Área de Investigación en Vacunas, Centro Superior de Investigación en Salud Pública (CSISP), Valencia, Spain.
Vaccine. 2013 Aug 20;31(37):3995-4002. doi: 10.1016/j.vaccine.2013.05.070. Epub 2013 Jun 1.
Adjuvanted influenza vaccines offer greater and broader immunogenicity to older adults than conventional vaccines. Studies assessing the comparative effectiveness of adjuvanted influenza vaccines in this age group are lacking.
We conducted a retrospective cohort study to estimate the comparative effectiveness of MF59-adjuvanted trivalent influenza vaccine (TIV) and virosomal-TIV for prevention of influenza hospitalization in adults aged ≥65 years. We obtained administrative data on immunization status and influenza hospitalization for the 2010-2011 influenza season. We used Cox regression models to assess comparative effectiveness; crude and adjusted by age, sex, comorbidity, deprivation, type of insurance, and travel time to hospital. We accounted for data clustering at the hospital level by using a multilevel random effects model.
Overall, 373,798 vaccinated subjects were evaluated. There were 40 hospitalizations for influenza among 176,618 subjects, contributing 4,288,109 person-weeks at risk in the virosomal-TIV group, and 37 hospitalizations for influenza among 197,180 subjects, contributing 4,786,360 person-weeks at risk in the MF59-TIV group. The crude hazard ratio (HR) was 0.83 (0.53-1.30), and the adjusted Cox estimated HR of MF59-TIV relative to virosomal-TIV was 0.86 (0.55-1.35). After accounting for data clustering, the HR of influenza hospitalization associated with MF59-TIV relative to virosomal-TIV was 0.94 (0.37-2.38).
During the 2010-2011 influenza season, we found no differences in the risk of influenza hospitalization in subjects aged ≥65 years vaccinated with MF59-TIV compared with those vaccinated with virosomal-TIV.
与传统疫苗相比,佐剂流感疫苗能为老年人提供更强和更广泛的免疫原性。目前缺乏评估此类人群中佐剂流感疫苗相对有效性的研究。
我们进行了一项回顾性队列研究,以评估 MF59 佐剂三价流感疫苗(TIV)和病毒体-TIV 预防 65 岁及以上成年人流感住院的相对有效性。我们获得了 2010-2011 流感季节的免疫接种状态和流感住院的行政数据。我们使用 Cox 回归模型评估相对有效性;通过年龄、性别、合并症、贫困程度、保险类型和到医院的旅行时间进行调整。我们通过多级随机效应模型考虑了医院层面的数据聚类。
总体而言,评估了 373798 名接种疫苗的受试者。在病毒体-TIV 组中,40 例流感住院发生在 176618 例受试者中,贡献了 4288109 人周的风险,197180 例受试者中有 37 例流感住院,贡献了 4786360 人周的风险在 MF59-TIV 组中。粗危害比(HR)为 0.83(0.53-1.30),MF59-TIV 相对于病毒体-TIV 的调整后的 Cox 估计 HR 为 0.86(0.55-1.35)。在考虑数据聚类后,MF59-TIV 与病毒体-TIV 相关的流感住院风险 HR 为 0.94(0.37-2.38)。
在 2010-2011 流感季节,我们发现 65 岁及以上接种 MF59-TIV 的受试者与接种病毒体-TIV 的受试者相比,流感住院的风险没有差异。