Comparison of Ticagrelor Versus Prasugrel to Prevent Periprocedural Myonecrosis in Acute Coronary Syndromes

Guidelines recommend a ticagrelor loading dose (LD) before PCI or a prasugrel LD at the time of percutaneous coronary intervention (PCI) in intermediate and high-risk non–ST-elevation acute coronary syndrome (NSTE-ACS). However, achieving an optimal PR inhibition at the time of PCI is critical to pr...

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Veröffentlicht in:The American journal of cardiology 2015-08, Vol.116 (3), p.339-343
Hauptverfasser: Bonello, Laurent, MD, PhD, Laine, Marc, MD, Cluzel, Marion, MD, Frere, Corinne, MD, PhD, Mancini, Julien, MD, PhD, Hasan, Aurasse, MD, Thuny, Franck, MD, PhD, Gaubert, Mélanie, MD, Guieu, Régis, MD, PhD, Dignat-George, Françoise, PhD, Michelet, Pierre, MD, PhD, Paganelli, Franck, MD, PhD, Kerbaul, François, MD, PhD
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container_end_page 343
container_issue 3
container_start_page 339
container_title The American journal of cardiology
container_volume 116
creator Bonello, Laurent, MD, PhD
Laine, Marc, MD
Cluzel, Marion, MD
Frere, Corinne, MD, PhD
Mancini, Julien, MD, PhD
Hasan, Aurasse, MD
Thuny, Franck, MD, PhD
Gaubert, Mélanie, MD
Guieu, Régis, MD, PhD
Dignat-George, Françoise, PhD
Michelet, Pierre, MD, PhD
Paganelli, Franck, MD, PhD
Kerbaul, François, MD, PhD
description Guidelines recommend a ticagrelor loading dose (LD) before PCI or a prasugrel LD at the time of percutaneous coronary intervention (PCI) in intermediate and high-risk non–ST-elevation acute coronary syndrome (NSTE-ACS). However, achieving an optimal PR inhibition at the time of PCI is critical to prevent adverse events and depends on the timing of LD intake in relation to PCI. We aimed to compare the rate of myonecrosis related to PCI in patients with NSTE-ACS receiving ticagrelor pretreatment versus prasugrel at the time of intervention. We prospectively randomized 213 patients with NSTE-ACS to a 180 mg of ticagrelor LD given as soon as possible after admission and before PCI or to a 60 mg LD of prasugrel given at the time of PCI. The primary end point was the rate of periprocedural myonecrosis as defined by an increase of >5 times the ninety-ninth percentiles in troponin-negative patients or a 20% increase in troponin-positive patients. The 2 groups were similar regarding baseline characteristics including clinical setting (p = 0.2). Procedural characteristics were also identical including the number of treated vessels and stenting procedures. Patients in the prasugrel group more often required emergent PCI (p = 0.001). Patients in the ticagrelor group had less periprocedural myonecrosis compared with those in the prasugrel group (19.8% vs 38.3%; p = 0.03). The rate of major adverse cardiovascular events and Bleeding Academic Research Consortium ≥2 at 1-month follow-up was low and similar between the 2 groups. In conclusion, a ticagrelor LD as soon as possible before PCI is superior to prasugrel at the time of PCI to prevent periprocedural myonecrosis in NSTE-ACS.
doi_str_mv 10.1016/j.amjcard.2015.04.050
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However, achieving an optimal PR inhibition at the time of PCI is critical to prevent adverse events and depends on the timing of LD intake in relation to PCI. We aimed to compare the rate of myonecrosis related to PCI in patients with NSTE-ACS receiving ticagrelor pretreatment versus prasugrel at the time of intervention. We prospectively randomized 213 patients with NSTE-ACS to a 180 mg of ticagrelor LD given as soon as possible after admission and before PCI or to a 60 mg LD of prasugrel given at the time of PCI. The primary end point was the rate of periprocedural myonecrosis as defined by an increase of &gt;5 times the ninety-ninth percentiles in troponin-negative patients or a 20% increase in troponin-positive patients. The 2 groups were similar regarding baseline characteristics including clinical setting (p = 0.2). Procedural characteristics were also identical including the number of treated vessels and stenting procedures. Patients in the prasugrel group more often required emergent PCI (p = 0.001). Patients in the ticagrelor group had less periprocedural myonecrosis compared with those in the prasugrel group (19.8% vs 38.3%; p = 0.03). The rate of major adverse cardiovascular events and Bleeding Academic Research Consortium ≥2 at 1-month follow-up was low and similar between the 2 groups. 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Patients in the prasugrel group more often required emergent PCI (p = 0.001). Patients in the ticagrelor group had less periprocedural myonecrosis compared with those in the prasugrel group (19.8% vs 38.3%; p = 0.03). The rate of major adverse cardiovascular events and Bleeding Academic Research Consortium ≥2 at 1-month follow-up was low and similar between the 2 groups. 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identifier ISSN: 0002-9149
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issn 0002-9149
1879-1913
language eng
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source MEDLINE; Elsevier ScienceDirect Journals; ProQuest Central UK/Ireland
subjects Acute Coronary Syndrome - complications
Acute Coronary Syndrome - diagnosis
Acute Coronary Syndrome - drug therapy
Acute coronary syndromes
Adenosine - administration & dosage
Adenosine - analogs & derivatives
Adolescent
Adult
Aged
Cardiology
Cardiovascular
Consortia
Dose-Response Relationship, Drug
Drug dosages
Electrocardiography
Female
Follow-Up Studies
Heart attacks
Humans
Male
Middle Aged
Myocardial Infarction - etiology
Myocardial Infarction - prevention & control
Piperazines - administration & dosage
Prasugrel Hydrochloride
Prospective Studies
Purinergic P2Y Receptor Antagonists - administration & dosage
Stroke
Studies
Thiophenes - administration & dosage
Treatment Outcome
Young Adult
title Comparison of Ticagrelor Versus Prasugrel to Prevent Periprocedural Myonecrosis in Acute Coronary Syndromes
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