Abstract

BackgroundPatients with heightened platelet reactivity in response to antiplatelet agents are at an increased risk of recurrent ischemic events. However, there is a lack of diagnostic criteria for increased response to combined aspirin/clopidogrel therapy. The challenge is to identify patients at risk of bleeding. This study sought to characterize bleeding tendency in patients treated with aspirin and clopidogrel.Patients/methodsIn a single-center prospective study, 100 patients under long-term aspirin/clopidogrel treatment, the effect of therapy was assayed by template bleeding time (BT) and the inhibition of platelet aggregation (IPA) by light transmission aggregometry (LTA). Arachidonic acid (0.625 mmol/L) and adenosine diphosphate (ADP; 2, 4, and 8 μmol/L) were used as platelet agonists.ResultsBleeding episodes (28 nuisance, 2 hematuria [1 severe], 1 severe proctorrhagia, 1 severe epistaxis) were significantly more frequent in patients with longer BT. Template BT ≥ 24 min was associated with bleeding episodes (28 of 32). Risk of bleeding increased 17.4% for each 1 min increase in BT. Correlation was found between BT and IPAmax in response to ADP 2 μmol/L but not to ADP 4 or 8 μmol/L.ConclusionIn patients treated with dual aspirin/clopidogrel therapy, nuisance and internal bleeding were significantly associated with template BT and with IPAmax in response to ADP 2 μmol/L but not in response to ADP 4 μmol/L or 8 μmol/L.

Highlights

  • Until recently, long-term antiplatelet therapy for the prevention of atherothrombotic disease was limited to aspirin (ASA)

  • Correlation was found between bleeding time (BT) and IPAmax in response to adenosine diphosphate (ADP) 2 μmol/L but not to ADP 4 or 8 μmol/L

  • In patients treated with dual aspirin/clopidogrel therapy, nuisance and internal bleeding were significantly associated with template BT and with IPAmax in response to ADP 2 μmol/L but not in response to ADP 4 μmol/L or 8 μmol/L

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Summary

Introduction

Long-term antiplatelet therapy for the prevention of atherothrombotic disease was limited to aspirin (ASA). Despite the use of available antiplatelet therapies, the recurrence of ischemic events in patients. The current gold standard for testing platelet function is light transmission platelet aggregometry (LTA), which is used to categorize patients receiving ASA and/or CLOP therapy as responders or nonresponders. Patients with heightened platelet reactivity in response to antiplatelet agents are at an increased risk of recurrent ischemic events. There is a lack of diagnostic criteria for increased response to combined aspirin/clopidogrel therapy. This study sought to characterize bleeding tendency in patients treated with aspirin and clopidogrel. Patients/methods: In a single-center prospective study, 100 patients under long-term aspirin/clopidogrel treatment, the effect of therapy was assayed by template bleeding time (BT) and the inhibition of platelet aggregation (IPA) by light transmission aggregometry (LTA). Arachidonic acid (0.625 mmol/L) and adenosine diphosphate (ADP; 2, 4, and 8 μmol/L) were used as platelet agonists

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