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1例新冠疫苗接种后发生迟发性过敏反应的病例报告

A Case Report of Prolonged Anaphylaxis after COVID-19 Vaccine.

作者信息

Armstrong Lisa, Maguire Nicole

机构信息

RWJ Barnabas Health-Community Medical Center, Department of Emergency Medicine, Toms River, New Jersey.

出版信息

Clin Pract Cases Emerg Med. 2022 Feb;6(1):21-24. doi: 10.5811/cpcem.2021.9.53690.

DOI:10.5811/cpcem.2021.9.53690
PMID:35226841
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8885233/
Abstract

INTRODUCTION

As the medical community and world have combatted the coronavirus disease 2019 (COVID-19) pandemic, a significant advance was the development of a vaccine against the virus that has already claimed over 4.5 million lives worldwide. Vaccines manufactured by Pfizer-BioNTech and Moderna were the first two COVID-19 vaccines given emergency use authorization by the United States Food and Drug Administration. Preliminary data demonstrated not only the vaccines' efficacy rates of greater than 95% after a second dose, but also marked safety. Initial data showed only 21 cases of anaphylaxis of greater than 1.8 million doses administered. The majority of those patients had a history of anaphylaxis and presented within the first 15 minutes after administration of the vaccine.

CASE REPORT

We describe a patient who had an anaphylactic reaction to her second dose of the Pfizer BioNTech severe acute respiratory syndrome coronavirus 2 (SARS CoV-2) vaccine with no prior history of allergic reactions or anaphylaxis. This reaction required multiple doses of epinephrine and a four-day hospitalization. We review both the available reports of anaphylaxis to the SAR CoV-2 vaccine and information on other prolonged cases of anaphylaxis.

CONCLUSION

Our case report is unique in that the patient, despite no prior history of anaphylaxis, had a prolonged course requiring a four-day hospitalization. To our knowledge this is one of the first case reports of prolonged anaphylaxis after the second dose of Pfizer BioNTech COVID-19 vaccine in a patient with no history of prior anaphylaxis.

摘要

引言

在医学界和全球抗击2019冠状病毒病(COVID-19)大流行的过程中,一项重大进展是研发出了针对该病毒的疫苗,这种病毒已在全球夺走了超过450万人的生命。辉瑞-生物科技公司和莫德纳公司生产的疫苗是首批获得美国食品药品监督管理局紧急使用授权的两种COVID-19疫苗。初步数据显示,不仅第二剂疫苗后的有效率超过95%,而且安全性也很显著。初步数据显示,在接种的超过180万剂疫苗中,仅有21例过敏反应。这些患者大多数有过敏反应史,且在接种疫苗后的前15分钟内出现症状。

病例报告

我们描述了一名患者,她在接种第二剂辉瑞生物科技公司的严重急性呼吸综合征冠状病毒2(SARS-CoV-2)疫苗后发生过敏反应,此前并无过敏反应或过敏史。该反应需要多次注射肾上腺素,并住院四天。我们回顾了关于SARS-CoV-2疫苗过敏反应的现有报告以及其他过敏反应延长病例的信息。

结论

我们的病例报告具有独特性,即该患者尽管此前没有过敏史,但过敏反应病程延长,需要住院四天。据我们所知,这是首例关于无过敏史患者在接种第二剂辉瑞生物科技公司COVID-19疫苗后出现过敏反应延长的病例报告之一。

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