Key result
NOACs offer advantages over VKAs in stable ACS due to faster action and no monitoring.
Why the study?
Despite progress in ACS management, morbidity and mortality remain high after discharge, and the role of new oral anticoagulants in stable ACS patients requires evaluation.
Do new oral anticoagulants (dabigatran, apixaban, rivaroxaban, darexaban) improve outcomes in stable patients after acute coronary syndrome?
Do new oral anticoagulants (dabigatran, apixaban, rivaroxaban, darexaban) improve outcomes in stable patients after acute coronary syndrome?
This review evaluates the evidence and practical consequences of using new oral anticoagulants (dabigatran, apixaban, rivaroxaban, darexaban) in stable ACS patients.
Does not support routine NOAC use in stable ACS; leaves open need for dedicated RCTs before practice change.
Despite tremendous progress in the management of patients with an acute coronary syndrome (ACS), morbidity and mortality remains high even in stable patients after discharge. The benefit of adding vitamin K antagonists (VKA) on top of antiplatelet therapy to prevent recurrent ischaemic events after an ACS has been successfully studied in the past. Because of their need for frequent monitoring and drug and food interactions, however, systematic long-term use of VKA has not been recommended in this setting. The new oral anticoagulants offer several advantages compared to VKA, including a faster onset and offset of action and the absence of frequent monitoring. In this review, we evaluate the current evidence and practical consequences of using the oral direct thrombin inhibitor dabigatran or the oral anti factor Xa inhibitors apixaban, rivaroxaban, and darexaban in stable ACS patients.
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Sinnaeve et al. (2012) conducted a review in Acute coronary syndrome (ACS). New oral anticoagulants (dabigatran, apixaban, rivaroxaban, darexaban) vs. Vitamin K antagonists (VKA) was evaluated. New oral anticoagulants, including dabigatran, apixaban, rivaroxaban, and darexaban, offer advantages over vitamin K antagonists in stable ACS patients due to faster action and no monitoring need.
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