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A prospective observational safety study on ChAdOx1 nCoV-19 corona virus vaccine (recombinant) use in healthcare workers- first results from India.一项关于医护人员使用ChAdOx1 nCoV-19冠状病毒疫苗(重组)的前瞻性观察性安全性研究——来自印度的初步结果。
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泰国首次接种ChAdOx1 nCoV-19疫苗后急性不良反应的发生率、类型及相关因素。

Rates, types, and associated factors of acute adverse effects after the first dose of ChAdOx1 nCoV-19 vaccine administration in Thailand.

作者信息

Watcharananan Sirapat Arthur, Nadee Chalermlap, Kongsuwattanaleart Patis, Sangthong Nussara, Ngorsakun Punpen, Vimonvattaravetee Pornpimon, Phuphuakrat Angsana, Udomsubpayakul Umaporn

机构信息

Choate Rosemary Hall, Wallingford, Connecticut, USA.

Praram 9 Hospital, Bangkok, Thailand.

出版信息

IJID Reg. 2022 Mar;2:35-39. doi: 10.1016/j.ijregi.2021.11.008. Epub 2021 Nov 27.

DOI:10.1016/j.ijregi.2021.11.008
PMID:35721432
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8626869/
Abstract

OBJECTIVES

Effective vaccines are prioritized to curtail the transmission and burden of coronavirus disease 2019. Nevertheless, monitoring the safety of vaccines is crucial. As Thailand began the ChAdOx1 nCoV-19 vaccination, our study examined the acute adverse effects and associated factors after the first dose of vaccination.

METHODS

A mobile self-report questionnaire was employed to assess the rates and types of different side-effects within 3 days of the first dose of ChAdOx1 nCoV-19 vaccine administration. The risk factors associated with these side-effects were analyzed.

RESULTS

In total, 774 participants were included in the survey, with a mean (± standard deviation) age of 49.5 (± 17.2) years. The majority (57.8%) were females, and 59.1% were anxious before the vaccination. Side-effects after the vaccination were a common occurrence (65.2%), but most (42.6%) were mild. Side-effects were significantly associated (odds ratio [95% confidence interval]) with younger age (4.32 [2.26-8.23]; < 0.001; age < 30 years vs ≥ 60 years), female sex (1.66 [1.19-2.30],  = 0.003), anxiousness (2.10 [1.06-4.13];  = 0.033; moderate-severe anxiousness vs none), and allergic disease (2.60 [1.07-6.31];  = 0.035).

CONCLUSIONS

After the ChAdOx1 nCoV-19 vaccination, most acute adverse effects were mild and often noted among participants with younger age, female sex, anxiousness, and allergic disease.

摘要

目的

优先使用有效的疫苗来减少2019冠状病毒病的传播和负担。然而,监测疫苗安全性至关重要。随着泰国开始接种ChAdOx1 nCoV-19疫苗,我们的研究调查了首剂疫苗接种后的急性不良反应及相关因素。

方法

采用移动自我报告问卷评估首剂ChAdOx1 nCoV-19疫苗接种后3天内不同副作用的发生率和类型。分析与这些副作用相关的危险因素。

结果

共有774名参与者纳入调查,平均(±标准差)年龄为49.5(±17.2)岁。大多数(57.8%)为女性,59.1%在接种前感到焦虑。接种疫苗后出现副作用很常见(65.2%),但大多数(42.6%)为轻度。副作用与较年轻的年龄(4.32[2.26 - 8.23];<0.001;年龄<30岁与≥60岁相比)、女性(1.66[1.19 - 2.30],=0.003)、焦虑(2.10[1.06 - 4.13];=0.033;中度 - 重度焦虑与无焦虑相比)以及过敏性疾病(2.60[1.07 - 6.31];=0.035)显著相关(优势比[95%置信区间])。

结论

接种ChAdOx1 nCoV-19疫苗后,大多数急性不良反应为轻度,且在年龄较小、女性、焦虑和患有过敏性疾病的参与者中较为常见。