Duration of Ticagrelor (Brilinta) After Drug-Eluting Stent in CAD
For patients with coronary artery disease who received drug-eluting stents for acute coronary syndrome, ticagrelor should be continued for at least 12 months; for stable coronary disease, at least 6 months is required. 1, 2
Standard Duration Based on Clinical Presentation
Acute Coronary Syndrome (ACS)
- Ticagrelor 90 mg twice daily must be continued for a minimum of 12 months after DES implantation 1, 2
- This 12-month recommendation applies regardless of stent type (bare metal or drug-eluting) 1
- Ticagrelor is preferred over clopidogrel for maintenance therapy in ACS patients 1, 2
- Aspirin 81 mg daily (range 75-100 mg) should be continued alongside ticagrelor 1, 2
Stable Ischemic Heart Disease (SIHD)
- Minimum duration is 6 months after DES implantation 1, 2
- Some guidelines suggest 1-6 months depending on bleeding risk, with 6 months being standard for patients without high bleeding risk 1
- Aspirin 81 mg daily should be maintained indefinitely 1, 2
Extension Beyond Standard Duration
When to Consider Prolonged Therapy (>12 months)
Continuation beyond 12 months may be reasonable if ALL of the following criteria are met: 1, 2, 3
- Patient has tolerated DAPT without any bleeding complications during the initial 12 months
- Patient is NOT at high bleeding risk (no prior bleeding on DAPT, no coagulopathy, no oral anticoagulant use)
- Patient has not experienced significant overt bleeding
For extended therapy beyond 12 months, consider reducing ticagrelor dose to 60 mg twice daily (not 90 mg) for long-term secondary prevention 3
High-Risk Features Favoring Extended Therapy
Patients with complex coronary disease may benefit from prolonged DAPT: 3
- Multivessel disease including left main involvement
- Prior myocardial infarction
- Chronic kidney disease
- History of stent thrombosis
- Complex PCI (multivessel stenting, >30 mm stent length, bifurcation lesions)
Early Discontinuation Scenarios
ACS Patients with High Bleeding Risk
Discontinuation after 6 months may be reasonable if: 1, 2
- Patient develops high bleeding risk (e.g., requires oral anticoagulation therapy)
- Patient is at high risk of severe bleeding complications (e.g., major intracranial surgery planned)
- Patient develops significant overt bleeding
SIHD Patients with High Bleeding Risk
Discontinuation after 3 months may be reasonable if: 1, 2
- Patient develops treatment indication requiring oral anticoagulation
- Patient faces high risk of severe bleeding complications
- Significant overt bleeding occurs
General Principle for Early Discontinuation
If the morbidity risk from bleeding clearly outweighs the anticipated ischemic benefit, earlier discontinuation is reasonable 1
Critical Management Points
Aspirin Dosing
- Use 81 mg daily (acceptable range 75-100 mg) when combined with ticagrelor 1, 2
- Higher aspirin doses increase bleeding without improving efficacy 1, 3
- Aspirin should be continued indefinitely after stopping ticagrelor 1, 3
If CABG is Required
- Stop ticagrelor at least 3 days before elective CABG 1, 3
- Resume ticagrelor as soon as possible after CABG to complete the 12-month course in ACS patients 1, 3
- Aspirin should be continued throughout the perioperative period 1
Common Pitfalls to Avoid
Do not stop ticagrelor before 12 months in ACS patients without compelling bleeding reasons - this dramatically increases thrombotic risk including stent thrombosis 1, 2, 3
Do not use ticagrelor 90 mg twice daily for therapy extending beyond 12 months - the approved dose for long-term secondary prevention is 60 mg twice daily 3
Do not discontinue therapy without discussing with the interventional cardiologist - premature cessation is a leading cause of stent thrombosis 2
Do not use aspirin doses >100 mg daily with ticagrelor - this increases bleeding without additional benefit 1, 3
Do not abruptly stop aspirin after discontinuing ticagrelor - aspirin monotherapy should continue for life 1, 3
Do not prescribe prasugrel instead of ticagrelor if the patient has prior stroke or TIA - prasugrel is contraindicated in these patients 1, 3