COVID-19疫苗接种时间关联致死性不良反应分析以提高COVID-19疫苗接种安全性

IF 1 Q3 MEDICINE, GENERAL & INTERNAL The Egyptian Journal of Internal Medicine Pub Date : 2023-01-01 DOI:10.1186/s43162-023-00191-7
Shahnawaz Muslim, Gulam Mustafa, Nasrin Nasrin, Aaisha Firdaus, Shambhu Kumar Singh
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引用次数: 1

摘要

COVID-19的病原体SARS-CoV-2在很短的时间内夺去了多人的生命。鉴于形势的紧迫性,疫苗在前所未有的时间框架内开发出来。疫苗在临床试验中肯定通过了安全性和有效性的测试,但大规模接种疫苗后的数据显示,在接种疫苗的时间关联中存在致命的不良反应。这种时间关联并不能保证死亡是由于接种疫苗,但与此同时,它确实引起了人们的关注。为了克服这一担忧并提高疫苗接种的安全性,我们回顾了文献并收集了15项研究的数据,其中包括22例与COVID-19疫苗接种时间相关的致命不良反应/死亡病例。对这些资料的分析表明,许多死亡的人(40.90%)以前是健康的人。所有死亡病例均在接种疫苗后3周内出现症状或住院。86.36%的死亡病例发生在接种疫苗/就诊/入院/干预后3周内。导致死亡的并发症为CVST、血小板减少症/血栓形成/VITT、DIC和出血,占81.18%。81.81%的死亡病例与ChAdOx1 nCoV-19疫苗的时间相关。68.18%的人在首次服药后出现症状。死亡以女性多见(59.09%),最常见的年龄组为20 ~ 60岁(86.36%)。了解疫苗接种时间关联的致命不良条件将有助于很好地解决这些情况,并进一步提高疫苗接种的安全性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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An analysis of fatal adverse conditions in temporal association of COVID-19 vaccination to boost the safety of vaccination for COVID-19.

SARS-CoV-2, the causative agent of COVID-19, claimed multiple lives in a very short span of time. Seeing the urgency of situation, vaccines were developed in hitherto unseen time frame. Vaccines definitely passed the test of safety and efficacy in clinical trials, but post mass vaccination data revealed cases of fatal adverse conditions in the temporal association of vaccination. The temporal association does not guarantee that the fatality is due to vaccination, but at the same time, it does create a concern. To overcome this concern and improve the safety of vaccination, we reviewed literature and collected data of 15 studies comprising of total 22 cases of fatal adverse condition/death in the temporal association of COVID-19 vaccination. Analysis of these data shows that many persons (40.90%) who succumbed were previously healthy individuals. All those who died developed symptoms or were admitted to hospital within a period of 3 weeks after vaccination. 86.36% cases of death took place within a period of 3 weeks after vaccination/presentation/admission/intervention. Complications which lead to death were CVST, thrombocytopenia/thrombosis /VITT, DIC and haemorrhage in 81.18% of cases. 81.81% cases of death were noted in the temporal association with ChAdOx1 nCoV-19 vaccine. 68.18% persons developed symptoms after first dose. Death was more common in females (59.09%), and the most commonly affected age group was 20 to 60 years (86.36%). Knowledge of fatal adverse conditions in the temporal association of vaccination will help to tackle these situations well and improve the safety of vaccination drive further.

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