Back to Search Start Over

Six-month clinical and angiographic results of the STENTYS® self-apposing stent in bifurcation lesions

Authors :
Thierry Lefèvre
Pierfrancesco Agostoni
Hector M. Garcia-Garcia
Karl Eugen Hauptmann
Stefan Verheye
Steve Ramcharitar
René Spaargaren
Marcus Wiemer
Jan Kovac
Patrick W. Serruys
Bernhard Witzenbichler
Joachim Schofer
Robert-Jan van Geuns
Eberhard Grube
Cardiology
Radiology & Nuclear Medicine
Source :
EuroIntervention, 7(5), 580-587. EuroPCR
Publication Year :
2011
Publisher :
Europa Digital & Publishing, 2011.

Abstract

Aims: We report the clinical and angiographic results of the OPEN I study, a multicentre prospective single-arm study evaluating both the drug-eluting and bare metal STENTYS (R) stents in the treatment of coronary bifurcation lesions. Methods and results: The STENTYS (R) stent is a provisional, self-expanding, nitinol stent with small interconnections that can be disconnected by balloon angioplasty in between the stent struts to provide access to the side branch (SB) and full ostium coverage. In nine European centres, 60 stents (33 BMS, 27 DES) were implanted in 63 patients (procedural success of 95.2%). Angiographic QCA and IVUS were used to measure acute gain and late loss. The Medina classification showed 35 patients (58%) had disease affecting the SB (true bifurcations) and 19 patients (32%) had disease in all three arms. The average bifurcation angulation pre-stenting was 60 degrees +/- 21 degrees. Post-stenting, disconnection was performed on 90% of the stents implanted. In 18 cases, disconnection was followed by SB stenting with all SB stents successfully implanted. Post-stenting, the bifurcation angle was 51 degrees. The primary clinical endpoint, cumulative MACE at six months, was low for DES (3.7%) but higher for BMS (27.3%) with the latter driven exclusively by clinically-driven TLR rates (3.7% vs. 24.2%). No cardiac deaths were recorded at six months and one patient had a non-Q wave infarct. The secondary angiographic endpoint of late luminal loss (LLL) was measured for both DES (paclitaxel) and BMS stents in the proximal main branch (MB), MB, distal MB as well as the SB. The values for DES were 0.39 mm, 0.42 mm, 0.40 mm and 0.16 mm, respectively. The values for BMS were 0.86 mm, 0.87 mm, 0.85 mm and 0.54 mm, respectively. Observed results using matched IVUS analysis at six months revealed an increase in mean stent area (mm(2)) for DES from 7.52 +/- 1.86 at baseline to 12.32 +/- 2.90 at six month follow-up (p

Details

ISSN :
1774024X
Volume :
7
Database :
OpenAIRE
Journal :
EuroIntervention
Accession number :
edsair.doi.dedup.....c56ff66c2e5304b48f5e60fa2f133d55