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在全国性被动流行病学监测计划背景下对 SARS-CoV-2 疫苗的过敏反应。

Anaphylaxis to SARS-CoV-2 Vaccines in the Setting of a Nationwide Passive Epidemiological Surveillance Program.

机构信息

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.

出版信息

J Clin Immunol. 2022 Nov;42(8):1593-1599. doi: 10.1007/s10875-022-01350-1. Epub 2022 Aug 17.

Abstract

BACKGROUND

Information on anaphylaxis among recipients of vaccines against the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) remains scarce.

OBJECTIVE

To identify the observed incidence of anaphylaxis in recipients of different anti-SARS-CoV-2 vaccines.

METHODS

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.

RESULTS

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.

CONCLUSIONS

In our population, anaphylactic reactions were infrequent. Our study provides further evidence supporting the security of these newly developed vaccines.

摘要

背景

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。

目的

确定不同 SARS-CoV-2 疫苗接种者中观察到的过敏反应发生率。

方法

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。

结果

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%。

结论

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2601/9382604/5a3ce98a4027/10875_2022_1350_Fig1_HTML.jpg

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