Communicable Disease Branch, Centre for Health Protection, Department of Health, Hong Kong Special Administrative Region.
Communicable Disease Branch, Centre for Health Protection, Department of Health, Hong Kong Special Administrative Region.
Vaccine. 2021 Jun 8;39(25):3372-3378. doi: 10.1016/j.vaccine.2021.04.059. Epub 2021 May 18.
Effectiveness of seasonal influenza vaccine (SIV) varies with the degree of matching with the vaccine and circulating viruses. We continued our SIV effectiveness against medically-attended influenza-like illness (ILI) under the Department of Health Hong Kong's sentinel private medical practitioners (PMP) network, using the test-negative case-control design, for the 2018/19 and 2019/20 season. In addition, we studied the potential interference between SIV and ILI caused by non-influenza respiratory viruses (NIRV) based on data collated from 2017/18 to 2019/20 seasons. 3404 patients were analysed. Across the 2017/18 to 2019/20 seasons, the vaccine effectiveness (VE) of SIV was 44% (95% CI 30-56%) against pan-negative controls, 57% (95%CI. 42-68%) against NIRV controls and 50% (95%CI 38-59%) against both. SIV was moderately effective against medically-attended ILI caused by influenza A/B in both 2018/19 and 2019/20 winter seasons (53.2% (95%CI 36.7-65.5%) and 41.8% (95%CI 6.3-64.1%), respectively). The VE against the main circulating subtype, influenza A(H1), was higher for the 2018/19 season (57.2% (95%CI 39.8-69.9%), compared to 34.6% (95%CI -9.6-61.4%) in the 2019/20 season). When compared to pan negative controls, those with single NIRV infections were similarly likely to have received SIV (OR 1.05 (95%CI 0.72-1.54) within the influenza season; OR 0.97 (95%CI 0.73-1.29) when including non-influenza seasons). Analyses by type of virus showed no increased risk of SIV identified among those with single infections of EV/RV, HMPV and parainfluenza but a 2-fold increased risk was shown for those with single infections of adenovirus and parainfluenza virus (adenovirus: OR 2.54 (95%CI 1.24-5.14) within influenza season and OR 1.78 (95%CI 1.01-3.09) for the whole period; parainfluenza virus: OR 2.01 (95%CI 1.22-3.29) within influenza season and OR 1.89 (95%CI 1.29-2.76) for the whole period). SIV programme and surveillance of influenza and NIRV, including SARS-CoV-2, should continue during the COVID-19 pandemic.
季节性流感疫苗(SIV)的有效性因疫苗与流行病毒的匹配程度而异。我们继续在香港卫生署的监测私人执业医生网络中,使用病例对照研究,对 2018/19 和 2019/20 两个季节中因医疗就诊的流感样疾病(ILI)进行 SIV 有效性评估。此外,我们还基于 2017/18 至 2019/20 两个季节的数据,研究了 SIV 与非流感呼吸道病毒(NIRV)引起的 ILI 之间的潜在干扰。共分析了 3404 名患者。在 2017/18 至 2019/20 两个季节中,SIV 的疫苗有效性(VE)分别为 44%(95%CI 30-56%)对 pan-negative 对照,57%(95%CI. 42-68%)对 NIRV 对照和 50%(95%CI 38-59%)对两者。SIV 在 2018/19 和 2019/20 两个冬季对流感 A/B 引起的因医疗就诊的 ILI 均有中度有效性(53.2%(95%CI 36.7-65.5%)和 41.8%(95%CI 6.3-64.1%))。SIV 对主要流行亚型流感 A(H1)的有效性在 2018/19 季节更高(57.2%(95%CI 39.8-69.9%),而在 2019/20 季节则较低(34.6%(95%CI -9.6-61.4%))。与 pan-negative 对照相比,那些单一感染 NIRV 的患者同样可能接种了 SIV(在流感季节中,SIV 的比值比(OR)为 1.05(95%CI 0.72-1.54);在包括非流感季节时,OR 为 0.97(95%CI 0.73-1.29))。按病毒类型进行的分析显示,在单一感染 EV/RV、HMPV 和副流感病毒的患者中,SIV 并没有增加风险,但单一感染腺病毒和副流感病毒的患者中,SIV 风险增加了两倍(腺病毒:在流感季节中,OR 为 2.54(95%CI 1.24-5.14);在整个期间,OR 为 1.78(95%CI 1.01-3.09);副流感病毒:在流感季节中,OR 为 2.01(95%CI 1.22-3.29);在整个期间,OR 为 1.89(95%CI 1.29-2.76))。在 COVID-19 大流行期间,应继续开展 SIV 计划和对流感及非流感呼吸道病毒(包括 SARS-CoV-2)的监测。