Ikematsu Hideyuki, Kawai Naoki, Iwaki Norio, Kashiwagi Seizaburo, Ishikawa Yusuke, Yamaguchi Hiroki, Shiosakai Kazuhito
Japan Physicians Association, Tokyo, Japan.
Japan Physicians Association, Tokyo, Japan.
J Infect Chemother. 2018 Sep;24(9):718-724. doi: 10.1016/j.jiac.2018.04.013. Epub 2018 Jun 1.
The duration of fever and symptoms after laninamivir octanoate hydrate (laninamivir) inhalation were investigated in the Japanese 2016/17 influenza season and the results were compared with those of the 2011/12 to 2015/16 seasons. A total of 1278 patients were evaluated for the duration of fever and symptoms in the six studied seasons. In the 2016/17 season, the influenza types/subtypes of the patients were 6 A (H1N1)pdm09 (2.9%), 183 A (H3N2) (87.6%), and 20 B (9.6%). The respective median durations of fever for A (H1N1)pdm09, A (H3N2), and B were 38.0, 33.0, and 38.5 h, without significant difference (p = 0.9201), and the median durations of symptoms were 86.5, 73.0, and 99.0 h, with significant difference (p = 0.0342). The median durations of fever and symptoms after laninamivir inhalation were quite consistent for the six studied seasons for A (H1N1)pdm09, A (H3N2), and B, without any significant differences. The percentage of patients with unresolved fever patients displayed a similar pattern through the six studied seasons for all these virus types. There was no significant difference in the duration of fever or symptoms between the Victoria and Yamagata lineages in the 2016/17 season and those of the previous studied seasons. Over the seasons tested, ten adverse drug reactions (ADRs) were reported from 1341 patients. The most frequent ADR was diarrhea and all ADRs were self-resolving and not serious. These results indicate the continuing clinical effectiveness of laninamivir against influenza A (H1N1)pdm09, A (H3N2), and B, with no safety issues.
在日本2016/17流感季,对吸入八水合拉尼米韦(laninamivir)后的发热及症状持续时间进行了调查,并将结果与2011/12至2015/16季的结果进行了比较。在六个研究季节中,共对1278例患者的发热及症状持续时间进行了评估。在2016/17季,患者的流感型别/亚型为6例甲型(H1N1)pdm09(2.9%)、183例甲型(H3N2)(87.6%)和20例乙型(9.6%)。甲型(H1N1)pdm09、甲型(H3N2)和乙型流感的发热中位数持续时间分别为38.0、33.0和38.5小时,无显著差异(p = 0.9201),症状中位数持续时间分别为86.5、73.0和99.0小时,有显著差异(p = 0.0342)。在六个研究季节中,吸入拉尼米韦后甲型(H1N1)pdm09、甲型(H3N2)和乙型流感的发热及症状中位数持续时间相当一致,无任何显著差异。在所有这些病毒型别的六个研究季节中,未退热患者的百分比呈现出类似模式。2016/17季维多利亚系和山形系的发热或症状持续时间与之前研究季节相比无显著差异。在测试的各个季节中,1341例患者报告了10例药物不良反应(ADR)。最常见的ADR是腹泻,所有ADR均自行缓解且不严重。这些结果表明拉尼米韦对甲型(H1N1)pdm09、甲型(H3N2)和乙型流感持续具有临床疗效,且无安全性问题。