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Published on: February 28, 2012
Rivaroxaban in atrial fibrillation cardioversion: insights from the X-VeRT trial
1Department of Cardiology, East & North Hertfordshire NHS Trust, Hertfordshire, UK.
Abstract:
ABSTRACT Vitamin K antagonists (VKAs) have traditionally been the standard of care for the thromboprophylactic anticoagulation of patients with nonvalvular atrial fibrillation (NVAF) undergoing cardioversion. X-VeRT was the first prospective trial to explore the safety and efficacy of one of the non-VKA oral anticoagulants, rivaroxaban, compared with dose-adjusted VKA as thromboprophylaxis in patients with NVAF scheduled to undergo cardioversion. The protocol allowed either early (1-5 days) or delayed (3-8 weeks) cardioversion to be performed. Rivaroxaban use (20 mg once daily or 15 mg if creatinine clearance was 30-49 ml/min) was associated with a similar incidence of adverse cardiovascular events and bleeding as VKA use; however, rivaroxaban significantly reduced the time to cardioversion in those undergoing delayed cardioversion. Thus, rivaroxaban is a safe alternative to VKAs for thromboprophylaxis in patients with NVAF undergoing elective cardioversion.
Insights
Rivaroxaban offers a safe and effective alternative to traditional warfarin for preventing blood clots in nonvalvular atrial fibrillation (NVAF) patients undergoing cardioversion. This study found rivaroxaban comparable to VKAs for safety while potentially speeding up cardioversion procedures.
Area of Science:
- Cardiology
- Pharmacology
- Clinical Trials
Background:
- Vitamin K antagonists (VKAs) are the standard for thromboprophylaxis in nonvalvular atrial fibrillation (NVAF) patients undergoing cardioversion.
- Non-VKA oral anticoagulants (NOACs) offer potential alternatives, necessitating safety and efficacy evaluations.
Purpose of the Study:
- To compare the safety and efficacy of rivaroxaban versus dose-adjusted VKAs for thromboprophylaxis in NVAF patients scheduled for cardioversion.
- To assess the impact of rivaroxaban on the timing of cardioversion procedures.
Main Methods:
- Prospective trial (X-VeRT) comparing rivaroxaban (20 mg daily or 15 mg if CrCl 30-49 ml/min) with dose-adjusted VKAs.
- Patients with NVAF undergoing cardioversion were randomized.
- Cardioversion timing was either early (1-5 days) or delayed (3-8 weeks).
Main Results:
- Rivaroxaban demonstrated a similar incidence of adverse cardiovascular events and bleeding compared to VKA.
- Rivaroxaban significantly reduced the time to cardioversion in patients undergoing delayed cardioversion.
- No significant difference in the primary safety endpoint between rivaroxaban and VKA groups.
Conclusions:
- Rivaroxaban is a safe and effective alternative to VKAs for thromboprophylaxis in NVAF patients undergoing elective cardioversion.
- Rivaroxaban may facilitate earlier cardioversion in certain patient subgroups.
- The findings support the use of rivaroxaban in this clinical setting.
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