Clinical Outcomes in Real-World Patients With Small Vessel Disease Treated With XIENCE V® Everolimus-Eluting Stents: One Year Results From the XIENCE V® USA Condition of Approval Post-Market Study

被引:19
作者
Hermiller, James B. [1 ]
Rutledge, David R. [2 ]
Mao, Vivian W. [2 ]
Zhao, Weiying [2 ]
Wang, Jin [2 ]
Gruberg, Luis [3 ]
Lombardi, William [4 ,5 ]
Sharma, Samin K. [6 ]
Krucoff, Mitchell W. [7 ,8 ]
机构
[1] St Vincent Heart Ctr Indiana, Div Cardiol, Indianapolis, IN 46290 USA
[2] Abbott Vasc, Dept Clin Res, Santa Clara, CA USA
[3] SUNY Stony Brook, Med Ctr, Div Cardiol, Stony Brook, NY 11794 USA
[4] North Cascade Cardiol, Div Cardiol, Washington, DC USA
[5] St Joseph Hosp, Washington, DC USA
[6] Mt Sinai Sch Med, Div Cardiol, New York, NY USA
[7] Duke Univ, Sch Med, Duke Clin Res Inst, Durham, NC USA
[8] Duke Univ, Sch Med, Div Cardiol, Durham, NC USA
关键词
drug-eluting stent; everolimus; small vessel; 1; year; CORONARY-ARTERY-DISEASE; SPIRIT III; FOLLOW-UP; MYOCARDIAL-INFARCTION; RANDOMIZED-TRIAL; 2-YEAR OUTCOMES; REGISTRY; LESIONS; SYSTEM; REVASCULARIZATION;
D O I
10.1002/ccd.25325
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objectives: The purpose of this study was to evaluate the 1-year clinical outcomes of more complex XIENCE V USA real-world patients with small versus nonsmall vessel lesions. Background: Patients with small vessel lesions undergoing coronary stent placement are at higher risk of major adverse cardiac events. Improved safety and efficacy of XIENCE V everolimus eluting stents (EES) have been previously demonstrated in selected low-risk small vessel populations in randomized clinical trials. Methods: The XIENCE V USA study was a condition of approval, single-arm study in unselected real-world patients. Baseline and 1-year clinical outcomes were compared between XIENCE V USA patients who received a single 2.5 mm stent (small vessel group, N=838) and patients implanted with a single >2.5 mm stent (non-small vessel group, N=2,015). Mean reference vessel diameter was 2.55 +/- 0.36 and 3.25 +/- 0.46 mm in the small and non-small vessel groups, respectively (P<0.001). Results: Small vessel group had more females, presented with a higher rate of diabetes, and had more complex lesion characteristics. The definite or probable ST rates analyzed using Kaplan-Meier method were low and not significantly different between the groups at 0.37 and 0.40% for the small and nonsmall vessel group (P=0.88), respectively. The composite rate of cardiac death or MI was comparable at 4.5% for the small and 5.1% for the non-small vessel 1 groups (P=0.57). The 1-year target lesion revascularization rate was also comparable in the small vessel group (3.8% vs. 3.0%, P=0.35). Conclusions: Despite gender difference, higher prevalence of diabetes and more complex lesions in the small vessel groups, the 1-year clinical outcomes were similar in both small and nonsmall vessel groups. These results demonstrate the therapeutic benefit of XIENCE V EES in a real-world all inclusive patient population with small vessel disease. (C) 2013 Wiley Periodicals, Inc.
引用
收藏
页码:7 / 16
页数:10
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