To the Editor Puymirat and colleagues report the APERITIF randomized clinical trial evaluating rivaroxaban, 2.5 mg, twice daily for 4 weeks added to dual antiplatelet therapy (DAPT) to prevent left ventricular (LV) thrombus after anterior ST-segment elevation myocardial infarction (STEMI). The primary end point—LV thrombus on contrast-enhanced cardiac magnetic resonance (CMR) at 1 month—was neutral, while minor bleeding (Bleeding Academic Research Consortium [BARC] type 1) was increased in the rivaroxaban group.
| # | Наименование новости | Тональность | Информативность | Дата публикации |
|---|---|---|---|---|
| 1 | Interpreting the APERITIF Randomized Clinical Trial—Reply | 0 | 10.38 | 01-08-2026 |
| 2 | Dual Antiplatelet Therapy Duration in Patients at High Bleeding Risk | 0 | 7.22 | 01-08-2026 |
| 3 | Prasugrel—The Default P2Y12 Inhibitor After PCI for ACS? | 0 | 7.98 | 01-08-2026 |
| 4 | Right Ventricular Metrics as End Points in Clinical Trials | 0 | 5.8 | 01-08-2026 |
| 5 | Coronary Artery Calcium Progression—A Useful Outcome in Clinical Trials? | 0 | 9.46 | 01-08-2026 |
| 6 | Lipoprotein(a), Inflammation, and Risk of Coronary Artery Disease and Aortic Valve Stenosis | 0 | 8.36 | 01-08-2026 |
| 7 | Twenty-Five–Year Follow-Up of Quantified Mitral Regurgitation | 0 | 15.41 | 29-07-2026 |
| 8 | Error in Figure | 0 | 14.84 | 01-08-2026 |
| 9 | Toward a Lifetime Strategy for Aortic Valve Replacement—Ariadne’s Thread | 0 | 7.65 | 01-08-2026 |
| 10 | JAMA Cardiology | 0 | 7.83 | 01-08-2026 |