Atrial fibrillation (AF) is a devastating disease in the
United States and affects almost 12% of patients who are between the ages of 75
to 84. Having AF almost increases the risk of stroke by 5-fold, and therefore,
anticoagulation therapy is essential for the prevention of stroke in patients
with AF. Warfarin has been the sole oral anticoagulation available for decades.
From 2010 to 2012, 3 additional novel oral anticoagulation (NOAC) came onto the
market, which includes dabigatran, rivaroxaban, and apixaban and offered viable
alternatives to warfarin for the management of AF. In January 2015, the FDA
approved edoxaban, a factor Xa inhibitor, to come onto the market for the
prevention of stroke in AF patients. Edoxaban is the third factor Xa inhibitor
currently available, in addition to rivaroxaban and apixaban.
Efficacy of edoxaban for the management of AF was
investigated in the ENGAGE-AF TIMI 48 trial. Patients were randomized toreceive warfarin, edoxaban 30 mg, or edoxaban 60 mg daily. Doses of warfarin
were adjusted to target international normalized ratio (INR) of 2 to 3.

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