Related Experiment Video
Updated: May 16, 2026

The WATCHMAN Left Atrial Appendage Closure Device for Atrial Fibrillation
Published on: February 28, 2012
Rivaroxaban and atrial fibrillation: continue to use warfarin or in some cases, dabigatran
Warfarin, at a dose adjusted according to the INR, is the standard prophylactic anticoagulant for patients with atrial fibrillation and a major risk of thrombosis. Dabigatran, a thrombin inhibitor, is an alternative when warfarin fails to maintain the INR within the therapeutic range most of the time. Warfarin and aspirin are reasonable choices for patients at moderate risk of thrombosis. Rivaroxaban, a factor Xa inhibitor, has been approved for the treatment of patients with atrial fibrillation and a moderate or major risk of thrombosis, but with no associated valve abnormalities. Clinical evaluation of rivaroxaban is mainly based on a double-blind, randomised, non-inferiority trial comparing rivaroxaban (20 or 15 mg taken once daily, according to renal function) versus adjusted-dose warfarin in 14 264 patients at high risk of thrombosis. Most patients were treated for at least 18 months. Overall mortality was not significantly different between the 2 groups (about 5% annually), nor was the incidence of stroke or systemic embolism (2% annually). Note that the dose of warfarin was not optimised in this trial. Indirect comparison with dabigatran is too fraught with methodological flaws to provide meaningful results. Overall, data on rivaroxaban are less convincing than those on dabigatran. About 35% of patients in the 2 groups stopped treatment prematurely, mainly because of adverse effects or withdrawal of consent. The overall incidence of bleeding was similar with rivaroxaban and warfarin (about 15%), including the incidence of serious bleeding (3.5%). Rivaroxaban was associated with fewer bleeding-related deaths (0.24% versus 0.48%), more cases of serious gastrointestinal bleeding (3.2% versus 2.02%) and fewer cases of intracranial haemorrhage (0.8% versus 1.2%). Combination with cytochrome P450 or P-glycoprotein inhibitors, or with drugs affecting renal function, boosts the effects of rivaroxaban. Combination with other antithrombotic drugs should be avoided. In practice, warfarin remains the standard prophylactic drug for patients with atrial fibrillation and a major risk of thrombosis, while dabigatran is an alternative in cases that are difficult to manage. In mid-2012, the data on rivaroxaban are not sufficiently convincing to challenge this standard.
Warfarin, at a dose adjusted according to the INR, is the standard prophylactic anticoagulant for patients with atrial fibrillation and a major risk of thrombosis. Dabigatran, a thrombin inhibitor, is an alternative when warfarin fails to maintain the INR within the therapeutic range most of the time. Warfarin and aspirin are reasonable choices for patients at moderate risk of thrombosis. Rivaroxaban, a factor Xa inhibitor, has been approved for the treatment of patients with atrial fibrillation and a moderate or major risk of thrombosis, but with no associated valve abnormalities. Clinical evaluation of rivaroxaban is mainly based on a double-blind, randomised, non-inferiority trial comparing rivaroxaban (20 or 15 mg taken once daily, according to renal function) versus adjusted-dose warfarin in 14 264 patients at high risk of thrombosis. Most patients were treated for at least 18 months. Overall mortality was not significantly different between the 2 groups (about 5% annually), nor was the incidence of stroke or systemic embolism (2% annually). Note that the dose of warfarin was not optimised in this trial. Indirect comparison with dabigatran is too fraught with methodological flaws to provide meaningful results. Overall, data on rivaroxaban are less convincing than those on dabigatran. About 35% of patients in the 2 groups stopped treatment prematurely, mainly because of adverse effects or withdrawal of consent. The overall incidence of bleeding was similar with rivaroxaban and warfarin (about 15%), including the incidence of serious bleeding (3.5%). Rivaroxaban was associated with fewer bleeding-related deaths (0.24% versus 0.48%), more cases of serious gastrointestinal bleeding (3.2% versus 2.02%) and fewer cases of intracranial haemorrhage (0.8% versus 1.2%). Combination with cytochrome P450 or P-glycoprotein inhibitors, or with drugs affecting renal function, boosts the effects of rivaroxaban. Combination with other antithrombotic drugs should be avoided. In practice, warfarin remains the standard prophylactic drug for patients with atrial fibrillation and a major risk of thrombosis, while dabigatran is an alternative in cases that are difficult to manage. In mid-2012, the data on rivaroxaban are not sufficiently convincing to challenge this standard.
Related Concept Videos
Anticoagulant Drugs: Vitamin K Antagonists and Direct Oral Anticoagulants
Warfarin, a prominent vitamin K antagonist family member, exerts its effect by inhibiting the enzyme VKORC1 (vitamin K epoxide reductase complex 1). By hindering this enzyme, warfarin...
Anticoagulant Drugs: Low-Molecular-Weight Heparins
Venous Thrombosis III: Interprofessional Care
Antiplatelet Drugs: Prostaglandin Synthesis, P2Y12 and Glycoprotein IIb/IIIa Inhibitors
Prostaglandin synthesis inhibitors, exemplified by the widely known aspirin, wield their power by irreversibly acetylating...
Antiarrhythmic Drugs: Class IV Agents as Calcium Channel Blockers
Verapamil, a calcium channel blocker, inhibits calcium movement across myocardial cell membranes and vascular smooth muscle. This results in the dilation of coronary and...
Venous Thrombosis IV: Nursing Management
