Key result
Rivaroxaban matches warfarin for resolving acute left ventricular thrombus, with ~96% clearance at 12 weeks.
Why the study?
Warfarin is the standard treatment for left ventricular thrombus, but direct oral anticoagulants like rivaroxaban are increasingly considered because of fixed dosing and lack of routine monitoring.
Does rivaroxaban result in noninferior resolution of acute left ventricular thrombus following myocardial infarction compared to warfarin?
RCT (n=261)
Open-label
2:1
No
Does rivaroxaban result in noninferior resolution of acute left ventricular thrombus following myocardial infarction compared to warfarin?
Relative Risk: 0.992 (95% CI 0.942–1.044)
Absolute Event Rate: 95.8% vs 96.6%
p-value: p=0.017 for noninferiority
Rivaroxaban was noninferior to warfarin for the resolution of acute left ventricular thrombus at 12 weeks post-myocardial infarction, with significantly higher rates of early resolution at 4 weeks.
Supports rivaroxaban as alternative to warfarin for post-MI left ventricular thrombus; provides first randomized confirmation of noninferiority.
BACKGROUND: Vitamin K antagonists, such as warfarin, are the standard treatment for left ventricular thrombus (LVT). However, direct oral anticoagulants, such as rivaroxaban, are increasingly being considered due to their fixed dosing and lack of routine monitoring requirements. OBJECTIVES: This study aimed to compare the effectiveness of rivaroxaban vs warfarin in treating post-myocardial infarction (MI) acute LVT at 12 weeks. METHODS: We conducted an open-label, noninferiority, randomized controlled trial involving patients with acute LVT diagnosed during initial MI hospitalization. Participants were randomized 2:1 to receive either rivaroxaban (20 mg daily) or warfarin (target international normalized ratio 2-3) for 12 weeks. The primary endpoint, LVT resolution, was assessed by echocardiography at 4 and 12 weeks. RESULTS: A total of 261 patients were randomized, with 171 in the rivaroxaban group and 90 in the warfarin group. The groups were similar in sex, age, and MI subtype, with most having ST-segment elevation MI and severe LV dysfunction. At 4 weeks, LVT resolution was higher in the rivaroxaban group (20% vs 8%; P = 0.017), with similar resolution at 12 weeks (95.8% vs 96.6%; P = 0.759). The cumulative all-cause mortality was comparable (3.5% vs 3.3%; P = 0.921). Major bleeding occurred in 2.3% of rivaroxaban patients vs 1.1% of the warfarin group (P = 0.491). CONCLUSIONS: Rivaroxaban demonstrated similar efficacy to warfarin in treating post-MI LVT, with >95% resolution in both groups. Future multicenter trials with longer follow-up are needed to validate these findings (Rivaroxaban in Left Ventricular Thrombus; NCT04970576).
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Shah et al. (2025) conducted an RCT in Acute left ventricular thrombus following acute myocardial infarction (n=261). Rivaroxaban vs. Warfarin (target INR 2-3) was evaluated on Complete resolution of LVT at 12 weeks (RR 0.992, 95% CI 0.942-1.044, p=0.017 for noninferiority). Rivaroxaban was noninferior to warfarin for the complete resolution of acute left ventricular thrombus at 12 weeks (95.8% vs 96.6%; RR 0.992, P=0.017 for noninferiority) with similar safety profiles.
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