Cath Lab Digest -
[Cached Version]
Published on: 1/1/2002
Last Visited: 6/30/2005
"We recently reported data from the RAVEL clinical study showing virtually no late loss and zero restenosis in previously untreated, or de novo, lesions six months following placement of the CYPHER Sirolimus-eluting Stent," said Prof. J. Eduardo Sousa, M.D., Ph.D., Co-principal Investigator, and Professor of Interventional Cardiology at Dante Pazzanese Institute of Cardiology, Sao Paulo, Brazil."Now we have evidence this stent may show a similar effect in preventing reblockages in previously stented arteries," he said.According to Dr. Sousa, results from the study indicate extremely low in-stent late loss (0.08 mm in minimum lumen diameter) at four-month follow-up in the 25 ISR patients treated at his hospital center.In-stent late loss is a sensitive and specific measure of the amount of tissue proliferation that can result in reblockage of the vessel.Additionally, the study's results show 0.0% restenosis, 0.0% TLR (target lesion revascularization), no thrombosis, and no deaths.The reference vessel diameter was 2.8 mm, with a mean diameter stenosis of 7.7%.Results were documented using intravenous ultrasound (IVUS) and quantitative coronary angiography evaluated by independent Core Laboratories."We were particularly impressed by the efficacy of the CYPHER Sirolimus-eluting Stent against a wide variety of restenotic lesions," said Dr. Sousa.
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