Immunomodulatory Therapy for MIS-C.


Journal

Pediatrics
ISSN: 1098-4275
Titre abrégé: Pediatrics
Pays: United States
ID NLM: 0376422

Informations de publication

Date de publication:
01 Jul 2023
Historique:
accepted: 04 04 2023
medline: 3 7 2023
pubmed: 28 6 2023
entrez: 28 6 2023
Statut: ppublish

Résumé

Studies comparing initial therapy for multisystem inflammatory syndrome in children (MIS-C) provided conflicting results. To compare outcomes in MIS-C patients treated with intravenous immunoglobulin (IVIG), glucocorticoids, or the combination thereof. Medline, Embase, CENTRAL and WOS, from January 2020 to February 2022. Randomized or observational comparative studies including MIS-C patients <21 years. 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. 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). Nonrandomized nature of included studies. 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.

Identifiants

pubmed: 37376963
pii: 192425
doi: 10.1542/peds.2022-061173
pii:
doi:

Substances chimiques

Glucocorticoids 0
Immunoglobulins, Intravenous 0

Types de publication

Meta-Analysis Journal Article

Langues

eng

Sous-ensembles de citation

IM

Auteurs

Naïm Ouldali (N)

Division of Infectious diseases, Department of Pediatric Infectious Diseases, Sainte Justine University Hospital, University of Montreal, Quebec, Canada.
Infection, Antimicrobials, Modelling, Evolution, Inserm, UMR 1137, Paris University, Paris, France.
Association Clinique et, Thérapeutique Infantile du Val-de-Marne, St Maur-des-Fossés, France.

Mary Beth F Son (MBF)

Department of Pediatrics, Harvard Medical School, Boston, Massachusetts.
Division of Immunology, Boston Children's Hospital, Boston, Massachusetts.

Andrew J McArdle (AJ)

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

Ortensia Vito (O)

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

Esther Vaugon (E)

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

Alexandre Belot (A)

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

Claire Leblanc (C)

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

Nancy L Murray (NL)

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

Manish M Patel (MM)

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

Michael Levin (M)

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

Adrienne G Randolph (AG)

Department of Pediatrics, Harvard Medical School, Boston, Massachusetts.
Department of Department of Anesthesiology, Critical Care, and Pain Medicine, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts.

François Angoulvant (F)

Department of General Pediatrics, Pediatric Infectious Disease and Internal Medicine, Robert Debré University Hospital, Assistance Publique-Hôpitaux de Paris, Université De Paris, Paris, France.
Service of Pediatrics, Department Women-Mother-Child, Lausanne University Hospital, Lausanne, Switzerland.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH