Ikematsu Hideyuki, Kawai Naoki, Iwaki Norio, Kashiwagi Seizaburo
Department of Clinical Trials, Center for Advanced Medical Innovation, Kyushu University, Japan; Japan Physicians Association, Tokyo, Japan.
Japan Physicians Association, Tokyo, Japan.
J Infect Chemother. 2014 Feb;20(2):81-5. doi: 10.1016/j.jiac.2013.07.013. Epub 2013 Dec 11.
Laninamivir octanoate hydrate (laninamivir) is a long-acting, single inhalation neuraminidase inhibitor that was approved in Japan in 2010 for the treatment of influenza A and B virus infection. We investigated the duration of fever and other symptoms after the initiation of laninamivir in the Japanese 2011-2012 influenza season. Virus isolation was done and the 50% inhibitory concentration (IC₅₀) was measured for the virus isolates at days 1 and 5. For 211 patients (A(H3N2): 190, B: 21), the median durations of fever of A(H3N2) and B patients were 33.0 and 50.0 h, respectively (p = 0.0989). Fever was resolved within 72 h after inhalation by 89.7% of the A(H3N2) patients and by 81.0% of the patients with B. The median durations of symptoms for A(H3N2) and B patients were 89.0 and 94.0 h, respectively (p = 0.5809). On day 5, the influenza virus-positive rates for A(H3N2) and B patients were significantly different: 25.8% (40/155) and 70.6% (12/17), respectively (p < 0.0001). No significant change in IC₅₀ value was found between day 1 and day 5 for any of the four tested neuraminidase inhibitors, and no IC₅₀ value exceeded 50 nM. The incidence of adverse drug reactions was 1.3% (3/234), with no serious reactions reported. These results show that laninamivir was effective for the treatment of both influenza A(H3N2) and B in this study, with no safety issues. The clinical effectiveness of laninamivir for A(H3N2) was superior to that for B.
八水合奥司他韦(奥司他韦)是一种长效单剂量吸入型神经氨酸酶抑制剂,于2010年在日本获批用于治疗甲型和乙型流感病毒感染。我们在日本2011 - 2012年流感季节研究了奥司他韦开始使用后发热及其他症状的持续时间。进行了病毒分离,并在第1天和第5天测定了病毒分离株的50%抑制浓度(IC₅₀)。对于211例患者(甲型(H3N2):190例,乙型:21例),甲型(H3N2)和乙型患者发热的中位持续时间分别为33.0小时和50.0小时(p = 0.0989)。89.7%的甲型(H3N2)患者和81.0%的乙型患者在吸入后72小时内退热。甲型(H3N2)和乙型患者症状的中位持续时间分别为89.0小时和94.0小时(p = 0.5809)。在第5天,甲型(H3N2)和乙型患者的流感病毒阳性率有显著差异:分别为25.8%(40/155)和70.6%(12/17)(p < 0.0001)。在所测试的四种神经氨酸酶抑制剂中,第1天和第5天之间IC₅₀值均未发现显著变化,且没有IC₅₀值超过50 nM。药物不良反应发生率为1.3%(3/234),未报告严重反应。这些结果表明,在本研究中奥司他韦对甲型(H3N2)和乙型流感均有效,且无安全性问题。奥司他韦对甲型(H3N2)的临床疗效优于乙型。