Treatment of Coronary Artery Dissection in Patients with Antiphospholipid Syndrome
For patients with antiphospholipid syndrome who have experienced a coronary artery dissection, anticoagulation with warfarin targeting an INR of 2.0-3.0 is recommended as the primary treatment strategy.
Pathophysiology and Risk Assessment
Antiphospholipid syndrome (APS) is characterized by persistent presence of antiphospholipid antibodies and clinical manifestations including arterial or venous thrombosis. Coronary artery dissection represents a unique challenge in these patients due to the dual risk of thrombosis and bleeding.
Key considerations in management:
- APS increases thrombotic risk, which can complicate coronary artery dissection healing
- Coronary dissections themselves carry risk of propagation and thrombosis
- Balancing antithrombotic therapy to prevent thrombosis while allowing vessel healing is critical
Treatment Algorithm
1. Anticoagulation Strategy
Primary recommendation: Warfarin with target INR 2.0-3.0 1
Duration of therapy:
2. Antiplatelet Considerations
For acute coronary dissection management:
Avoid triple therapy (warfarin + dual antiplatelet therapy) due to excessive bleeding risk 1, 3
3. Special Considerations
If PCI with stenting was performed:
For patients with "triple positive" antiphospholipid antibodies:
Monitoring and Follow-up
- Regular INR monitoring to maintain target range 2.0-3.0 1
- Assess for signs of recurrent thrombosis or bleeding complications
- Consider proton pump inhibitor co-therapy to reduce GI bleeding risk in patients requiring combination therapy 1
Pitfalls and Caveats
Avoid DOACs in APS patients with arterial thrombosis
Avoid excessive anticoagulation intensity
Be cautious with antiplatelet discontinuation timing
By following this evidence-based approach, the dual risks of thrombosis and bleeding can be optimally managed in patients with antiphospholipid syndrome who have experienced coronary artery dissection.