首页> 外文期刊>Journal of neurovirology >Clinical effectiveness of neuraminidase inhibitors-oseltamivir, zanamivir, laninamivir, and peramivir-for treatment of influenza A(H3N2) and A(H1N1)pdm09 infection: an observational study in the 2010-2011 influenza season in Japan
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Clinical effectiveness of neuraminidase inhibitors-oseltamivir, zanamivir, laninamivir, and peramivir-for treatment of influenza A(H3N2) and A(H1N1)pdm09 infection: an observational study in the 2010-2011 influenza season in Japan

机译:神经氨酸酶抑制剂奥司他韦,扎那米韦,拉尼那韦和帕拉米韦对治疗A(H3N2)和A(H1N1)pdm09流感的疗效:一项在2010-2011年日本流感季节的观察性研究

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The clinical effectiveness of the newly released neuraminidase inhibitors (NAIs) laninamivir and peramivir has not been sufficiently evaluated in influenza-infected patients in clinical and practical settings. In this study, we analyzed the clinical data of 211 patients infected with influenza A virus subtype H3N2 (A(H3N2)) and 45 patients infected with influenza A virus subtype H1N1pdm (A(H1N1)pdm09) who received the NAIs oseltamivir, zanamivir, laninamivir, or peramivir during the 2010-2011 influenza season. The duration of fever from the first dose of the NAI to fever alleviation to < 37.5 A degrees C was evaluated as an indicator of the clinical effectiveness of the NAIs in the influenza-infected patients. For the A(H3N2)-infected patients, Kaplan-Meier analysis showed the peramivir treatment group had the fastest time of fever alleviation to < 37.5 A degrees C (median 17.0 h, 95 % confidence interval [CI] 7.2-26.8 h) of the four treatment groups. No significant difference was found in the time to fever alleviation among the other antivirals, oseltamivir, zanamivir, and laninamivir. Results of multivariate analysis, using a Cox proportional-hazards model (hazard ratio 3.321) adjusted for the factors age, sex, body weight, vaccination status, time from onset to the clinic visit, and body temperature showed significantly faster fever alleviation in the peramivir treatment group compared with the oseltamivir treatment group. For the A(H1N1)pdm09-infected patients, only the oseltamivir and zanamivir treatment groups were compared, and no significant difference in time to alleviation of fever was observed between the two groups. Based on a cycling probe real-time polymerase chain reaction (PCR) assay, none of the A(H1N1)pdm09 strains in this study had the H275Y mutation conferring oseltamivir resistance. Further evaluation of the clinical effectiveness of the newly released NAIs for influenza-infected patients, including those infected with A(H1N1)pdm09, is needed.
机译:在临床和实际环境中,尚未对流感感染的患者充分评估新发布的神经氨酸酶抑制剂(NAIs)兰尼米韦和帕拉米韦的临床疗效。在这项研究中,我们分析了接受NAIs oseltamivir,zanamivir,NAI laninamivir或peramivir,在2010-2011年流感季节。从首次服用NAI到发烧缓解至<37.5 A摄氏度的发烧持续时间被评估为NAI在流感感染患者中临床有效性的指标。对于感染了A(H3N2)的患者,Kaplan-Meier分析显示,培拉米韦治疗组的缓解发热最快时间为<37.5 A摄氏度(中值17.0 h,95%置信区间[CI] 7.2-26.8 h)。四个治疗组。在其他抗病毒药物奥司他韦,扎那米韦和兰那米韦之间,在缓解发烧时间上没有发现显着差异。使用Cox比例风险模型(风险比3.321)进行多变量分析的结果,该模型针对年龄,性别,体重,疫苗接种状况,发病时间至就诊时间以及体温进行了调整,从而显示出Peramivir缓解发热的速度明显加快治疗组与奥司他韦治疗组相比。对于感染了A(H1N1)pdm09的患者,仅比较了奥司他韦和扎那米韦治疗组,两组之间在缓解发烧时间上没有显着差异。根据循环探针实时聚合酶链反应(PCR)分析,本研究中的A(H1N1)pdm09菌株均未出现可赋予奥司他韦抗性的H275Y突变。需要进一步评估新发布的NAI对流感感染患者(包括感染了A(H1N1)pdm09的患者)的临床有效性。

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