Evidence map›Paper›PMID 35216660›Full record

ArticleThe Lancet. Child & adolescent health2022

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.

Anna R Yousaf, Margaret M Cortese, Allan W Taylor, Karen R Broder, Matthew E Oster, Joshua M Wong, Alice Y Guh, David W McCormick, Satoshi Kamidani, Elizabeth P Schlaudecker and 10 more

Open access · greenAbstract read
In one paragraph

Article in The Lancet. Child & adolescent health, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 84 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
84citing papers in PubMed, 2 pooled it
26.4field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

84 citing papers in PubMed, 2 syntheses or guidelines pooled it, 122 citations in OpenAlex.

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24 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

20 authors at 6 institutions in 1 country.

Anna R YousafCDC COVID-19 Response Team, US Centers for Disease Control and Prevention, Atlanta, GA, USA. Electronic address: pgy6@cdc.gov.
Margaret M CorteseCDC COVID-19 Response Team, US Centers for Disease Control and Prevention, Atlanta, GA, USA.
Allan W TaylorCDC COVID-19 Response Team, US Centers for Disease Control and Prevention, Atlanta, GA, USA.
Karen R BroderCDC COVID-19 Response Team, US Centers for Disease Control and Prevention, Atlanta, GA, USA.
Matthew E OsterDivision of Cardiology, Children's Healthcare of Atlanta, Department of Pediatrics, Emory University School of Medicine, Atlanta, GA, USA.
Joshua M WongCDC 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.
Alice Y GuhCDC COVID-19 Response Team, US Centers for Disease Control and Prevention, Atlanta, GA, USA.
David W McCormickCDC 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.
Satoshi KamidaniCenter for Childhood Infections and Vaccines, Children's Healthcare of Atlanta, Department of Pediatrics, Emory University School of Medicine, Atlanta, GA, USA.
Elizabeth P SchlaudeckerDivision of Infectious Diseases, Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA.
Kathryn M EdwardsDivision of Infectious Diseases, Department of Pediatrics, Vanderbilt University Medical Center, Nashville, TN, USA.
C Buddy CreechVanderbilt Vaccine Research Program, Department of Pediatrics, Vanderbilt University Medical Center, Nashville, TN, USA.
Mary A StaatDivision of Infectious Diseases, Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA.
Ermias D BelayCDC COVID-19 Response Team, US Centers for Disease Control and Prevention, Atlanta, GA, USA.
Paige MarquezCDC COVID-19 Response Team, US Centers for Disease Control and Prevention, Atlanta, GA, USA.
John R SuCDC COVID-19 Response Team, US Centers for Disease Control and Prevention, Atlanta, GA, USA.
Mark B SalzmanKaiser Permanente West Los Angeles Medical Center, Los Angeles, CA, USA.
Deborah ThompsonUS Food and Drug Administration, Center for Biologics Evaluation and Research, Silver Spring, MD, USA.
Angela P CampbellCDC COVID-19 Response Team, US Centers for Disease Control and Prevention, Atlanta, GA, USA.
MIS-C Investigation Authorship Group
Centers for Disease Control and Prevention · USEmory University · USUniversity of Cincinnati · USVanderbilt University Medical Center · USCenter for Biologics Evaluation and Research · USKaiser Permanente West Los Angeles Medical Center · US

Funding

CDC HHS
6 · The paper itself

Abstract

backgroundMultisystem 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).

methodsIn 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.

findingsUsing 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.

interpretationHere, 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.

fundingUS Centers for Disease Control and Prevention.

Indexed as

COVID-19COVID-19 VaccinesAdolescentChildFemaleHumansMaleSARS-CoV-2Systemic Inflammatory Response SyndromeUnited StatesYoung AdultCOVID-19 Vaccines

Identifiers

PMID35216660
PMCPMC8864018
OpenAlexW4214518533

What OpenQuestion holds

Textmetadata
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.