Outcomes of SARS-CoV-2 infection among children and young people with pre-existing rheumatic and musculoskeletal diseases.

Kearsley-Fleet, LORCID logo; Chang, MORCID logo; Lawson-Tovey, SORCID logo; Costello, RORCID logo; Fingerhutová, ŠORCID logo; Švestková, N; Belot, AORCID logo; Aeschlimann, FAORCID logo; Melki, IORCID logo; Koné-Paut, IORCID logo; +17 more...Eulert, SORCID logo; Kallinich, TORCID logo; Berkun, YORCID logo; Uziel, YORCID logo; Raffeiner, BORCID logo; Oliveira Ramos, F; Clemente, DORCID logo; Dackhammar, CORCID logo; Wulffraat, NMORCID logo; Waite, HORCID logo; Strangfeld, AORCID logo; Mateus, EFORCID logo; Machado, PMORCID logo; CARRA Registry Investigators; COVID-19 Global Pediatric Rheumatology Database Investigators; Natter, MORCID logo; Hyrich, KLORCID logo and (2022) Outcomes of SARS-CoV-2 infection among children and young people with pre-existing rheumatic and musculoskeletal diseases. Annals of the Rheumatic Diseases, 81 (7). pp. 998-1005. ISSN 0003-4967 DOI: 10.1136/annrheumdis-2022-222241
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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.


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