Impact of time to treatment on the effects of bivalirudin vs. glycoprotein IIb/IIIa inhibitors and heparin in patients undergoing primary percutaneous coronary intervention: insights from the HORIZONS-AMI trial

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Impact of time to treatment on the effects of bivalirudin vs. glycoprotein IIb/IIIa inhibitors and heparin in patients undergoing primary percutaneous coronary intervention: insights from the HORIZONS-AMI trial. / Schoos, Mikkel M; De Luca, Giuseppe; Dangas, George D; Clemmensen, Peter; Ayele, Girma Minalu; Mehran, Roxana; Stone, Gregg W.

In: EUROINTERVENTION, Vol. 12, No. 9, 20.10.2016, p. 1144-1153.

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@article{c6a8b5d04efb43cdbf4a1c8ea9240e17,
title = "Impact of time to treatment on the effects of bivalirudin vs. glycoprotein IIb/IIIa inhibitors and heparin in patients undergoing primary percutaneous coronary intervention: insights from the HORIZONS-AMI trial",
abstract = "AIMS: In the HORIZONS-AMI trial, bivalirudin compared to unfractionated heparin (UFH) plus a glycoprotein IIb/IIIa inhibitor (GPI) improved net clinical outcomes in patients undergoing primary percutaneous coronary intervention (PCI) at the cost of an increased rate of acute stent thrombosis. We sought to examine whether these effects are dependent on time to treatment.METHODS AND RESULTS: The interaction between anticoagulation regimen and symptom onset to first balloon inflation time (SBT) on the 30-day and three-year rates of major adverse cardiac events (MACE) was examined in 3,199 randomised patients according to SBT ≤3 hours versus >3 hours. Among patients with an SBT ≤3 hours, bivalirudin resulted in higher 30-day rates of MACE compared to UFH plus a GPI. Non-significant differences were observed in patients with an SBT >3 hours. Similar results were found for MACE at three years and stent thrombosis and reinfarction at 30 days and three years. By multivariable analysis, bivalirudin was an independent predictor of MACE at 30 days and three years in patients with an SBT ≤3 hours, but not in patients with SBT >3 hours.CONCLUSIONS: Bivalirudin compared to UFH plus a GPI is associated with an increased rate of stent thrombosis and MACE in patients with short SBTs, but not in those with longer SBTs.",
keywords = "Aged, Anticoagulants/therapeutic use, Antithrombins/therapeutic use, Cause of Death, Drug Therapy, Combination, Female, Graft Occlusion, Vascular/epidemiology, Heparin/therapeutic use, Hirudins, Humans, Male, Middle Aged, Mortality, Myocardial Infarction/epidemiology, Myocardial Revascularization/statistics & numerical data, Peptide Fragments/therapeutic use, Percutaneous Coronary Intervention/methods, Platelet Glycoprotein GPIIb-IIIa Complex/antagonists & inhibitors, Postoperative Complications/epidemiology, Recombinant Proteins/therapeutic use, Recurrence, ST Elevation Myocardial Infarction/therapy, Stroke/epidemiology, Thrombosis/epidemiology, Time-to-Treatment/statistics & numerical data, Treatment Outcome",
author = "Schoos, {Mikkel M} and {De Luca}, Giuseppe and Dangas, {George D} and Peter Clemmensen and Ayele, {Girma Minalu} and Roxana Mehran and Stone, {Gregg W}",
year = "2016",
month = oct,
day = "20",
doi = "10.4244/EIJV12I9A186",
language = "English",
volume = "12",
pages = "1144--1153",
journal = "EUROINTERVENTION",
issn = "1774-024X",
publisher = "EUROPA EDITION",
number = "9",

}

RIS

TY - JOUR

T1 - Impact of time to treatment on the effects of bivalirudin vs. glycoprotein IIb/IIIa inhibitors and heparin in patients undergoing primary percutaneous coronary intervention: insights from the HORIZONS-AMI trial

