Adverse events following COVID-19 vaccination: first 90 days of experience from a tertiary care teaching hospital in South India.

Q2 Medicine
Therapeutic Advances in Vaccines and Immunotherapy Pub Date : 2021-11-22 eCollection Date: 2021-01-01 DOI:10.1177/25151355211055833
Chetak Kadabasal Basavaraja, Juny Sebastian, Mandyam Dhati Ravi, Sheba Baby John
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引用次数: 15

Abstract

Background: The COVID-19 vaccination program was introduced in India on 16 January 2021. The Government-issued fact sheet was the only source of information regarding Adverse Events Following Immunizations (AEFIs) for these vaccines. The objective of this study was to assess the AEFIs reported following COVID-19 vaccination in a tertiary care teaching hospital.

Materials and methods: The spontaneous reporting method was used for data collection for a period of 3 months. A data collection form was designed to collect the data from the study population who reported adverse events. Collected data were analyzed and categorized by severity and seriousness. The causality assessment team performed causality assessment of the AEFIs using the World Health Organization's causality assessment algorithm.

Results: A total of 11,656 doses of COVID-19 vaccine were administered at the study site during the study period, of which 9292 doses were COVISHIELD™ and 2364 doses were COVAXIN™. In all, 445 AEFIs were reported from 269 subjects with an incidence rate of 3.48%. The majority of the subjects with AEFIs belonged to the age group of 18-45 years. Out of the total 445 AEFIs, 418 AEFIs were expected as per the fact sheets, 409 with COVISHIELD™ and 9 with COVAXIN™. Most of the AEFIs [62.02% (n = 276)] were observed at the system organ class of 'General disorders and administration site conditions'. After the causality assessment, out of 433 AEFIs to COVISHIELDTM vaccine, 94.22% (n = 408) of events were categorized to have 'consistent causal association with immunization'. Out of 12 adverse events following COVAXIN™, 8 (66.66%) events were categorized as 'consistent causal association with immunization'. All of them recovered from their adverse events without any sequelae.

Conclusion: Spontaneous reporting is one of the cheapest methods that can be used for the reporting of AEFI. This method helps health care professionals to identify rare events and potential signals.

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COVID-19疫苗接种后的不良事件:来自南印度一家三级保健教学医院的头90天经验
背景:印度于2021年1月16日开始实施COVID-19疫苗接种规划。政府发布的情况说明书是关于这些疫苗接种后不良事件的唯一信息来源。本研究的目的是评估三级保健教学医院COVID-19疫苗接种后报告的aefi。材料和方法:采用自发报告法收集数据,为期3个月。设计了一份数据收集表,从报告不良事件的研究人群中收集数据。对收集的数据进行分析并按严重程度和严重性分类。因果关系评估小组使用世界卫生组织的因果关系评估算法对急性呼吸系统疾病进行了因果关系评估。结果:在研究期间,研究地点共接种了11,656剂COVID-19疫苗,其中9292剂为COVISHIELD™,2364剂为COVAXIN™。269例受试者共报告急性脑梗死445例,发生率3.48%。aefi患者以18-45岁年龄组居多。在总共445个aefi中,418个aefi根据情况说明书预计,409个使用COVISHIELD™,9个使用COVAXIN™。大多数aefi [62.02% (n = 276)]发生在“一般疾病和给药部位状况”的系统器官类别。经过因果关系评估,在433例COVISHIELDTM疫苗的不良事件中,94.22% (n = 408)的事件被归类为“与免疫接种有一致的因果关系”。在COVAXIN™后的12个不良事件中,8个(66.66%)事件被归类为“与免疫接种一致的因果关联”。所有患者均从不良事件中恢复,无任何后遗症。结论:自发性报告是报告急性脑损伤最经济的方法之一。这种方法有助于卫生保健专业人员识别罕见事件和潜在信号。
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来源期刊
Therapeutic Advances in Vaccines and Immunotherapy
Therapeutic Advances in Vaccines and Immunotherapy Medicine-Pharmacology (medical)
CiteScore
5.10
自引率
0.00%
发文量
15
审稿时长
8 weeks
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