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Multisystem Inflammatory Syndrome in Children Associated with Severe Acute Respiratory Syndrome Coronavirus 2: A Systematic Review.
Abrams, Joseph Y; Godfred-Cato, Shana E; Oster, Matthew E; Chow, Eric J; Koumans, Emilia H; Bryant, Bobbi; Leung, Jessica W; Belay, Ermias D.
Afiliação
  • Abrams JY; COVID-19 Response, Centers for Disease Control and Prevention, Atlanta, GA. Electronic address: jabrams@cdc.gov.
  • Godfred-Cato SE; COVID-19 Response, Centers for Disease Control and Prevention, Atlanta, GA.
  • Oster ME; COVID-19 Response, Centers for Disease Control and Prevention, Atlanta, GA.
  • Chow EJ; COVID-19 Response, Centers for Disease Control and Prevention, Atlanta, GA.
  • Koumans EH; COVID-19 Response, Centers for Disease Control and Prevention, Atlanta, GA.
  • Bryant B; COVID-19 Response, Centers for Disease Control and Prevention, Atlanta, GA.
  • Leung JW; COVID-19 Response, Centers for Disease Control and Prevention, Atlanta, GA.
  • Belay ED; COVID-19 Response, Centers for Disease Control and Prevention, Atlanta, GA.
J Pediatr ; 226: 45-54.e1, 2020 Nov.
Article em En | MEDLINE | ID: mdl-32768466
ABSTRACT

OBJECTIVE:

To develop a more comprehensive description of multisystem inflammatory syndrome in children (MIS-C), a novel syndrome linked to severe acute respiratory syndrome coronavirus 2, by conducting a systematic analysis of studies from different settings that used various inclusion criteria. STUDY

DESIGN:

MIS-C studies were identified by searching PubMed and Embase as well as preprint repositories and article references to identify studies of MIS-C cases published from April 25, 2020, through June 29, 2020. MIS-C study metadata were assessed and information on case demographics, clinical symptoms, laboratory measurements, treatments, and outcomes were summarized and contrasted between studies.

RESULTS:

Eight studies were identified representing a total of 440 MIS-C cases. Inclusion criteria varied by study 3 studies selected patients diagnosed with Kawasaki disease, 2 required cardiovascular involvement, and 3 had broader multisystem inclusion criteria. Median age of patients by study ranged from 7.3 to 10 years, and 59% of patients were male. Across all studies, the proportion of patients with positive results for severe acute respiratory syndrome coronavirus 2 reverse transcriptase-polymerase chain reaction tests ranged from 13% to 69% and for serology, from 75% to 100%. Patients with MIS-C had high prevalence of gastrointestinal (87%), dermatologic/mucocutaneous (73%), and cardiovascular (71%) symptoms. Prevalence of cardiovascular, neurologic, and respiratory system involvement significantly differed by study inclusion criteria. All studies reported elevated C-reactive protein, interleukin-6, and fibrinogen levels for at least 75% of patients in each study.

CONCLUSIONS:

This systematic review of MIS-C studies assists with understanding this newly identified syndrome and may be useful in developing a refined, universal case definition of MIS-C.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Síndrome de Resposta Inflamatória Sistêmica / COVID-19 Tipo de estudo: Diagnostic_studies / Prognostic_studies / Risk_factors_studies / Systematic_reviews Limite: Child / Humans Idioma: En Revista: J Pediatr Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Síndrome de Resposta Inflamatória Sistêmica / COVID-19 Tipo de estudo: Diagnostic_studies / Prognostic_studies / Risk_factors_studies / Systematic_reviews Limite: Child / Humans Idioma: En Revista: J Pediatr Ano de publicação: 2020 Tipo de documento: Article