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在意大利住院老年患者中,含佐剂与不含佐剂季节性流感疫苗针对严重实验室确诊流感的相对有效性。

Relative effectiveness of the adjuvanted vs non-adjuvanted seasonal influenza vaccines against severe laboratory-confirmed influenza among hospitalized Italian older adults.

机构信息

Hygiene Unit, San Martino Policlinico Hospital - IRCCS for Oncology and Neurosciences, Genoa, Italy.

Department of Health Sciences, University of Genoa, Genoa, Italy; Interuniversity Research Center on Influenza and Other Transmissible Infections (CIRI-IT), Genoa, Italy.

出版信息

Int J Infect Dis. 2022 Dec;125:164-169. doi: 10.1016/j.ijid.2022.10.041. Epub 2022 Nov 2.

DOI:10.1016/j.ijid.2022.10.041
PMID:36332902
Abstract

OBJECTIVES

In this study, we aimed to investigate the relative vaccine effectiveness (rVE) of the MF59-adjuvanted trivalent (aTIV) and non-adjuvanted quadrivalent (QIVe) egg-based standard-dose vaccines against severe laboratory-confirmed influenza.

METHODS

This test-negative case-control study was conducted in a hospital setting during four recent Italian influenza seasons (from 2018/19 to 2021/22). The clinical outcome was severe acute respiratory infection (SARI) with laboratory confirmation diagnosed among subjects aged ≥65 years. rVE of aTIV versus QIVe was estimated through propensity score matching followed by logistic regression.

RESULTS

The influenza virus circulated to a significant extent only during the 2018/19 and 2019/20 seasons. The final population included 512 vaccinated older adults, of which 83 were cases and 429 were test-negative controls. aTIV and QIVe users differed substantially from the point of view of several baseline characteristics. The propensity score adjusted rVE of aTIV vs QIVe was 59.2% (95% CI: 14.6%, 80.5%), 54.7% (95% CI: -28.7%, 84.0%) and 56.9% (95% CI: -7.8%, 82.8%) against any influenza, A(H1N1)pdm09 and A(H3N2), respectively.

CONCLUSION

aTIV was more effective than QIVe in preventing laboratory-confirmed SARI. The benefits of aTIV may be obscured by confounding indication.

摘要

目的

本研究旨在探讨 MF59 佐剂三价(aTIV)和非佐剂四价(QIVe)流感疫苗对严重实验室确诊流感的相对疫苗有效性(rVE)。

方法

这是一项在医院环境中进行的病例对照研究,涵盖了四个意大利流感季节(2018/19 年至 2021/22 年)。临床结局为年龄≥65 岁的患者中经实验室确诊的严重急性呼吸道感染(SARI)。通过倾向评分匹配和逻辑回归来估计 aTIV 与 QIVe 的 rVE。

结果

流感病毒仅在 2018/19 年和 2019/20 年期间广泛传播。最终纳入了 512 名接种疫苗的老年患者,其中 83 例为病例,429 例为阴性对照。从几个基线特征来看,aTIV 和 QIVe 的使用者存在显著差异。调整倾向评分后,aTIV 相对于 QIVe 的 rVE 分别为 59.2%(95%CI:14.6%,80.5%)、54.7%(95%CI:-28.7%,84.0%)和 56.9%(95%CI:-7.8%,82.8%),分别针对任何流感、A(H1N1)pdm09 和 A(H3N2)。

结论

aTIV 在预防实验室确诊的 SARI 方面比 QIVe 更有效。aTIV 的益处可能因混杂的指示而被掩盖。

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