Suppr超能文献

2021 年 7 月至 8 月,在欧洲主要德尔塔(Delta)传播期间,初级保健和社区层面针对 COVID-19 的完全初级疫苗接种的有效性:多中心分析,I-MOVE-COVID-19 和 ECDC 网络。

Effectiveness of complete primary vaccination against COVID-19 at primary care and community level during predominant Delta circulation in Europe: multicentre analysis, I-MOVE-COVID-19 and ECDC networks, July to August 2021.

机构信息

Epiconcept, Paris, France.

Nivel, Utrecht, the Netherlands.

出版信息

Euro Surveill. 2022 May;27(21). doi: 10.2807/1560-7917.ES.2022.27.21.2101104.

Abstract

IntroductionIn July and August 2021, the SARS-CoV-2 Delta variant dominated in Europe.AimUsing a multicentre test-negative study, we measured COVID-19 vaccine effectiveness (VE) against symptomatic infection.MethodsIndividuals with COVID-19 or acute respiratory symptoms at primary care/community level in 10 European countries were tested for SARS-CoV-2. We measured complete primary course overall VE by vaccine brand and by time since vaccination.ResultsOverall VE was 74% (95% CI: 69-79), 76% (95% CI: 71-80), 63% (95% CI: 48-75) and 63% (95% CI: 16-83) among those aged 30-44, 45-59, 60-74 and ≥ 75 years, respectively. VE among those aged 30-59 years was 78% (95% CI: 75-81), 66% (95% CI: 58-73), 91% (95% CI: 87-94) and 52% (95% CI: 40-61), for Comirnaty, Vaxzevria, Spikevax and COVID-19 Vaccine Janssen, respectively. VE among people 60 years and older was 67% (95% CI: 52-77), 65% (95% CI: 48-76) and 83% (95% CI: 64-92) for Comirnaty, Vaxzevria and Spikevax, respectively. Comirnaty VE among those aged 30-59 years was 87% (95% CI: 83-89) at 14-29 days and 65% (95% CI: 56-71%) at ≥ 90 days between vaccination and onset of symptoms.ConclusionsVE against symptomatic infection with the SARS-CoV-2 Delta variant varied among brands, ranging from 52% to 91%. While some waning of the vaccine effect may be present (sample size limited this analysis to only Comirnaty), protection was 65% at 90 days or more between vaccination and onset.

摘要

简介

2021 年 7 月和 8 月,SARS-CoV-2 德尔塔变异株在欧洲占主导地位。

目的

本研究采用多中心病例对照研究,测量了 COVID-19 疫苗对有症状感染的有效性(VE)。

方法

在欧洲 10 个国家的基层医疗/社区层面,对出现 COVID-19 或急性呼吸道症状的个体进行 SARS-CoV-2 检测。我们通过疫苗品牌和接种后时间来衡量完全初级疗程的总体 VE。

结果

在年龄为 30-44、45-59、60-74 和≥75 岁的个体中,总体 VE 分别为 74%(95%CI:69-79)、76%(95%CI:71-80)、63%(95%CI:48-75)和 63%(95%CI:16-83)。在 30-59 岁的个体中,Comirnaty、Vaxzevria、Spikevax 和 COVID-19 Vaccine Janssen 的 VE 分别为 78%(95%CI:75-81)、66%(95%CI:58-73)、91%(95%CI:87-94)和 52%(95%CI:40-61)。60 岁及以上人群中,Comirnaty、Vaxzevria 和 Spikevax 的 VE 分别为 67%(95%CI:52-77)、65%(95%CI:48-76)和 83%(95%CI:64-92)。在 30-59 岁的个体中,Comirnaty 在接种后 14-29 天的 VE 为 87%(95%CI:83-89),在接种后 90 天或以上的 VE 为 65%(95%CI:56-71%)。

结论

针对 SARS-CoV-2 德尔塔变异株的有症状感染,不同品牌的 VE 差异较大,从 52%到 91%不等。虽然疫苗效果可能存在一定程度的衰减(由于样本量限制,该分析仅针对 Comirnaty),但在接种后 90 天或以上,保护率为 65%。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9a35/9137272/58ba0c88a1c7/2101104-f1.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验