Department of Molecular and Clinical Pharmacology, Institute of Translational Medicine, University of Liverpool, Liverpool, UK.
Department of Pharmacy, NHS Greater Glasgow and Clyde, Glasgow, UK.
Drugs R D. 2021 Mar;21(1):9-27. doi: 10.1007/s40268-020-00333-0. Epub 2020 Dec 17.
In December 2019, an outbreak of a novel severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) began, resulting in a number of antivirals and immune modulators being repurposed to treat the associated coronavirus disease 2019 (COVID-19). Many patients requiring treatment for COVID-19 may have either pre-existing renal or hepatic disease or experience acute renal/hepatic injury as a result of the acute infection. Altered renal or hepatic function can significantly affect drug concentrations of medications due to impaired drug metabolism and excretion, resulting in toxicity or reduced efficacy. The aim of this paper is to review the pharmacokinetics and available study data for the experimental COVID-19 therapies in patients with any degree of renal or hepatic impairment to make recommendations for dosing.
COVID-19 agents included in these recommendations were listed as primaries on the University of Liverpool COVID-19 drug interaction website ( www.covid19-druginteractions.org ), initially identified from Clinicialtrials.gov and ChicCTR.org.cn. A literature search was performed using PubMed and EMBASE as well as product licences and pharmacokinetic databases.
Remdesivir, dexamethasone, azithromycin, favipiravir, lopinavir/ritonavir, atazanavir, hydroxychloroquine, interferon beta, ribavirin, tocilizumab, anakinra and sarilumab were identified as experimental drugs being used in COVID-19 trials as of November 2020. Limited study data was found for these drugs in patients with renal or hepatic impairment for COVID-19 or other indications. Recommendations were made based on available data, consideration of pharmacokinetic properties (including variability), the dosing and anticipated treatment duration of each regimen in COVID-19 and known toxicities.
Dosing of drugs used to treat COVID-19 in patients with renal or hepatic impairment is complex. These recommendations were produced to provide guidance to clinicians worldwide who are treating patients with COVID-19, many of whom will have some degree of acute or chronic renal or hepatic impairment.
2019 年 12 月,一种新型严重急性呼吸系统综合征冠状病毒 2(SARS-CoV-2)的爆发导致许多抗病毒药物和免疫调节剂被重新用于治疗相关的 2019 年冠状病毒病(COVID-19)。许多需要治疗 COVID-19 的患者可能存在预先存在的肾脏或肝脏疾病,或者由于急性感染而出现急性肾/肝损伤。改变的肾功能或肝功能会因药物代谢和排泄受损而显著影响药物的药物浓度,从而导致毒性或疗效降低。本文的目的是回顾在任何程度的肾功能或肝功能不全的 COVID-19 患者中,实验性 COVID-19 治疗药物的药代动力学和现有研究数据,为剂量推荐提供建议。
这些建议中包括的 COVID-19 药物最初是根据利物浦大学 COVID-19 药物相互作用网站(www.covid19-druginteractions.org)的主要药物列出的,这些药物最初是从 Clinicialtrials.gov 和 ChicCTR.org.cn 确定的。使用 PubMed 和 EMBASE 以及产品许可证和药代动力学数据库进行文献检索。
截至 2020 年 11 月,瑞德西韦、地塞米松、阿奇霉素、法匹拉韦、洛匹那韦/利托那韦、阿扎那韦、羟氯喹、干扰素β、利巴韦林、托珠单抗、阿那白滞素和沙利鲁单抗被确定为 COVID-19 试验中使用的实验性药物。对于 COVID-19 或其他适应症的肾功能或肝功能不全患者,这些药物的研究数据有限。根据可用数据、药代动力学特性(包括变异性)、COVID-19 中每种方案的剂量和预期治疗持续时间以及已知毒性提出了建议。
在肾功能或肝功能不全的 COVID-19 患者中使用的药物的剂量复杂。这些建议的目的是为全球治疗 COVID-19 患者的临床医生提供指导,其中许多患者将有一定程度的急性或慢性肾功能或肝功能不全。