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Treatment of Multisystem Inflammatory Syndrome in Children
Andrew J McArdle1, Ortensia Vito1, Harsita Patel1
1From the Department of Infectious Disease, Section of Pediatric Infectious Disease (A.J.M., O.V., H.P., E.G.S., P.S., C.W., C.B., R.N., T.D., E.W., J.A.H., M.K., A.J.C., M.L.), and the Inflammation, Repair, and Development Section, National Heart and Lung Institute, Faculty of Medicine (D.M.), Imperial College London, the Department of Pediatrics, Imperial College Healthcare NHS Trust (R.N., E.W., J.A.H., A.J.C., M.L.), and the Department of Women and Children's Health, School of Life Course Sciences, King's College London, St. Thomas' Hospital (M.J.C.), London, and the Genomic Informatics Group, University of Southampton, Southampton (E.G.S.) - all in the United Kingdom; the Translational Genomics Group, Broad Institute of MIT and Harvard, Cambridge, MA (E.G.S.); the Department of Pediatrics, University of California, San Diego, and Rady Children's Hospital, San Diego (A.H.T.); the Department of Pediatrics and Pediatric Infectious Diseases, Sechenov University, Moscow (D.M.); Servicio de Infectología, Hospital Nacional de Niños Dr. Carlos Sáenz Herrera, Centro de Ciencias Médicas, Caja Costarricense de Seguro Social, San José, Costa Rica (R.U.-G.); and the Department of Genetics and Genomic Sciences, Icahn School of Medicine at Mount Sinai, New York (C.H.).
Treatment for multisystem inflammatory syndrome in children (MIS-C) using intravenous immune globulin (IVIG) alone, with glucocorticoids, or both showed no significant differences in recovery. Further data may reveal subtle variations in MIS-C outcomes with different immunomodulatory therapies.
Area of Science:
- Pediatric critical care
- Infectious diseases
- Immunology
Background:
- Multisystem inflammatory syndrome in children (MIS-C) is a serious condition linked to SARS-CoV-2.
- Urgent evidence is needed to guide treatment decisions for pediatric MIS-C.
- Current treatment strategies lack definitive comparative data.
Purpose of the Study:
- To compare the effectiveness of different primary immunomodulatory treatments for MIS-C.
- To evaluate intravenous immune globulin (IVIG) alone versus IVIG plus glucocorticoids and glucocorticoids alone.
- To assess key clinical outcomes including need for support and disease severity reduction.
Main Methods:
- International observational cohort study of suspected MIS-C cases.
- Data collected via a web-based physician-reported database.
- Inverse-probability weighting and generalized linear models used for comparative analysis.
Main Results:
- 490 children meeting WHO criteria for MIS-C were analyzed from 614 suspected cases.
- No significant differences in the composite outcome of inotropic support, mechanical ventilation, or death were observed between treatment groups.
- Adjusted odds ratios for reduction in disease severity were similar across IVIG alone, IVIG plus glucocorticoids, and glucocorticoids alone groups.
Conclusions:
- Current data show no clear evidence of differential recovery based on primary treatment with IVIG alone, IVIG plus glucocorticoids, or glucocorticoids alone for MIS-C.
- The study highlights the need for continued data collection as potential differences may emerge with larger sample sizes.
- Findings support the ongoing evaluation of immunomodulatory therapies in pediatric critical care settings.
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