Dual antiplatelet therapy after TAVR: A drop in the bucket?

Marco Ferlini1, Silvia Mauri1, Roberta Rossini2

  • 1Division of Cardiology, Fondazione IRCCS Policlinico San Matteo, Italy.

Insights

Dual antiplatelet therapy (DAPT) after TAVR increases bleeding without improving efficacy. Aspirin alone shows similar effectiveness with less bleeding, and oral anticoagulants may prevent future events.

Area of Science:

  • Cardiology
  • Interventional Cardiology
  • Cardiovascular Research

Background:

  • Current guidelines suggest 3-6 months of dual antiplatelet therapy (DAPT) post-transcatheter aortic valve replacement (TAVR).
  • Oral anticoagulant agents (OAC) are recommended if pre-existing indications exist.
  • Recent evidence challenges DAPT's necessity and explores alternatives for TAVR patients.

Purpose of the Study:

  • To evaluate the efficacy and safety of aspirin monotherapy versus DAPT after TAVR.
  • To explore the potential role of OAC in preventing post-TAVR cerebrovascular events.
  • To inform guideline updates regarding antithrombotic therapy following TAVR.

Main Methods:

  • Comparative analysis of studies comparing aspirin monotherapy with DAPT.
  • Review of data on cerebrovascular events post-TAVR, including causes like atrial fibrillation and subclinical leaflet thrombosis.
  • Theoretical consideration of OAC use in specific TAVR patient subgroups.

Main Results:

  • Aspirin monotherapy demonstrated comparable efficacy to DAPT with a significant reduction in major bleeding events.
  • A substantial proportion of late cerebrovascular events (>24h post-TAVR) may be linked to new-onset atrial fibrillation or subclinical leaflet thrombosis.
  • OAC may offer a protective effect against these specific cerebrovascular events compared to antiplatelet therapy.

Conclusions:

  • Aspirin monotherapy appears to be a safer alternative to DAPT in many TAVR patients.
  • The potential benefit of OAC in preventing specific post-TAVR cerebrovascular events warrants further investigation.
  • In the absence of high bleeding risk or recent PCI, OAC could be considered over antiplatelet strategies pending clinical trial results.

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