Literature DB >> 26060087

Final results of a self-apposing paclitaxel-eluting stent fOr the PErcutaNeous treatment of de novo lesions in native bifurcated coronary arteries study.

Christoph K Naber1, Stylianos A Pyxaras, Holger Nef, Alexander J IJsselmuiden, Carlo Briguori, Christian Schlundt, Joanna Wykrzykowska, Franz R Eberli, Helge Möllmann, Søren Galatius, Johannes Rieber, Philippe Commeau, Robert-Jan van Geuns, David Bouchez, Harald Mudra.   

Abstract

AIMS: We aimed to evaluate the long-term safety and efficacy of the STENTYS self-apposing paclitaxeleluting stent (STENTYS-PES) in bifurcation lesions in routine clinical practice. METHODS AND
RESULTS: The primary endpoint of the study was the composite major adverse cardiac events (MACE: cardiac death, myocardial infarction, clinically driven target lesion revascularisation, or emergent bypass surgery) assessed at six months after enrolment. This was reported in 21 patients (10.1%), mainly due to clinically driven target lesion revascularisation (TLR). At 12 months, 27 patients experienced MACE (13.0%).
CONCLUSIONS: The long-term results of OPEN II show that the STENTYS-PES is safe and effective in the treatment of all-comers with coronary bifurcation lesions.

Entities:  

Mesh:

Substances:

Year:  2016        PMID: 26060087     DOI: 10.4244/EIJY15M06_02

Source DB:  PubMed          Journal:  EuroIntervention        ISSN: 1774-024X            Impact factor:   6.534


  3 in total

1.  Comparison between the STENTYS self-apposing bare metal and paclitaxel-eluting coronary stents for the treatment of saphenous vein grafts (ADEPT trial).

Authors:  A J J IJsselmuiden; C Simsek; A G van Driel; D Bouchez; G Amoroso; P Vermeersch; P P Karjalainen
Journal:  Neth Heart J       Date:  2018-02       Impact factor: 2.380

2.  Five-year clinical follow-up of the STENTYS self-apposing stent in complex coronary anatomy: a single-centre experience with report of specific angiographic indications.

Authors:  H Lu; R J Bekker; M J Grundeken; P Woudstra; J J Wykrzykowska; J G P Tijssen; R J de Winter; K T Koch
Journal:  Neth Heart J       Date:  2018-05       Impact factor: 2.380

3.  Defining a COPD composite safety endpoint for demonstrating efficacy in clinical trials: results from the randomized, placebo-controlled UPLIFT® trial.

Authors:  Bartolomé R Celli; Marc Decramer; Dacheng Liu; Norbert Metzdorf; Guus M Asijee; Donald P Tashkin
Journal:  Respir Res       Date:  2016-05-04
  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.