奥司他韦
神经氨酸酶
医学
神经氨酸酶抑制剂
抗病毒药物
药代动力学
药品
药效学
病毒学
免疫学
重症监护医学
病毒
甲型流感病毒
抗病毒治疗
大流行
体外膜肺氧合
法维皮拉维
药理学
药物治疗
正粘病毒科
2019年冠状病毒病(COVID-19)
人类免疫缺陷病毒(HIV)
作者
Lindsey E Hastings,Edward P. Acosta,David Winston Kimberlin
标识
DOI:10.1093/infdis/jiaf258
摘要
Owing to its decades of use among patients of all ages and health conditions, oseltamivir has the most widely described pharmacokinetics (PK) and pharmacodynamics (PD) of all the modern influenza antivirals. Despite this, there remain numerous questions regarding optimal PK/PD parameters for oseltamivir and other neuraminidase inhibitors in populations at the highest risk for influenza-related complications including infants, young children, pregnant people, immunocompromised individuals, and those with altered clearance and drug distribution from critical illness, extracorporeal membrane oxygenation, and renal replacement therapies. Even less is known regarding the PK/PD of baloxavir-the first widely available cap-dependent endonuclease inhibitor-and the role that baloxavir may have alone and in combination with neuraminidase inhibitors for treating influenza in these populations. Support for further influenza antiviral PK and PD studies is needed to diversify and bolster our arsenal so that we may better protect and treat our most vulnerable patients.
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