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on November 2, 2009

Circulation. 2009
Published online before print November 2, 2009, doi: 10.1161/CIRCULATIONAHA.109.874057
A more recent version of this article appeared on November 17, 2009
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Submitted on April 19, 2009
Accepted on August 19, 2009

Comparison of Plaque Sealing With Paclitaxel-Eluting Stents Versus Medical Therapy for the Treatment of Moderate Nonsignificant Saphenous Vein Graft Lesions. The Moderate VEin Graft LEsion Stenting With the Taxus Stent and Intravascular Ultrasound (VELETI) Pilot Trial

Josep Rodés-Cabau MD, FESC*, Olivier F. Bertrand MD, PhD, Eric Larose MD, Jean-Pierre Déry MD, Stéphane Rinfret MD, Rodrigo Bagur MD, Guy Proulx MD, Can M. Nguyen MD, Mélanie Côté MSc, Marie-Claude Landcop RN, Jean-Rock Boudreault MD, Jacques Rouleau MD, Louis Roy MD, Onil Gleeton MD, Gérald Barbeau MD, Bernard Noël MD, Javier Courtis MD, Gilles R. Dagenais MD, Jean-Pierre Després PhD, and Robert DeLarochellière MD

From the Institut Universitaire de Cardiologie et de Pneumologie de Québec, Québec, Québec, Canada.

* To whom correspondence should be addressed. E-mail: josep.rodes{at}criucpq.ulaval.ca.

Background—The presence of moderate saphenous vein graft (SVG) lesions is a major predictor of cardiac events late after coronary artery bypass grafting. We determined the effects of sealing moderate nonsignificant SVG lesions with paclitaxel-eluting stents (PES) on the prevention of SVG atherosclerosis progression.

Methods and Results—Patients with at least 1 moderate SVG lesion (30% to 60% diameter stenosis) were randomized either to stenting the moderate SVG lesion with a PES (n=30, PES group) or to medical treatment alone (n=27, medical treatment group). Patients had an angiographic and intravascular ultrasound evaluation of the SVG at baseline and at 12-month follow-up. The primary end points were (1) the ultrasound SVG minimal lumen area at follow-up and (2) the changes in ultrasound atheroma volume in an angiographically nondiseased SVG segment. Mean time from coronary artery bypass grafting was 12±6 years, and mean low-density lipoprotein cholesterol level was 73±31 mg/dL. A total of 70 moderate SVG lesions (39±7% diameter stenosis) were evaluated. Significant disease progression occurred in the medical treatment group at the level of the moderate SVG lesion (decrease in minimal lumen area from 6.3±3.0 to 5.6±3.1 mm2; P<0.001), leading to a severe flow-limiting lesion or SVG occlusion in 22% of the patients compared with none in the PES group (P=0.014). In the PES group, mean minimal lumen area increased (P<0.001) from 6.1±2.2 to 8.6±2.9 mm2 at follow-up (P=0.001 compared with the medical treatment group at 12 months). There were no cases of restenosis or stent thrombosis. No significant atherosclerosis progression occurred at the nonstented SVG segments. At 12-month follow-up, the cumulative incidence of major adverse cardiac events related to the target SVG was 19% in the medical treatment group versus 3% in the PES group (P=0.091).

Conclusions—Stenting moderate nonsignificant lesions in old SVGs with PES was associated with a lower rate of SVG disease progression and a trend toward a lower incidence of major adverse cardiac events at 1-year follow-up compared with medical treatment alone, despite very low low-density lipoprotein cholesterol values. This pilot study supports further investigation into the role of plaque sealing in SVGs.

Clinical Trial Registration—URL: http://www.clinicaltrials.gov. Unique identifier: NCT002289835.


Key words: atherosclerosis • coronary disease • stents


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S. A. Parikh and M. A. Costa
Secondary Prevention, the Interventional Way: Prophylactic Drug-Eluting Stents for Nonobstructive Saphenous Vein Graft Disease
Circulation, November 17, 2009; 120(20): 1940 - 1942.
[Full Text] [PDF]