Hans Christian Andersen Children's Hospital, Odense University Hospital, Odense C, Denmark; Clinical Pharmacology, Pharmacy and Environmental Medicine, Department of Public Health, University of Southern Denmark, DK-5000 Odense C, Denmark.
Clinical Pharmacology, Pharmacy and Environmental Medicine, Department of Public Health, University of Southern Denmark, DK-5000 Odense C, Denmark.
Lancet Child Adolesc Health. 2023 Dec;7(12):852-862. doi: 10.1016/S2352-4642(23)00225-0. Epub 2023 Oct 25.
Scant evidence exists on the real-world effectiveness of quadrivalent live attenuated influenza vaccines (LAIV-4) in younger children. We aimed to assess the real-world effectiveness of LAIV-4 against influenza-related hospital contacts and admission and morbidity.
Using nationwide Danish health-care registries, we designed a cohort study that emulates a target trial, comparing LAIV-4 to no vaccination in children aged 2-6 years. Eligible children vaccinated from Oct 1, 2021, to Jan 15, 2022, were matched to unvaccinated controls in a 1:1 ratio according to demographic characteristics and risk groups for influenza, and followed-up until May 31, 2022. Primary study outcomes any hospital contact for influenza and influenza-related hospital admissions more than 12 h in duration, while hospital admission for respiratory tract infections, or for wheezing or asthma, and antibiotic prescriptions were evaluated as secondary outcomes. We estimated incidence rate ratios (IRRs) and 95% CIs using Poisson regression for each outcome. Vaccine effectiveness was calculated as 1 - IRR.
Among 308 520 Danish children aged 2-6 years, 95 434 vaccinated children were matched with 95 434 unvaccinated children who acted as controls. Receipt of LAIV-4 compared with no vaccination was associated with a reduced IRR of 0·36 (95% CI 0·27 to 0·46) and estimated vaccine effectiveness of 64·3% (53·6 to 72·6) against influenza-related hospital contacts (76 vs 210 events). The corresponding IRR and vaccine effectiveness against influenza-related hospital admissions were 0·63 (0·38 to 1·05) and 36·9% (-5·2 to 62·1; 24 vs 38 events), respectively. LAIV-4 was not associated with reductions in admission rates for respiratory tract infections (IRR 1·14, 95% CI 0·94 to 1·38), wheezing or asthma (1·04, 0·83 to 1·31), or antibiotic prescriptions for respiratory tract infections (0·97, 0·93 to 1·00). Vaccine effectiveness assessed across risk groups for influenza showed similar effectiveness in children with and without coexisting risk factors for severe influenza.
LAIV-4 offered moderate protection in younger children against influenza-related hospital contacts during a season dominated by influenza A(H3N2); however vaccination was not associated with reductions in secondary outcomes. This real-world study thereby supports trial evidence of moderate vaccine effectiveness of LAIV-4 against influenza-related outcomes when implementing broad vaccination schedules in younger children.
Beckett-Fonden.
关于四价减毒活流感疫苗(LAIV-4)在幼儿中的真实世界有效性,证据有限。本研究旨在评估 LAIV-4 对流感相关住院接触、住院和发病的真实世界有效性。
使用丹麦全国性的医疗保健登记处,我们设计了一项队列研究,对 2-6 岁儿童进行了目标试验的模拟,将 LAIV-4 与未接种疫苗进行了比较。2021 年 10 月 1 日至 2022 年 1 月 15 日接种疫苗的合格儿童按人口统计学特征和流感高危人群与未接种疫苗的儿童以 1:1 的比例进行匹配,并随访至 2022 年 5 月 31 日。主要研究结果为任何与流感相关的住院接触和持续超过 12 小时的流感相关住院,而呼吸道感染、喘息或哮喘住院以及抗生素处方则作为次要结果进行评估。我们使用泊松回归对每个结果计算发病率比(IRR)和 95%置信区间(CI)。疫苗有效性计算为 1-IRR。
在 308520 名 2-6 岁丹麦儿童中,有 95434 名接种疫苗的儿童与 95434 名未接种疫苗的儿童相匹配,作为对照组。与未接种疫苗相比,接种 LAIV-4 与 0.36 的 IRR(95%CI 0.27-0.46)和 64.3%(53.6-72.6)的估计疫苗有效性相关,可预防流感相关的住院接触(76 例 vs 210 例)。相应的 IRR 和针对流感相关住院的疫苗有效性分别为 0.63(0.38-1.05)和 36.9%(-5.2-62.1;24 例 vs 38 例)。LAIV-4 与呼吸道感染(IRR 1.14,95%CI 0.94-1.38)、喘息或哮喘(1.04,0.83-1.31)或呼吸道感染的抗生素处方(0.97,0.93-1.00)的住院率降低无关。在流感高危人群中评估的疫苗有效性显示,在伴有或不伴有严重流感高危因素的儿童中,疫苗均具有相似的有效性。
在甲型流感病毒(H3N2)占主导的季节,LAIV-4 为幼儿提供了针对流感相关住院接触的中等程度保护;然而,接种疫苗与降低次要结果无关。这项真实世界研究支持了临床试验证据,即广泛为幼儿接种 LAIV-4 可对流感相关结果产生中等程度的疫苗有效性。
Beckett 基金会。