Strut Coverage and Vessel Wall Response to a New-Generation Paclitaxel-Eluting Stent With an Ultrathin Biodegradable Abluminal Polymer Optical Coherence Tomography Drug-Eluting Stent Investigation (OCTDESI)

被引:56
作者
Guagliumi, Giulio [1 ]
Sirbu, Vasile [1 ]
Musumeci, Giuseppe [1 ]
Bezerra, Hiram G. [2 ]
Aprile, Alessandro [1 ]
Kyono, Hiroyuki [2 ]
Fiocca, Luigi [1 ]
Matiashvili, Aleksandre [1 ]
Lortkipanidze, Nikoloz [1 ]
Vassileva, Angelina [1 ]
Popma, Jeffrey J. [4 ]
Allocco, Dominic J. [3 ]
Dawkins, Keith D. [3 ]
Valsecchi, Orazio [1 ]
Costa, Marco A. [2 ]
机构
[1] Ospedali Riuniti Bergamo, Cardiovasc Dept, Div Cardiol, I-24128 Bergamo, Italy
[2] Case Western Reserve Univ, Sch Med, Univ Hosp Case Med Ctr, Cleveland, OH USA
[3] Boston Sci Corp, Natick, MA USA
[4] Beth Israel Deaconess Med Ctr, Boston, MA 02215 USA
关键词
optical coherence tomography; biodegradable polymer; drug-eluting stent; stent thrombosis; paclitaxel; DURABLE POLYMER; CORONARY-ARTERY; BARE-METAL; FOLLOW-UP; IMPLANTATION; THROMBOSIS; TRIAL; ULTRASOUND; DISEASE; LEADERS;
D O I
10.1161/CIRCINTERVENTIONS.110.950154
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background-Polymer-coated drug-eluting stents are effective in preventing restenosis but have been associated with delayed healing and incomplete strut coverage. It is unknown whether paclitaxel-eluting stents (PES) with minimal biodegradable abluminal coating enhances strut coverage while preventing neointimal hyperplasia. Using optical coherence tomography (OCT) as a primary imaging modality, we assessed the proportion of uncovered struts at 6-month follow-up in PES coated with durable versus ultrathin (<1 mu m) biodegradable abluminal polymers. Methods and Results-In this pilot trial, 60 patients with de novo lesions (<= 25 mm) in native coronary vessels were randomly assigned to receive either TAXUS Liberte PES or JACTAX PES, a Liberte stent with polymer deposited abluminally as microdots (JACTAX HD: 9.2 mu g each of polymer and paclitaxel per 16-mm stent; JACTAX LD: 5 mu g each). OCT follow-up occurred at 6 months with clinical follow-up through 1 year. The primary end point was percent uncovered struts by OCT. An independent core laboratory blinded to stent assignment analyzed images. The 6-month rate of uncovered struts per patient was 5.3 +/- 14.7% for TAXUS Liberte, 7.0 +/- 12.2% for JACTAX HD, and 4.6 +/- 7.3% for JACTAX LD (P=0.81); percent malapposed struts was 1.4 +/- 4.4%, 0.8 +/- 1.9%, and 1.1 +/- 2.8%, respectively (P=0.86). Strut-level intimal thickness was 0.20 +/- 0.10, 0.22 +/- 0.15, and 0.24 +/- 0.15 mm (P=0.64); percent volume obstruction by OCT was 22.2 +/- 12.8, 22.5 +/- 16.2, and 25.8 +/- 15.2 (P=0.69). There were no deaths, Q-wave myocardial infarctions, or stent thromboses through 1 year. Conclusions-JACTAX PES with an ultrathin microdot biodegradable abluminal polymer did not result in improved strut coverage at 6 months compared with TAXUS Liberte
引用
收藏
页码:367 / U154
页数:12
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