Clinical and Angiographic Outcomes With Sirolimus-Eluting Stents in Total Coronary Occlusions The ACROSS/TOSCA-4 (Approaches to Chronic Occlusions With Sirolimus-Eluting Stents/Total Occlusion Study of Coronary Arteries-4) Trial

被引:56
作者
Kandzari, David E. [1 ]
Rao, Sunil V. [2 ]
Moses, Jeffrey W. [3 ,4 ]
Dzavik, Vladimir [5 ]
Strauss, Bradley H. [6 ]
Kutryk, Michael J. [7 ]
Simonton, Charles A. [8 ]
Garg, Jyotsna [2 ]
Lokhnygina, Yuliya [2 ]
Mancini, G. B. John [9 ]
Yeoh, Eunice [9 ]
Buller, Christopher E. [10 ]
机构
[1] Scripps Clin, Div Cardiovasc Dis, La Jolla, CA 92037 USA
[2] Duke Clin Res Inst, Durham, NC USA
[3] Columbia Univ, Med Ctr, New York, NY USA
[4] Cardiovasc Res Fdn, New York, NY USA
[5] Univ Toronto, Univ Hlth Network, Toronto, ON, Canada
[6] Univ Toronto, Sunnybrook Hlth Sci Ctr, Toronto, ON, Canada
[7] Univ Toronto, St Michaels Hosp, Roy & Ann Foss Intervent Cardiol Program, Toronto, ON, Canada
[8] Carolinas Med Ctr, Charlotte, NC 28203 USA
[9] Univ British Columbia, Vancouver, BC V5Z 1M9, Canada
[10] Vancouver Hlth Sci Ctr, Vancouver, BC, Canada
关键词
total coronary occlusion; sirolimus-eluting stent; drug-eluting stent; fracture; PROPENSITY SCORE; IMPLANTATION; REDUCTION; IMPACT;
D O I
10.1016/j.jcin.2008.10.013
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objectives We sought to examine angiographic and clinical outcomes with sirolimus-eluting stents (SES) in total coronary occlusion (TCO) revascularization. Background Despite evaluation of drug-eluting stents beyond approved indications, few studies have evaluated their clinical benefit in TCO revascularization. Methods Among 15 centers in North America, 200 consecutive TCO patients (78.8% >6 weeks TCO age) were enrolled for treatment with SES. The primary end point was 6-month angiographic binary restenosis within the treated segment. Results Patient characteristics included: diabetes, 24.5%; prior infarction, 33.5%; and stent length, 45.9 mm median (quartile 1, 30.2 mm; quartile 2, 62.1 mm). A total of 199 patients (99.5%) were treated with SES, and procedural success was 98.0%. The 6-month binary restenosis rates were 9.5% in-stent, 12.4% in-segment, and 22.6% in-"working length" representing the entire treatment segment. Rates of 1-year target lesion revascularization, myocardial infarction, and target vessel failure were 9.8%, 1.0%, and 10.9%, respectively. Stent thrombosis occurred in 2 patients (1.0%). Using logistic regression modeling with propensity score adjustment, the absolute reduction in binary restenosis with SES compared with a historical bare-metal stent control was 37.7% (95% confidence interval [CI]: 27.2% to 48.3%, p < 0.001; odds ratio: 0.17, 95% CI: 0.09 to 0.30, p < 0.0001). Among 32 patients (16%) identified with stent fracture, target lesion revascularization was more common than patients without fracture (25.0% vs. 6.7%, p = 0.005). Conclusions Despite greater lesion complexity than prior TCO trials, percutaneous revascularization with SES appears safe and results in substantial reductions in angiographic restenosis and failed patency and a low rate of repeat revascularization. These findings support the use of SES in TCO revascularization. (The ACROSS/TOSCA Trial; NCT00378612). (J Am Coll Cardiol Intv 2009;2:97-106) (C) 2009 by the American College of Cardiology Foundation
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收藏
页码:97 / 106
页数:10
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