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葡萄牙二价mRNA疫苗对COVID-19住院和死亡的长期有效性:一项基于电子健康记录的队列研究

Long term bivalent mRNA vaccine effectiveness against COVID-19 hospitalisations and deaths in Portugal: a cohort study based on electronic health records.

作者信息

Machado Ausenda, Kislaya Irina, Soares Patricia, Magalhães Sarah, Nunes Baltazar

机构信息

Departamento de Epidemiologia, Instituto Nacional de Saúde Doutor Ricardo Jorge, Lisbon, Portugal.

Centro de Investigação em Saúde Pública, Universidade NOVA de Lisboa, Lisbon, Portugal.

出版信息

BMC Infect Dis. 2025 Apr 23;25(1):590. doi: 10.1186/s12879-025-10866-x.

Abstract

BACKGROUND

In Autumn 2022, there were recommendations for a COVID-19 booster vaccination with adapted bivalent vaccines to eligible population. Evaluating vaccine effectiveness (VE), in a short period after the vaccination, is key to guide public health decisions on the vaccine performance, allowing implementation of mitigation strategies promptly. However, to assess long-term protection post-vaccination and evaluate the need for additional boosters, it is crucial to conduct studies that span the maximum duration of the vaccination program. This study aims to estimate the VE of bivalent mRNA vaccines against COVID-19-related hospitalisation and death in the Portuguese population aged 65 years or older, from September 2022 to May 2023.

METHODS

We used a cohort approach to analyse six electronic health registries using deterministic linkage, with a follow-up period of eight months. Severe outcomes included COVID-19-related hospitalisations and death, classified using discharge ICD-10 codes as proxies. The exposure of interest was the bivalent mRNA vaccine. VE was estimated for 14-97, 98-181 and 182-240 days after bivalent vaccination. Confounder-adjusted hazard ratio (aHR) was obtained by fitting a time-dependent Cox regression model with time-dependent vaccination status, adjusted for sociodemographic, history of influenza and pneumococcus vaccination, previous SARS-CoV-2 tests and infection, and comorbidities. VE was estimated by one minus the aHR between vaccinated with bivalent vaccine person-years versus those without bivalent vaccine person-years.

RESULTS

The cohort included 2,151,531 individuals aged 65 or older (27.8% with 80 or more years). In the ≥ 80 years old, VE was 41.3% (95%CI: 34.5-47.5%) and 50.3% (95%CI: 44.6-55.3%) against COVID-19-related hospitalisation and death, respectively. In the 65-79 years old, VE was 58.5% (95%CI: 51.9-64.2%) against COVID-19-related hospitalisation, and 65.1% (95%CI: 59.0-70.4%) against COVID-19-related death. VE waned for both age groups and outcomes. Among adults aged 65 years or older, we observed long-term moderate VE estimates against severe COVID-19-related outcomes.

CONCLUSIONS

These results support the need for yearly boosters of COVID-19 vaccination to maximise the protection of the senior population against COVID-19 severe disease. Additional (spring boosters) during a vaccination campaign should be evaluated considering the epidemiological context and results from long-term VE studies.

摘要

背景

2022年秋季,有建议向符合条件的人群提供经调整的二价疫苗作为新冠病毒加强针。在接种疫苗后的短时间内评估疫苗效力(VE),对于指导有关疫苗性能的公共卫生决策至关重要,从而能够迅速实施缓解策略。然而,为了评估接种疫苗后的长期保护效果并评估额外加强针的必要性,开展涵盖疫苗接种计划最长持续时间的研究至关重要。本研究旨在估计2022年9月至2023年5月期间,二价mRNA疫苗对葡萄牙65岁及以上人群中与新冠病毒相关的住院和死亡的疫苗效力。

方法

我们采用队列研究方法,通过确定性链接分析六个电子健康记录,随访期为八个月。严重结局包括与新冠病毒相关的住院和死亡,使用出院ICD-10编码作为替代指标进行分类。感兴趣的暴露因素是二价mRNA疫苗。在接种二价疫苗后的14 - 97天、98 - 181天和182 - 240天估计疫苗效力。通过拟合一个具有时间依赖性接种状态的时间依赖性Cox回归模型获得混杂因素调整后的风险比(aHR),并对社会人口统计学、流感和肺炎球菌疫苗接种史、既往SARS-CoV-2检测和感染情况以及合并症进行调整。疫苗效力通过1减去接种二价疫苗的人年与未接种二价疫苗的人年之间的aHR来估计。

结果

该队列包括2,151,531名65岁及以上的个体(27.8%为80岁及以上)。在80岁及以上人群中,二价疫苗对与新冠病毒相关的住院和死亡的疫苗效力分别为41.3%(95%CI:34.5 - 47.5%)和50.3%(95%CI:44.6 - 55.3%)。在65 - 79岁人群中,二价疫苗对与新冠病毒相关的住院的疫苗效力为58.5%(95%CI:51.9 - 64.2%),对与新冠病毒相关的死亡的疫苗效力为65.1%(95%CI:59.0 - 70.4%)。两个年龄组的疫苗效力均出现下降。在65岁及以上的成年人中,我们观察到二价疫苗对严重新冠病毒相关结局的长期中等效力估计。

结论

这些结果支持每年进行新冠病毒加强针接种的必要性,以最大限度地保护老年人群免受新冠病毒严重疾病的侵害。在疫苗接种活动期间额外接种(春季加强针)应根据流行病学情况和长期疫苗效力研究结果进行评估。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9b90/12020219/efb4ca8ff786/12879_2025_10866_Fig1_HTML.jpg

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