Early anakinra treatment improves cardiac outcome of multisystem inflammatory syndrome in children regardless of disease severity.
MIS-C
SARS-CoV-2
anakinra
cardiac outcome
children
Journal
Rheumatology (Oxford, England)
ISSN: 1462-0332
Titre abrégé: Rheumatology (Oxford)
Pays: England
ID NLM: 100883501
Informations de publication
Date de publication:
30 Aug 2023
30 Aug 2023
Historique:
received:
02
03
2023
revised:
13
06
2023
accepted:
10
07
2023
medline:
30
8
2023
pubmed:
30
8
2023
entrez:
30
8
2023
Statut:
aheadofprint
Résumé
The main aim of this study was to define the best treatment option for multisystem inflammatory syndrome in children (MIS-C) and to analyze the role of anakinra. This is a multicentre retrospective cohort study. Patients were treated according to the attending physician's decision. The patients were divided in 4 groups on the basis of the first treatment at time of admittance: i) intravenous immunoglobulins (IVIG), ii) IVIG and methylprednisolone (≤ 2 mg/kg/day), iii) IVIG with high dose methylprednisolone (>2 mg/kg/day) and iv) anakinra with or without IVIG and/or methylprednisolone. Primary outcomes were defined as the presence of at least one of the following features: death, the failure of initial treatment, meaning the need of additional treatment for clinical worsening and cardiac involvement at the end of follow-up. Two hundred thirty-nine patients were recruited. At univariate analysis, persistent heart involvement at discharge was more frequent in those not receiving anakinra as initial treatment (3/21 vs 66/189; p= 0.047). After comparison of the 4 treatment regimens adjusting for the propensity score, we observed that early treatment with anakinra was associated with a lower probability to develop persistent heart disease at the end of follow-up (OR: 0.6; 95% CI: 0.4-1.0). We report that early treatment with anakinra is safe and very effective in patients with severe MIS-C. In addition, our study suggests that early treatment with anakinra is the most favorable option for patients with a higher risk to develop a severe disease outcome.
Identifiants
pubmed: 37647645
pii: 7255901
doi: 10.1093/rheumatology/kead381
pii:
doi:
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Informations de copyright
© The Author(s) 2023. Published by Oxford University Press on behalf of the British Society for Rheumatology. All rights reserved. For permissions, please email: journals.permissions@oup.com.