Direct Oral Anticoagulants Versus Vitamin K Antagonists for the Management of Left Ventricular Thrombus After Myocardial Infarction: A Meta-Analysis

Am J Cardiol. 2024 Dec 1:232:18-25. doi: 10.1016/j.amjcard.2024.09.008. Epub 2024 Sep 11.

Abstract

Left ventricular (LV) thrombus formation remains a post-acute myocardial infarction (AMI) complication even in the modern era of early reperfusion. The optimal anticoagulation regimen in this clinical scenario is poorly defined. The present meta-analysis sought to investigate the efficacy and safety profile of direct oral anticoagulants (DOACs) compared with vitamin K antagonists (VKAs) for the management of LV thrombus after AMI. A systematic literature review was conducted in electronic databases to identify studies reporting efficacy and safety outcome data regarding the use of DOACs versus VKAs for patients with LV thrombus after AMI. Odds ratios (ORs) and 95% confidence intervals (CIs) were calculated, and random-effects meta-analyses were conducted to synthesize pooled ORs. Eight studies comprising a total of 605 patients were included. DOACs were associated with an almost twofold higher likelihood of thrombus resolution compared with VKAs (pooled OR 1.95 [1.25 to 3.04], p = 0.003, I2 = 0%), and decreased the risk of systemic embolism by 70% (pooled OR 0.30 [0.12 to 0.75]; p = 0.01, I2 = 0%). The use of DOACs was associated with a 54% lower risk of bleeding compared with VKAs (pooled OR 0.46 [0.26 to 0.84], p = 0.01, I2 = 0%). Overall, patients receiving DOACs had a 63% lower risk of reaching the composite outcome of safety and efficacy compared with patients using VKAs (pooled OR 0.37 [0.23 to 0.60], p <0.0001, I2 = 0%). In conclusion, DOACs appear to have a more favorable efficacy and safety profile compared with VKAs for the management of LV thrombus related to AMI.

Keywords: direct oral anticoagulants; left ventricular thrombus; meta-analysis; myocardial infarction; vitamin K antagonists.

Publication types

  • Comparative Study
  • Meta-Analysis

MeSH terms

  • Administration, Oral
  • Anticoagulants* / therapeutic use
  • Factor Xa Inhibitors / therapeutic use
  • Heart Diseases / complications
  • Heart Diseases / drug therapy
  • Heart Diseases / etiology
  • Heart Ventricles*
  • Humans
  • Myocardial Infarction* / complications
  • Myocardial Infarction* / drug therapy
  • Thrombosis* / drug therapy
  • Thrombosis* / etiology
  • Vitamin K* / antagonists & inhibitors

Substances

  • Anticoagulants
  • Factor Xa Inhibitors
  • Vitamin K