Meta-Analysis Comparing Single Versus Dual Antiplatelet Therapy Following Transcatheter Aortic Valve Implantation

Frédéric Maes1, Eugenio Stabile2, Gian Paolo Ussia3

  • 1Department of Cardiology, Quebec Heart & Lung Institute, Laval University, Quebec City, Quebec, Canada.

Insights

Dual antiplatelet therapy (DAPT) after transcatheter aortic valve implantation (TAVI) increases bleeding risk without reducing ischemic events compared to single antiplatelet therapy (SAPT). These findings challenge current DAPT recommendations post-TAVI.

Area of Science:

  • Cardiology
  • Interventional Cardiology
  • Thrombosis Research

Background:

  • Transcatheter aortic valve implantation (TAVI) is a growing procedure for aortic stenosis.
  • Optimal antithrombotic therapy post-TAVI remains debated, with current guidelines often recommending dual antiplatelet therapy (DAPT).
  • Concerns exist regarding the balance between preventing thrombotic events and increasing bleeding risk with DAPT.

Purpose of the Study:

  • To compare the efficacy and safety of DAPT versus single antiplatelet therapy (SAPT) following TAVI.
  • To evaluate the impact of DAPT versus SAPT on ischemic events, bleeding events, and mortality.
  • To inform optimal antithrombotic strategies after TAVI procedures.

Main Methods:

  • Patient-level meta-analysis of three randomized controlled trials comparing DAPT and SAPT post-TAVI.
  • Inclusion of 421 patients (210 DAPT, 211 SAPT).
  • Primary endpoint: composite of death, major/life-threatening bleeding, and major vascular complications at 30 days, adjudicated by Valve Academic Research Consortium 2 criteria.

Main Results:

  • The 30-day composite primary endpoint was significantly higher in the DAPT group (17.6%) compared to the SAPT group (10.9%).
  • Major or life-threatening bleeding events were significantly increased with DAPT (11.4%) versus SAPT (5.2%).
  • No significant differences were observed between DAPT and SAPT for death, global ischemic events, or stroke.

Conclusions:

  • DAPT following TAVI is associated with a higher rate of major adverse events, primarily driven by increased bleeding risk.
  • DAPT did not demonstrate a significant benefit in reducing ischemic events compared to SAPT after TAVI.
  • Current recommendations for DAPT post-TAVI may need reevaluation based on these findings, favoring SAPT in many cases.

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