Oral Anticoagulation for the Prevention of Thromboembolic Events in Patients With Anterior ST-Segment Elevation

Laurie-Anne Boivin-Proulx, Simon-Pierre Demers, Fabrice Ieroncig

  • 1Montreal Heart Institute, 5000 Belanger, Montreal, QC, Canada, H1T 1C8. guillaume.marquis.gravel@umontreal.ca.

Insights

Triple therapy (TT) with dual-antiplatelet therapy (DAPT) plus oral anticoagulant (OAC) did not significantly reduce net adverse clinical events (NACE) compared to DAPT alone in STEMI patients with wall-motion abnormalities. Both treatments showed similar ischemic and bleeding event risks.

Area of Science:

  • Cardiology
  • Interventional Cardiology
  • Cardiovascular Research

Background:

  • Patients with ST-segment elevation myocardial infarction (STEMI) and new-onset anterior/apical wall-motion abnormalities (WMAs) may benefit from oral anticoagulants (OAC) to prevent left ventricular thrombus and cardioembolic events.
  • Assessing the comparative effectiveness and safety of dual-antiplatelet therapy (DAPT) versus triple therapy (TT) (DAPT + OAC) is crucial for optimizing treatment strategies.

Purpose of the Study:

  • To compare the effectiveness and safety of DAPT versus TT in patients with anterior STEMI and new-onset anterior/apical WMAs undergoing primary percutaneous coronary intervention (PCI).
  • To evaluate the composite endpoint of net adverse clinical events (NACE) at 6 months, including mortality, myocardial infarction, stroke, and major bleeding.

Main Methods:

  • A multicenter, retrospective cohort study included 1666 patients with anterior STEMI and WMAs treated with primary PCI.
  • Patients were divided into two groups: those discharged on TT (n=627) and those on DAPT (n=1039), excluding those with a concomitant indication for OAC.
  • Adjusted Cox proportional hazards analysis and inverse probability of treatment weighting were used to compare outcomes.

Main Results:

  • The incidence of NACE at 6 months was 6.03 per 100 patient-years in the TT group and 7.18 per 100 patient-years in the DAPT group (adjusted hazard ratio, 0.86; 95% CI, 0.55-1.32).
  • There were no significant differences in the adjusted risks of individual components of the primary endpoint, including ischemic events and major bleeding (BARC type 3 or 5), between the TT and DAPT groups (P>.05 for all).

Conclusions:

  • The addition of OAC to DAPT in anterior STEMI patients with new-onset WMAs treated with PCI was not associated with a significant reduction in NACE.
  • Treatment strategies involving TT or DAPT alone demonstrated similar safety and efficacy profiles regarding major adverse clinical and bleeding events in this specific patient cohort.
Abstract

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