Ticagrelor in Acute Coronary Syndrome: Recommended Use and Dosage
For patients with acute coronary syndrome (ACS), ticagrelor should be administered at a loading dose of 180 mg followed by 90 mg twice daily for 12 months, regardless of initial treatment strategy. 1
Indications and Patient Selection
Ticagrelor is recommended for:
- All ACS patients (STEMI and NSTE-ACS) as a P2Y12 inhibitor in addition to aspirin 1
- STEMI patients managed with primary PCI 1
- NSTE-ACS patients regardless of whether they undergo PCI or are managed conservatively 1
- Patients previously on clopidogrel should be switched to ticagrelor (discontinue clopidogrel when ticagrelor is started) 1
Dosing Protocol
- Loading dose: 180 mg orally 1
- Maintenance dose: 90 mg twice daily 1
- Duration: 12 months unless contraindicated due to excessive bleeding risk 1
- Aspirin co-administration: 75-100 mg daily (never exceed 100 mg when combined with ticagrelor) 1, 2
Contraindications
Ticagrelor should not be used in patients with:
- Previous intracranial hemorrhage
- Ongoing active bleeding 1
Clinical Evidence Supporting Recommendation
The PLATO trial demonstrated that ticagrelor significantly reduced the composite endpoint of cardiovascular death, myocardial infarction, or stroke compared to clopidogrel (9.8% vs. 11.7%, HR 0.84) 3. Specifically:
- Reduced myocardial infarction (5.8% vs. 6.9%, p=0.005)
- Reduced cardiovascular mortality (4.0% vs. 5.1%, p=0.001)
- Reduced all-cause mortality (4.5% vs. 5.9%, p<0.001) 3
Special Considerations
- Timing of administration: In NSTE-ACS patients planned for an invasive strategy with angiography anticipated >24 hours, upstream treatment with ticagrelor may be considered 1
- Switching from clopidogrel: Patients previously exposed to clopidogrel should be switched to ticagrelor early after hospital admission with a loading dose of 180 mg, regardless of timing and loading dose of clopidogrel 1
- Bleeding risk assessment: Consider using the PRECISE-DAPT score (≥25 indicates high bleeding risk) when determining duration of therapy 1
- Perioperative management: Discontinue ticagrelor at least 3-5 days before planned surgery to minimize bleeding risk 2
Monitoring and Side Effects
- Dyspnea: Occurs in up to 15% of patients, usually mild to moderate in severity 2
- Ventricular pauses: May occur but are largely asymptomatic 4
- Bleeding risk: Similar overall major bleeding compared to clopidogrel, but higher non-CABG-related bleeding (4.5% vs. 3.8%, p=0.03) 3
Comparison with Other P2Y12 Inhibitors
- Prasugrel: In NSTE-ACS patients undergoing PCI, prasugrel should be considered in preference to ticagrelor 1
- Clopidogrel: Ticagrelor is superior to clopidogrel in reducing cardiovascular events in ACS patients 3 but clopidogrel should be used when ticagrelor is unavailable, not tolerated, or contraindicated 1
Important Cautions
- Avoid high-dose aspirin (>100 mg daily) as it may reduce ticagrelor's effectiveness 2
- Emphasize the importance of twice-daily dosing and adherence to prevent thrombotic events 2
- Monitor for bleeding complications, especially in patients with risk factors for bleeding
By following these evidence-based recommendations for ticagrelor use in ACS patients, clinicians can optimize outcomes by reducing mortality and recurrent ischemic events while managing bleeding risk.