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七种欧洲国家老年人中针对 Omicron BA.2.86/JN.1 流行期间住院和死亡的单价 XBB.1.5 COVID-19 疫苗有效性:VEBIS-EHR 网络研究。

Monovalent XBB.1.5 COVID-19 vaccine effectiveness against hospitalisations and deaths during the Omicron BA.2.86/JN.1 period among older adults in seven European countries: A VEBIS-EHR network study.

机构信息

Department of Epidemiology, Epiconcept, Paris, France.

Vaccine Preventable Diseases and Immunisation, European Centre for Disease Prevention and Control (ECDC), Solna, Sweden.

出版信息

Expert Rev Vaccines. 2024 Jan-Dec;23(1):1085-1090. doi: 10.1080/14760584.2024.2428800. Epub 2024 Nov 25.

Abstract

BACKGROUND

We aimed to estimate XBB.1.5 vaccine effectiveness (VE) against COVID-19-related hospitalizations and deaths during BA.2.86/JN.1 predominance, among EU/EEA individuals with ≥65-years.

RESEARCH DESIGN AND METHODS

We linked electronic health records to create historical cohorts in Belgium, Denmark, Italy, Navarre (Spain), Norway, Portugal and Sweden. We included individuals aged ≥65-years eligible for the autumnal 2023 COVID-19 vaccine. Follow-up started when ≥80% of country-specific sequenced viruses were BA.2.86/JN.1 (4/dec/23 to 08/jan/24) and ended 25 February 2024. At study site level, we estimated the vaccine confounder-adjusted hazard ratio (aHR) of COVID-19 hospitalizations and deaths between individuals with ≥14 days after vaccination versus unvaccinated in autumn 2023, overall, by time since vaccination and age groups. VE was estimated as (1-pooled aHR)x100 with a random-effects model.

RESULTS

XBB.1.5 VE against COVID-19 hospitalizations was 50% (95%CI: 45 to 55) and 41% (95%CI: 35 to 46) in 65-79-year-olds and in ≥80-year-olds, respectively. VE against COVID19-related-death was 58% (95%CI: 42 to 69) and 48% (95%CI: 38 to 57), respectively, in both age groups. VE estimates against each outcome declined in all age groups over time.

CONCLUSION

Monovalent XBB.1.5 vaccine had a moderate protective effect against severe and fatal COVID-19 likely caused by BA.2.86/JN.1 during the 2023/2024 winter, among persons aged ≥65.

摘要

背景

我们旨在评估 XBB.1.5 疫苗对欧盟/欧洲经济区≥65 岁人群在 BA.2.86/JN.1 流行期间与 COVID-19 相关住院和死亡的有效性。

研究设计和方法

我们将电子健康记录链接起来,在比利时、丹麦、意大利、纳瓦拉(西班牙)、挪威、葡萄牙和瑞典创建了历史队列。我们纳入了有资格在 2023 年秋季接种 COVID-19 疫苗的≥65 岁人群。随访始于当≥80%的国家特定测序病毒为 BA.2.86/JN.1(2023 年 12 月 4 日至 2024 年 1 月 8 日)时开始,并于 2024 年 2 月 25 日结束。在研究点水平上,我们根据疫苗调整混杂因素后的风险比(aHR)估计了 2023 年秋季接种疫苗后≥14 天与未接种疫苗的个体之间 COVID-19 住院和死亡的情况,整体上按疫苗接种后时间和年龄组进行了估计。疫苗有效性(VE)通过随机效应模型计算为(1-汇总 aHR)x100。

结果

XBB.1.5 对 COVID-19 住院的有效性在 65-79 岁和≥80 岁的人群中分别为 50%(95%CI:45 至 55)和 41%(95%CI:35 至 46)。XBB.1.5 对 COVID19 相关死亡的有效性在这两个年龄组中分别为 58%(95%CI:42 至 69)和 48%(95%CI:38 至 57)。随着时间的推移,两个年龄组中针对每种结果的 VE 估计值均呈下降趋势。

结论

在 2023/2024 年冬季,单价 XBB.1.5 疫苗对由 BA.2.86/JN.1 引起的≥65 岁人群的严重和致命 COVID-19 具有中等保护作用。

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