What is the recommended duration of dual antiplatelet therapy (DAPT) with Brillinta (ticagrelor) and Aspirin in patients with stent restenosis?

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Last updated: December 5, 2025View editorial policy

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Duration of DAPT with Brillinta (Ticagrelor) and Aspirin for In-Stent Restenosis

For patients undergoing angioplasty for in-stent restenosis, dual antiplatelet therapy with aspirin and clopidogrel should be continued for at least 6 months, with strong consideration for extending to 24 months in patients who tolerate DAPT without bleeding complications. 1, 2

Standard Duration Recommendation

  • Aspirin 81 mg daily (range 75-100 mg) should be continued indefinitely in all patients after treatment for in-stent restenosis 1, 3

  • A P2Y12 inhibitor (clopidogrel 75 mg daily) should be given for at least 6 months as the minimum duration after angioplasty for in-stent restenosis 1

  • Clopidogrel is the preferred P2Y12 inhibitor for in-stent restenosis treatment, not ticagrelor or prasugrel 1

Important Clarification About Ticagrelor (Brillinta)

Ticagrelor is NOT the standard P2Y12 inhibitor for in-stent restenosis. The guidelines specifically recommend clopidogrel for this indication 1. Ticagrelor is preferentially recommended for acute coronary syndrome patients undergoing PCI, but in-stent restenosis is typically managed differently unless it presents as ACS 3.

Evidence-Based Duration Strategy

Extended DAPT (Beyond 6 Months)

  • In patients who tolerate DAPT without bleeding complications and are not at high bleeding risk, continuation beyond 6 months may be reasonable 1, 3

  • The PRODIGY trial substudy demonstrated significant benefit with 24-month DAPT versus 6-month DAPT in patients treated for in-stent restenosis, showing reduced death and MI (6.5% vs. 15.5%; p=0.03) without increased bleeding 2

  • The cumulative incidence of death, MI, or stroke at 24 months was 7.3% with long DAPT versus 16.7% with short DAPT (p=0.034), providing the strongest evidence for extended therapy in this specific population 2

Shortened DAPT (Less Than 6 Months)

  • In patients who develop high bleeding risk (e.g., requiring oral anticoagulation) or significant overt bleeding, discontinuation after 3 months may be reasonable 1, 3

  • For patients at very high bleeding risk, discontinuation after 1 month may be considered in select cases, though this carries higher ischemic risk 1

Risk Stratification Algorithm

Factors Favoring Extended DAPT (12-24 months):

  • No bleeding complications during initial 6 months 1, 2
  • Low bleeding risk (PRECISE-DAPT score <25) 3
  • High ischemic risk (diabetes, multivessel disease, prior MI, complex lesions) 3
  • Good medication adherence 1

Factors Favoring Shortened DAPT (3-6 months):

  • High bleeding risk (PRECISE-DAPT score ≥25) 3
  • Need for oral anticoagulation 3, 1
  • History of gastrointestinal bleeding 3
  • Advanced age with frailty 3
  • Planned major surgery 3

Critical Pitfalls to Avoid

  • The risk of stent thrombosis is highest in the first days to weeks after stent implantation, making DAPT adherence particularly crucial during the initial period 1

  • Never discontinue DAPT before discussing with the treating cardiologist, as premature cessation is associated with catastrophic stent thrombosis 3

  • Do not use prasugrel in patients with prior stroke or TIA (Class III recommendation) 3

Gastrointestinal Protection

  • Proton pump inhibitors (PPIs) should be used in patients with history of gastrointestinal bleeding who require DAPT 3, 1

  • PPIs are reasonable in patients with increased bleeding risk (advanced age, concomitant warfarin, steroids, NSAIDs, H. pylori infection) 3, 1

Context-Specific Modifications

If the in-stent restenosis presented as an acute coronary syndrome, then the standard ACS DAPT duration applies: 12 months of DAPT with ticagrelor or prasugrel preferred over clopidogrel 3. However, for elective treatment of in-stent restenosis discovered on surveillance or stable symptoms, clopidogrel for 6-24 months is the evidence-based approach 1, 2.

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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