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Randomized Trial of a GPIIb/IIIa Platelet Receptor Blocker in Refractory Unstable Angina

 

作者: Maarten Simoons,   Menko de Boer,   Marcel van den Brand,   Addy van Miltenburg,   Jan Hoorntje,   Guy Heyndrickx,   L. van der Wieken,   David De Bono,   Wolfgang Rutsch,   Thomas Schaible,   Harlan Weisman,   Peter Klootwijk,   Karin Nijssen,   Jeanne Stibbe,   Pim de Feyter,  

 

期刊: Circulation  (OVID Available online 1994)
卷期: Volume 89, issue 2  

页码: 596-603

 

ISSN:0009-7322

 

年代: 1994

 

出版商: OVID

 

关键词: angina;platelets;glycoproteins

 

数据来源: OVID

 

摘要:

BackgroundPatients with unstable angina despite intensive medical therapy, ie, refractory angina, are at high risk for developing thrombotic complications: myocardial infarction or coronary occlusion during percutaneous transluminal coronary angioplasty (PTCA). Chimeric 7E3 (c7E3) Fab is an antibody fragment that blocks the platelet glycoprotein (GP) Ib/IIIa receptor and potently inhibits platelet aggregation.Methods and ResultsTo evaluate whether potent platelet inhibition could reduce these complications, 60 patients with dynamic ST-T changes and recurrent pain despite intensive medical therapy were randomized toc7E3 Fab or placebo. After initial angiography had demonstrated a culprit lesion suitable for PTCA, placebo orc7E3 Fab was administered as 0.25 mg/kg bolus injection followed by 10 μg/min for 18 to 24 hours until 1 hour after completion of second angiography and PTCA. During study drug infusion, ischemia occurred in 9c7E3 Fab and 16 placebo patients (P= .06). During hospital stay, 12 major events occurred in 7 placebo patients (23%), including 1 death, 4 infarcts, and 7 urgent interventions. In thec7E3 Fab group, only 1 event (an infarct) occurred (3%,P= .03). Angiography showed improved TIMI flow in 4 placebo and 6c7E3 Fab patients and worsening of flow in 3 placebo patients but in none of thec7E3 Fab patients. Quantitative analysis showed significant improvement of the lesion in the patients treated with c7E3 Fab, which was not observed in the placebo group, although the difference between the two treatment groups was not significant. Measurement of platelet function and bleeding time demonstrated >90% blockade of GPIIb/IIIa receptors, >90% reduction of ex vivo platelet aggregation to ADP, and a significantly prolonged bleeding time during c7E3 Fab infusion, without excess bleeding.ConclusionsCombined therapy withc7E3 Fab, heparin, and aspirin appears safe. These pilot study results support the concept that effective blockade of the platelet GPIIb/IIIa receptors can reduce myocardial infarction and facilitate PTCA in patients with refractory unstable angina.

 

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