Long Lesion Study Demonstrates Supera Stent Efficacy in SFA and Popliteal Arteries


June 3, 2011

June 3, 2011 - IDEV Technologies announced that data from a long lesion study of 182 patients with significantly diseased superficial femoral arteries and popliteal arteries showed high patency rates and no stent fractures after treatment with the Supera Veritas Peripheral Vascular Stent System. The data were presented at the Vaatdagen 2011 (Vascular Days) Conference based on analysis by Andre Molenaar, M.D., and Peter Haarbrink, M.D., interventional radiologists at Canisius-Wilhelmina Ziekenhuis (CWZ) hospital, a leading teaching and high volume medical center in Nijmegen, The Netherlands.

The patients were treated and followed over a two-year period, and represented an extremely challenging patient cohort with highly calcified and long lesions in the superficial femoral artery (SFA) which at times encompassed the proximal popliteal artery and/or popliteal artery alone. The results were achieved in vessels with significant disease and atypical extremely long lesion lengths with no Plavix used.

The SFA plus proximal popliteal treated artery cohort consisted of 159 patients, with an average lesion length of 240 mm, 40 percent Tasc D classification, and 57 percent total occlusions with an average of nearly two stents per patient. A high patency rate of 74 percent was achieved at 12 months as measured by duplex ultrasound (DU). A group of 23 patients were treated with a Supera stent in the popliteal artery, with an average stent length of 142 mm and a patency rate of 83 percent at 12 months, again measured by DU. A subgroup analysis by X-ray at 24 months showed no stent fractures. These data compare favorably to standard nitinol stent performance in patients with significantly shorter lesions.

"These are outstanding and noteworthy results which demonstrate that Supera is a market-changing technology when used appropriately," stated Molenaar. "The average stent length deployed was 240 mm, ranging from 40 to 550 mm. Compared with other stent trials, and even the Leipzig Supera registry, these are much longer lesions with significant disease," added Haarbrink.

Molenaar added that no concomitant treatment occurred with antiplatelet medication. "Patients received aspirin post procedure but none of these patients received Plavix following their stent procedures. We can assume the results would have had an even more dramatic improvement from baseline had we supplemented our procedure with this treatment. It is also clear to us that we utilize Supera for the most challenging cases, constantly testing the device and still receive exceptional results. We look forward to continuing our analysis of Supera.

For more information: www.idevmd.com