COVID-19 Response, Centers for Disease Control and Prevention, Atlanta, GeorgiaUSA.
Epidemic Intelligence Service, Centers for Disease Control and Prevention, Atlanta, Georgia, USA.
Clin Infect Dis. 2022 Aug 24;75(1):e741-e748. doi: 10.1093/cid/ciab936.
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.
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.
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.
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.
成年人多系统炎症综合征(MIS-A)与 2019 年冠状病毒病(COVID-19)大流行有关。MIS-A 被列入 COVID-19 疫苗紧急使用授权需要监测的不良事件清单。
评估 COVID-19 疫苗可用后疾病预防控制中心(CDC)收到的 MIS-A 患者报告。收集的患者数据包括临床和人口统计学特征及其疫苗接种情况。还审查了疫苗不良事件报告系统(VAERS)中可能的 MIS-A 病例。
从 2020 年 12 月 14 日至 2021 年 4 月 30 日,向 CDC 报告了 20 例符合 MIS-A 病例定义的患者。他们的中位年龄为 35 岁(范围 21-66 岁),13 例(65%)为男性。总体而言,16 例(80%)患者在 MIS-A 发病前中位时间 26 天(范围 11-78 天)前有 COVID-19 样疾病。所有 20 例患者均有严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)感染的实验室证据。7 例 MIS-A 患者(35%)在 MIS-A 发病前中位时间 10 天(范围 6-45 天)接种 COVID-19 疫苗;3 例患者在 MIS-A 发病前 4、17 和 22 天接种第二剂 COVID-19 疫苗。MIS-A 患者主要表现为胃肠道和心脏表现以及低血压或休克。
尽管有 7 例患者报告接种 COVID-19 疫苗,但所有患者均有 SARS-CoV-2 感染的证据。鉴于 COVID-19 疫苗的广泛使用,没有报告单独接种疫苗与 MIS-A 相关,且无 SARS-CoV-2 感染的证据,这令人感到欣慰。