The TRAPIST Study - A multicentre randomized placebo controlled clinical trial of trapidil for prevention of restenosis after coronary stenting, measured by 3-D intravascular ultrasound

被引:34
作者
Serruys, PW
Foley, DP
Pieper, M
Kleijne, JA
de Feyter, PJ
机构
[1] Erasmus Med Ctr, Thoraxctr, Dept Intervent Cardiol, NL-3015 GD Rotterdam, Netherlands
[2] Cardialysis, Rotterdam, Netherlands
[3] Heartctr Bodensee, Kreuzlingen, Switzerland
关键词
restenosis; stent; trapidil; intravascular ultrasound; quantitative coronary angiography; randomized trial;
D O I
10.1053/euhj.2001.2627
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background Studies have reported benefit of oral therapy with the phosphodiesterase inhibitor. trapidil, in reducing restenosis after coronary angioplasty, Coronary stenting is associated with improved late outcome compared with balloon angioplasty, but significant neointimal hyperplasia still occurs in a considerable proportion of patients. The aim of this study was to investigate the safety and efficacy of trapidil 200 mg in preventing in-stent restenosis. Methods Patients with a single native coronary lesion requiring revascularization were randomized to placebo or trapidil at least 1 h before, and continuing for 6 months after, successful implantation of a coronary Wallstent. The primary end-point was in-stent neointimal volume measured by three-dimensional reconstruction of intravascular ultrasound images recorded at the 6 month follow-up catheterization. Results Of 312 patients randomized at 21 centres in nine countries, 303 (148 trapidil, 155 placebo) underwent successful Wallstent implantation, and 139 patients (90%) in the placebo group and 130 (88%) in the trapidil group had repeat catheterization at 26 +/- 2 weeks. There was nosignificant difference between trapidil and placebo-treated patients regarding in-stent neointimal volume (108.6 +/- 95.6 mm(3) vs 93.3 +/- 79.1 mm(3): P=0.16) or obstruction volume (38 +/- 18% vs 36 +/- 21%. P=0-32), in angiographic minimal luminal diameter at follow-up (1.63 +/- 0.61 mm vs 1.74 +/- 0.69mm; P=0.17), restenosis rate (31% vs 24%, P=0.24), cumulative incidence of major adverse cardiac events at 7 months (22% vs 20%, P=0.71) or anginal complaints (30%, vs 24%; P=0.29). Conclusion Oral trapidil 600 mg daily for 6 months did not reduce in-stent hyperplasia or improve clinical outcome after successful Wallstent implantation and is not indicated for this purpose. (C) 2001 The European Society of Cardiology.
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页码:1938 / 1947
页数:10
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