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本文引用的文献

1
Potential Drug Interaction Between Favipiravir and Warfarin in Patients With COVID-19: A Real-World Observational Study.新型冠状病毒肺炎患者使用法匹拉韦与华法林潜在的药物相互作用:一项真实世界观察性研究。
J Clin Pharmacol. 2023 Mar;63(3):338-344. doi: 10.1002/jcph.2161. Epub 2022 Oct 17.
2
Mechanism of action of favipiravir against SARS-CoV-2: Mutagenesis or chain termination?法匹拉韦对新型冠状病毒的作用机制:诱变还是链终止?
Innovation (Camb). 2021 Nov 28;2(4):100165. doi: 10.1016/j.xinn.2021.100165. Epub 2021 Sep 8.
3
Elevated INR in a COVID-19 patient after concomitant administration of favipiravir and warfarin: A case report.COVID-19 患者同时使用法匹拉韦和华法林后 INR 升高:病例报告。
J Clin Pharm Ther. 2022 Mar;47(3):407-410. doi: 10.1111/jcpt.13499. Epub 2021 Aug 2.
4
Blood coagulation parameter abnormalities in hospitalized patients with confirmed COVID-19 in Ethiopia.在埃塞俄比亚,住院的 COVID-19 确诊患者存在凝血参数异常。
PLoS One. 2021 Jun 21;16(6):e0252939. doi: 10.1371/journal.pone.0252939. eCollection 2021.
5
Randomized, placebo-controlled trial of orally administered vitamin K1 for warfarin-associated coagulopathy in Chinese patients with mechanical heart valves.随机、安慰剂对照试验:口服维生素 K1 治疗中国机械心脏瓣膜患者华法林相关凝血功能障碍
Eur J Clin Pharmacol. 2021 Sep;77(9):1333-1339. doi: 10.1007/s00228-021-03127-8. Epub 2021 Mar 30.
6
2020 ESC Guidelines for the diagnosis and management of atrial fibrillation developed in collaboration with the European Association for Cardio-Thoracic Surgery (EACTS): The Task Force for the diagnosis and management of atrial fibrillation of the European Society of Cardiology (ESC) Developed with the special contribution of the European Heart Rhythm Association (EHRA) of the ESC.2020年欧洲心脏病学会(ESC)与欧洲心胸外科学会(EACTS)合作制定的心房颤动诊断和管理指南:欧洲心脏病学会(ESC)心房颤动诊断和管理特别工作组,由ESC欧洲心律协会(EHRA)特别贡献制定。
Eur Heart J. 2021 Feb 1;42(5):373-498. doi: 10.1093/eurheartj/ehaa612.
7
Analysis of Factors That Interrupt With INR Control in the First Anticoagulation Clinic Monitoring Jordanian Patients.分析影响约旦首诊抗凝监测患者 INR 控制的中断因素。
Clin Appl Thromb Hemost. 2019 Jan-Dec;25:1076029619870252. doi: 10.1177/1076029619870252.
8
The effect of simvastatin on warfarin anticoagulation: a Swedish register-based nationwide cohort study.辛伐他汀对华法林抗凝的影响:一项基于瑞典登记的全国队列研究。
Eur J Clin Pharmacol. 2019 Oct;75(10):1387-1392. doi: 10.1007/s00228-019-02703-3. Epub 2019 Jun 14.
9
High INR on warfarin.华法林治疗期间国际标准化比值(INR)升高
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10
The CARE Guidelines: Consensus-based Clinical Case Reporting Guideline Development.《CARE指南:基于共识的临床病例报告指南制定》
Glob Adv Health Med. 2013 Sep;2(5):38-43. doi: 10.7453/gahmj.2013.008.

法匹拉韦与华法林之间的药物相互作用:病例系列

Drug Interaction Between Favipiravir and Warfarin: A Case Series.

作者信息

Pornwattanakavee Suphannika, Priksri Watcharapong, Aonkhum Authakorn, Leelakanok Nattawut, Sapapsap Bannawich

机构信息

Burapha University, Chonburi, Thailand.

Chonburi Hospital, Chonburi, Thailand.

出版信息

Hosp Pharm. 2024 Jun;59(3):264-271. doi: 10.1177/00185787231214428. Epub 2023 Dec 29.

DOI:10.1177/00185787231214428
PMID:38764984
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11097932/
Abstract

Initiating favipiravir in COVID-19 patients with long-term warfarin use can lead to increased INR. However, data on the onset and duration of the increasing INR are limited. We reviewed patient charts to include COVID-19 adult patients who received favipiravir for at least 5 days and used warfarin at the same dose for at least 12 weeks. Data on demographics, comorbidities, other medical characteristics, international normalized ratio (INR), and signs of bleeding were collected. Eight patients, with a mean age of 70.88 ± 8.49 years old, received the standard dose of favipiravir. The mean maximum INR (4.30 ± 1.26) was statistically different from the baseline INR ( = .00029) and the change was observed within 4.38 ± 1.99 days after initiating favipiravir. Warfarin was then discontinued without favipiravir discontinuation in most patients, allowing the INR to gradually decrease within 2 to 3 days. Concurrent use of favipiravir and warfarin led to INR prolongation within approximately 4 days. The effect of such interaction can be acute as the prolongation occurred within 1 day in 1 of the patients.

摘要

在长期使用华法林的新冠肺炎患者中启用法匹拉韦可导致国际标准化比值(INR)升高。然而,关于INR升高的起始时间和持续时间的数据有限。我们查阅了患者病历,纳入了接受法匹拉韦治疗至少5天且以相同剂量使用华法林至少12周的成年新冠肺炎患者。收集了人口统计学、合并症、其他医学特征、国际标准化比值(INR)和出血迹象的数据。8名平均年龄为70.88±8.49岁的患者接受了标准剂量的法匹拉韦。平均最大INR(4.30±1.26)与基线INR在统计学上有差异(P = 0.00029),且在启用法匹拉韦后4.38±1.99天内观察到了变化。然后在大多数患者中停用了华法林而未停用 法匹拉韦,使INR在2至3天内逐渐下降。法匹拉韦和华法林的同时使用导致INR在约4天内延长。这种相互作用的影响可能是急性的,因为有1名患者在1天内就出现了延长情况。