Immunomodulatory Therapy for MIS-C

Author:

Ouldali Naïm123,Son Mary Beth F.45,McArdle Andrew J.6,Vito Ortensia6,Vaugon Esther1,Belot Alexandre7,Leblanc Claire8,Murray Nancy L.9,Patel Manish M.9,Levin Michael6,Randolph Adrienne G.410,Angoulvant François811,

Affiliation:

1. aDivision of Infectious diseases, Department of Pediatric Infectious Diseases, Sainte Justine University Hospital, University of Montreal, Quebec, Canada

2. bInfection, Antimicrobials, Modelling, Evolution, Inserm, UMR 1137, Paris University, Paris, France

3. cAssociation Clinique et, Thérapeutique Infantile du Val-de-Marne, St Maur-des-Fossés, France

4. dDepartment of Pediatrics, Harvard Medical School, Boston, Massachusetts

5. eDivision of Immunology, Boston Children's Hospital, Boston, Massachusetts

6. fSection of Pediatrics, Division of Infectious Diseases, Department of Medicine, Imperial College London, London, United Kingdom

7. gHospices Civils de Lyon, Pediatric Nephrology, Rheumatology, Dermatology, Hopital Femme, Mère Enfant, Centre International de Recherche en Infectiologie/INSERM U1111, Bron, France

8. hDepartment of General Pediatrics, Pediatric Infectious Disease and Internal Medicine, Robert Debré University Hospital, Assistance Publique–Hôpitaux de Paris, Université De Paris, Paris, France

9. iCOVID-19 Response Team, Centers for Disease Control and Prevention, Atlanta, Georgia

10. jDepartment of Department of Anesthesiology, Critical Care, and Pain Medicine, Boston Children’s Hospital, Harvard Medical School, Boston, Massachusetts

11. kService of Pediatrics, Department Women-Mother-Child, Lausanne University Hospital, Lausanne, Switzerland

Abstract

CONTEXT Studies comparing initial therapy for multisystem inflammatory syndrome in children (MIS-C) provided conflicting results. OBJECTIVE To compare outcomes in MIS-C patients treated with intravenous immunoglobulin (IVIG), glucocorticoids, or the combination thereof. DATA SOURCES Medline, Embase, CENTRAL and WOS, from January 2020 to February 2022. STUDY SELECTION Randomized or observational comparative studies including MIS-C patients <21 years. DATA EXTRACTION Two reviewers independently selected studies and obtained individual participant data. The main outcome was cardiovascular dysfunction (CD), defined as left ventricular ejection fraction < 55% or vasopressor requirement ≥ day 2 of initial therapy, analyzed with a propensity score-matched analysis. RESULTS Of 2635 studies identified, 3 nonrandomized cohorts were included. The meta-analysis included 958 children. IVIG plus glucocorticoids group as compared with IVIG alone had improved CD (odds ratio [OR] 0.62 [0.42–0.91]). Glucocorticoids alone group as compared with IVIG alone did not have improved CD (OR 0.57 [0.31–1.05]). Glucocorticoids alone group as compared with IVIG plus glucocorticoids did not have improved CD (OR 0.67 [0.24–1.86]). Secondary analyses found better outcomes associated with IVIG plus glucocorticoids compared with glucocorticoids alone (fever ≥ day 2, need for secondary therapies) and better outcomes associated with glucocorticoids alone compared with IVIG alone (left ventricular ejection fraction < 55% ≥ day 2). LIMITATIONS Nonrandomized nature of included studies. CONCLUSIONS In a meta-analysis of MIS-C patients, IVIG plus glucocorticoids was associated with improved CD compared with IVIG alone. Glucocorticoids alone was not associated with improved CD compared with IVIG alone or IVIG plus glucocorticoids.

Publisher

American Academy of Pediatrics (AAP)

Subject

Pediatrics, Perinatology and Child Health

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