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直接口服抗凝剂(DOACs)的药物相互作用:从药理学到临床实践

Drug-Drug Interactions of Direct Oral Anticoagulants (DOACs): From Pharmacological to Clinical Practice.

作者信息

Ferri Nicola, Colombo Elisa, Tenconi Marco, Baldessin Ludovico, Corsini Alberto

机构信息

Department of Medicine, University of Padova, 35100 Padua, Italy.

Department of Pharmacological and Biomolecular Sciences, University of Milan, 20133 Milan, Italy.

出版信息

Pharmaceutics. 2022 May 24;14(6):1120. doi: 10.3390/pharmaceutics14061120.

Abstract

The direct oral anticoagulants (DOACs), dabigatran, rivaroxaban, apixaban, and edoxaban, are becoming the most commonly prescribed drugs for preventing ischemic stroke in patients with non-valvular atrial fibrillation (NVAF) and for the treatment and prevention of venous thromboembolism (VTE). Rivaroxaban was also recently approved for the treatment of patients with a recent acute coronary syndrome (ACS). Their use demonstrated to have a favorable risk-benefit profile, with significant reductions in stroke, intracranial hemorrhage, and mortality compared to warfarin, but with increased gastrointestinal bleeding. Nevertheless, their safety profile is compromised in multimorbidity patients requiring contemporary administration of several drugs. Comorbidity and polypharmacy have a high prevalence in elderly patients, who are also more susceptible to bleeding events. The combination of multiple treatments can cause relevant drug-drug interactions (DDIs) by affecting the exposure or the pharmacological activities of DOACs. Although important differences of the pharmacokinetic (PK) properties can be observed between DOACs, all of them are substrate of P-glycoprotein (P-gp) and thus may interact with strong inducers or inhibitors of this drug transporter. On the contrary, rivaroxaban and, to a lower extent, apixaban, are also susceptible to drugs altering the cytochrome P450 isoenzyme (CYP) activities. In the present review, we summarize the potential DDI of DOACs with several classes of drugs that have been reported or have characteristics that may predict clinically significant DDIs when administered together with DOACs. Possible strategies, including dosage reduction, avoiding concomitant administration, or different time of treatment, will be also discussed to reduce the incidence of DDI with DOACs. Considering the available data from specific clinical trials or registries analysis, the use of DOACs is associated with fewer clinically relevant DDIs than warfarin, and their use represents an acceptable clinical choice. Nevertheless, DDIs can be significant in certain patient conditions so a careful evaluation should be made before prescribing a specific DOAC.

摘要

直接口服抗凝剂(DOACs),如达比加群、利伐沙班、阿哌沙班和依度沙班,正成为预防非瓣膜性心房颤动(NVAF)患者缺血性卒中以及治疗和预防静脉血栓栓塞(VTE)最常用的药物。利伐沙班最近还被批准用于治疗近期急性冠脉综合征(ACS)患者。与华法林相比,它们的使用显示出具有良好的风险效益比,卒中、颅内出血和死亡率显著降低,但胃肠道出血有所增加。然而,在需要同时服用多种药物的多病共存患者中,它们的安全性受到影响。合并症和多药联用在老年患者中很常见,而老年患者也更容易发生出血事件。多种治疗方法的联合使用可能会通过影响DOACs的暴露量或药理活性而导致相关的药物相互作用(DDIs)。尽管在DOACs之间可以观察到药代动力学(PK)特性的重要差异,但它们都是P-糖蛋白(P-gp)的底物,因此可能与这种药物转运体的强效诱导剂或抑制剂相互作用。相反,利伐沙班以及在较低程度上阿哌沙班,也易受改变细胞色素P450同工酶(CYP)活性的药物影响。在本综述中,我们总结了DOACs与几类药物潜在的药物相互作用,这些药物已有相关报道,或者具有与DOACs联用时可能预测具有临床显著药物相互作用的特征。还将讨论包括减少剂量、避免同时给药或不同治疗时间等可能的策略,以降低与DOACs发生药物相互作用的发生率。考虑到来自特定临床试验或登记分析的现有数据,与华法林相比,DOACs的使用与较少的临床相关药物相互作用相关,并且它们的使用是一种可接受的临床选择。然而,在某些患者情况下,药物相互作用可能很显著,因此在开具特定的DOAC之前应进行仔细评估。

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