Multisystem Inflammatory Syndrome in Adults After Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) Infection and Coronavirus Disease 2019 (COVID-19) Vaccination

Author:

Belay Ermias D1ORCID,Godfred Cato Shana1,Rao Agam K1,Abrams Joseph1,Wyatt Wilson W12,Lim Sarah3,Newton-Cheh Christopher4,Melgar Michael1,DeCuir Jennifer12,Webb Brandon5,Marquez Paige1,Su John R1,Meng Lu1,Grome Heather N2,Schlaudecker Elizabeth6,Talaat Kawsar7,Edwards Kathryn8,Barnett Elizabeth9,Campbell Angela P1,Broder Karen R1,Bamrah Morris Sapna1

Affiliation:

1. COVID-19 Response, Centers for Disease Control and Prevention, Atlanta, GeorgiaUSA

2. Epidemic Intelligence Service, Centers for Disease Control and Prevention, Atlanta, Georgia, USA

3. Minnesota Department of Health, St Paul, Minnesota, USA

4. Massachusetts General Hospital, Cardiovascular Research Center, Boston, Massachusetts, USA

5. Intermountain Healthcare, Murray, Utah, USA

6. Cincinnati Children’s Hospital Medical Center, University of Cincinnati College of Medicine, Cincinnati, Ohio, USA

7. Johns Hopkins University, Baltimore, Maryland, USA

8. Vanderbilt University Medical Center, Nashville, Tennessee, USA

9. Boston Medical Center, Boston, Massachusetts, USA

Abstract

Abstract Background Multisystem inflammatory syndrome in adults (MIS-A) was reported in association with the coronavirus disease 2019 (COVID-19) pandemic. MIS-A was included in the list of adverse events to be monitored as part of the emergency use authorizations issued for COVID-19 vaccines. Methods Reports of MIS-A patients received by the Centers for Disease Control and Prevention (CDC) after COVID-19 vaccines became available were assessed. Data collected on the patients included clinical and demographic characteristics and their vaccine status. The Vaccine Adverse Events Reporting System (VAERS) was also reviewed for possible cases of MIS-A. Results From 14 December 2020 to 30 April 2021, 20 patients who met the case definition for MIS-A were reported to CDC. Their median age was 35 years (range, 21–66 years), and 13 (65%) were male. Overall, 16 (80%) patients had a preceding COVID-19-like illness a median of 26 days (range 11–78 days) before MIS-A onset. All 20 patients had laboratory evidence of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection. Seven MIS-A patients (35%) received COVID-19 vaccine a median of 10 days (range, 6–45 days) before MIS-A onset; 3 patients received a second dose of COVID-19 vaccine 4, 17, and 22 days before MIS-A onset. Patients with MIS-A predominantly had gastrointestinal and cardiac manifestations and hypotension or shock. Conclusions Although 7 patients were reported to have received COVID-19 vaccine, all had evidence of prior SARS-CoV-2 infection. Given the widespread use of COVID-19 vaccines, the lack of reporting of MIS-A associated with vaccination alone, without evidence of underlying SARS-CoV-2 infection, is reassuring.

Funder

Centers for Disease Control and Prevention

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Microbiology (medical)

Reference22 articles.

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