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Updated Case Definition of MIS-C and Implications for Clinical Care.
Day-Lewis, Megan; Berbert, Laura; Baker, Annette; Dionne, Audrey; Newburger, Jane W; Son, Mary Beth F.
Afiliación
  • Day-Lewis M; Division of Immunology, Boston Children's Hospital, Boston, Massachusetts.
  • Berbert L; Institute Centers for Clinical and Translational Research, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts.
  • Baker A; Department of Cardiology, Boston Children's Hospital, Boston, Massachusetts.
  • Dionne A; Department of Cardiology, Boston Children's Hospital, Boston, Massachusetts.
  • Newburger JW; Department of Cardiology, Boston Children's Hospital, Boston, Massachusetts.
  • Son MBF; Department of Pediatrics, Boston Children's Hospital, Boston, Massachusetts.
Pediatrics ; 153(2)2024 Jan 01.
Article en En | MEDLINE | ID: mdl-38204335
ABSTRACT

OBJECTIVES:

A broad, surveillance case definition was implemented when multisystem inflammatory syndrome in children (MIS-C) emerged in 2020. In 2023, a revised MIS-C case definition was constructed to improve specificity and reduce misclassification with other pediatric inflammatory conditions. This study aims to describe the impact of the updated definition on the classification of patients with MIS-C and Kawasaki Disease (KD).

METHODS:

Patients hospitalized from March 2020 to November 2022 with clinician-diagnosed KD and MIS-C at a single center were studied retrospectively. Specificity and positive predictive value were assessed; McNemar test was used to compare specificity.

RESULTS:

Among 119 patients with MIS-C per the 2020 definition, 20 (17%) did not fulfill the 2023 definition. Six of these 20 (30%) had shock or cardiac involvement. Of 59 KD patients, 10 (17%) met the 2020 MIS-C definition. Five patients (8%) met the 2023 MIS-C definition. Specificity for the 2020 and 2023 MIS-C definitions among KD patients were 83.1% and 91.5% respectively (McNemar, P = .0736). Positive predictive value was higher for the 2023 MIS-C case definition compared with the 2020 MIS-C case definition (95.2% vs 92.2%).

CONCLUSIONS:

Approximately 1 in 5 patients diagnosed with MIS-C using the 2020 case definition did not meet the 2023 definition, including patients with cardiovascular dysfunction. Overlap persisted between patients meeting KD and 2023 MIS-C case definitions, with a false positive rate of 8%. Implications for treatment should be considered, particularly in settings where presumed MIS-C may be treated with corticosteroid monotherapy.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: COVID-19 / Síndrome Mucocutáneo Linfonodular Tipo de estudio: Observational_studies / Risk_factors_studies Límite: Child / Humans Idioma: En Revista: Pediatrics Año: 2024 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: COVID-19 / Síndrome Mucocutáneo Linfonodular Tipo de estudio: Observational_studies / Risk_factors_studies Límite: Child / Humans Idioma: En Revista: Pediatrics Año: 2024 Tipo del documento: Article