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Multisystem inflammatory syndrome in children during the COVID-19 waves: data from the Juvenile Inflammatory Rheumatism cohort.
Kechiche, Robin; Borocco, Charlotte; Bajolle, Fanny; Belot, Alexandre; Poignant, Sylvaine; Lachaume, Noémie; Percheron, Lucas; Meinzer, Ulrich; Mertes, Clara; Despert, Véronique; Morin, Luc; Lambert, Virginie; Dusser, Perrine; Matsa, Nassima; Hentgen, Véronique; Kone-Paut, Isabelle; Galeotti, Caroline.
  • Kechiche R; Department of Pediatric Rheumatology, Reference Centre for Autoinflammatory Diseases and Amyloidosis (CEREMAIA), Bicêtre University Hospital, Assistance Publique-Hôpitaux de Paris (AP-HP), Paris-Saclay University, Le Kremlin-Bicêtre, France.
  • Borocco C; Department of Pediatric Rheumatology, Reference Centre for Autoinflammatory Diseases and Amyloidosis (CEREMAIA), Bicêtre University Hospital, Assistance Publique-Hôpitaux de Paris (AP-HP), Paris-Saclay University, Le Kremlin-Bicêtre, France.
  • Bajolle F; Department of Pediatric Cardiology, M3C-Necker, Necker-Enfants Malades Hospital, AP-HP, Paris Cité University, Paris, France.
  • Belot A; Department of Pediatric Nephrology, Rheumatology, Dermatology, Reference Centre of Inflammatory Rheumatism and Rare Autoimmune Diseases in Children (RAISE), Hôpital Femme-Mère-Enfant, Hospices Civils de Lyon, Bron, France.
  • Poignant S; Department of Pediatrics, Nantes University Hospital, Nantes, France.
  • Lachaume N; Department of Pediatrics, Louis Mourier University Hospital, AP-HP, Paris-Cité University, Colombe, France.
  • Percheron L; Pediatrics-Nephrology, Internal Medicine and Hypertension, Children Hospital-Toulouse University Hospital, Toulouse, France.
  • Meinzer U; Department of General Pediatrics, Pediatric Rheumatology and Infectious Diseases, National Reference Centre for Rare Pediatric Inflammatory Rheumatisms and Systemic Autoimmune Diseases (RAISE), Robert Debré University Hospital, Assistance Publique-Hôpitaux de Paris, Paris, France.
  • Mertes C; Department of Pediatrics, Strasbourg University Hospital, Strasbourg, France.
  • Despert V; Department of Pediatrics, Rennes University Hospital, Rennes, France.
  • Morin L; Pediatric Intensive Care Unit, Bicêtre University Hospital, AP-HP, Paris-Saclay University, Le Kremlin-Bicêtre, France.
  • Lambert V; Department of Pediatric Radiology, Bicêtre University Hospital, AP-HP, Paris-Saclay University, Le Kremlin-Bicêtre, France.
  • Dusser P; Pediatric Cardiology, Institut Mutualiste Montsouris, Paris, France.
  • Matsa N; Department of Pediatric Rheumatology, Reference Centre for Autoinflammatory Diseases and Amyloidosis (CEREMAIA), Bicêtre University Hospital, Assistance Publique-Hôpitaux de Paris (AP-HP), Paris-Saclay University, Le Kremlin-Bicêtre, France.
  • Hentgen V; Department of Pediatric Rheumatology, Reference Centre for Autoinflammatory Diseases and Amyloidosis (CEREMAIA), Bicêtre University Hospital, Assistance Publique-Hôpitaux de Paris (AP-HP), Paris-Saclay University, Le Kremlin-Bicêtre, France.
  • Kone-Paut I; Department of Pediatrics, Reference Centre for Autoinflammatory Diseases and Amyloidosis (CEREMAIA), Versailles Hospital, Versailles, France.
  • Galeotti C; Department of Pediatric Rheumatology, Reference Centre for Autoinflammatory Diseases and Amyloidosis (CEREMAIA), Bicêtre University Hospital, Assistance Publique-Hôpitaux de Paris (AP-HP), Paris-Saclay University, Le Kremlin-Bicêtre, France.
Front Pediatr ; 11: 1126985, 2023.
Artículo en Inglés | MEDLINE | ID: covidwho-20237752
ABSTRACT

Introduction:

Multisystem inflammatory syndrome in children (MIS-C) is a new condition that first appeared in children and adolescents during the COVID-19 pandemic. We aimed to describe the diagnostic course, clinical and biological manifestations, and treatment of MIS-C during the first three COVID-19 waves.

Methods:

We extracted patient data from the Juvenile Inflammatory Rheumatism (JIR) cohort. We analyzed data for patients meeting the World Health Organization diagnostic criteria for MIS-C from the start of the COVID-19 pandemic from March 2020 to June 30, 2021. We then compared data for patients in wave one to those in waves two and three.

Results:

We identified 136 patients with MIS-C. The median age decreased but not significantly during the waves, from 9.9 years to 7.3 years (p = 0.105). Boys represented 52.2% (n = 71) of patients, and 46% (n = 41) of patients originated from sub-Saharan Africa (p < 0.001). Patients presented less diarrhea (p = 0.004), respiratory distress (p < 0.001), and myocarditis (p < 0.001) with progressive waves. Biological inflammation also decreased, namely, C-reactive protein level (p < 0.001), neutrophil count (p = 0.004), and albumin level (p < 0.001). Patients received more corticosteroids (p < 0.001) and required less ventilation support (p < 0.01) and less inotrope treatment (p < 0.001) in the later waves. The duration of hospitalization gradually decreased (p < 0.001), as did critical care unit admissions (p = 0.002).

Conclusion:

Over the three COVID-19 waves, with a change in the management of MIS-C, children in the JIR cohort in France showed a less severe disease course, in particular, a greater use of corticosteroids. This observation may reflect the impact of both improved management and different SARS-CoV-2 variant.
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Texto completo: Disponible Colección: Bases de datos internacionales Base de datos: MEDLINE Tipo de estudio: Estudio de cohorte / Estudio observacional / Estudio pronóstico Tópicos: Variantes Idioma: Inglés Revista: Front Pediatr Año: 2023 Tipo del documento: Artículo País de afiliación: Fped.2023.1126985

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Texto completo: Disponible Colección: Bases de datos internacionales Base de datos: MEDLINE Tipo de estudio: Estudio de cohorte / Estudio observacional / Estudio pronóstico Tópicos: Variantes Idioma: Inglés Revista: Front Pediatr Año: 2023 Tipo del documento: Artículo País de afiliación: Fped.2023.1126985