Comparison of Direct Oral Anticoagulants vs Vitamin K Antagonists After Transcatheter Mitral Valve Replacement

Nathan El Bèze1, Dominique Himbert2, Gaspard Suc2

  • 1Department of Cardiology, Bichat Claude Bernard Hospital-Paris City University, Paris, France.

Insights

Direct oral anticoagulants (DOACs) show reduced bleeding and shorter hospital stays post-transcatheter mitral valve replacement (TMVR) compared to vitamin K antagonists (VKAs). This study suggests DOACs may be a safer option for TMVR patients without increasing thrombotic risks.

Area of Science:

  • Cardiology
  • Interventional Cardiology
  • Medical Devices

Background:

  • No established antithrombotic treatment guidelines exist for transcatheter mitral valve replacement (TMVR).
  • Vitamin K antagonists (VKAs) are currently the predominant treatment, based on analogy with surgical mitral bioprostheses.

Purpose of the Study:

  • To compare bleeding and thrombotic events in patients undergoing transseptal TMVR with either direct oral anticoagulants (DOACs) or VKAs.
  • To evaluate the safety and efficacy of DOACs versus VKAs in the TMVR population.

Main Methods:

  • Prospective cohort study of 156 patients who underwent transseptal TMVR with a SAPIEN prosthesis (2011-2023).
  • Patients received VKAs until October 2019, followed by DOACs.
  • Primary outcome was bleeding events; median follow-up was 4.7 months.

Main Results:

  • DOAC use was associated with a significantly lower incidence of bleeding events (9% in DOAC group vs. 40% in VKA group; adjusted HR: 0.21).
  • DOAC treatment correlated with a shorter hospital stay.
  • No significant differences were observed in thrombotic events, major vascular complications, stroke, or mortality between the groups.

Conclusions:

  • Direct oral anticoagulants (DOACs) may reduce bleeding complications following transcatheter mitral valve replacement (TMVR) compared to VKAs.
  • DOACs appear to decrease length of hospital stay without increasing thrombotic event risk.
  • DOACs represent a potentially safer antithrombotic strategy for TMVR patients.
Abstract

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