Antiplatelet Therapy After Percutaneous Coronary Intervention (PCI)
Dual antiplatelet therapy (DAPT) consisting of aspirin 75-100 mg and a P2Y12 inhibitor is recommended for up to 6 months as the default antithrombotic strategy after PCI with drug-eluting stents in patients with chronic coronary syndrome (CCS), with duration adjustments based on individual bleeding and ischemic risk profiles. 1
Standard DAPT Recommendations After PCI
For Acute Coronary Syndrome (ACS) Patients:
- DAPT with aspirin and a P2Y12 inhibitor is indicated for at least 12 months 1
- Ticagrelor or prasugrel is recommended in preference to clopidogrel for ACS patients undergoing PCI 1
- Loading dose followed by daily maintenance:
For Chronic Coronary Syndrome (CCS) Patients:
- DAPT with aspirin 75-100 mg and clopidogrel 75 mg daily for up to 6 months 1
- In patients at high bleeding risk but not high ischemic risk, discontinue DAPT 1-3 months after PCI and continue single antiplatelet therapy 1
- Stopping DAPT after 1-3 months may be considered in patients who are neither at high bleeding nor high ischemic risk 1
Risk-Based DAPT Duration Adjustments
Shorter DAPT Duration (1-3 months):
- Indicated for patients at high bleeding risk 1
- Recent evidence suggests short DAPT (≤3 months) followed by P2Y12 inhibitor monotherapy (particularly ticagrelor) reduces net adverse clinical events and bleeding without increasing ischemic events 4
Extended DAPT Duration (>6-12 months):
- Consider for patients at enhanced ischemic risk without high bleeding risk 1
- Extended DAPT (18-48 months) compared to 6-12 months shows:
- Decreased MI (OR: 0.67; 95% CI: 0.47 to 0.95)
- Decreased stent thrombosis (OR: 0.45; 95% CI: 0.24 to 0.74)
- Increased major hemorrhage (OR: 1.58; 95% CI: 1.20 to 2.09) 1
Special Populations
Patients Requiring Oral Anticoagulation:
- For patients with atrial fibrillation requiring PCI:
- Initial low-dose aspirin plus OAC and clopidogrel is recommended 1
- Early cessation of aspirin (≤1 week) followed by OAC plus clopidogrel for up to 6 months (or 12 months if high ischemic risk) 1
- Continuation of aspirin up to 1 month may be considered in patients at high ischemic risk 1
- Direct oral anticoagulants (DOACs) are preferred over vitamin K antagonists 1
High Thrombotic Risk PCI:
- For complex left main, 2-stent bifurcation, suboptimal stenting result, prior stent thrombosis, or known CYP2C19 *2/*3 polymorphisms:
- Consider prasugrel or ticagrelor (instead of clopidogrel) for the first month, up to 3-6 months 1
Bleeding Risk Reduction Strategies
- Proton pump inhibitor is recommended for patients at risk of gastrointestinal bleeding 1, 2
- Radial approach is preferred over femoral approach to reduce bleeding and vascular complications 1
- For patients on ticagrelor who have tolerated DAPT, transition to ticagrelor monotherapy is recommended ≥1 month after PCI 1
Common Pitfalls and Considerations
- Premature DAPT discontinuation: Increases risk of stent thrombosis, particularly in the first months after PCI
- Inadequate patient counseling: Poor adherence to DAPT is associated with increased adverse events
- Failure to consider both bleeding and ischemic risks: Both must be assessed to determine optimal DAPT duration
- Overlooking drug interactions: Some medications may affect P2Y12 inhibitor metabolism or increase bleeding risk
Algorithm for DAPT Duration Decision-Making
- Assess patient's baseline ischemic risk (ACS vs. CCS, complex PCI, diabetes, prior MI)
- Assess patient's bleeding risk (age >75, weight <60kg, prior bleeding, oral anticoagulant use)
- Determine DAPT duration:
- High bleeding risk: 1-3 months DAPT, then single antiplatelet therapy
- Standard risk: 6 months for CCS, 12 months for ACS
- High ischemic risk without high bleeding risk: Consider extended DAPT >12 months
The evolution of stent technology and growing evidence base has led to more personalized approaches to antiplatelet therapy after PCI, with a careful balance between preventing thrombotic complications and minimizing bleeding risk.