Pretreatment with Dual Antiplatelet Therapy in Patients with Non-ST-Segment Elevation Acute Coronary Syndromes undergoing Percutaneous Coronary Intervention

Background - Although dual antiplatelet therapy is the standard of care in non-ST-segment elevation acute coronary syndromes (NSTEACS), it remains unclear when a second antiplatelet agent should be initiated. We sought to assess the safety and efficacy of pretreatment with clopidogrel in patients wi...

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Main Authors: Yudi, M., Eccleston, D., Andrianpoulos, N., Farouque, O., Duffy, S., Brennan, A., Reid, Christopher, Clark, D., Ajani, A.
Format: Journal Article
Published: Blackwell Publishing 2015
Online Access:http://hdl.handle.net/20.500.11937/47581
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author Yudi, M.
Eccleston, D.
Andrianpoulos, N.
Farouque, O.
Duffy, S.
Brennan, A.
Reid, Christopher
Clark, D.
Ajani, A.
author_facet Yudi, M.
Eccleston, D.
Andrianpoulos, N.
Farouque, O.
Duffy, S.
Brennan, A.
Reid, Christopher
Clark, D.
Ajani, A.
author_sort Yudi, M.
building Curtin Institutional Repository
collection Online Access
description Background - Although dual antiplatelet therapy is the standard of care in non-ST-segment elevation acute coronary syndromes (NSTEACS), it remains unclear when a second antiplatelet agent should be initiated. We sought to assess the safety and efficacy of pretreatment with clopidogrel in patients with NSTEACS undergoing percutaneous coronary intervention (PCI). Methods - We analyzed baseline clinical and procedural characteristics of 6,817 patients with NSTEACS who underwent PCI from the Melbourne Interventional Group registry from 2005-2012. Patients were included in the pretreatment group if clopidogrel was administered prior to cardiac catheterisation. We assessed 30-day mortality, myocardial infarction (MI) and major adverse cardiovascular events (MACE). The safety endpoint was in-hospital bleeding. Results - Of the 6,817 patients, only 2,951 (43%) received pretreatment with clopidogrel. Patients in the pretreatment group were more likely to present with unstable angina (70.8% vs. 68.2%, p=0.02) and have a history of myocardial infarction (35.6% vs. 23.6%, p < 0.01) but were less likely to have PCI within 24 hours of admission (17.2% vs. 25.2%, p <0.01). There was no difference between the groups in 30-day mortality (0.9% vs. 1.4%, p=0.06), MI (2.0% vs. 2.2%, p=0.52) or MACE (3.7% vs. 4.2%, p=0.25). There was no difference in bleeding complications (1.9% vs. 1.9%, p=0.94). Conclusions - Pretreatment with dual antiplatelet therapy in NSTEACS is not routine clinical practice in Australia. Pretreatment appears safe but is not associated with improved short-term clinical outcomes.
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spelling curtin-20.500.11937-475812017-09-13T14:10:55Z Pretreatment with Dual Antiplatelet Therapy in Patients with Non-ST-Segment Elevation Acute Coronary Syndromes undergoing Percutaneous Coronary Intervention Yudi, M. Eccleston, D. Andrianpoulos, N. Farouque, O. Duffy, S. Brennan, A. Reid, Christopher Clark, D. Ajani, A. Background - Although dual antiplatelet therapy is the standard of care in non-ST-segment elevation acute coronary syndromes (NSTEACS), it remains unclear when a second antiplatelet agent should be initiated. We sought to assess the safety and efficacy of pretreatment with clopidogrel in patients with NSTEACS undergoing percutaneous coronary intervention (PCI). Methods - We analyzed baseline clinical and procedural characteristics of 6,817 patients with NSTEACS who underwent PCI from the Melbourne Interventional Group registry from 2005-2012. Patients were included in the pretreatment group if clopidogrel was administered prior to cardiac catheterisation. We assessed 30-day mortality, myocardial infarction (MI) and major adverse cardiovascular events (MACE). The safety endpoint was in-hospital bleeding. Results - Of the 6,817 patients, only 2,951 (43%) received pretreatment with clopidogrel. Patients in the pretreatment group were more likely to present with unstable angina (70.8% vs. 68.2%, p=0.02) and have a history of myocardial infarction (35.6% vs. 23.6%, p < 0.01) but were less likely to have PCI within 24 hours of admission (17.2% vs. 25.2%, p <0.01). There was no difference between the groups in 30-day mortality (0.9% vs. 1.4%, p=0.06), MI (2.0% vs. 2.2%, p=0.52) or MACE (3.7% vs. 4.2%, p=0.25). There was no difference in bleeding complications (1.9% vs. 1.9%, p=0.94). Conclusions - Pretreatment with dual antiplatelet therapy in NSTEACS is not routine clinical practice in Australia. Pretreatment appears safe but is not associated with improved short-term clinical outcomes. 2015 Journal Article http://hdl.handle.net/20.500.11937/47581 10.1111/imj.12818 Blackwell Publishing restricted
spellingShingle Yudi, M.
Eccleston, D.
Andrianpoulos, N.
Farouque, O.
Duffy, S.
Brennan, A.
Reid, Christopher
Clark, D.
Ajani, A.
Pretreatment with Dual Antiplatelet Therapy in Patients with Non-ST-Segment Elevation Acute Coronary Syndromes undergoing Percutaneous Coronary Intervention
title Pretreatment with Dual Antiplatelet Therapy in Patients with Non-ST-Segment Elevation Acute Coronary Syndromes undergoing Percutaneous Coronary Intervention
title_full Pretreatment with Dual Antiplatelet Therapy in Patients with Non-ST-Segment Elevation Acute Coronary Syndromes undergoing Percutaneous Coronary Intervention
title_fullStr Pretreatment with Dual Antiplatelet Therapy in Patients with Non-ST-Segment Elevation Acute Coronary Syndromes undergoing Percutaneous Coronary Intervention
title_full_unstemmed Pretreatment with Dual Antiplatelet Therapy in Patients with Non-ST-Segment Elevation Acute Coronary Syndromes undergoing Percutaneous Coronary Intervention
title_short Pretreatment with Dual Antiplatelet Therapy in Patients with Non-ST-Segment Elevation Acute Coronary Syndromes undergoing Percutaneous Coronary Intervention
title_sort pretreatment with dual antiplatelet therapy in patients with non-st-segment elevation acute coronary syndromes undergoing percutaneous coronary intervention
url http://hdl.handle.net/20.500.11937/47581