Literature DB >> 15976780

The early glycoprotein IIb/IIIa inhibition in non-ST-segment elevation acute coronary syndrome (EARLY ACS) trial: a randomized placebo-controlled trial evaluating the clinical benefits of early front-loaded eptifibatide in the treatment of patients with non-ST-segment elevation acute coronary syndrome--study design and rationale.

Robert P Giugliano1, L Kristin Newby, Robert A Harrington, C Michael Gibson, Frans Van de Werf, Paul Armstrong, Gilles Montalescot, James Gilbert, John T Strony, Robert M Califf, Eugene Braunwald.   

Abstract

BACKGROUND: The recent North American and European practice guidelines in patients with non-ST-segment elevation acute coronary syndrome (nSTE ACS) recommend glycoprotein IIb/IIIa (GpIIb-IIIa) inhibition in patients undergoing an early invasive treatment strategy. However, the guidelines are not explicit regarding the timing of initiation of GpIIb-IIIa antagonists, and there is marked variation in clinical practice regarding their use. STUDY
DESIGN: The EARLY ACS trial will enroll 10,500 patients in a prospective, randomized, double blind, international, multicenter investigation of early eptifibatide compared with placebo (with provisional eptifibatide in the catheterization laboratory) in patients with high-risk nSTE ACS in whom an invasive strategy is planned no sooner than the next calendar day. The primary efficacy end point is the 96-hour composite of all-cause mortality, nonfatal myocardial infarction, recurrent ischemia requiring urgent revascularization, or need for thrombotic bailout with GpIIb-IIIa inhibitor during percutaneous coronary intervention. The key secondary end point is the composite of death or nonfatal myocardial infarction within 30 days of enrollment. IMPLICATIONS: The EARLY ACS trial will be the largest study to date to evaluate the utility of early GpIIb-IIIa inhibition in patients with nSTE ACS in whom an invasive approach is planned. This trial will provide important evidence regarding the benefit of initiating eptifibatide early after presentation with high-risk ACS versus delayed provisional use after coronary angiography. Furthermore, it will explore the ability of biomarkers to identify high-risk patients who may benefit from such an early aggressive approach.

Entities:  

Mesh:

Substances:

Year:  2005        PMID: 15976780     DOI: 10.1016/j.ahj.2005.03.029

Source DB:  PubMed          Journal:  Am Heart J        ISSN: 0002-8703            Impact factor:   4.749


  6 in total

Review 1.  Non ST segment elevation acute coronary syndromes: A simplified risk-orientated algorithm.

Authors:  David H Fitchett; Bjug Borgundvaag; Warren Cantor; Eric Cohen; Sanjay Dhingra; Stephen Fremes; Milan Gupta; Michael Heffernan; Heather Kertland; Mansoor Husain; Anatoly Langer; Eric Letovsky; Shaun G Goodman
Journal:  Can J Cardiol       Date:  2006-06       Impact factor: 5.223

2.  Effects of platelet glycoprotein IIb/IIIa receptor blockers in non-ST segment elevation acute coronary syndromes: benefit and harm in different age subgroups.

Authors:  Adrián V Hernández; Cynthia M Westerhout; Ewout W Steyerberg; John P A Ioannidis; Héctor Bueno; Harvey White; Pierre Theroux; David J Moliterno; Paul W Armstrong; Robert M Califf; Lars C Wallentin; Maarten L Simoons; Eric Boersma
Journal:  Heart       Date:  2006-10-25       Impact factor: 5.994

Review 3.  Eptifibatide: a review of its use in patients with acute coronary syndromes and/or undergoing percutaneous coronary intervention.

Authors:  Monique P Curran; Gillian M Keating
Journal:  Drugs       Date:  2005       Impact factor: 9.546

4.  Routine upstream versus selective down stream use of tirofiban in non-ST elevation myocardial infarction patients scheduled for early invasive therapy; a randomized comparison.

Authors:  Saman Rasoul; Jan Paul Ottervanger; Menko Jan de Boer; Jan Henk E Dambrink; Harry Suryapranata; Jan C A Hoorntje; A T Marcel Gosselink; Arnoud W J van 't Hof
Journal:  J Thromb Thrombolysis       Date:  2007-03-02       Impact factor: 2.300

Review 5.  Antiplatelet agents for chronic kidney disease.

Authors:  Patrizia Natale; Suetonia C Palmer; Valeria M Saglimbene; Marinella Ruospo; Mona Razavian; Jonathan C Craig; Meg J Jardine; Angela C Webster; Giovanni Fm Strippoli
Journal:  Cochrane Database Syst Rev       Date:  2022-02-28

6.  Stroke Outcomes With Vorapaxar Versus Placebo in Patients With Acute Coronary Syndromes: Insights From the TRACER Trial.

Authors:  Leo Ungar; Robert M Clare; Fatima Rodriguez; Bradley J Kolls; Paul W Armstrong; Philip Aylward; Claes Held; David J Moliterno; John Strony; Frans Van de Werf; Lars Wallentin; Harvey D White; Pierluigi Tricoci; Robert A Harrington; Kenneth W Mahaffey; Chiara Melloni
Journal:  J Am Heart Assoc       Date:  2018-12-18       Impact factor: 5.501

  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.