Ritonavir- or cobicistat-boosted antiretroviral therapy and direct oral anticoagulants: A case for apixaban

被引:14
作者
Nisly, Sarah A. [1 ]
Stevens, Brooke N. [2 ]
机构
[1] Wingate Univ, Sch Pharm, Wake Forest Baptist Hlth, Internal Med, 515 N Main St, Wingate, NC 28174 USA
[2] Indiana Univ Hlth, Indianapolis, IN USA
关键词
Antiretroviral therapy; direct oral anticoagulant; human immunodeficiency virus; interaction; PHARMACOKINETICS; DABIGATRAN; RIVAROXABAN;
D O I
10.1177/0956462419832099
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The potential for drug-drug interactions (DDIs) between direct oral anticoagulants and antiretroviral therapy (ART) is vast. Ritonavir and cobicistat are used as pharmacokinetic enhancers with either concurrent protease inhibitors or the integrase strand transfer inhibitor, elvitegravir, to optimize therapeutic concentrations by cytochrome P450 (CYP) inhibition. To date, only rivaroxaban and dabigatran have reported cases of use with ritonavir-boosted ART. Apixaban is metabolized similarly to rivaroxaban, but offers a dose reduction in the case of major DDIs. We report the successful use of reduced-dose apixaban to treat and prevent thromboembolic complications in six persons living with human immunodeficiency virus (HIV) on ritonavir- or cobicistat-boosted ART. This case series and available literature support the use of apixaban or dabigatran, depending on the boosted ART regimen.
引用
收藏
页码:718 / 722
页数:5
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