Individualization of Duration of Dual Antiplatelet Therapy after Coronary Stenting: A Comprehensive, Evidence-Based Review

Author:

Carciotto Gabriele1ORCID,Costa Francesco2ORCID,Garcia-Ruiz Victoria3,Galli Mattia4ORCID,Soraci Emmanuele5,Magliarditi Alberto5,Teresi Lucio1,Nasso Enrica6,Carerj Scipione6,Di Bella Gianluca6,Micari Antonio2,De Luca Giuseppe67ORCID

Affiliation:

1. Division of Cardiology, Policlinico G Martino, 98125 Messina, Italy

2. BIOMORF Department, University of Messina, 98122 Messina, Italy

3. Division of Cardiology, GIOMI Hospital, 98165 Messina, Italy

4. Maria Cecilia Hospital, GVM Care & Research, 48033 Cotignola, Italy

5. U.O.S. Emodinamica, Department of Medicine, Ospedale Barone Romeo di Patti, 98066 Messina, Italy

6. Department of Clinical and Experimental Medicine, University of Messina, 98122 Messina, Italy

7. Division of Cardiology, IRCCS Hospital Galeazzi-Sant’Ambrogio, 20157 Milan, Italy

Abstract

Dual antiplatelet therapy (DAPT), comprising aspirin and a P2Y12 receptor inhibitor, is the cornerstone of post-percutaneous coronary intervention treatment to prevent stent thrombosis and reduce the risk of adverse cardiovascular events. The selection of an optimal DAPT regimen, considering the interplay of various antiplatelet agents, patient profiles, and procedural characteristics, remains an evolving challenge. Traditionally, a standard duration of 12 months has been recommended for DAPT in most patients. While contemporary guidelines provide general frameworks, DAPT modulation with longer or shorter treatment courses followed by aspirin or P2Y12 inhibitor monotherapy are evolving towards an individualized strategy to optimize the balance between efficacy and safety. This review comprehensively examines the current landscape of DAPT strategies after coronary stenting, with a focus on emerging evidence for treatment individualization.

Publisher

MDPI AG

Subject

General Medicine

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