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Association of Intravenous Immunoglobulins Plus Methylprednisolone vs Immunoglobulins Alone With Course of Fever in Multisystem Inflammatory Syndrome in Children.
Ouldali, Naïm; Toubiana, Julie; Antona, Denise; Javouhey, Etienne; Madhi, Fouad; Lorrot, Mathie; Léger, Pierre-Louis; Galeotti, Caroline; Claude, Caroline; Wiedemann, Arnaud; Lachaume, Noémie; Ovaert, Caroline; Dumortier, Morgane; Kahn, Jean-Emmanuel; Mandelcwajg, Alexis; Percheron, Lucas; Biot, Blandine; Bordet, Jeanne; Girardin, Marie-Laure; Yang, David Dawei; Grimaud, Marion; Oualha, Mehdi; Allali, Slimane; Bajolle, Fanny; Beyler, Constance; Meinzer, Ulrich; Levy, Michael; Paulet, Ana-Maria; Levy, Corinne; Cohen, Robert; Belot, Alexandre; Angoulvant, François.
  • Ouldali N; Assistance Publique-Hôpitaux de Paris, Department of General Paediatrics, Paediatric Infectious Disease and Internal Medicine, Robert Debré University Hospital, Université de Paris, Paris, France.
  • Toubiana J; ACTIV, Association Clinique et Thérapeutique Infantile du Val-de-Marne, Créteil, France.
  • Antona D; Université de Paris, INSERM UMR 1123, ECEVE, Paris, France.
  • Javouhey E; Assistance Publique-Hôpitaux de Paris, Department of General Paediatrics and Paediatric Infectious Diseases, Necker-Enfants-Malades University Hospital, Université de Paris, Paris, France.
  • Madhi F; Institut Pasteur, Biodiversity and Epidemiology of Bacterial Pathogens, Paris, France.
  • Lorrot M; Santé Publique France, Agence Nationale de Santé Publique, Saint-Maurice, France.
  • Léger PL; Hospices Civils de Lyon, Paediatric Intensive Care Unit, Hopital Femme, Mère Enfant, University of Lyon, Bron, France.
  • Galeotti C; EA 7426 Pathophysiology of Injury-Induced Immunosuppression, University Claude Bernard Lyon 1, Hospices Civils of Lyon, Lyon, France.
  • Claude C; Centre Hospitalier Intercommunal, Paediatric Department, Université Paris Est, IMRB-GRC GEMINI, Créteil, France.
  • Wiedemann A; Assistance Publique-Hôpitaux de Paris, Department of General Paediatric, Armand Trousseau University Hospital, Sorbonne Université, Paris, France.
  • Lachaume N; Assistance Publique-Hôpitaux de Paris, Paediatric Intensive Care Unit, Armand Trousseau University Hospital, Sorbonne Université, Paris, France.
  • Ovaert C; Assistance Publique-Hôpitaux de Paris, Department of Paediatric Rheumatology, Reference Centre for Autoinflammatory Diseases and Amyloidosis (CEREMAIA), Bicêtre University Hospital, Université de Paris Saclay, Le Kremlin-Bicêtre, France.
  • Dumortier M; Assistance Publique-Hôpitaux de Paris, Paediatric Intensive Care Unit, Bicêtre University Hospital, Université de Paris Saclay, Le Kremlin-Bicêtre, France.
  • Kahn JE; Children's Hospital, University Hospital of Nancy, Paediatric Department, Université de Lorraine, Vandoeuvre les Nancy, France.
  • Mandelcwajg A; INSERM UMRS 1256 NGERE, Nutrition, Genetics, and Environmental Risk Exposure, National Center of Inborn Errors of Metabolism, Université de Lorraine, Vandoeuvre les Nancy, France.
  • Percheron L; Assistance Publique-Hôpitaux de Paris, Paediatric Emergency Departement, Louis Mourier University Hospital, Colombes, France.
  • Biot B; Assistance Publique-Hôpitaux de Marseille, Paediatric and Congenital Cardiology, Timone Hospital Marseille, University Hospital, Marseille, France.
  • Bordet J; INSERM, Marseille Medical Genetics, UMR 1251, Aix Marseille Université, Marseille, France.
  • Girardin ML; Hôpital Femme Enfant Adolescent, Department of Paediatrics and Paediatric Emergency, University Hospital, Nantes, France.
  • Yang DD; Assistance Publique-Hôpitaux de Paris, Internal Medicine Department, Ambroise Paré University Hospital, Université Versailles-Saint Quentin-en-Yvelines, Boulogne-Billancourt, France.
  • Grimaud M; Paediatric Department, Hôpital Delafontaine, Saint Denis, France.
  • Oualha M; Hôpital des Enfants, Paediatric Nephrology Department, Purpan University Hospital, Toulouse, France.
  • Allali S; Paediatric Department, Hôpital de Valence, Valence, France.
  • Bajolle F; Strasbourg University Hospital, Paediatric Cardiology Department, Hautepierre University Hospital, Strasbourg, France.
  • Beyler C; Paediatric Intensive Care Unit, Strasbourg University Hospital, Hautepierre University Hospital, Strasbourg, France.
  • Meinzer U; Assistance Publique-Hôpitaux de Paris, Paediatric Emergency Department, Necker-Enfants Malades University Hospital, Université de Paris, Paris, France.
  • Levy M; Assistance Publique-Hôpitaux de Paris, Paediatric Intensive Care Unit, Necker-Enfants Malades University Hospital, EA7323, Université de Paris, Paris, France.
  • Paulet AM; Assistance Publique-Hôpitaux de Paris, Paediatric Intensive Care Unit, Necker-Enfants Malades University Hospital, EA7323, Université de Paris, Paris, France.
  • Levy C; Assistance Publique-Hôpitaux de Paris, Department of General Paediatrics and Paediatric Infectious Diseases, Necker-Enfants-Malades University Hospital, Université de Paris, Paris, France.
  • Cohen R; Assistance Publique-Hôpitaux de Paris, M3C Department, Necker-Enfants Malades University Hospital, Université de Paris, Paris, France.
  • Belot A; Assistance Publique-Hôpitaux de Paris, Cardiopaediatric Unit, Robert Debré University Hospital, Université de Paris, Paris, France.
  • Angoulvant F; Assistance Publique-Hôpitaux de Paris, Department of General Paediatrics, Paediatric Infectious Disease and Internal Medicine, Robert Debré University Hospital, Université de Paris, Paris, France.
JAMA ; 325(9): 855-864, 2021 03 02.
Article in English | MEDLINE | ID: covidwho-1135043
ABSTRACT
Importance Multisystem inflammatory syndrome in children (MIS-C) is the most severe pediatric disease associated with severe acute respiratory syndrome coronavirus 2 infection, potentially life-threatening, but the optimal therapeutic strategy remains unknown.

