(Circulation. 1999;100:1609-1615.)
© 1999 American Heart Association, Inc.
Clinical Investigation and Reports |
From the University of Washington School of Medicine (X.-Q.Z.), Seattle, Wash; Montreal Heart Institute (P.T.), Québec, Canada; and Merck Research Laboratories (S.M.S., F.L.S.), West Point, Pa.
Correspondence to Xue-Qiao Zhao, MD, University of Washington, 1914 N 34th St, Suite 105, Seattle, WA 98103. E-mail xueqiao{at}u.washington.edu
BackgroundThe present study describes the effects of tirofiban, a nonpeptide platelet glycoprotein (GP) IIb/IIIa receptor blocker, on the characteristics of culprit lesions in patients with unstable angina (UA) or nonQ-wave myocardial infarction (NQWMI).
Methods and ResultsOf 1915 patients enrolled in PRISM-PLUS, 1491 had a readable film obtained a median of 65 hours after randomization. A core laboratory examined the culprit lesions for intracoronary thrombus burden (primary end point) and for TIMI flow grade distribution and severity of the obstruction and of underlying coronary artery disease (secondary end points). The combination of tirofiban plus heparin compared with heparin alone significantly reduced the intracoronary thrombus burden of the culprit lesions (OR=0.77, P=0.022), improved the perfusion grade (OR=0.65, P=0.002), and decreased the severity of the obstruction (P=0.037), but it did not influence the severity of the underlying plaque. Persistence of a thrombus in 45% of patients was associated with a 2.4-fold increase in the odds of death at 30 days (P=0.005) and a 2-fold increase in the odds of myocardial infarction (P=0.002).
ConclusionsThe addition of tirofiban to heparin reduced the thrombus burden of the culprit lesion and improved distal perfusion in patients with UA or NQWMI, which supports the clinical benefit observed with the combination treatment.
Key Words: thrombus angiography platelet aggregation inhibitors prognosis
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