Changes in Coagulation and Platelet Activation Markers Following Transcatheter Left Atrial Appendage Closure

Josep Rodés-Cabau1, Gilles O'Hara1, Jean-Michel Paradis1

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

Insights

Left atrial appendage closure (LAAC) activates the coagulation system, as shown by increased prothrombin fragment 1+2 and thrombin-antithrombin levels post-procedure. However, platelet activation markers did not significantly change after LAAC.

Area of Science:

  • Cardiology
  • Hematology
  • Medical Devices

Background:

  • Antithrombotic treatment recommendations post-left atrial appendage closure (LAAC) lack empirical data.
  • Changes in hemostatic markers following LAAC are not well-documented.

Purpose of the Study:

  • To investigate the presence, degree, and timing of changes in platelet and coagulation activation markers after LAAC.
  • To assess the impact of LAAC on hemostatic balance.

Main Methods:

  • A study of 43 patients undergoing successful LAAC with Watchman or Amplatzer Cardiac Plug devices.
  • Hemostatic markers (prothrombin fragment 1+2, thrombin-antithrombin III, soluble P-selectin, soluble CD40 ligand) were measured at baseline, and at 7, 30, and 180 days post-LAAC.
  • Patients received dual or single antiplatelet therapy post-procedure.

Main Results:

  • Coagulation activation markers (prothrombin fragment 1+2 and thrombin-antithrombin III) significantly increased at 7 days post-LAAC, then returned towards baseline levels by 30 and 180 days (p <0.001).
  • No clinical or procedural factors correlated with increased coagulation marker levels.
  • Platelet activation markers (soluble P-selectin and soluble CD40 ligand) showed no significant changes throughout the study period.

Conclusions:

  • Transcatheter LAAC is associated with significant activation of the coagulation system.
  • LAAC does not appear to induce significant platelet activation.
  • Further research is needed to optimize antithrombotic strategies post-LAAC.

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