Updates in antithrombotic therapy in coronary and peripheral artery disease

Amy West Pollak1

  • 1Department of Cardiovascular Medicine, Mayo Clinic, Jacksonville, FL.

Insights

Dual-pathway inhibition, combining antiplatelet and antithrombotic therapies, can improve cardiovascular outcomes for patients with atherosclerotic cardiovascular disease (ASCVD), including coronary artery disease (CAD) and peripheral artery disease (PAD). This review outlines patient selection for this treatment approach.

Area of Science:

  • Cardiology
  • Vascular Medicine
  • Pharmacology

Background:

  • Atherosclerotic cardiovascular disease (ASCVD) includes coronary artery disease (CAD) and peripheral artery disease (PAD), often coexisting.
  • Platelet activation and thrombin generation are key pathophysiological mechanisms in acute ischemic events within ASCVD.
  • Dual-pathway inhibition, a combination of antiplatelet and antithrombotic agents, is an emerging strategy for managing ASCVD.

Purpose of the Study:

  • To review the role of dual-pathway inhibition in improving cardiovascular outcomes for patients with ASCVD.
  • To identify patients with CAD and PAD who may benefit from dual-pathway inhibition.
  • To provide an overview of the clinical presentations of stable CAD and lower extremity PAD.

Main Methods:

  • Literature review focusing on dual-pathway inhibition in ASCVD.
  • Analysis of studies evaluating antiplatelet and antithrombotic therapy combinations.
  • Synthesis of clinical data on CAD and PAD presentations.

Main Results:

  • Dual-pathway inhibition demonstrates potential for improving cardiovascular outcomes in ASCVD patients.
  • Understanding patient profiles with coexisting CAD and PAD is crucial for treatment selection.
  • Clinical presentations of CAD and PAD inform therapeutic strategies.

Conclusions:

  • Dual-pathway inhibition is a promising therapeutic approach for select ASCVD patients.
  • Personalized treatment strategies considering coexisting CAD and PAD are essential.
  • Further research may refine patient selection for dual-pathway inhibition.

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