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Until recently, vitamin K antagonists (VKAs) were the only available oral anticoagulants evaluated for long-term treatment of patients with coronary heart disease (CHD), particularly after an acute coronary syndrome (ACS). Despite efficacy in this setting, VKAs are rarely used because they are cumbersome to administer. Instead, the more readily manageable antiplatelet agents are the mainstay of prevention in ACS patients. This situation has the potential to change with the introduction of non-VKA oral anticoagulants (NOACs), which are easier to administer than VKAs because they can be given in fixed doses without routine coagulation monitoring. The NOACs include dabigatran, which inhibits thrombin, and apixaban, rivaroxaban and edoxaban, which inhibit factor Xa. Apixaban and rivaroxaban were evaluated in phase III trials for prevention of recurrent ischaemia in ACS patients, most of whom were also receiving dual antiplatelet therapy with aspirin and clopidogrel. Although at the doses tested rivaroxaban was effective and apixaban was not, both agents increased major bleeding. The role for the NOACs in ACS management, although promising, is therefore complicated, because it is uncertain how they compare with newer antiplatelet agents, such as prasugrel, ticagrelor or vorapaxar, and because their safety in combination with these other drugs is unknown. Ongoing studies are also now evaluating the use of NOACs in non-valvular atrial fibrillation patients, where their role is established, with coexistent ACS or coronary stenting. Focusing on CHD, we review the results of clinical trials with the NOACs and provide a perspective on their future incorporation into clinical practice.

Original publication

DOI

10.1160/TH15-09-0703

Type

Journal article

Journal

Thromb Haemost

Publication Date

04/2016

Volume

115

Pages

685 - 711

Keywords

Anticoagulants, acute coronary syndrome, apixaban, coronary heart disease, dabigatran etexilate, edoxaban, non-vitamin K antagonist oral anticoagulants, rivaroxaban, vitamin K antagonists, Administration, Oral, Animals, Anticoagulants, Clinical Trials as Topic, Coronary Artery Disease, Dabigatran, Drug Interactions, Humans, Platelet Aggregation Inhibitors, Pyrazoles, Pyridines, Pyridones, Rivaroxaban, Thiazoles