Assessment of adverse events following vaccination with AstraZeneca Coronavirus Disease 2019 vaccine in Greater Kampala, Uganda, March-April 2021

Author:

Komakech Allan1

Affiliation:

1. Uganda Public Health Fellowship Program

Abstract

Abstract Background Tracking of adverse events following vaccination is important for evaluating vaccine safety. During March 2021, Uganda began COVID-19 vaccination using the Astra-Zeneca vaccine targeting teachers, health workers, security personnel, and the elderly. We assessed adverse events following AstraZeneca vaccination in Greater Kampala, Uganda to track the safety of the vaccine. Methods We used vaccination registers to identify persons who received ≥ 1 dose of the AstraZeneca COVID-19 vaccine during March 10–April 30, 2021. Adverse events following vaccination were defined as an untoward medical occurrence after vaccination (not necessarily causally related to the vaccine). Serious adverse events were defined as any event considered life-threatening, resulting in hospitalization, persistent disability ˃28 days, death, or congenital anomaly. We extracted telephone contacts for a systematic random sample of vaccinated individuals and their next of kin where necessary. We then conducted phone interviews to collect data on demographics and details of adverse events where they occurred. We used logistic regression analysis to establish relationships between variables and our outcome of interest (developing an adverse event following vaccination). Results Among 374 subjects interviewed, mean age was 41 years; range 20–85 years; 176 (47%) were female. Of these, 235 (63%) received only one dose and 139 (37%) received two doses. In total, 516 adverse events occurred in 286 (77%) individuals, including in 255 (68%) individuals after the first dose and in 45 (32%) individuals after the second. The most common adverse events were redness/pain/itching at the injection site (34%) and headache (32%). None of the events were classified as serious. Persons aged 20–29 years (AOR 4.7; 95% CI: 2.0–10.2), 30–39 years (AOR 3.7; 95% CI: 1.8–7.4) and 40–49 years (AOR 2.8; 95% CI 1.3–5.0) were more likely to develop adverse events than those aged ≥ 50 years. Conclusion Most individuals experienced ≥ 1 adverse event. No serious adverse events were reported. Younger age (˂50 years) was associated with adverse event. We recommend use of the AstraZeneca COVID-19 vaccine in Uganda based on its safety.

Publisher

Research Square Platform LLC

Reference35 articles.

1. Coronavirus disease (COVID-19) [Internet]. [cited 2021 Oct 13]. Available from: https://www.who.int/emergencies/diseases/novel-coronavirus-2019

2. Comas-Herrera A, Ashcroft EC, Lorenz-Dant K, Ashcroft EC. International examples of measures to prevent and manage COVID-19 outbreaks in residential care and nursing home settings. 2020 [cited 2021 Oct 13]; Available from: https://www.nejm.org/doi/full/10.1056/NEJMoa2008457

3. Maqbool A, Khan NZ. Analyzing barriers for implementation of public health and social measures to prevent the transmission of COVID-19 disease using DEMATEL method. Diabetes Metab Syndr Clin Res Rev. 2020 Sep 1;14(5):887–92.

4. Reeves DB, Bracis C, Swan DA, Moore M, Dimitrov D, Schiffer JT. Rapid vaccination and early reactive partial lockdown will minimize deaths from emerging 4 highly contagious SARS-CoV-2 variants 5. medRxiv [Internet]. 2021 Feb 3 [cited 2021 Apr 16];2021.02.02.21250985. Available from: https://doi.org/10.1101/2021.02.02.21250985

5. Prüβ BM. Current State of the First COVID-19 Vaccines. Vaccines 2021, Vol 9, Page 30 [Internet]. 2021 Jan 8 [cited 2021 Nov 3];9(1):30. Available from: https://www.mdpi.com/2076-393X/9/1/30/htm

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3