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Abbreviated Dual Antiplatelet Therapy in Patients Undergoing Percutaneous Coronary Intervention: A Systematic Review and Meta-Analysis of Randomized Controlled Trials Publisher Pubmed



Soleimani H1 ; Karimi E1 ; Mahalleh M1, 2 ; Entezari FJ1 ; Nasrollahizadeh A1, 3 ; Nasrollahizadeh A1, 3 ; Rafiee H1 ; Kalhor P1 ; Alazizi KM4 ; Rios LHP5 ; Aronow WS6 ; Ambrosy AP7 ; Hosseini K1
Authors
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Authors Affiliations
  1. 1. Tehran Heart Center, Cardiovascular Diseases Research Institute, Tehran University of Medical Sciences, Tehran, Iran
  2. 2. Rheumatology Research Center, Tehran University of Medical Sciences, Tehran, Iran
  3. 3. Faculty of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran
  4. 4. Department of Cardiology, Baylor Scott and White The Heart Hospital, Plano, TX, United States
  5. 5. Division of Cardiology, Rooney Heart Institute, Naples, FL, United States
  6. 6. Departments of Cardiology and Medicine, Westchester Medical Center and New York Medical College, Valhalla, 10595, NY, United States
  7. 7. Department of Cardiology, Kaiser Permanente San Francisco Medical Center, San Francisco, CA, United States

Source: BMC Cardiovascular Disorders Published:2025


Abstract

Background: Dual antiplatelet therapy (DAPT), combining aspirin and a P2Y12 receptor inhibitor, is a standard post-percutaneous coronary intervention (PCI) treatment to reduce thrombosis and ischemic events. However, the optimal DAPT duration remains unclear, with concerns about bleeding risks associated with long-term potent P2Y12 inhibitors. This systematic review and meta-analysis investigates the safety and efficacy of shortened DAPT regimens. Methods: A comprehensive search of PubMed, Scopus, and EMBASE identified randomized controlled trials (RCTs) comparing conventional DAPT (≥ 12 months) and abbreviated DAPT (≤ 3 months) post-PCI. Primary outcomes were 1-year all-cause mortality and bleeding, assessed using the Bleeding Academic Research Consortium (BARC) classification. Secondary outcomes included cardiovascular mortality, non-fatal myocardial infarction (MI), stroke, and major adverse cardiovascular events (MACE). Risk of bias was assessed with the Cochrane tool, and meta-analyses used random-effects models. Results: Forty studies involving 54,233 participants were included. Abbreviated DAPT significantly reduced all-cause mortality (RR: 0.90, 95%CI: 0.82–0.98) and bleeding (BARC 3 or 5: RR: 0.77, 95%CI: 0.60–0.97). No significant differences were observed in cardiovascular mortality, stroke, non-fatal MI, revascularization, or in-stent thrombosis. Subgroup analyses showed lower mortality with 1-month DAPT and reduced bleeding in patients with high bleeding risk, acute coronary syndrome (ACS), and complex PCI. Conclusions: Abbreviated DAPT post-PCI is associated with lower all-cause mortality and bleeding without compromising ischemic protection, supporting its use in specific patient populations. Individualized DAPT durations should be considered to balance bleeding and ischemic risks. © The Author(s) 2025.