No routine monitoring |
No reliable, readily available measurement assay |
Improved safety profile |
Dose reduction or avoidance in renal impairment and avoidance in moderate or severe hepatic impairment |
Rapid onset (may preclude the need for induction or bridging therapy) |
No specific antidote |
Short half-life (advantageous for invasive procedures or in the setting of active bleed) |
Short half-life (mandates strict adherence) |
Fixed dosing |
Less flexibility in dosing |
Greater convenience, patient satisfaction and quality of life |
Fewer studies and approved indications (e.g., contraindicated in mechanical valve replacement) |
Potentially more cost-effective from health system perspective |
Potentially higher drug acquisition costs for patients |
Fewer drug, disease and diet interactions |
DOAC drug interactions do exist that may preclude use |