What is the recommended dosage of Brillinta (ticagrelor) after percutaneous coronary intervention (PCI) with stent placement?

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Last updated: September 4, 2025View editorial policy

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Recommended Dosage of Ticagrelor After Stent Placement

For patients who have undergone percutaneous coronary intervention (PCI) with stent placement, ticagrelor should be administered at a loading dose of 180 mg followed by a maintenance dose of 90 mg twice daily for at least 12 months.

Dosing Protocol for Ticagrelor After PCI

Initial Loading Dose

  • A loading dose of 180 mg ticagrelor should be given as early as possible before or at the time of PCI 1
  • This loading dose ensures rapid platelet inhibition when it's most critical

Maintenance Dosing

  • Following the loading dose, patients should receive 90 mg of ticagrelor twice daily 2
  • This maintenance dose should be continued for at least 12 months in patients who received a stent during PCI for acute coronary syndrome (ACS) 2

Duration of Therapy Based on Clinical Scenario

For ACS Patients

  • Ticagrelor 90 mg twice daily should be given for at least 12 months in combination with aspirin 2
  • Ticagrelor is preferred over clopidogrel in ACS patients due to superior outcomes 2

For Stable Coronary Artery Disease (CAD) Patients

  • For drug-eluting stents (DES) in non-ACS patients: Typically clopidogrel 75 mg daily is used for at least 12 months 2
  • For bare-metal stents (BMS) in non-ACS patients: P2Y12 inhibitor for a minimum of 1 month and ideally up to 12 months 2
  • Ticagrelor may be considered in selected stable CAD patients at high ischemic/thrombotic risk and low bleeding risk 1

Aspirin Co-administration

  • Low-dose aspirin (81 mg daily) should be used in combination with ticagrelor 2
  • Higher aspirin doses should be avoided as they may reduce ticagrelor's effectiveness

Special Considerations

High Bleeding Risk Patients

  • If the risk of bleeding outweighs the anticipated benefit of 12 months of ticagrelor therapy, earlier discontinuation (< 12 months) may be reasonable 2
  • Recent evidence suggests that after 3 months of dual antiplatelet therapy (DAPT), continuing with ticagrelor monotherapy (without aspirin) may reduce bleeding while maintaining anti-thrombotic efficacy 3

Renal Impairment

  • No dose adjustment is required for patients with renal impairment 4
  • Ticagrelor can provide benefits in patients with impaired renal function without increased bleeding risk

Contraindications and Precautions

  • Ticagrelor should be discontinued at least 5 days before planned surgery 1
  • Contraindications include history of intracranial hemorrhage, active pathological bleeding, and severe hepatic impairment 1

Monitoring

  • Routine platelet function testing to adjust ticagrelor dosing is not recommended 2
  • Patients should be counseled about the importance of medication adherence, especially with the twice-daily dosing schedule

Remember that premature discontinuation of ticagrelor significantly increases the risk of stent thrombosis, myocardial infarction, and death. Patient education about the importance of adherence to the prescribed regimen is crucial for optimal outcomes.

References

Guideline

Antiplatelet Therapy in Coronary Artery Disease

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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