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(Circulation. 2006;114:1736-1744.)
© 2006 American Heart Association, Inc.
Controversies in Cardiovascular Medicine |
From the Division of Cardiology, Beth Israel Deaconess Medical Center, Boston, Mass (J.R.), and Saint Lukes Mid America Heart Institute, Kansas City, Mo (D.J.C.).
Correspondence to David J. Cohen, MD, MSc, Cardiovascular Research, Saint Lukes Mid America Heart Institute, 4401 Wornall Rd, Kansas City, MO 64111. E-mail dcohen@saint-lukes.org
An extract of the first 250 words of the full text is provided, because this article has no abstract. |
| Introduction |
|---|
15% to 20% of patients treated with BMS required
1 repeat revascularization procedure within the 6 to 12 months after stent implantation.1 Despite numerous attempts at systemic pharmacotherapy, device modification, and even use of ionizing radiation, the rate of restenosis after BMS implantation remained largely unaffected.
Response by Eisenberg p 1744
Over the past 5 years, effective DES have become the first device to substantially reduce the incidence of restenosis after stent implantation. By delivering high concentrations of either antiproliferative or immunomodulatory compounds directly to the site of arterial injury and by controlling this delivery through polymer-based drug release, both sirolimus- and paclitaxel-eluting stents have safely and effectively inhibited the proliferative process that results in in-stent restenosis. In pivotal clinical trials, both sirolimus- and paclitaxel-eluting stents have reduced rates of angiographic restenosis by 70% to 90% compared with conventional BMS designs, with parallel reductions in the need for clinically driven target vessel revascularization (TVR).24 As a result, in April 2003, DES were approved for use in clinical practice in the United States. Within 9 months of their introduction, DES made
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