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Published on: February 28, 2012
Novel Oral Anticoagulants for DC Cardioversion Procedures: Utilization and Clinical Outcomes Compared with Warfarin
Corey M Coleman1, Shaden Khalaf1, Steven Mould1
1From the Department of Cardiovascular Medicine, Cleveland Clinic, Cleveland, Ohio.
Background:
Novel oral anticoagulant (NOAC) agents dabigatran, rivaroxaban, and apixaban are increasingly utilized as thromboembolic prevention for patients with atrial fibrillation undergoing direct current cardioversion (DCCV) with post hoc analyses of clinical trials suggesting satisfactory safety and efficacy. This study characterizes utilization, effectiveness, and complications of NOAC agents for stroke prophylaxis in the setting of DCCV.
Methods:
Comparison of warfarin and NOAC agents as periprocedural anticoagulation for DCCV procedures performed at Cleveland Clinic from January 2009 through December 2013. Variables of interest include utilization rates for each NOAC agent stratified by clinical parameters including CHADS2 score, and associated clinical outcomes including cerebrovascular accident (CVA), transient ischemic attack (TIA), peripheral arterial embolism (PAE), and bleeding events during 8 weeks of postprocedure follow-up.
Results:
Among 5,320 DCCV procedures, 673 (12.6%) cases were excluded due to inadequate follow-up. Warfarin was utilized in 3,721 (80.1%), dabigatran in 719 (15.5%), rivaroxaban in 159 (3.4%), and apixaban in 48 (1.0%) with a steady increase in NOAC utilization from 2011 to 2013. There were low rates of CVA/TIA (warfarin: 0.97% vs NOAC 1.62%, P = 0.162) and bleeding (warfarin: 1.02% vs NOAC: 0.5%, P = 0.247) and no significant differences detected between agents. Higher CHADS2 /CHA2 DS2 -VASC scores were associated with thromboembolic and bleeding risk. Increasing age, chronic kidney disease, diabetes, coronary disease, and deep vein thrombosis/pulmonary embolism were associated with increased bleeding risk.
Conclusion:
In a high-volume, single-center experience, NOAC utilization has grown to account for over a third of cardioversion procedures, and these agents appear safe and effective compared to warfarin with low rates of thromboembolic and bleeding complications.
Insights
Novel oral anticoagulants (NOACs) are increasingly used for atrial fibrillation patients undergoing cardioversion, showing comparable safety and effectiveness to warfarin. These agents are associated with low rates of stroke and bleeding complications.
Area of Science:
- Cardiology
- Pharmacology
- Clinical Medicine
Background:
- Novel oral anticoagulants (NOACs) are increasingly used for thromboembolic prevention in patients with atrial fibrillation undergoing direct current cardioversion (DCCV).
- Previous analyses suggest NOACs are safe and effective, but real-world utilization and outcomes require further characterization.
Purpose of the Study:
- To characterize the utilization, effectiveness, and complications of NOAC agents versus warfarin for stroke prophylaxis in patients undergoing DCCV.
- To analyze trends in NOAC adoption and compare outcomes stratified by patient clinical parameters.
Main Methods:
- A retrospective analysis of DCCV procedures at Cleveland Clinic from 2009-2013 comparing warfarin and NOACs.
- Data collected included NOAC utilization rates, cerebrovascular accident (CVA), transient ischemic attack (TIA), peripheral arterial embolism (PAE), and bleeding events within 8 weeks post-procedure.
Main Results:
- NOAC utilization increased steadily from 2011-2013, accounting for over a third of procedures by the study's end.
- Rates of CVA/TIA and bleeding were low and not significantly different between warfarin and NOACs (CVA/TIA: 0.97% vs 1.62%, P=0.162; Bleeding: 1.02% vs 0.5%, P=0.247).
- Higher CHADS2/CHA2DS2-VASC scores, age, chronic kidney disease, diabetes, coronary disease, and DVT/PE were associated with increased thromboembolic and bleeding risks.
Conclusions:
- NOACs are increasingly utilized and demonstrate comparable safety and effectiveness to warfarin in a high-volume DCCV setting.
- The study confirms low rates of thromboembolic and bleeding complications with NOACs in this patient population.
- Risk factors for thromboembolic events and bleeding were identified, emphasizing the need for individualized patient management.
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