• Matthew T Roe, Robert H Christenson, E Magnus Ohman, Raymond Bahr, Francis M Fesmire, Alan Storrow, Michael Mollod, W Frank Peacock, Jeffrey A Rosenblatt, Hongqiu Yang, Elizabeth S Fraulo, James W Hoekstra, W Brian Gibler, EARLY Investigators, and Emergency Medicine Cardiac Research and Education Group.
• Duke Clinical Research Institute, Durham, NC 27715, USA. roe00001@mc.duke.edu
• Am. Heart J. 2003 Dec 1; 146 (6): 993-8.

BackgroundThe acute benefits of platelet glycoprotein IIb/IIIa inhibitors for non-ST-segment elevation acute coronary syndromes (NSTE ACS) remain unclear.MethodsIn this pilot trial, 311 patients with NSTE ACS were randomly assigned in the emergency department to double-blinded therapy with eptifibatide or placebo for 12 to 24 hours before crossover to open-label eptifibatide. Serial creatine-kinase MB (CK-MB) and quantitative cardiac troponin T levels were collected during the first 24 hours to assess the impact of early platelet glycoprotein IIb/IIIa blockade on infarct size as measured by cardiac markers.ResultsMedian peak CK-MB (10.3 vs 11.8 ng/mL; P =.71) and peak quantitative cardiac troponin T levels (0.2 vs 0.3 ng/mL; P =.95) were similar between treatment groups, respectively. Median calculated peak CK-MB values (41 vs 40 ng/mL; P =.72) and area under the CK-MB curve measurements (980 vs 764 microg/min/L; P =.68) from curve-fitting analyses that could be performed in 106 of 311 patients were also similar.ConclusionsIn this pilot trial, early administration of eptifibatide in the emergency department did not modulate serologic measurements of infarct size in patients with NSTE ACS.

37 keywords...

hide…