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Reported cases of multisystem inflammatory syndrome in children aged 12-20 years in the USA who received a COVID-19 vaccine, December, 2020, through August, 2021: a surveillance investigation.
Yousaf, Anna R; Cortese, Margaret M; Taylor, Allan W; Broder, Karen R; Oster, Matthew E; Wong, Joshua M; Guh, Alice Y; McCormick, David W; Kamidani, Satoshi; Schlaudecker, Elizabeth P; Edwards, Kathryn M; Creech, C Buddy; Staat, Mary A; Belay, Ermias D; Marquez, Paige; Su, John R; Salzman, Mark B; Thompson, Deborah; Campbell, Angela P.
Afiliação
  • Yousaf AR; CDC COVID-19 Response Team, US Centers for Disease Control and Prevention, Atlanta, GA, USA. Electronic address: pgy6@cdc.gov.
  • Cortese MM; CDC COVID-19 Response Team, US Centers for Disease Control and Prevention, Atlanta, GA, USA.
  • Taylor AW; CDC COVID-19 Response Team, US Centers for Disease Control and Prevention, Atlanta, GA, USA.
  • Broder KR; CDC COVID-19 Response Team, US Centers for Disease Control and Prevention, Atlanta, GA, USA.
  • Oster ME; Division of Cardiology, Children's Healthcare of Atlanta, Department of Pediatrics, Emory University School of Medicine, Atlanta, GA, USA.
  • Wong JM; CDC COVID-19 Response Team, US Centers for Disease Control and Prevention, Atlanta, GA, USA; Epidemic Intelligence Service, US Centers for Disease Control and Prevention, Atlanta, GA, USA.
  • Guh AY; CDC COVID-19 Response Team, US Centers for Disease Control and Prevention, Atlanta, GA, USA.
  • McCormick DW; CDC COVID-19 Response Team, US Centers for Disease Control and Prevention, Atlanta, GA, USA; Epidemic Intelligence Service, US Centers for Disease Control and Prevention, Atlanta, GA, USA.
  • Kamidani S; Center for Childhood Infections and Vaccines, Children's Healthcare of Atlanta, Department of Pediatrics, Emory University School of Medicine, Atlanta, GA, USA.
  • Schlaudecker EP; Division of Infectious Diseases, Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA.
  • Edwards KM; Division of Infectious Diseases, Department of Pediatrics, Vanderbilt University Medical Center, Nashville, TN, USA.
  • Creech CB; Vanderbilt Vaccine Research Program, Department of Pediatrics, Vanderbilt University Medical Center, Nashville, TN, USA.
  • Staat MA; Division of Infectious Diseases, Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA.
  • Belay ED; CDC COVID-19 Response Team, US Centers for Disease Control and Prevention, Atlanta, GA, USA.
  • Marquez P; CDC COVID-19 Response Team, US Centers for Disease Control and Prevention, Atlanta, GA, USA.
  • Su JR; CDC COVID-19 Response Team, US Centers for Disease Control and Prevention, Atlanta, GA, USA.
  • Salzman MB; Kaiser Permanente West Los Angeles Medical Center, Los Angeles, CA, USA.
  • Thompson D; US Food and Drug Administration, Center for Biologics Evaluation and Research, Silver Spring, MD, USA.
  • Campbell AP; CDC COVID-19 Response Team, US Centers for Disease Control and Prevention, Atlanta, GA, USA.
Lancet Child Adolesc Health ; 6(5): 303-312, 2022 05.
Article em En | MEDLINE | ID: mdl-35216660
ABSTRACT

BACKGROUND:

Multisystem inflammatory syndrome in children (MIS-C) is a hyperinflammatory condition associated with antecedent SARS-CoV-2 infection. In the USA, reporting of MIS-C after vaccination is required under COVID-19 vaccine emergency use authorisations. We aimed to investigate reports of individuals aged 12-20 years with MIS-C after COVID-19 vaccination reported to passive surveillance systems or through clinician outreach to the US Centers for Disease Control and Prevention (CDC).

METHODS:

In this surveillance activity, we investigated potential cases of MIS-C after COVID-19 vaccination reported to CDC's MIS-C national surveillance system, the Vaccine Adverse Event Reporting System (co-administered by CDC and the US Food and Drug Administration), and CDC's Clinical Immunization Safety Assessment Project. A multidisciplinary team adjudicated cases by use of the CDC MIS-C definition. Any positive SARS-CoV-2 serology test satisfied case criteria; although anti-nucleocapsid antibodies indicate previous SARS-CoV-2 infection, anti-spike protein antibodies indicate either past or recent infection or COVID-19 vaccination. We describe the demographic and clinical features of cases, stratified by laboratory evidence of SARS-CoV-2 infection. To calculate the reporting rate of MIS-C, we divided the count of all individuals meeting the MIS-C case definition, and of those without evidence of SARS-CoV-2 infection, by the number of individuals aged 12-20 years in the USA who received one or more COVID-19 vaccine doses up to Aug 31, 2021, obtained from CDC national vaccine surveillance data.

FINDINGS:

Using surveillance results from Dec 14, 2020, to Aug 31, 2021, we identified 21 individuals with MIS-C after COVID-19 vaccination. Of these 21 individuals, median age was 16 years (range 12-20); 13 (62%) were male and eight (38%) were female. All 21 were hospitalised 12 (57%) were admitted to an intensive care unit and all were discharged home. 15 (71%) of 21 individuals had laboratory evidence of past or recent SARS-CoV-2 infection, and six (29%) did not. As of Aug 31, 2021, 21 335 331 individuals aged 12-20 years had received one or more doses of a COVID-19 vaccine, making the overall reporting rate for MIS-C after vaccination 1·0 case per million individuals receiving one or more doses in this age group. The reporting rate in only those without evidence of SARS-CoV-2 infection was 0·3 cases per million vaccinated individuals.

INTERPRETATION:

Here, we describe a small number of individuals with MIS-C who had received one or more doses of a COVID-19 vaccine before illness onset; the contribution of vaccination to these illnesses is unknown. Our findings suggest that MIS-C after COVID-19 vaccination is rare. Continued reporting of potential cases and surveillance for MIS-C illnesses after COVID-19 vaccination is warranted.

FUNDING:

US Centers for Disease Control and Prevention.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Vacinas contra COVID-19 / COVID-19 Tipo de estudo: Prognostic_studies / Screening_studies Limite: Adolescent / Adult / Child / Female / Humans / Male País/Região como assunto: America do norte Idioma: En Revista: Lancet Child Adolesc Health Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Vacinas contra COVID-19 / COVID-19 Tipo de estudo: Prognostic_studies / Screening_studies Limite: Adolescent / Adult / Child / Female / Humans / Male País/Região como assunto: America do norte Idioma: En Revista: Lancet Child Adolesc Health Ano de publicação: 2022 Tipo de documento: Article