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2023 - 2024年流感季节期间,对美国65岁及以上医疗保险受益人的流感疫苗接种后健康结果进行安全监测。

Safety monitoring of health outcomes following influenza vaccination during the 2023-2024 season among U.S. Medicare beneficiaries aged 65 years and older.

作者信息

Lloyd Patricia C, Acharya Gyanada, Zhao Henu, Shah Nimesh, Anguzu Godwin, Ambarsoomzadeh Derick, Clarke Tainya C, Ng Xinyi, Hu Mao, Chillarige Yoganand, Forshee Richard A, Anderson Steven A

机构信息

Office of Biostatistics and Pharmacovigilance, Center for Biologics Evaluation and Research, U.S. Food & Drug Administration, 10903 New Hampshire Ave., Building 71, Silver Spring, MD 20993, United States.

Acumen, LLC, 500 Airport Blvd. Suite 100, Burlingame, CA 94010, United States.

出版信息

Vaccine. 2025 Apr 19;53:127069. doi: 10.1016/j.vaccine.2025.127069. Epub 2025 Apr 8.

Abstract

BACKGROUND

Influenza vaccination is widely recommended for individuals aged 6 months and older in the United States. While the safety of annual influenza vaccines is well established, FDA conducts routine monitoring and safety evaluations. This study assessed the safety of 2023-2024 influenza vaccines among elderly Medicare beneficiaries.

METHODS

A self-controlled case series (SCCS) analysis compared incidence rate ratios (IRR) of anaphylaxis, encephalitis/encephalomyelitis/acute disseminated encephalomyelitis, Guillain-Barré syndrome (GBS), transverse myelitis, hemorrhagic stroke, non-hemorrhagic stroke, transient ischemic attack (TIA), and non-hemorrhagic stroke/TIA, following 2023-2024 seasonal influenza vaccinations in risk and control intervals among Medicare beneficiaries aged 65 years and older. We used conditional Poisson regression to estimate IRRs and 95 % confidence intervals (CIs) adjusted for event-dependent observation time for certain outcomes, seasonality, and uncertainty from outcome misclassification where feasible. For health outcomes with statistically significant associations, we stratified results by concomitant vaccination status.

RESULTS

We observed 20,258,006 influenza vaccinees, and no statistically significant elevations of risk for anaphylaxis, encephalitis/encephalomyelitis (with ADEM), GBS, hemorrhagic stroke, or transverse myelitis. For the combined non-hemorrhagic stroke/TIA outcome (22-42-day risk window), we observed a small elevation in risk that was statistically significant in both the Fee-for-Service (IRR: 1.07; 95 % CI: 1.01, 1.14) and Medicare Advantage (IRR: 1.10; 95 % CI: 1.02, 1.17) populations that received a high-dose vaccine. This was also observed among Medicare Advantage beneficiaries that received any influenza vaccine (IRR: 1.11; 95 % CI: 1.01, 1.22). Additionally, we observed a small statistically significant risk for the individual TIA outcome (22-42-day risk window) among the Medicare Advantage population that received any influenza vaccine.

CONCLUSION

The benefits of seasonal influenza vaccines established by past studies likely outweigh the risks found in this study. The small, elevated risk of stroke outcomes must be carefully considered in light of the known benefits of influenza vaccination.

摘要

背景

在美国,广泛建议6个月及以上的人群接种流感疫苗。虽然每年流感疫苗的安全性已得到充分证实,但美国食品药品监督管理局(FDA)仍进行常规监测和安全性评估。本研究评估了2023 - 2024年流感疫苗在老年医疗保险受益人群中的安全性。

方法

采用自控病例系列(SCCS)分析,比较了65岁及以上医疗保险受益人群在2023 - 2024年季节性流感疫苗接种后,在风险期和对照期内发生过敏反应、脑炎/脑脊髓炎/急性播散性脑脊髓炎、吉兰 - 巴雷综合征(GBS)、横贯性脊髓炎、出血性中风、非出血性中风、短暂性脑缺血发作(TIA)以及非出血性中风/TIA的发病率比(IRR)。我们使用条件泊松回归来估计IRR以及95%置信区间(CI),并针对某些结局的事件依赖观察时间、季节性以及结局错误分类的不确定性(如可行)进行调整。对于具有统计学显著关联的健康结局,我们按同时接种疫苗的状态对结果进行分层。

结果

我们观察了20,258,006名流感疫苗接种者,未发现过敏反应、脑炎/脑脊髓炎(伴急性播散性脑脊髓炎)、GBS、出血性中风或横贯性脊髓炎的风险有统计学显著升高。对于非出血性中风/TIA合并结局(22 - 42天风险窗口),我们观察到风险有小幅升高,在接受高剂量疫苗的按服务收费人群(IRR:1.07;95% CI:1.01,1.14)和医疗保险优势人群(IRR:1.10;95% CI:1.02,1.17)中均具有统计学显著性。在接受任何流感疫苗的医疗保险优势受益人群中也观察到了这一情况(IRR:1.11;95% CI:1.01,1.22)。此外,在接受任何流感疫苗的医疗保险优势人群中,我们观察到个体TIA结局(22 - 至42天风险窗口)存在小的统计学显著风险。

结论

既往研究确立的季节性流感疫苗的益处可能超过本研究中发现的风险。鉴于流感疫苗已知的益处,中风结局的小幅风险升高必须仔细权衡。

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