Skip to main content
Journal cover image

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.

Publication ,  Journal Article
Giugliano, RP; Newby, LK; Harrington, RA; Gibson, CM; Van de Werf, F; Armstrong, P; Montalescot, G; Gilbert, J; Strony, JT; Califf, RM ...
Published in: Am Heart J
June 2005

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.

Duke Scholars

Published In

Am Heart J

DOI

EISSN

1097-6744

Publication Date

June 2005

Volume

149

Issue

6

Start / End Page

994 / 1002

Location

United States

Related Subject Headings

  • Time Factors
  • Syndrome
  • Research Design
  • Randomized Controlled Trials as Topic
  • Prospective Studies
  • Platelet Glycoprotein GPIIb-IIIa Complex
  • Peptides
  • Myocardial Infarction
  • Multicenter Studies as Topic
  • Middle Aged
 

Citation

APA
Chicago
ICMJE
MLA
NLM
Giugliano, Robert P., L Kristin Newby, Robert A. Harrington, C Michael Gibson, Frans Van de Werf, Paul Armstrong, Gilles Montalescot, et al. “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.Am Heart J 149, no. 6 (June 2005): 994–1002. https://doi.org/10.1016/j.ahj.2005.03.029.
Journal cover image

Published In

Am Heart J

DOI

EISSN

1097-6744

Publication Date

June 2005

Volume

149

Issue

6

Start / End Page

994 / 1002

Location

United States

Related Subject Headings

  • Time Factors
  • Syndrome
  • Research Design
  • Randomized Controlled Trials as Topic
  • Prospective Studies
  • Platelet Glycoprotein GPIIb-IIIa Complex
  • Peptides
  • Myocardial Infarction
  • Multicenter Studies as Topic
  • Middle Aged