Acumen LLC, Burlingame, CA, USA.
U.S. Food and Drug Administration, Silver Spring, MD, USA.
Vaccine. 2024 May 31;42(15):3486-3492. doi: 10.1016/j.vaccine.2024.04.051. Epub 2024 May 3.
While safety of influenza vaccines is well-established, some studies have suggested potential associations between influenza vaccines and certain adverse events (AEs). This study examined the safety of the 2022-2023 influenza vaccines among U.S. adults ≥ 65 years.
A self-controlled case series compared incidence rates of anaphylaxis, encephalitis/encephalomyelitis, Guillain-Barré Syndrome (GBS), and transverse myelitis following 2022-2023 seasonal influenza vaccinations (i.e., any, high-dose or adjuvanted) in risk and control intervals among Medicare beneficiaries ≥ 65 years. We used conditional Poisson regression to estimate incidence rate ratios (IRRs) and 95 % confidence intervals (CIs) adjusted for event-dependent observation time and seasonality. Analyses also accounted for uncertainty from outcome misclassification where feasible. For AEs with any statistically significant associations, we stratified results by concomitant vaccination status.
Among 12.7 million vaccine recipients, we observed 76 anaphylaxis, 276 encephalitis/encephalomyelitis, 134 GBS and 75 transverse myelitis cases. Only rates of anaphylaxis were elevated in risk compared to control intervals. With all adjustments, an elevated, but non-statistically significant, anaphylaxis rate was observed following any (IRR: 2.40, 95% CI: 0.96-6.03), high-dose (IRR: 2.31, 95% CI: 0.67-7.91), and adjuvanted (IRR: 3.28, 95% CI: 0.71-15.08) influenza vaccination; anaphylaxis IRRs were 2.54 (95% CI: 0.49-13.05) and 1.64 (95% CI: 0.38-7.05) for persons with and without concomitant vaccination, respectively.
Rates of encephalitis/encephalomyelitis, GBS, or transverse myelitis were not elevated following 2022-2023 seasonal influenza vaccinations among U.S. adults ≥ 65 years. There was an increased rate of anaphylaxis following influenza vaccination that may have been influenced by concomitant vaccination.
流感疫苗的安全性已得到充分证实,但一些研究表明流感疫苗与某些不良事件(AE)之间可能存在关联。本研究在美国≥ 65 岁的成年人中检查了 2022-2023 年流感疫苗的安全性。
通过自我对照病例系列研究,在 Medicare 受益人≥ 65 岁中,比较了 2022-2023 年季节性流感疫苗(即任何、高剂量或佐剂)接种前后过敏反应、脑炎/脑脊髓炎、格林-巴利综合征(GBS)和横贯性脊髓炎的发生率在风险和对照间隔内。我们使用条件泊松回归来估计调整事件相关观察时间和季节性的发病率比(IRR)和 95%置信区间(CI)。在可行的情况下,分析还考虑了结果分类错误的不确定性。对于任何具有统计学显著关联的 AE,我们根据伴随疫苗接种状态对结果进行分层。
在 1270 万疫苗接种者中,我们观察到 76 例过敏反应、276 例脑炎/脑脊髓炎、134 例 GBS 和 75 例横贯性脊髓炎病例。与对照间隔相比,仅风险间隔内的过敏反应发生率升高。经过所有调整,观察到任何(IRR:2.40,95%CI:0.96-6.03)、高剂量(IRR:2.31,95%CI:0.67-7.91)和佐剂(IRR:3.28,95%CI:0.71-15.08)流感疫苗接种后过敏反应率升高,但无统计学意义;同时接种和不同时接种的过敏反应 IRR 分别为 2.54(95%CI:0.49-13.05)和 1.64(95%CI:0.38-7.05)。
在美国≥ 65 岁的成年人中,接种 2022-2023 年季节性流感疫苗后,脑炎/脑脊髓炎、GBS 或横贯性脊髓炎的发生率并未升高。流感疫苗接种后过敏反应发生率增加,可能与同时接种疫苗有关。