Effect of pravastatin on angiographic restenosis after coronary balloon angioplasty

被引:116
|
作者
Bertrand, ME
McFadden, EP
Fruchart, JC
VanBelle, E
Commeau, P
Grollier, G
Bassand, JP
Machecourt, J
Cassagnes, J
Mossard, JM
Vacheron, A
Castaigne, A
Danchin, N
Lablanche, JM
机构
[1] CLIN ST MARTIN, CAEN, FRANCE
[2] CHU CAEN, F-14000 CAEN, FRANCE
[3] CHU BESANCON, F-25030 BESANCON, FRANCE
[4] CHU GRENOBLE, F-38043 GRENOBLE, FRANCE
[5] CHU CLERMONT FERRAND, CLERMONT FERRAND, FRANCE
[6] CHU STRASBOURG, F-67000 STRASBOURG, FRANCE
[7] CHU NECKER, NECKER, PARIS, FRANCE
[8] CHU CRETEIL, CRETEIL, FRANCE
[9] CHU NANCY, NANCY, FRANCE
关键词
D O I
10.1016/S0735-1097(97)00259-3
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objectives. This study sought to determine whether pravastatin affects clinical or angiographic restenosis after coronary balloon angioplasty. Background. Experimental data and preliminary clinical studies suggest that lipid-lowering drugs might have a beneficial effect on restenosis after coronary angioplasty. Methods. In a multicenter, randomized, double blind trial, 695 patients were randomized to receive pravastatin (40 mg/day) or placebo for 6 months after successful balloon angioplasty. All patients received aspirin (100 mg/day). The primary angiographic end point was minimal lumen diameter (MLD) at follow-up, assessed by quantitative coronary angiography. A sample size of 313 patients per group was required to demonstrate a difference of 0.13 mm in MLD between groups (allowing for a two-failed alpha error of 0.05 and a beta error of 0.20). To allow for incomplete angiographic follow-up (estimated lost to follow up rate of 10%), 690 randomized patients were required. Secondary end points were angiographic restenosis rate (restenosis assessed as a categoric variable, >50% stenosis) and clinical events (death, myocardial infarction, target vessel revascularization). Results. At baseline, clinical, demographic, angiographic and lipid variables did not differ significantly between groups. In patients treated with pravastatin, there was a significant reduction in total and low density lipoprotein cholesterol and triglyceride levels and a significant increase in high density lipoprotein cholesterol levels. At follow-up the MLD (mean +/- SD) was 1.47 +/- 0.62 mm in the placebo group and 1.54 +/- 0.66 mm in the pravastatin group (p = 0.21). Similarly, late loss and net gain did not differ significantly between groups. The restenosis rate (recurrence >50% stenosis) was 43.8% in the placebo group and 39.2% in the pravastatin group (p = 0.26). Clinical restenosis did not differ significantly between groups. Conclusions. Although pravastatin has documented efficacy in reducing clinical events anti angiographic disease progression in patients with coronary atherosclerosis, this study shows that it has no effect on angiographic outcome at the target site 6 months after coronary angioplasty. (C) 1997 by the American College of Cardiology.
引用
收藏
页码:863 / 869
页数:7
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