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首页> 外文期刊>Eurosurveillance >Low and decreasing vaccine effectiveness against influenza A(H3) in 2011/12 among vaccination target groups in Europe: results from the I-MOVE multicentre case–control study
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Low and decreasing vaccine effectiveness against influenza A(H3) in 2011/12 among vaccination target groups in Europe: results from the I-MOVE multicentre case–control study

机译:在欧洲预防接种目标人群中,2011/12年针对甲型H3流感的疫苗效力较低且在下降:I-MOVE多中心病例对照研究的结果

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Within the Influenza Monitoring Vaccine Effectiveness in Europe (I-MOVE) project we conducted a multicentre case-control study in eight European Union (EU) Member States to estimate the 2011/12 influenza vaccine effectiveness against medically attended influenza-like illness (ILI) laboratory-confirmed as influenza A(H3) among the vaccination target groups. Practitioners systematically selected ILI / acute respiratory infection patients to swab within seven days of symptom onset. We restricted the study population to those meeting the EU ILI case definition and compared influenza A(H3) positive to influenza laboratory-negative patients. We used logistic regression with study site as fixed effect and calculated adjusted influenza vaccine effectiveness (IVE), controlling for potential confounders (age group, sex, month of symptom onset, chronic diseases and related hospitalisations, number of practitioner visits in the previous year). Adjusted IVE was 25% (95% confidence intervals (CI): -6 to 47) among all ages (n=1,014), 63% (95% CI: 26 to 82) in adults aged between 15 and 59 years and 15% (95% CI: -33 to 46) among those aged 60 years and above. Adjusted IVE was 38% (95%CI: -8 to 65) in the early influenza season (up to week 6 of 2012) and -1% (95% CI: -60 to 37) in the late phase. The results suggested a low adjusted IVE in 2011/12. The lower IVE in the late season could be due to virus changes through the season or waning immunity. Virological surveillance should be enhanced to quantify change over time and understand its relation with duration of immunological protection. Seasonal influenza vaccines should be improved to achieve acceptable levels of protection. .
机译:在欧洲流感监测疫苗有效性(I-MOVE)项目中,我们在八个欧盟(EU)成员国中进行了多中心病例对照研究,以评估2011/12年流感疫苗对医治类流感样疾病(ILI)的有效性在疫苗接种目标人群中,实验室确认为甲型H3流感。从业人员系统地选择ILI /急性呼吸道感染患者以在症状发作后7天内进行拭子检查。我们将研究人群限制为符合EU ILI病例定义的人群,并将A(H3)流感阳性与实验室阴性的流感患者进行比较。我们将逻辑回归与研究地点作为固定作用,并计算调整后的流感疫苗效力(IVE),控制潜在的混杂因素(年龄组,性别,症状发作月份,慢性病和相关住院,上一年的就诊人数) 。在所有年龄段(n = 1,014)中,校正后的IVE为25%(95%置信区间(CI):-6至47),在15至59岁之间的成年人中为63%(95%CI:26至82),而15% (60%或以上)(95%CI:-33至46)。在流感早期(截至2012年第6周),调整后的IVE为38%(95%CI:-8至65),在后期则为-1%(95%CI:-60至37)。结果表明,2011/12年调整后的IVE低。夏季末的IVE较低可能是由于整个季节的病毒变化或免疫力下降。应加强病毒学监测,以量化随时间变化的变化,并了解其与免疫保护时间的关系。应改进季节性流感疫苗,以达到可接受的防护水平。 。

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