Pretreatment with dual antiplatelet therapy in patients with ST-elevation myocardial infarction.

BACKGROUND: The optimal time to administer P2Y12 inhibitors in patients with ST-elevation myocardial infarction (STEMI) remains to be defined. We sought to assess whether a pretreatment strategy was associated with improved coronary reperfusion and clinical outcomes. METHODS: Consecutive patients fr...

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Main Authors: Yudi, M., Farouque, O., Andrianopoulos, N., Ajani, A., Brennan, A., Lefkovits, J., Reid, Christopher, Chan, W., Duffy, S., Clark, D., Melbourne Interventional Group.
Format: Journal Article
Published: 2017
Online Access:http://hdl.handle.net/20.500.11937/57317
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author Yudi, M.
Farouque, O.
Andrianopoulos, N.
Ajani, A.
Brennan, A.
Lefkovits, J.
Reid, Christopher
Chan, W.
Duffy, S.
Clark, D.
Melbourne Interventional Group.
author_facet Yudi, M.
Farouque, O.
Andrianopoulos, N.
Ajani, A.
Brennan, A.
Lefkovits, J.
Reid, Christopher
Chan, W.
Duffy, S.
Clark, D.
Melbourne Interventional Group.
author_sort Yudi, M.
building Curtin Institutional Repository
collection Online Access
description BACKGROUND: The optimal time to administer P2Y12 inhibitors in patients with ST-elevation myocardial infarction (STEMI) remains to be defined. We sought to assess whether a pretreatment strategy was associated with improved coronary reperfusion and clinical outcomes. METHODS: Consecutive patients from the Melbourne Interventional Group registry (2005-2014) who presented with STEMI and underwent primary PCI were included. Those who received any P2Y12 inhibitor prior to arrival in the cardiac catheterisation laboratory were included in the pretreatment group. The primary endpoints were the proportion of patients with initial TIMI flow grade <3 and in-hospital bleeding. The secondary endpoints were 12-month mortality and major adverse cardiovascular events (MACE). RESULTS: Of the 2,807 patients included, 892(31.8%) received pretreatment. Clopidogrel was the most common P2Y12 inhibitor used (79.6%). Pretreatment was associated with less thromboaspiration and GPIIb/IIIa inhibitor use (both P?<?0.01). Pretreatment was not associated with lower rates of TIMI flow <3 on initial angiogram (78.0% vs. 80.7%, P?=?0.18) nor with increased in-hospital bleeding (3.6% vs. 3.9%, P?=?0.67). Pretreatment was associated with lower 12-month mortality (4.7% vs. 7.0%, P?=?0.02) but similar MACE rate (13.0% vs. 14.1%, P?=?0.43). Multivariate analysis revealed pretreatment was not an independent predictor of 12-month mortality (OR 0.79; 95% CI 0.5-1.3, P?=?0.32). CONCLUSION: Pretreatment with a P2Y12 inhibitor in patients with STEMI was not routine practice in our Australian cohort and was not associated with improved coronary reperfusion or clinical outcomes. Larger studies are required to definitively ascertain the risk/benefit ratio of dual antiplatelet therapy pretreatment in STEMI.
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spelling curtin-20.500.11937-573172017-10-30T08:35:13Z Pretreatment with dual antiplatelet therapy in patients with ST-elevation myocardial infarction. Yudi, M. Farouque, O. Andrianopoulos, N. Ajani, A. Brennan, A. Lefkovits, J. Reid, Christopher Chan, W. Duffy, S. Clark, D. Melbourne Interventional Group. BACKGROUND: The optimal time to administer P2Y12 inhibitors in patients with ST-elevation myocardial infarction (STEMI) remains to be defined. We sought to assess whether a pretreatment strategy was associated with improved coronary reperfusion and clinical outcomes. METHODS: Consecutive patients from the Melbourne Interventional Group registry (2005-2014) who presented with STEMI and underwent primary PCI were included. Those who received any P2Y12 inhibitor prior to arrival in the cardiac catheterisation laboratory were included in the pretreatment group. The primary endpoints were the proportion of patients with initial TIMI flow grade <3 and in-hospital bleeding. The secondary endpoints were 12-month mortality and major adverse cardiovascular events (MACE). RESULTS: Of the 2,807 patients included, 892(31.8%) received pretreatment. Clopidogrel was the most common P2Y12 inhibitor used (79.6%). Pretreatment was associated with less thromboaspiration and GPIIb/IIIa inhibitor use (both P?<?0.01). Pretreatment was not associated with lower rates of TIMI flow <3 on initial angiogram (78.0% vs. 80.7%, P?=?0.18) nor with increased in-hospital bleeding (3.6% vs. 3.9%, P?=?0.67). Pretreatment was associated with lower 12-month mortality (4.7% vs. 7.0%, P?=?0.02) but similar MACE rate (13.0% vs. 14.1%, P?=?0.43). Multivariate analysis revealed pretreatment was not an independent predictor of 12-month mortality (OR 0.79; 95% CI 0.5-1.3, P?=?0.32). CONCLUSION: Pretreatment with a P2Y12 inhibitor in patients with STEMI was not routine practice in our Australian cohort and was not associated with improved coronary reperfusion or clinical outcomes. Larger studies are required to definitively ascertain the risk/benefit ratio of dual antiplatelet therapy pretreatment in STEMI. 2017 Journal Article http://hdl.handle.net/20.500.11937/57317 10.1002/ccd.27325 restricted
spellingShingle Yudi, M.
Farouque, O.
Andrianopoulos, N.
Ajani, A.
Brennan, A.
Lefkovits, J.
Reid, Christopher
Chan, W.
Duffy, S.
Clark, D.
Melbourne Interventional Group.
Pretreatment with dual antiplatelet therapy in patients with ST-elevation myocardial infarction.
title Pretreatment with dual antiplatelet therapy in patients with ST-elevation myocardial infarction.
title_full Pretreatment with dual antiplatelet therapy in patients with ST-elevation myocardial infarction.
title_fullStr Pretreatment with dual antiplatelet therapy in patients with ST-elevation myocardial infarction.
title_full_unstemmed Pretreatment with dual antiplatelet therapy in patients with ST-elevation myocardial infarction.
title_short Pretreatment with dual antiplatelet therapy in patients with ST-elevation myocardial infarction.
title_sort pretreatment with dual antiplatelet therapy in patients with st-elevation myocardial infarction.
url http://hdl.handle.net/20.500.11937/57317