Imran Mahrukh, Mills Carrie W, McDermott Kimberly W, Dean Alex, Bogdanov Alina, McGovern Ian, Haag Mendel D M
Center for Outcomes Research & Epidemiology, CSL Seqirus, Kirkland, Quebec, Canada.
Real World Evidence, Veradigm, Chicago, Illinois, USA.
Open Forum Infect Dis. 2024 Aug 16;11(8):ofae459. doi: 10.1093/ofid/ofae459. eCollection 2024 Aug.
This study estimated the relative vaccine effectiveness (rVE) of the MF59-adjuvanted trivalent influenza vaccine (aTIV) versus high-dose trivalent inactivated influenza vaccine (HD-TIV) for prevention of influenza-related medical encounters (IRMEs) during the 2019-2020 United States (US) influenza season stratified by the cumulative number of influenza risk factors. A secondary objective evaluated outpatient IRMEs and influenza- and pneumonia-related hospitalizations.
This retrospective cohort study included US adults ≥65 years old vaccinated with aTIV or HD-TIV between 1 August 2019 and 31 January 2020. Electronic health records linked to claims were used to ascertain exposure, covariates, risk factors, and outcomes. Multivariable adjusted odds ratios (ORs) were derived using inverse probability of treatment-weighted samples to calculate rVEs independently for individuals with 0, ≥1, 1-2, or ≥3 risk factors.
The study included 1 115 725 aTIV and 2 561 718 HD-TIV recipients. For the primary outcome of any IRME, the analysis found comparable effectiveness between aTIV and HD-TIV (rVE, 5.2% [95% confidence interval {CI}, -5.9% to 15.1%]) among those with 0 risk factors, whereas aTIV was more effective than HD-TIV among patients with ≥1, 1-2, or ≥3 risk factors (12.5% [95% CI, 10.0%-15.0%], 18.4% [95% CI, 13.7%-22.9%], and 10.4% [7.4%-13.3%], respectively). The same trends were observed for the secondary outcomes.
This study demonstrated comparable effectiveness of aTIV and HD-TIV among individuals with no identified risk factors and higher effectiveness of aTIV compared with HD-TIV in preventing any IRMEs, outpatient IRMEs, and influenza- or pneumonia-related hospitalizations among those with at least 1 or multiple high-risk factors in adults ≥65 years old.
本研究评估了MF59佐剂三价流感疫苗(aTIV)与高剂量三价灭活流感疫苗(HD-TIV)在美国2019 - 2020流感季预防流感相关医疗就诊(IRMEs)方面的相对疫苗效力(rVE),并按流感风险因素累积数量进行分层。次要目标是评估门诊IRMEs以及流感和肺炎相关住院情况。
这项回顾性队列研究纳入了2019年8月1日至2020年1月31日期间接种aTIV或HD-TIV的65岁及以上美国成年人。利用与索赔相关联的电子健康记录来确定暴露情况、协变量、风险因素和结局。使用治疗加权样本的逆概率得出多变量调整比值比(ORs),以便分别为具有0个、≥1个、1 - 2个或≥3个风险因素的个体计算rVE。
该研究纳入了1115725名aTIV接种者和2561718名HD-TIV接种者。对于任何IRME的主要结局,分析发现,在无风险因素的人群中,aTIV和HD-TIV的效力相当(rVE,5.2% [95%置信区间{CI},-5.9%至15.1%]);而在具有≥1个、1 - 2个或≥3个风险因素的患者中,aTIV比HD-TIV更有效(分别为12.5% [95% CI,10.0% - 15.0%]、18.4% [95% CI,13.7% - 22.9%]和10.4% [7.4% - 13.3%])。次要结局也观察到了相同趋势。
本研究表明,在65岁及以上成年人中,对于未发现风险因素的个体,aTIV和HD-TIV的效力相当;而在预防至少有1个或多个高风险因素的个体发生任何IRMEs、门诊IRMEs以及流感或肺炎相关住院方面,aTIV比HD-TIV更有效。