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《瑞典 COVID-19 疫苗接种登记研究的安全性概况(CoVacSafe-SE)》。

The profile of the COvid-19 VACcination register SAFEty study in Sweden (CoVacSafe-SE).

机构信息

Swedish Medical Products Agency, Uppsala, Sweden.

出版信息

Ups J Med Sci. 2021 Dec 10;126. doi: 10.48101/ujms.v126.8136. eCollection 2021.

Abstract

BACKGROUND

The coronavirus disease 2019 (COVID-19) vaccines have been rapidly implemented in national vaccination programs world-wide after accelerated approval processes. The large population exposure achieved in very short time requires systematic monitoring of safety. The Swedish Medical Products Agency has launched a project platform for epidemiological surveillance to detect and characterise suspected adverse effects of COVID-19 vaccines in Sweden.

METHODS

The platform includes all individuals 12 years or older in Sweden in 2021 and will be updated annually. Data, including vaccine and COVID-19 disease data, socioeconomic and demographic data, comorbidity, prescribed medicines and healthcare utilisation outcomes, are obtained from several national registers in collaboration with other Swedish Government agencies. Data from 2015 to 2019 are used as a historical comparison cohort unexposed to both the COVID-19 pandemic and to the COVID-19 vaccines.

RESULTS

The primary study cohort includes 8,305,978 adults 18 years and older permanently residing in Sweden on 31 December 2020. The historical control cohort includes 8,679,641 subjects. By 31 July 2021, around 50% of those 18 years and older and two-thirds of those 50 years and older were vaccinated with at least one dose, 90% of those 70 years or older had two doses.

CONCLUSIONS

The nationwide register-based study cohort created by the Swedish Medical Products Agency with regular updates of individual level linkage of COVID-19 vaccination exposure data to other health data registers will facilitate both safety signal detection and evaluation and other pharmacoepidemiological studies.

摘要

背景

在加速审批程序后,新型冠状病毒病 2019(COVID-19)疫苗已在全球各国的疫苗接种计划中迅速实施。在短时间内实现了大量人群接种,这需要系统监测安全性。瑞典药品管理局已启动了一个项目平台,用于开展流行病学监测,以发现和描述瑞典 COVID-19 疫苗的疑似不良反应。

方法

该平台包括 2021 年瑞典所有 12 岁及以上的人群,每年将进行更新。数据包括疫苗和 COVID-19 疾病数据、社会经济和人口统计学数据、合并症、处方药物和医疗保健利用结果,从几个国家登记处与其他瑞典政府机构合作获取。2015 年至 2019 年的数据被用作历史对照队列,既未接触过 COVID-19 大流行,也未接触过 COVID-19 疫苗。

结果

主要研究队列包括 2020 年 12 月 31 日永久居住在瑞典的 18 岁及以上的 8305978 名成年人。历史对照队列包括 8679641 名受试者。截至 2021 年 7 月 31 日,约 50%的 18 岁及以上人群和三分之二的 50 岁及以上人群已至少接种了一剂疫苗,90%的 70 岁及以上人群已接种了两剂疫苗。

结论

瑞典药品管理局创建的基于全国范围登记的研究队列,定期更新 COVID-19 疫苗接种暴露数据与其他健康数据登记的个体水平链接,将有助于发现和评估安全性信号以及开展其他药物流行病学研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/71fe/8693580/30c25826872a/UJMS-126-8136-g001.jpg

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