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首页> 外文期刊>Journal of infection and chemotherapy: official journal of the Japan Society of Chemotherapy >Continued effectiveness of laninamivir octanate hydrate for influenza treatment in Japan: Comparison between the 2011-2012 and 2012-2013 influenza seasons
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Continued effectiveness of laninamivir octanate hydrate for influenza treatment in Japan: Comparison between the 2011-2012 and 2012-2013 influenza seasons

机译:拉尼米韦辛酸水合物在日本治疗流感方面的持续有效性:2011-2012年和2012-2013年流感季节之间的比较

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The clinical effectiveness of Laninamivir octanoate hydrate (laninamivir) was investigated in the Japanese 2012-2013 influenza season for comparison with that of the Japanese 2011-2012 influenza season. A total of 235 patients were enrolled, of whom 210 were evaluated for the duration of fever and other symptoms. The median durations of fever for A(H3N2) were 32.0 and 38.0 h and the median durations of symptoms for the A(H3N2) were 102.0 and 84.0 h for patients aged under 10 and 10 years or older, respectively. All four influenza B patients were 10 years or older, and their median duration of fever was 43.0 h and the median duration of symptoms was 71.0 h. There was no significant difference in the duration of fever or symptoms between the two seasons. The rates of patients A(H3N2) virus positive at day 5 were 37.2% (16/43) and 12.8% (18/141) for those aged under 10 years and 10 years or older, respectively. The virus positive rate was significantly higher for the patients under 10 years than for the patients aged 10 years or older (p < 0.0001). No significant change in IC50 value was found between days 1 and 5. Adverse drug reactions were reported by 2 of the 231 patients (0.87%), but neither was serious. These results suggest that laninamivir continued to be effective against influenza A(H3N2) with no safety issues and that it is unlikely that the clinical use of laninamivir will lead to virus resistance. (C) 2014, Japanese Society of Chemotherapy and The Japanese Association for Infectious Diseases. Published by Elsevier Ltd. All rights reserved.
机译:在日本2012-2013年流感季节调查了Laninamivir辛酸水合物(laninamivir)的临床有效性,以与日本2011-2012年流感季节进行比较。总共招募了235位患者,其中210位接受了发烧持续时间和其他症状的评估。 10岁以下和10岁以上患者的A(H3N2)发烧中位数分别为32.0和38.0 h,A(H3N2)症状发烧中位数分别为102.0和84.0 h。所有四名乙型流感患者均年龄在10岁或以上,其平均发烧时间为43.0小时,症状的平均时间为71.0小时。在两个季节之间,发烧时间或症状没有显着差异。 10岁以下和10岁以上的患者在第5天的A(H3N2)病毒阳性率分别为37.2%(16/43)和12.8%(18/141)。 10岁以下患者的病毒阳性率显着高于10岁或10岁以上患者(p <0.0001)。在第1天和第5天之间,IC50值未见明显变化。231例患者中有2例报告了药物不良反应(0.87%),但均未见严重。这些结果表明,Laninamivir继续有效地对抗A型流感(H3N2),没有安全问题,并且Laninamivir的临床使用不太可能导致病毒耐药。 (C)2014年,日本化学治疗学会和日本传染病协会。由Elsevier Ltd.出版。保留所有权利。

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