Volume 70, Issue 5 pp. 635-639
Coronary Artery Disease

Three-year clinical outcomes after coronary stenting of chronic total occlusion using sirolimus-eluting stents: Insights from the rapamycin-eluting stent evaluated at rotterdam cardiology hospital—(RESEARCH) registry

Héctor M. García-García MD, MSC

Héctor M. García-García MD, MSC

Thoraxcenter, Erasmus Medical Center, Rotterdam, Netherlands

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Joost Daemen MD

Joost Daemen MD

Thoraxcenter, Erasmus Medical Center, Rotterdam, Netherlands

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Neville Kukreja MRCP

Neville Kukreja MRCP

Thoraxcenter, Erasmus Medical Center, Rotterdam, Netherlands

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Shuzou Tanimoto MD

Shuzou Tanimoto MD

Thoraxcenter, Erasmus Medical Center, Rotterdam, Netherlands

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Carlos A.G. van Mieghem MD

Carlos A.G. van Mieghem MD

Thoraxcenter, Erasmus Medical Center, Rotterdam, Netherlands

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Martin van der Ent MD, PhD

Martin van der Ent MD, PhD

Thoraxcenter, Erasmus Medical Center, Rotterdam, Netherlands

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Ron T. van Domburg PhD

Ron T. van Domburg PhD

Thoraxcenter, Erasmus Medical Center, Rotterdam, Netherlands

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Patrick W. Serruys MD, PhD

Corresponding Author

Patrick W. Serruys MD, PhD

Thoraxcenter, Erasmus Medical Center, Rotterdam, Netherlands

Thoraxcenter, Ba-583, Dr. Molewaterplein 40, 3015 GD Rotterdam, NetherlandsSearch for more papers by this author
First published: 29 October 2007
Citations: 26

Abstract

Background: We previously reported that the 1-year survival-free from target lesion revascularization was 97.4% in patients with chronic total occlusion (CTO) treated with sirolimus-eluting stents (SES). There are currently no long-term results of the efficacy of SES in this subset of lesions. We assessed the 3-year clinical outcomes of 147 patients with CTO treated with either SES or bare metal stents (BMS). Methods and Results: A total of 147 (BMS = 71, SES = 76) patients were included. Four patients died in the BMS group while five patients died in the SES group, P = 0.8; two myocardial infarctions occurred in both groups, P = 0.9; and target vessel revascularization was performed in nine patients in the BMS and seven in the SES group, P = 0.5. The cumulative event-free survival of MACE was 81.7% in BMS group and 84.2% in SES group, P = 0.7. Two patients of the SES group had a coronary aneurism at 3-year angiographic follow-up. Conclusions: The use of SES was no longer associated with significantly lower rates of target vessel revascularization and major adverse cardiac events in patients with CTOs after 3 years of follow-up compared with BMSs. © 2007 Wiley-Liss, Inc.

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