Key result
NOACs linked to ~2.3-fold higher likelihood of ventricular thrombus resolution vs. VKAs at 12 months.
Why the study?
To evaluate the utilization of NOACs, VKAs, or APT in ventricular thrombus patients and analyze factors associated with thrombus resolution and clinical outcomes.
Does NOAC therapy improve thrombus resolution in patients with ventricular thrombus compared to VKAs or antiplatelet therapy?
Observational (n=463)
No
Does NOAC therapy improve thrombus resolution in patients with ventricular thrombus compared to VKAs or antiplatelet therapy?
Hazard Ratio: 2.28 (95% CI 1.57–3.31)
Absolute Event Rate: 86.79% vs 77.17%
p-value: p=<0.001
NOACs appear to be a safe and effective alternative to VKAs for resolving ventricular thrombus, warranting further investigation in prospective randomized trials.
May support NOAC preference over VKAs for ventricular thrombus in practice; hypothesis-generating and requires RCT confirmation before guideline changes.
Aim of the Study . To evaluate the utilization of oral antithrombotic agents, non‐vitamin K antagonist oral anticoagulants (NOACs), vitamin K antagonists (VKAs), or antiplatelet therapy (APT), in ventricular thrombus (VT) patients and to analyze factors for thrombus resolution and clinical outcomes. Methods . This retrospective observational study was conducted from 2010 to 2019 in National Center of Cardiovascular Diseases of China. We included patients with VT confirmed by imaging. The primary outcome was the rate of thrombus resolution. Hazard ratio (HR) was calculated with or without adjustment for covariates using Cox proportional hazards regression models. Results . 463 patients were included. 43.0% received VKAs, 16.6% received NOACs, and 40.4% received APT. Over a median of 468 days’ follow‐up, NOACs group was more likely to have the thrombus resolved within 12 months’ follow‐up than VKAs (HR 2.28, 95% CI 1.57 to 3.31) or APT (HR 2.92, 95% CI 1.97 to 4.33). After adjustment for baseline variables, the significance remained in the comparison of NOACs versus VKAs (HR 2.13, 95% CI 1.41 to 3.22) as well as NOACs versus APT (HR 2.55, 95% CI 1.53 to 4.27). No significant differences were identified in bleeding rate, thromboembolism rate, or all‐cause death in 12 months’ follow‐up. Conclusion . Our findings showed that patients who were male, diagnosed with MI with or without ventricular aneurysm, or diagnosed with coronary artery diseases medical history had a risk of thrombus unresolved. Patients with NOACs had a higher resolution and a similar safety profile comparing VKAs or APT, which persisted after adjusting for other factors. Large randomized controlled trials are required urgently. This trial is registered with NCT05006677 .
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Yang et al. (2022) conducted an observational in Ventricular thrombus (n=463). Non-vitamin K antagonist oral anticoagulants (NOACs) vs. Vitamin K antagonists (VKAs) was evaluated on Thrombus resolution within 12 months (HR 2.28, 95% CI 1.57 to 3.31, p=<0.001). NOACs were associated with a significantly higher likelihood of ventricular thrombus resolution within 12 months compared to VKAs (HR 2.28, p < 0.001).
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