EpiConcept, Paris, France.
Euro Surveill. 2015 Jan 15;20(2):21011. doi: 10.2807/1560-7917.es2015.20.2.21011.
While influenza vaccines aim to decrease the incidence of severe influenza among high-risk groups, evidence of influenza vaccine effectiveness (IVE) among the influenza vaccine target population is sparse. We conducted a multicentre test-negative case-control study to estimate IVE against hospitalised laboratory-confirmed influenza in the target population in 18 hospitals in France, Italy, Lithuania and the Navarre and Valencia regions in Spain. All hospitalised patients aged ≥18 years, belonging to the target population presenting with influenza-like illness symptom onset within seven days were swabbed. Patients positive by reverse transcription polymerase chain reaction for influenza virus were cases and those negative were controls. Using logistic regression, we calculated IVE for each influenza virus subtype and adjusted it for month of symptom onset, study site, age and chronic conditions. Of the 1,972 patients included, 116 were positive for influenza A(H1N1)pdm09, 58 for A(H3N2) and 232 for influenza B. Adjusted IVE was 21.3% (95% confidence interval (CI): -25.2 to 50.6; n=1,628), 61.8% (95% CI: 26.8 to 80.0; n=557) and 43.1% (95% CI: 21.2 to 58.9; n=1,526) against influenza A(H1N1) pdm09, A(H3N2) and B respectively. Our results suggest that the 2012/13 IVE was moderate against influenza A(H3N2) and B and low against influenza A(H1N1) pdm09.
虽然流感疫苗旨在降低高危人群中严重流感的发病率,但针对流感疫苗目标人群的流感疫苗有效性(IVE)证据很少。我们在法国、意大利、立陶宛以及西班牙的纳瓦拉和瓦伦西亚地区的 18 家医院进行了一项多中心病例对照研究,以评估目标人群中针对住院确诊流感的 IVE。所有年龄≥18 岁、属于目标人群、出现流感样疾病症状且在 7 天内发病的住院患者都进行了拭子采样。经逆转录聚合酶链反应检测为流感病毒阳性的患者为病例,阴性患者为对照。我们使用逻辑回归计算了每种流感病毒亚型的 IVE,并根据症状出现月份、研究地点、年龄和慢性疾病进行了调整。在纳入的 1972 名患者中,116 例为 A(H1N1)pdm09 阳性,58 例为 A(H3N2)阳性,232 例为 B 型阳性。调整后的 IVE 分别为 21.3%(95%可信区间:-25.2 至 50.6;n=1628)、61.8%(95%可信区间:26.8 至 80.0;n=557)和 43.1%(95%可信区间:21.2 至 58.9;n=1526),分别针对 A(H1N1)pdm09、A(H3N2)和 B 型流感。我们的研究结果表明,2012/13 年的 IVE 对 A(H3N2)和 B 型流感的效果中等,对 A(H1N1)pdm09 的效果较低。