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Mid-season influenza vaccine effectiveness 2011-2012: A Department of Defense Global, Laboratory-based, Influenza Surveillance System case-control study estimate

机译:2011-2012年中期流感疫苗的有效性:美国国防部基于实验室的全球流感监测系统病例对照研究估计值

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Mid-season influenza vaccine effectiveness (VE) was estimated using data from surveillance conducted by the Department of Defense Global, Laboratory-based, Influenza Surveillance Program at the United States Air Force School of Aerospace Medicine. Respiratory specimens from geographically diverse military members and dependents who sought medical care 2 October 2011-3 March 2012 were analyzed by viral culture and real-time reverse transcriptase-polymerase chain reaction; influenza viruses were typed and sequenced. Controls were influenza test-negative. Overall, vaccine type and subtype-specific VE were estimated using logistic regression. Adjusted VE (95% confidence interval) was: overall 77 (57-87)%; live attenuated vaccine (LAIV) 74 (48-87)%; trivalent inactivated vaccine (TIV) 75 (48-88)%. H3 component-specific VE was: overall 77 (52-89)%; LAIV 78 (47-91)%; TIV 74 (38-89)%; data were insufficient for separate H1 and B estimates. Both vaccine types showed moderate to high VE, indicating significant protection against circulating influenza strains
机译:季中流感疫苗效力(VE)使用美国空军航空航天医学院基于实验室的国防部全球流感监测计划进行的监测数据进行估算。通过病毒培养和实时逆转录酶-聚合酶链反应分析2011年10月2日至2012年3月3日在各地就医的军人和家属的呼吸道标本。对流感病毒进行分型和测序。对照是流感测试阴性的。总体而言,疫苗类型和亚型特异性VE是通过逻辑回归估算的。调整后的VE(95%置信区间)为:总体77(57-87)%;减毒活疫苗(LAIV)74(48-87)%;三价灭活疫苗(TIV)75(48-88)%。 H3成分特异性VE为:总体77(52-89)%; LAIV 78(47-91)%; TIV 74(38-89)%;数据不足以分别进行H1和B估计。两种疫苗均显示中等至高VE,表明对流行的流感病毒株具有显着的保护作用

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