Muslim Shahnawaz, Mustafa Gulam, Nasrin Nasrin, Firdaus Aaisha, Singh Shambhu Kumar
Madhubani Medical College and Hospital, Madhubani, Bihar India.
College of Pharmacy, Shaqra University, Shaqra, 11961 Saudi Arabia.
Egypt J Intern Med. 2023;35(1):11. doi: 10.1186/s43162-023-00191-7. Epub 2023 Feb 7.
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.
新型冠状病毒肺炎(COVID-19)的病原体严重急性呼吸综合征冠状病毒2(SARS-CoV-2)在很短的时间内夺去了许多人的生命。鉴于形势紧迫,疫苗在前所未有的时间框架内得以研发。疫苗在临床试验中无疑通过了安全性和有效性测试,但大规模接种疫苗后的数据分析显示,在接种疫苗后的时间关联中出现了致命不良反应的病例。时间关联并不能保证死亡是由接种疫苗引起的,但同时,这确实引发了人们的担忧。为了消除这种担忧并提高疫苗接种的安全性,我们查阅了文献,并收集了15项研究的数据,这些研究共包括22例在COVID-19疫苗接种时间关联中的致命不良反应/死亡病例。对这些数据的分析表明,许多死亡者(40.90%)此前身体健康。所有死亡者在接种疫苗后的3周内出现症状或入院。86.36%的死亡病例发生在接种疫苗/出现症状/入院/干预后的3周内。导致死亡的并发症在81.18%的病例中为大脑静脉窦血栓形成(CVST)、血小板减少症/血栓形成/疫苗诱导的免疫性血小板减少症(VITT)、弥散性血管内凝血(DIC)和出血。81.81%的死亡病例与腺病毒载体新冠疫苗(ChAdOx1 nCoV-19)存在时间关联。68.18%的人在接种第一剂疫苗后出现症状。女性死亡更为常见(59.09%),最常受影响的年龄组为20至60岁(86.36%)。了解疫苗接种时间关联中的致命不良反应将有助于更好地应对这些情况,并进一步提高疫苗接种行动的安全性。