Pharmacodynamic effects of early aspirin withdrawal after percutaneous coronary intervention in patients with atrial fibrillation treated with ticagrelor or prasugrel

Dual antithrombotic therapy (DAT) without aspirin reduces bleeding compared with triple antithrombotic therapy (TAT) in patients with atrial fibrillation who have undergone percutaneous coronary intervention, without apparently increasing ischemic events. A prospective pharmacodynamic study was perf...

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Main Authors: Mark A. Sammut, Mohammed E. F. Rahman, Claire Bridge, Jessica Hanson, Heather Judge, Bethany Lynch, Emily Maz, Hannah McMellon, Janet Middle, Georgia Williamson, William A. E. Parker, Justin Lee, Robert F. Storey
Format: Article
Language:English
Published: Taylor & Francis Group 2025-12-01
Series:Platelets
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Online Access:https://www.tandfonline.com/doi/10.1080/09537104.2025.2507037
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author Mark A. Sammut
Mohammed E. F. Rahman
Claire Bridge
Jessica Hanson
Heather Judge
Bethany Lynch
Emily Maz
Hannah McMellon
Janet Middle
Georgia Williamson
William A. E. Parker
Justin Lee
Robert F. Storey
author_facet Mark A. Sammut
Mohammed E. F. Rahman
Claire Bridge
Jessica Hanson
Heather Judge
Bethany Lynch
Emily Maz
Hannah McMellon
Janet Middle
Georgia Williamson
William A. E. Parker
Justin Lee
Robert F. Storey
author_sort Mark A. Sammut
collection DOAJ
description Dual antithrombotic therapy (DAT) without aspirin reduces bleeding compared with triple antithrombotic therapy (TAT) in patients with atrial fibrillation who have undergone percutaneous coronary intervention, without apparently increasing ischemic events. A prospective pharmacodynamic study was performed to investigate the impact of aspirin on bleeding time, platelet function and fibrin clot analysis in this population. Patients receiving TAT (n = 16), comprising aspirin, ticagrelor/prasugrel and a direct-acting oral anticoagulant (DOAC), were compared with those receiving DAT without aspirin (n = 18). Bleeding time was reduced with DAT compared with TAT (median 27.8 vs 30.0 minutes, p = .005). Assessed by light transmission aggregometry, median platelet aggregation was significantly increased with DAT compared with TAT in response to arachidonic acid (63 vs 3%, p = .002) and collagen (72 vs 37%, p < .001) but not 5-μmol/L adenosine diphosphate (25 vs 27%, p = .966) or thrombin-receptor-activating peptide (37 vs 24%, p = .086). VerifyNow P2Y12 assay showed > 70% inhibition in all patients. Fibrin clot lysis time and maximum turbidity were similar between groups. Using P2Y12 inhibitors of consistent potency, DAT improves hemostasis through sparing cyclooxygenase-1-mediated platelet activation but has a comparable effect to TAT on other pathways and fibrin clot properties. DAT with ticagrelor/prasugrel and DOAC may provide sufficient antithrombotic effect without excessive anti-hemostatic effect.
