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首剂接种 4 种新冠疫苗后一周内的副作用。西班牙 ProVaVac 调查研究的结果,涉及 13837 人。

Side effects during the week after first dose vaccination with four Covid-19 vaccines. Results of the ProVaVac Survey Study with 13,837 people in Spain.

机构信息

Foundation for the Promotion of Health and Biomedical Research of the Valencia Community (FISABIO), Valencia, Spain.

General Directorate for Planning, Technological Efficiency and Patient Care, Department of Health, Valencia Government, Valencia, Spain; Universitat Politècnica de Valencia, UPV.

出版信息

Vaccine. 2022 Sep 29;40(41):5942-5949. doi: 10.1016/j.vaccine.2022.08.028. Epub 2022 Aug 29.

Abstract

BACKGROUND

In 2021, four vaccines against Covid-19 (BNT162b2, mRNA-1273, ChAdOx1nCoV-19, and JNJ-78436735) were employed in the region of Valencia, Spain. We conducted a survey to identify real-world, self-reported frequency and severity of side effects during the week after vaccination.

METHODS

Survey data was obtained from April 19, 2021, to October 6, 2021, at three different moments in time: day one, day three and day seven after vaccination. Answers were linked to individual-level, personal and clinical information. Respondents were stratified by the vaccine they received and reported effects were presented over time and stratified by severity. We compared our results per vaccine with the frequencies stated in each Summary of Product Characteristics (SmPC). We used binomial logistic models to identify associations between respondent characteristics and side effects.

RESULTS

No symptoms were reported by 1,986 respondents (14.35 %), 6,254 informed exclusively mild symptoms (45.20 %), 3,444 up to moderate symptoms (24.89 %), and 2,153 people (15.56 %) notified also severe symptoms. Among the latter, the more frequent were extreme tiredness (7.0 %), and nausea or vomiting (7.1 %). The reported frequency of facial paralysis (0.4 %) was much higher than reflected in SmPCs. Female sex, younger age, previous positive Active Infection Diagnostic Test, chronicity, and vaccination with other than the BNT162b2 vaccine were associated to an increased risk of side effects (p < 0.001).

CONCLUSIONS

Side effects after vaccination are common in the real-world. However, they are principally mild, and their frequency declines after a few days. Providing patients with dependable, beforehand information about side effects may improve outcomes and reinforce vaccination programs.

摘要

背景

2021 年,四种针对 COVID-19 的疫苗(BNT162b2、mRNA-1273、ChAdOx1nCoV-19 和 JNJ-78436735)在西班牙瓦伦西亚地区使用。我们进行了一项调查,以确定接种疫苗后一周内真实世界中自我报告的副作用频率和严重程度。

方法

调查数据于 2021 年 4 月 19 日至 2021 年 10 月 6 日分三个不同时间点获得:接种后第 1 天、第 3 天和第 7 天。答案与个体水平的个人和临床信息相关联。根据接种疫苗的不同,受访者被分层,并按时间和严重程度报告效果。我们将每种疫苗的结果与各产品特性总结(SmPC)中所述的频率进行比较。我们使用二项逻辑回归模型来确定受访者特征与副作用之间的关联。

结果

1986 名受访者(14.35%)报告无任何症状,6254 名受访者仅报告轻度症状(45.20%),3444 名受访者报告中度症状(24.89%),2153 名受访者(15.56%)报告严重症状。在后者中,更常见的是极度疲劳(7.0%)和恶心或呕吐(7.1%)。面瘫的报告频率(0.4%)远高于 SmPC 反映的频率。女性、年龄较小、先前的阳性主动感染诊断测试、慢性和接种除 BNT162b2 以外的疫苗与副作用风险增加相关(p < 0.001)。

结论

接种疫苗后的副作用在现实世界中很常见。然而,它们主要是轻度的,并且在几天后会减少。向患者提供有关副作用的可靠、事先信息可能会改善结果并加强疫苗接种计划。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d01f/9420721/98b8bd20072b/gr1_lrg.jpg

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