Duration of fever in children infected with influenza A(H1N1)pdm09, A(H3N2) or B virus and treated with baloxavir marboxil, oseltamivir, laninamivir, or zanamivir in Japan during the 2012–2013 and 2019–2020 influenza seasons

IF 4.5 2区 医学 Q1 PHARMACOLOGY & PHARMACY Antiviral research Pub Date : 2024-06-17 DOI:10.1016/j.antiviral.2024.105938
Yuyang Sun , Keita Wagatsuma , Reiko Saito , Isamu Sato , Takashi Kawashima , Tadashi Saito , Yashushi Shimada , Yasuhiko Ono , Fujio Kakuya , Michiyoshi Minato , Naoki Kodo , Eitaro Suzuki , Akito Kitano , Irina Chon , Wint Wint Phyu , Jiaming Li , Hisami Watanabe
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Abstract

We compared the duration of fever in children infected with A(H1N1)pdm09, A(H3N2), or influenza B viruses following treatment with baloxavir marboxil (baloxavir) or neuraminidase inhibitors (NAIs) (oseltamivir, zanamivir, or laninamivir). This observational study was conducted at 10 outpatient clinics across 9 prefectures in Japan during the 20122013 and 20192020 influenza seasons. Patients with influenza rapid antigen test positive were treated with one of four anti-influenza drugs. The type/subtype of influenza viruses were identified from MDCK or MDCK SIAT1 cell-grown samples using two-step real-time PCR. Daily self-reported body temperature after treatment were used to evaluate the duration of fever by treatment group and various underlying factors. Among 1742 patients <19 years old analyzed, 452 (26.0%) were A(H1N1)pdm09, 827 (48.0%) A(H3N2), and 463 (26.0%) influenza B virus infections. Among fours treatment groups, baloxavir showed a shorter median duration of fever compared to oseltamivir in univariate analysis for A(H1N1)pdm09 virus infections (baloxavir, 22.0 h versus oseltamivir, 26.7 h, P < 0.05; laninamivir, 25.5 h, and zanamivir, 25.0 h). However, this difference was not significant in multivariable analyses. For A(H3N2) virus infections, there were no statistically significant differences observed (20.3, 21.0, 22.0, and 19.0 h) uni- and multivariable analyses. For influenza B, baloxavir shortened the fever duration by approximately 15 h than NAIs (20.3, 35.0, 34.3, and 34.1 h), as supported by uni- and multivariable analyses. Baloxavir seems to have comparable clinical effectiveness with NAIs on influenza A but can be more effective for treating pediatric influenza B virus infections than NAIs.

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2012-2013年和2019-2020年流感季节日本儿童感染甲型(H1N1)pdm09、甲型(H3N2)或乙型流感病毒并接受巴洛沙韦、奥司他韦、拉尼他韦或扎那米韦治疗后的发烧持续时间。
我们比较了感染甲型(H1N1)pdm09、甲型(H3N2)或乙型流感病毒的儿童在接受巴洛沙韦(baloxavir marboxil,巴洛沙韦)或神经氨酸酶抑制剂(neuraminidase inhibitors,NAIs)(奥司他韦、扎那米韦或拉尼那韦)治疗后的发烧持续时间。这项观察性研究于2012-2013年和2019-2020年流感季节在日本9个都道府县的10家门诊诊所进行。流感快速抗原检测呈阳性的患者接受了四种抗流感药物中的一种治疗。使用两步实时 PCR 技术从 MDCK 或 MDCK SIAT1 细胞培养样本中鉴定流感病毒的类型/亚型。采用治疗后每日自我体温报告来评估不同治疗组的发热持续时间和各种潜在因素。在分析的 1742 名年龄小于 19 岁的患者中,452 人(26.0%)感染了甲型 H1N1 pdm09,827 人(48.0%)感染了甲型 H3N2,463 人(26.0%)感染了乙型流感病毒。在四个治疗组中,与奥司他韦相比,巴洛沙韦在甲型 H1N1 pdm09 病毒感染的单变量分析中显示出更短的发热中位持续时间(巴洛沙韦为 22.0 小时,奥司他韦为 26.7 小时,P < 0.05;拉尼那韦为 25.5 小时,扎那米韦为 25.0 小时)。然而,这一差异在多变量分析中并不显著。对于甲型 H3N2 病毒感染,在单变量和多变量分析中观察到的差异(20.3、21.0、22.0 和 19.0 小时)并无统计学意义。就乙型流感而言,巴洛沙韦比非那西丁类药物(20.3、35.0、34.3 和 34.1 小时)缩短了约 15 小时的发热持续时间,单变量和多变量分析也证实了这一点。巴洛沙韦对甲型流感的临床疗效似乎与非那西丁类药物相当,但在治疗小儿乙型流感病毒感染方面比非那西丁类药物更有效。
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来源期刊
Antiviral research
Antiviral research 医学-病毒学
CiteScore
17.10
自引率
3.90%
发文量
157
审稿时长
34 days
期刊介绍: Antiviral Research is a journal that focuses on various aspects of controlling viral infections in both humans and animals. It is a platform for publishing research reports, short communications, review articles, and commentaries. The journal covers a wide range of topics including antiviral drugs, antibodies, and host-response modifiers. These topics encompass their synthesis, in vitro and in vivo testing, as well as mechanisms of action. Additionally, the journal also publishes studies on the development of new or improved vaccines against viral infections in humans. It delves into assessing the safety of drugs and vaccines, tracking the evolution of drug or vaccine-resistant viruses, and developing effective countermeasures. Another area of interest includes the identification and validation of new drug targets. The journal further explores laboratory animal models of viral diseases, investigates the pathogenesis of viral diseases, and examines the mechanisms by which viruses avoid host immune responses.
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