TY - JOUR
T1 - Outcomes of SARS-CoV-2 infection among children and young people with pre-existing rheumatic and musculoskeletal diseases
AU - Kearsley-Fleet, Lianne
AU - Chang, Min Lee
AU - Lawson-Tovey, Saskia
AU - Costello, Ruth
AU - Fingerhutová, Šárka
AU - Švestková, Natálie
AU - Belot, Alexandre
AU - Aeschlimann, Florence A.
AU - Melki, Isabelle
AU - Koné-Paut, Isabelle
AU - Eulert, Sascha
AU - Kallinich, Tilmann
AU - Berkun, Yackov
AU - Uziel, Yosef
AU - Raffeiner, Bernd
AU - Oliveira Ramos, Filipa
AU - Clemente, Daniel
AU - Dackhammar, Christina
AU - Wulffraat, Nico M.
AU - Waite, Helen
AU - Strangfeld, Anja
AU - Mateus, Elsa F.
AU - Machado, Pedro M.
AU - Natter, Marc
AU - Hyrich, Kimme L.
N1 - Funding Information:
Twitter Lianne Kearsley-Fleet @KearsleyFleet, Saskia Lawson-Tovey @saskiaamber, Ruth Costello @RcostelloEpi, Pedro M Machado @pedrommcmachado and Kimme L Hyrich @khyrich Acknowledgements We wish to thank all rheumatology providers who entered data into the EULAR COVID-19 Registry, and the CARRA databases. We also wish to acknowledge the efforts provided by Anne Dennos and Dr. Timothy Beukelman for reviewing the CARRA Registry COVID-19 ESI reports. This work could not have been accomplished without the aid of the following organisations: The NIH’s National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS), the Arthritis Foundation and members of the Paediatric Rheumatology European Society (PReS). We would also like to thank all participants and hospital sites that recruited patients for the CARRA Registry. The authors thank the CARRA Registry and CARRA-sponsored COVID-19 Global Paediatric Database site principal investigators, sub-investigators and research coordinators (see supplementary materials). In Germany, the cases were collected via an add-on module of the national paediatric rheumatologic database (NPRD), which is currently funded by the German Research Foundation (Kick-COVID, MI 2760/1-1) and the companies Chugai, GSK and Novartis. We are grateful to all patients and their parents for participating in the NPRD and to all colleagues who contributed to this data collection (see online supplemental materials).
Funding Information:
Funding This publication was supported by funding from the European Alliance of Associations for Rheumatology (EULAR), and NIH/NCATS Colorado CTSA Grant Number UL1 TR002535, and CARRA. PPM is supported by the National Institute for Health Research (NIHR) University College London Hospitals (UCLH) Biomedical Research Centre. KLH is supported by the NIHR Manchester Biomedical Research Centre.
Publisher Copyright:
© Author(s) (or their employer(s)) 2022. No commercial re-use. See rights and permissions. Published by BMJ.
PY - 2022/7/1
Y1 - 2022/7/1
N2 - Objectives Some adults with rheumatic and musculoskeletal diseases (RMDs) are at increased risk of COVID-19-related death. Excluding post-COVID-19 multisystem inflammatory syndrome of children, children and young people (CYP) are overall less prone to severe COVID-19 and most experience a mild or asymptomatic course. However, it is unknown if CYP with RMDs are more likely to have more severe COVID-19. This analysis aims to describe outcomes among CYP with underlying RMDs with COVID-19. Methods Using the European Alliance of Associations for Rheumatology COVID-19 Registry, the Childhood Arthritis and Rheumatology Research Alliance (CARRA) Registry, and the CARRA-sponsored COVID-19 Global Paediatric Rheumatology Database, we obtained data on CYP with RMDs who reported SARS-CoV-2 infection (presumptive or confirmed). Patient characteristics and illness severity were described, and factors associated with COVID-19 hospitalisation were investigated. Results 607 CYP with RMDs <19 years old from 25 different countries with SARS-CoV-2 infection were included, the majority with juvenile idiopathic arthritis (JIA; n=378; 62%). Forty-three (7%) patients were hospitalised; three of these patients died. Compared with JIA, diagnosis of systemic lupus erythematosus, mixed connective tissue disease, vasculitis, or other RMD (OR 4.3; 95% CI 1.7 to 11) or autoinflammatory syndrome (OR 3.0; 95% CI 1.1 to 8.6) was associated with hospitalisation, as was obesity (OR 4.0; 95% CI 1.3 to 12). Conclusions This is the most significant investigation to date of COVID-19 in CYP with RMDs. It is important to note that the majority of CYP were not hospitalised, although those with severe systemic RMDs and obesity were more likely to be hospitalised.
AB - Objectives Some adults with rheumatic and musculoskeletal diseases (RMDs) are at increased risk of COVID-19-related death. Excluding post-COVID-19 multisystem inflammatory syndrome of children, children and young people (CYP) are overall less prone to severe COVID-19 and most experience a mild or asymptomatic course. However, it is unknown if CYP with RMDs are more likely to have more severe COVID-19. This analysis aims to describe outcomes among CYP with underlying RMDs with COVID-19. Methods Using the European Alliance of Associations for Rheumatology COVID-19 Registry, the Childhood Arthritis and Rheumatology Research Alliance (CARRA) Registry, and the CARRA-sponsored COVID-19 Global Paediatric Rheumatology Database, we obtained data on CYP with RMDs who reported SARS-CoV-2 infection (presumptive or confirmed). Patient characteristics and illness severity were described, and factors associated with COVID-19 hospitalisation were investigated. Results 607 CYP with RMDs <19 years old from 25 different countries with SARS-CoV-2 infection were included, the majority with juvenile idiopathic arthritis (JIA; n=378; 62%). Forty-three (7%) patients were hospitalised; three of these patients died. Compared with JIA, diagnosis of systemic lupus erythematosus, mixed connective tissue disease, vasculitis, or other RMD (OR 4.3; 95% CI 1.7 to 11) or autoinflammatory syndrome (OR 3.0; 95% CI 1.1 to 8.6) was associated with hospitalisation, as was obesity (OR 4.0; 95% CI 1.3 to 12). Conclusions This is the most significant investigation to date of COVID-19 in CYP with RMDs. It is important to note that the majority of CYP were not hospitalised, although those with severe systemic RMDs and obesity were more likely to be hospitalised.
KW - Arthritis
KW - Covid-19
KW - Infections
KW - Juvenile
UR - http://www.scopus.com/inward/record.url?scp=85132192631&partnerID=8YFLogxK
U2 - 10.1136/annrheumdis-2022-222241
DO - 10.1136/annrheumdis-2022-222241
M3 - Article
C2 - 35338032
AN - SCOPUS:85132192631
SN - 0003-4967
VL - 81
SP - 998
EP - 1005
JO - Annals of the rheumatic diseases
JF - Annals of the rheumatic diseases
IS - 7
ER -