Aspirin Plus Clopidogrel Versus Aspirin Alone After Coronary Artery Bypass Grafting

Author:

Kulik Alexander1,Le May Michel R.1,Voisine Pierre1,Tardif Jean-Claude1,DeLarochelliere Robert1,Naidoo Sarika1,Wells George A.1,Mesana Thierry G.1,Ruel Marc1

Affiliation:

1. From the Lynn Heart and Vascular Institute (A.K.), Boca Raton Regional Hospital, Boca Raton, Fla; the Divisions of Cardiac Surgery and Cardiology (A.K., M.R.L.M., S.N., T.G.M., M.R.), University of Ottawa Heart Institute, Ottawa, Ontario, Canada; the Departments of Cardiac Surgery and Cardiology (P.V., R.D.), Hôpital Laval, Quebec City, Quebec, Canada; the Department of Medicine (J.-C.T.), Montreal Heart Institute, Université de Montréal, Quebec, Canada; and the Department of Epidemiology and...

Abstract

Background— Clopidogrel inhibits intimal hyperplasia in animal studies and therefore may reduce saphenous vein graft (SVG) intimal hyperplasia after coronary artery bypass grafting. The Clopidogrel After Surgery for Coronary Artery DiseasE (CASCADE) study was undertaken to evaluate whether the addition of clopidogrel to aspirin inhibits SVG disease after coronary artery bypass grafting, as assessed at 1 year by intravascular ultrasound. Methods and Results— In this double-blind phase II trial, 113 patients undergoing coronary artery bypass grafting with SVGs were randomized to receive aspirin 162 mg plus clopidogrel 75 mg daily or aspirin 162 mg plus placebo daily for 1 year. The primary outcome was SVG intimal hyperplasia (mean intimal area) as determined by intravascular ultrasound at 1 year. Secondary outcomes were graft patency, major adverse cardiovascular events, and major bleeding. One-year intravascular ultrasound and coronary angiography were performed in 92 patients (81.4%). At 1 year, SVG intimal area did not differ significantly between the 2 groups (4.1±2.0 versus 4.5±2.1 mm 2 , aspirin-clopidogrel versus aspirin-placebo, P =0.44). Overall 1-year graft patency was 95.2% in the aspirin-clopidogrel group compared with 95.5% in the aspirin-placebo group ( P =0.90), and SVG patency was 94.3% in the aspirin-clopidogrel group versus 93.2% in the aspirin-placebo group ( P =0.69). Freedom from major adverse cardiovascular events at 1 year was 92.9±3.4% in the aspirin-clopidogrel group and 91.1±3.8% in the aspirin-placebo group ( P =0.76). The incidence of major bleeding at 1 year was similar for the 2 groups (1.8% versus 0%, aspirin-clopidogrel versus aspirin-placebo, P =0.50). Conclusions— Compared with aspirin monotherapy, the combination of aspirin plus clopidogrel did not significantly reduce the process of SVG intimal hyperplasia 1 year after coronary artery bypass grafting. Clinical Trial Registration— URL: http://www.clinicaltrials.gov . Unique identifier: NCT00228423.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Physiology (medical),Cardiology and Cardiovascular Medicine

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