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Vaccine Effectiveness Against Laboratory-confirmed Influenza in Healthy Young Children: A Case-Control Study.

机译:针对健康幼童的实验室确诊流感疫苗有效性:病例对照研究。

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BACKGROUND: the Western Australian Influenza Vaccine Effectiveness study commenced in 2008 to evaluate a new program to provide free influenza vaccine to all children aged 6 to 59 months. We aimed to assess the protective effect of inactivated influenza vaccination in these children. METHODS: We conducted a prospective case-control study in general practices and a hospital emergency department, testing all eligible patients for influenza and a range of other common respiratory viruses. Influenza vaccine effectiveness (VE) against laboratory-confirmed influenza was estimated with cases defined as children with an influenza-like illness who tested positive and controls as those with an influenza-like illness who tested negative for influenza virus. We calculated VE using the adjusted odds ratio from multivariate logistic regression. As a surrogate marker for adequate specimen collection, we explored the difference in VE point estimates defining controls as children in whom another respiratory virus was detected. RESULTS: a total of 75 children were enrolled from general practices and 214 through the emergency department, with 12 (27%) and 36 (17%), respectively, having laboratory-confirmed influenza. Using all the influenza-negative controls, the adjusted VE was 58% (95% confidence interval, 9-81). When controls were limited to those with another virus present, the adjusted VE was 68% (95% confidence interval, 26-86). CONCLUSIONS: VE estimates were higher when controls included only those children with another respiratory virus detected. Testing for other common respiratory viruses enables the control group to be restricted to those for whom an adequate sample is likely.
机译:背景:西澳大利亚州流感疫苗效力研究于2008年开始,以评估一项新计划,该计划为所有6至59个月大的儿童免费提供流感疫苗。我们旨在评估灭活流感疫苗对这些儿童的保护作用。方法:我们在一般实践和医院急诊科中进行了前瞻性病例对照研究,测试了所有符合条件的患者的流感和一系列其他常见呼吸道病毒。估计针对实验室确诊的流感的流感疫苗效力(VE),其病例定义为患有流感样疾病的儿童,其检测为阳性,而对照组则为那些患有流感样疾病的儿童,其流感病毒检测为阴性。我们使用多元logistic回归调整后的优势比计算VE。作为适当标本收集的替代标记,我们探索了VE点估计的差异,这些差异将对照定义为检测到另一种呼吸道病毒的儿童。结果:共有75名儿童从普通科招募,214名通过急诊科招募,分别有12名(27%)和36名(17%)患有实验室确诊的流感。使用所有流感阴性对照,调整后的VE为58%(95%置信区间9-81)。当对照组仅限于存在其他病毒的对照组时,调整后的VE为68%(95%置信区间26-86)。结论:当对照仅包括那些检测到另一种呼吸道病毒的儿童时,VE估计较高。对其他常见呼吸道病毒的检测可以使对照组仅限于可能有足够样本的人群。

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