Safety and Effectiveness of Everolimus-Eluting Stents in Chronic Total Coronary Occlusion Revascularization

被引:45
作者
Kandzari, David E. [1 ]
Kini, Annapoorna S. [2 ]
Karmpaliotis, Dimitri [3 ,4 ]
Moses, Jeffrey W. [3 ,4 ]
Tummala, Pradyumna E. [5 ]
Grantham, J. Aaron [6 ]
Orr, Charles [7 ]
Lombardi, William [8 ]
Nicholson, William J. [9 ]
Lembo, Nicholas J. [1 ]
Popma, Jeffrey J. [10 ]
Wang, Jin [11 ]
Larracas, Cristina [11 ]
Rutledge, David R. [11 ]
机构
[1] Piedmont Heart Inst, Atlanta, GA 30309 USA
[2] Mt Sinai Med Ctr, New York, NY 10029 USA
[3] Columbia Univ, Med Ctr, New York, NY USA
[4] Cardiovasc Res Fdn, New York, NY USA
[5] Northeast Georgia Heart Ctr, Gainesville, GA USA
[6] St Lukes Mid Amer Heart Inst, Kansas City, MO USA
[7] St Vincents Heart Ctr, Indianapolis, IN USA
[8] PeaceHlth St Joseph Med Ctr, Ctr Cardiovasc, North Cascade Cardiol, Bellingham, WA USA
[9] York Hosp, York, PA USA
[10] Beth Israel Deaconess Med Ctr, Boston, MA USA
[11] Abbott Vasc Inc, Santa Clara, CA USA
关键词
chronic total occlusion; drug-eluting stent; everolimus; percutaneous coronary intervention; IN-HOSPITAL OUTCOMES; CONSENSUS DOCUMENT; INTERVENTION; ARTERIES; RECANALIZATION; MULTICENTER; IMPACT; IMPLANTATION; METAANALYSIS; IMMEDIATE;
D O I
10.1016/j.jcin.2014.12.238
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
OBJECTIVES This study sought to evaluate procedural and clinical outcomes among patients undergoing chronic total occlusion (CTO) percutaneous coronary intervention (PCI) using contemporary methods and everolimus-eluting stents (EES). BACKGROUND Limited studies have detailed the procedural and late-term safety and efficacy of CTO revascularization among multiple centers applying modern techniques and with newer-generation drug-eluting stents. METHODS Among 20 centers, 250 consecutive patients were enrolled for attempted CTO PCI. Procedural and in-hospital clinical outcomes were examined in addition to the 1-year primary endpoint of death, myocardial infarction, and target lesion revascularization (major adverse cardiac events [MACE]). RESULTS Demographic, lesion, and procedural characteristics included prior bypass surgery: 9.9%; diabetes: 40.1%; lesion length: 36.1 +/- 18.5 mm; and stent length: 51.7 +/- 27.2 mm. Procedural success, defined as guidewire recanalization with no in-hospital MACE, was 96.4%. Success with antegrade-only methods was 97.9% and 86.2% by retrograde/combined methods, respectively. Compared with a pre-specified performance goal derived from 6 prior CTO drug-eluting stent trials (1-year MACE: 24.4%), treatment with EES was associated with significantly lower composite adverse events for both intent-to-treat (18.5%, 1-sided upper confidence interval: 23.4%, p = 0.025) and per-protocol populations (8.2%, 1-sided upper confidence interval: 12.3%, p < 0.0001). Target lesion revascularization at 1 year was 6.3%. Dual antiplatelet therapy adherence was 53.9% at 1 year, yet subacute definite stent thrombosis occurred in only 2 patients (0.9%), and late probable stent thrombosis occurred in 1 patient (0.5%). CONCLUSIONS In a multicenter registration trial representing contemporary technique and EES, favorable procedural success and late-term clinical outcomes support CTO PCI in a patient population with high lesion complexity. (EXPERT CTO: Evaluation of the XIENCE PRIME LL and XIENCE Nano Everolimus Eluting Coronary Stent Coronary Stents, Performance, and Technique in Chronic Total Occlusions; NCT01435031) (C) 2015 by the American College of Cardiology Foundation.
引用
收藏
页码:761 / 769
页数:9
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