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

被引:35
作者
Belay, Ermias D. [1 ]
Cato, Shana Godfred [1 ]
Rao, Agam K. [1 ]
Abrams, Joseph [1 ]
Wilson, W. Wyatt [1 ]
Lim, Sarah [2 ]
Newton-Cheh, Christopher [3 ]
Melgar, Michael [1 ]
DeCuir, Jennifer [1 ,4 ]
Webb, Brandon [5 ]
Marquez, Paige [1 ]
Su, John R. [1 ]
Meng, Lu
Grome, Heather N. [4 ]
Schlaudecker, Elizabeth
Talaat, Kawsar [7 ]
Edwards, Kathryn [6 ,8 ]
Barnett, Elizabeth [9 ]
Campbell, Angela P. [1 ]
Broder, Karen R. [1 ]
Morris, Sapna Bamrah [1 ]
机构
[1] Ctr Dis Control & Prevent, COVID 19 Response, Atlanta, GA USA
[2] Minnesota Dept Hlth, St Paul, MN USA
[3] Massachusetts Gen Hosp, Cardiovasc Res Ctr, Boston, MA 02114 USA
[4] Ctr Dis Control & Prevent, Epidem Intelligence Serv, Atlanta, GA USA
[5] Intermt Healthcare, Murray, UT USA
[6] Univ Cincinnati, Coll Med, Cincinnati Childrens Hosp Med Ctr, Cincinnati, OH USA
[7] Johns Hopkins Univ, Baltimore, MD USA
[8] Vanderbilt Univ, Med Ctr, Nashville, TN USA
[9] Boston Med Ctr, Boston, MA USA
关键词
coronavirus; COVID-19; MIS-A; MIS-C; multisystem inflammatory syndrome in adults;
D O I
10.1093/cid/ciab936
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
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. Seven of 20 MIS-A patients received COVID-19 vaccination before illness onset. All patients had evidence of prior SARS-CoV-2 infection. Given widespread COVID-19 vaccinations in the United States, the lack of reporting of MIS-A associated with vaccination alone is reassuring.
引用
收藏
页码:E741 / E748
页数:8
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