Title of article :
Clinical Outcome Following Stringent Discontinuation of Dual Antiplatelet Therapy After 12 Months in Real-World Patients Treated With Second-Generation Zotarolimus-Eluting Resolute and Everolimus-Eluting Xience V Stents: 2-Year Follow-Up of the Randomized
Author/Authors :
Mounir W.Z. and Tandjung، نويسنده , , Kenneth and Sen، نويسنده , , Hanim and Lam، نويسنده , , Ming Kai and Basalus، نويسنده , , Mounir W.Z. and Louwerenburg، نويسنده , , J. (Hans) W. and Stoel، نويسنده , , Martin G. and van Houwelingen، نويسنده , , K. Gert and de Man، نويسنده , , Frits H.A.F. and Linssen، نويسنده , , Gerard C.M. and Saïd، نويسنده , , Salah A.M. and Nienhuis، نويسنده , , Mark B. and Lِwik، نويسنده , , Marije M. and Verhorst، نويسنده , , Patrick M.J. and van der Palen، نويسنده , , Job and von Birgelen، نويسنده , , Clemens، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2013
Pages :
11
From page :
2406
To page :
2416
Abstract :
Objectives m of this study was to assess the safety and efficacy of the implantation of Resolute zotarolimus-eluting stents (ZES) (Medtronic Inc., Santa Rosa, California) and Xience V everolimus-eluting stents (EES) (Abbott Vascular, Santa Clara, California) following strict discontinuation of dual antiplatelet therapy (DAPT) after 12 months. ound imited long-term follow-up data are available from head-to-head comparisons of second-generation drug-eluting stents. s ndomized TWENTE (The Real-World Endeavor Resolute Versus Xience V Drug-Eluting Stent Study in Twente) trial is an investigator-initiated study performed in a population with many complex patients and lesions and only limited exclusion criteria. Patients were randomly assigned 1:1 to ZES (n = 697) or EES (n = 694). s ar follow-up information was available on all patients. The rate of continuation of DAPT beyond 12 months was very low (5.4%). The primary endpoint of target vessel failure, a composite of cardiac death, target vessel–related myocardial infarction, and target vessel revascularization, did not differ between ZES and EES (10.8% vs. 11.6, p = 0.65), despite fewer target lesion revascularizations in patients with EES (2.6% vs. 4.9%, p = 0.03). The patient-oriented composite endpoint was similar (16.4% vs. 17.1%, p = 0.75). Two-year rates of definite or probable stent thrombosis were 1.2% and 1.4%, respectively (p = 0.63). Very late definite or probable stent thrombosis occurred only in 2 patients in each study arm (0.3% vs. 0.3%, p = 1.00). sions 2 years of follow-up and stringent discontinuation of DAPT beyond 12 months, Resolute ZES and Xience V EES showed similar results in terms of safety and efficacy for treating patients with a majority of complex lesions and off-label indications for drug-eluting stents. (The Real-World Endeavor Resolute Versus Xience V Drug-Eluting Stent Study in Twente [TWENTE]; NCT01066650)
Keywords :
everolimus-eluting stent(s) , drug-eluting stent(s) , percutaneous coronary intervention , Revascularization , zotarolimus-eluting stent(s)
Journal title :
JACC (Journal of the American College of Cardiology)
Serial Year :
2013
Journal title :
JACC (Journal of the American College of Cardiology)
Record number :
1756807
Link To Document :
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