AU - Schoos, Mikkel M

AU - De Luca, Giuseppe

AU - Dangas, George D

AU - Clemmensen, Peter

AU - Ayele, Girma Minalu

AU - Mehran, Roxana

AU - Stone, Gregg W

PY - 2016/10/20

Y1 - 2016/10/20

N2 - AIMS: In the HORIZONS-AMI trial, bivalirudin compared to unfractionated heparin (UFH) plus a glycoprotein IIb/IIIa inhibitor (GPI) improved net clinical outcomes in patients undergoing primary percutaneous coronary intervention (PCI) at the cost of an increased rate of acute stent thrombosis. We sought to examine whether these effects are dependent on time to treatment.METHODS AND RESULTS: The interaction between anticoagulation regimen and symptom onset to first balloon inflation time (SBT) on the 30-day and three-year rates of major adverse cardiac events (MACE) was examined in 3,199 randomised patients according to SBT ≤3 hours versus >3 hours. Among patients with an SBT ≤3 hours, bivalirudin resulted in higher 30-day rates of MACE compared to UFH plus a GPI. Non-significant differences were observed in patients with an SBT >3 hours. Similar results were found for MACE at three years and stent thrombosis and reinfarction at 30 days and three years. By multivariable analysis, bivalirudin was an independent predictor of MACE at 30 days and three years in patients with an SBT ≤3 hours, but not in patients with SBT >3 hours.CONCLUSIONS: Bivalirudin compared to UFH plus a GPI is associated with an increased rate of stent thrombosis and MACE in patients with short SBTs, but not in those with longer SBTs.

AB - AIMS: In the HORIZONS-AMI trial, bivalirudin compared to unfractionated heparin (UFH) plus a glycoprotein IIb/IIIa inhibitor (GPI) improved net clinical outcomes in patients undergoing primary percutaneous coronary intervention (PCI) at the cost of an increased rate of acute stent thrombosis. We sought to examine whether these effects are dependent on time to treatment.METHODS AND RESULTS: The interaction between anticoagulation regimen and symptom onset to first balloon inflation time (SBT) on the 30-day and three-year rates of major adverse cardiac events (MACE) was examined in 3,199 randomised patients according to SBT ≤3 hours versus >3 hours. Among patients with an SBT ≤3 hours, bivalirudin resulted in higher 30-day rates of MACE compared to UFH plus a GPI. Non-significant differences were observed in patients with an SBT >3 hours. Similar results were found for MACE at three years and stent thrombosis and reinfarction at 30 days and three years. By multivariable analysis, bivalirudin was an independent predictor of MACE at 30 days and three years in patients with an SBT ≤3 hours, but not in patients with SBT >3 hours.CONCLUSIONS: Bivalirudin compared to UFH plus a GPI is associated with an increased rate of stent thrombosis and MACE in patients with short SBTs, but not in those with longer SBTs.

KW - Aged

KW - Anticoagulants/therapeutic use

KW - Antithrombins/therapeutic use

KW - Cause of Death

KW - Drug Therapy, Combination

KW - Female

KW - Graft Occlusion, Vascular/epidemiology

KW - Heparin/therapeutic use

KW - Hirudins

KW - Humans

KW - Male

KW - Middle Aged

KW - Mortality

KW - Myocardial Infarction/epidemiology

KW - Myocardial Revascularization/statistics & numerical data

KW - Peptide Fragments/therapeutic use

KW - Percutaneous Coronary Intervention/methods

KW - Platelet Glycoprotein GPIIb-IIIa Complex/antagonists & inhibitors

KW - Postoperative Complications/epidemiology

KW - Recombinant Proteins/therapeutic use

KW - Recurrence

KW - ST Elevation Myocardial Infarction/therapy

KW - Stroke/epidemiology

KW - Thrombosis/epidemiology

KW - Time-to-Treatment/statistics & numerical data

KW - Treatment Outcome

U2 - 10.4244/EIJV12I9A186

DO - 10.4244/EIJV12I9A186

M3 - SCORING: Journal article

C2 - 27753600

VL - 12

SP - 1144

EP - 1153

JO - EUROINTERVENTION

JF - EUROINTERVENTION

SN - 1774-024X

IS - 9

ER -