observational Health Data Sciences and Informatics (OHDSI)
KW - Observational Medical Outcomes Partnership (OMOP)
KW - autoimmune condition
KW - hospitalization
KW - mortality
KW - open science
UR - http://www.scopus.com/inward/record.url?scp=85111765204&partnerID=8YFLogxK
U2 - 10.1093/rheumatology/keab250
DO - 10.1093/rheumatology/keab250
M3 - Article
C2 - 33725121
SN - 1462-0324
VL - 60
SP - SI37-SI50
JO - Rheumatology
JF - Rheumatology
IS - SI
ER -