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spelling doaj-art-007c2c6fcde94c1bbac626ea8dd63c922025-08-20T02:23:12ZengTaylor & Francis GroupPlatelets0953-71041369-16352025-12-0136110.1080/09537104.2025.2507037Pharmacodynamic effects of early aspirin withdrawal after percutaneous coronary intervention in patients with atrial fibrillation treated with ticagrelor or prasugrelMark A. Sammut0Mohammed E. F. Rahman1Claire Bridge2Jessica Hanson3Heather Judge4Bethany Lynch5Emily Maz6Hannah McMellon7Janet Middle8Georgia Williamson9William A. E. Parker10Justin Lee11Robert F. Storey12Division of Clinical Medicine, School of Medicine and Population Health, University of Sheffield, Sheffield, UKDivision of Clinical Medicine, School of Medicine and Population Health, University of Sheffield, Sheffield, UKDivision of Clinical Medicine, School of Medicine and Population Health, University of Sheffield, Sheffield, UKDivision of Clinical Medicine, School of Medicine and Population Health, University of Sheffield, Sheffield, UKDivision of Clinical Medicine, School of Medicine and Population Health, University of Sheffield, Sheffield, UKDivision of Clinical Medicine, School of Medicine and Population Health, University of Sheffield, Sheffield, UKDivision of Clinical Medicine, School of Medicine and Population Health, University of Sheffield, Sheffield, UKDivision of Clinical Medicine, School of Medicine and Population Health, University of Sheffield, Sheffield, UKDivision of Clinical Medicine, School of Medicine and Population Health, University of Sheffield, Sheffield, UKDivision of Clinical Medicine, School of Medicine and Population Health, University of Sheffield, Sheffield, UKDivision of Clinical Medicine, School of Medicine and Population Health, University of Sheffield, Sheffield, UKSouth Yorkshire Cardiothoracic Centre, Sheffield Teaching Hospitals NHS Foundation Trust, Sheffield, UKDivision of Clinical Medicine, School of Medicine and Population Health, University of Sheffield, Sheffield, UKDual antithrombotic therapy (DAT) without aspirin reduces bleeding compared with triple antithrombotic therapy (TAT) in patients with atrial fibrillation who have undergone percutaneous coronary intervention, without apparently increasing ischemic events. A prospective pharmacodynamic study was performed to investigate the impact of aspirin on bleeding time, platelet function and fibrin clot analysis in this population. Patients receiving TAT (n = 16), comprising aspirin, ticagrelor/prasugrel and a direct-acting oral anticoagulant (DOAC), were compared with those receiving DAT without aspirin (n = 18). Bleeding time was reduced with DAT compared with TAT (median 27.8 vs 30.0 minutes, p = .005). Assessed by light transmission aggregometry, median platelet aggregation was significantly increased with DAT compared with TAT in response to arachidonic acid (63 vs 3%, p = .002) and collagen (72 vs 37%, p < .001) but not 5-μmol/L adenosine diphosphate (25 vs 27%, p = .966) or thrombin-receptor-activating peptide (37 vs 24%, p = .086). VerifyNow P2Y12 assay showed > 70% inhibition in all patients. Fibrin clot lysis time and maximum turbidity were similar between groups. Using P2Y12 inhibitors of consistent potency, DAT improves hemostasis through sparing cyclooxygenase-1-mediated platelet activation but has a comparable effect to TAT on other pathways and fibrin clot properties. DAT with ticagrelor/prasugrel and DOAC may provide sufficient antithrombotic effect without excessive anti-hemostatic effect.https://www.tandfonline.com/doi/10.1080/09537104.2025.2507037Acute coronary syndromeaspirinatrial fibrillationdual antithrombotic therapyticagrelortriple antithrombotic therapy
spellingShingle Mark A. Sammut
Mohammed E. F. Rahman
Claire Bridge
Jessica Hanson
Heather Judge
Bethany Lynch
Emily Maz
Hannah McMellon
Janet Middle
Georgia Williamson
William A. E. Parker
Justin Lee
Robert F. Storey
Pharmacodynamic effects of early aspirin withdrawal after percutaneous coronary intervention in patients with atrial fibrillation treated with ticagrelor or prasugrel
Platelets
Acute coronary syndrome
aspirin
atrial fibrillation
dual antithrombotic therapy
ticagrelor
triple antithrombotic therapy
title Pharmacodynamic effects of early aspirin withdrawal after percutaneous coronary intervention in patients with atrial fibrillation treated with ticagrelor or prasugrel
title_full Pharmacodynamic effects of early aspirin withdrawal after percutaneous coronary intervention in patients with atrial fibrillation treated with ticagrelor or prasugrel
title_fullStr Pharmacodynamic effects of early aspirin withdrawal after percutaneous coronary intervention in patients with atrial fibrillation treated with ticagrelor or prasugrel
title_full_unstemmed Pharmacodynamic effects of early aspirin withdrawal after percutaneous coronary intervention in patients with atrial fibrillation treated with ticagrelor or prasugrel
title_short Pharmacodynamic effects of early aspirin withdrawal after percutaneous coronary intervention in patients with atrial fibrillation treated with ticagrelor or prasugrel
title_sort pharmacodynamic effects of early aspirin withdrawal after percutaneous coronary intervention in patients with atrial fibrillation treated with ticagrelor or prasugrel
topic Acute coronary syndrome
aspirin
atrial fibrillation
dual antithrombotic therapy
ticagrelor
triple antithrombotic therapy
url https://www.tandfonline.com/doi/10.1080/09537104.2025.2507037
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