Objective:

To compare intravenous immunoglobulins (IVIG) plus methylprednisolone vs IVIG alone as initial therapy in MIS-C. Design, Setting, and

Participants:

Retrospective cohort study drawn from a national surveillance system with propensity score-matched analysis. All cases with suspected MIS-C were reported to the French National Public Health Agency. Confirmed MIS-C cases fulfilling the World Health Organization definition were included. The study started on April 1, 2020, and follow-up ended on January 6, 2021. Exposures IVIG and methylprednisolone vs IVIG alone. Main Outcomes and

Measures:

The primary outcome was persistence of fever 2 days after the introduction of initial therapy or recrudescence of fever within 7 days, which defined treatment failure. Secondary outcomes included a second-line therapy, hemodynamic support, acute left ventricular dysfunction after first-line therapy, and length of stay in the pediatric intensive care unit. The primary analysis involved propensity score matching with a minimum caliper of 0.1.

Results:

Among 181 children with suspected MIS-C, 111 fulfilled the World Health Organization definition (58 females [52%]; median age, 8.6 years [interquartile range, 4.7 to 12.1]). Five children did not receive either treatment. Overall, 3 of 34 children (9%) in the IVIG and methylprednisolone group and 37 of 72 (51%) in the IVIG alone group did not respond to treatment. Treatment with IVIG and methylprednisolone vs IVIG alone was associated with lower risk of treatment failure (absolute risk difference, -0.28 [95% CI, -0.48 to -0.08]; odds ratio [OR], 0.25 [95% CI, 0.09 to 0.70]; P = .008). IVIG and methylprednisolone therapy vs IVIG alone was also significantly associated with lower risk of use of second-line therapy (absolute risk difference, -0.22 [95% CI, -0.40 to -0.04]; OR, 0.19 [95% CI, 0.06 to 0.61]; P = .004), hemodynamic support (absolute risk difference, -0.17 [95% CI, -0.34 to -0.004]; OR, 0.21 [95% CI, 0.06 to 0.76]), acute left ventricular dysfunction occurring after initial therapy (absolute risk difference, -0.18 [95% CI, -0.35 to -0.01]; OR, 0.20 [95% CI, 0.06 to 0.66]), and duration of stay in the pediatric intensive care unit (median, 4 vs 6 days; difference in days, -2.4 [95% CI, -4.0 to -0.7]). Conclusions and Relevance Among children with MIS-C, treatment with IVIG and methylprednisolone vs IVIG alone was associated with a more favorable fever course. Study interpretation is limited by the observational design.
Subject(s)

Full text: Available Collection: International databases Database: MEDLINE Main subject: Methylprednisolone / Immunoglobulins, Intravenous / Systemic Inflammatory Response Syndrome / COVID-19 / Glucocorticoids Type of study: Cohort study / Observational study / Prognostic study Topics: Long Covid / Variants Limits: Adolescent / Child / Child, preschool / Female / Humans / Male Country/Region as subject: Europa Language: English Journal: JAMA Year: 2021 Document Type: Article Affiliation country: Jama.2021.0694

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Methylprednisolone / Immunoglobulins, Intravenous / Systemic Inflammatory Response Syndrome / COVID-19 / Glucocorticoids Type of study: Cohort study / Observational study / Prognostic study Topics: Long Covid / Variants Limits: Adolescent / Child / Child, preschool / Female / Humans / Male Country/Region as subject: Europa Language: English Journal: JAMA Year: 2021 Document Type: Article Affiliation country: Jama.2021.0694