Division of International Health (Public Health), Graduate School of Medical and Dental Sciences, Niigata University, Niigata, Japan.
Division of International Health (Public Health), Graduate School of Medical and Dental Sciences, Niigata University, Niigata, Japan.
Antiviral Res. 2024 Aug;228:105938. doi: 10.1016/j.antiviral.2024.105938. Epub 2024 Jun 17.
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 2012-2013 and 2019-2020 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.
我们比较了儿童在感染 A(H1N1)pdm09、A(H3N2)或乙型流感病毒后使用巴洛沙韦(baloxavir)或神经氨酸酶抑制剂(NAIs)(奥司他韦、扎那米韦或拉尼米韦)治疗的发热持续时间。这项观察性研究在日本 9 个县的 10 家门诊诊所进行,时间为 2012-2013 年和 2019-2020 年流感季节。流感快速抗原检测阳性的患者使用四种抗流感药物中的一种进行治疗。使用两步实时 PCR 从 MDCK 或 MDCK SIAT1 细胞培养样本中鉴定流感病毒的类型/亚型。根据治疗组和各种潜在因素,通过每日自我报告的治疗后体温来评估发热持续时间。在分析的 1742 名<19 岁的患者中,452 例(26.0%)为 A(H1N1)pdm09 病毒感染,827 例(48.0%)为 A(H3N2)病毒感染,463 例(26.0%)为乙型流感病毒感染。在四个治疗组中,对于 A(H1N1)pdm09 病毒感染,与奥司他韦相比,巴洛沙韦在单变量分析中表现出更短的发热中位持续时间(巴洛沙韦,22.0 小时;奥司他韦,26.7 小时;P<0.05;拉尼米韦,25.5 小时;扎那米韦,25.0 小时)。然而,多变量分析结果无统计学意义。对于 A(H3N2)病毒感染,单变量和多变量分析均未见统计学差异(20.3、21.0、22.0 和 19.0 小时)。对于乙型流感,巴洛沙韦与 NAIs 相比可将发热持续时间缩短约 15 小时(20.3、35.0、34.3 和 34.1 小时),单变量和多变量分析均支持这一结果。巴洛沙韦似乎与 NAIs 对甲型流感的临床疗效相当,但对治疗小儿乙型流感病毒感染可能比 NAIs 更有效。