9-Month Clinical, Angiographic, and Intravascular Ultrasound Results of a Prospective Evaluation of the Axxess Self-Expanding Biolimus A9-Eluting Stent in Coronary Bifurcation Lesions

被引:70
作者
Verheye, Stefan [1 ]
Agostoni, Pierfrancesco [1 ]
Dubois, Christophe L. [2 ]
Dens, Joseph [9 ]
Ormiston, John [8 ]
Worthley, Stephen [7 ]
Trauthen, Brett [6 ]
Hasegawa, Takao [5 ]
Koo, Bon-Kwon [5 ]
Fitzgerald, Peter J. [5 ]
Mehran, Roxana [3 ,4 ]
Lansky, Alexandra J. [3 ,4 ]
机构
[1] Ziekenhuis Netwerk Antwerpen, Antwerp Cardiovasc Inst Middelheim, B-2020 Antwerp, Belgium
[2] Univ Hosp Gasthuisberg, B-3000 Louvain, Belgium
[3] Cardiovasc Res Fdn, New York, NY USA
[4] Columbia Univ, Med Ctr, New York, NY USA
[5] Stanford Univ, Med Ctr, Stanford, CA 94305 USA
[6] Devax Inc, Lake Forest, CA USA
[7] Royal Adelaide Hosp, Adelaide, SA 5000, Australia
[8] Auckland City Hosp, Auckland, New Zealand
[9] Oost Limburg Hosp, Genk, Belgium
关键词
coronary artery disease; Biolimus A9-eluting stent; bifurcation lesion; restenosis; ELUTING STENT; CLASSIFICATION; TRIAL;
D O I
10.1016/j.jacc.2008.12.012
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objectives This study sought to assess the safety and performance of the Axxess (Devax Inc., Lake Forest, California) self-expanding drug-eluting stent in coronary bifurcation lesions. Background Percutaneous treatment of coronary bifurcations is a predictor of adverse late outcomes, in part because of the lack of dedicated devices. Methods Patients with de novo bifurcation lesions were prospectively enrolled in a multicenter study. The Axxess stent was deployed at the level of the carina followed by additional sirolimus-eluting stents in the distal parent vessel (PV) and/or side branch (SB). All patients underwent clinical follow-up at 9 months; 150 were to receive control angiography and 76 were to receive intravascular ultrasound. The primary end point was the rate of major adverse cardiac events (MACE): a composite of death, myocardial infarction (MI), and target lesion revascularization (TLR). Secondary end points included in-segment restenosis, late loss, and percent neointimal volume obstruction. Results Overall, 302 patients were treated with 299 Axxess stents (99%). Additional stenting of 1 branch was performed in 21.7% of patients (17.7% PV, 4% SB), and of both branches in 64.7%. At 9 months, 99.3% of patients returned for clinical follow-up; from the angiographic and IVUS substudies, 93.3% and 89.4% returned. The cumulative 9-month MACE rate was 7.7% (0.7% death, 3.3% non-Q-wave MI, 1.0% Q-wave MI, 4.3% TLR). Subacute and late stent thrombosis occurred in 0.7% and 0.3% of patients. Total restenosis was 6.4% (3.6% PV, 4.3% SB), late loss was 0.20 +/- 0.41 mm in the PV and 0.17 +/- 0.34 mm in the SB. In the Axxess stent segment, percent neointimal volume obstruction was 4.3 +/- 5.2%. Conclusions This prospective multicenter study confirms the safety and performance of the Axxess stent in bifurcation lesions. (Drug-Eluting Stent Intervention for Treating Side Branches Effectively; ACTRN12606000259549) (J Am Coll Cardiol 2009;53:1031-9) (C) 2009 by the American College of Cardiology Foundation
引用
收藏
页码:1031 / 1039
页数:9
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