Comisión Coordinadora de Institutos Nacionales de Salud Y Hospitales de Alta Especialidad, Mexico City, Mexico.
Instituto Nacional de Pediatría, Insurgentes Sur 3700c, Mexico City, Mexico.
J Clin Immunol. 2022 Nov;42(8):1593-1599. doi: 10.1007/s10875-022-01350-1. Epub 2022 Aug 17.
Information on anaphylaxis among recipients of vaccines against the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) remains scarce.
To identify the observed incidence of anaphylaxis in recipients of different anti-SARS-CoV-2 vaccines.
A nationwide observational study among recipients of 61,414,803 doses of seven different anti-SARS-CoV-2 vaccines, describing the incidence and characteristics of adult patients (age ≥ 18 years) who developed anaphylaxis as an adverse event following immunization (AEFI) against SARS-CoV-2 vaccines between December 24, 2020, and October 15, 2021, in Mexico.
Sixty-six patients developed anaphylaxis as an AEFI, for an overall observed incidence of 1.07 cases per 1,000,000 (95% CI 0.84-1.37) administered doses. Eighty-six percent of the patients were female, consistent with previous reports of AEFI to COVID-19 vaccines. mRNA-based vaccine recipients had the highest frequency of anaphylaxis, followed by adenovirus-vectored vaccines and inactivated virus recipients, with an observed incidence of 2.5, 0.7, and 0.2 cases per 1,000,000 doses administered, respectively. Only 46% of the patients received correct treatment with epinephrine as the first-line treatment through the appropriate route and dose. We detected one case of anaphylactic reaction-related death occurring 5 min following immunization with ChAdOx1 nCov-19 for a mortality rate of 1.5% among those who developed this AEFI.
In our population, anaphylactic reactions were infrequent. Our study provides further evidence supporting the security of these newly developed vaccines.
关于严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)疫苗接种者的过敏反应信息仍然很少。
确定不同 SARS-CoV-2 疫苗接种者中观察到的过敏反应发生率。
在墨西哥,对 61414803 剂 7 种不同 SARS-CoV-2 疫苗的接种者进行了一项全国性观察性研究,描述了 2020 年 12 月 24 日至 2021 年 10 月 15 日期间,成人(年龄≥18 岁)作为疫苗接种后不良事件(AEFI)出现过敏反应的患者的发生率和特征。
66 例患者发生过敏反应作为 AEFI,总体观察发生率为每 100 万剂 1.07 例(95%CI 0.84-1.37)。86%的患者为女性,与先前 COVID-19 疫苗 AEFI 的报告一致。基于 mRNA 的疫苗接种者过敏反应频率最高,其次是腺病毒载体疫苗和灭活病毒疫苗,观察到的每 100 万剂接种者的发生率分别为 2.5、0.7 和 0.2 例。只有 46%的患者接受了正确的治疗,即通过适当的途径和剂量给予肾上腺素作为一线治疗。我们检测到 1 例与过敏反应相关的死亡病例,在接种 ChAdOx1 nCov-19 后 5 分钟发生,该 AEFI 发生率为 1.5%。
在我们的人群中,过敏反应很少见。我们的研究进一步证明了这些新开发疫苗的安全性。