Detailed Information

Cited 0 time in webofscience Cited 0 time in scopus
Metadata Downloads

A Randomized, Double-Blind, Multicenter Comparison Study of Triple Antiplatelet Therapy With Dual Antiplatelet Therapy to Reduce Restenosis After Drug-Eluting Stent Implantation in Long Coronary Lesions Results From the DECLARE-LONG II (Drug-Eluting Stenting Followed by Cilostazol Treatment Reduces Late Restenosis in Patients with Long Coronary Lesions) Trial

Authors
Lee, Seung-WhanPark, Seong-WookKim, Young-HakYun, Sung-CheolPark, Duk-WooLee, Cheol WhanKang, Soo-JinPark, Seung-JungLee, Jae-HwanChoi, Si WanSeong, In-WhanLee, Nae-HeeCho, Yoon HaengShin, Won-YongLee, Seung-JinLee, Se-WhanHyon, Min-SuBang, Duk-WonChoi, Young-JinKim, Hyun-SookLee, Bong-KiLee, KeunPark, Hoon-KiPark, Chang-BumLee, Sang-GonKim, Min-KyuPark, Kyoung-HaPark, Woo-Jung
Issue Date
15-Mar-2011
Publisher
Elsevier BV
Keywords
cilostazol; coronary artery disease; triple antiplatelet therapy; zotarolimus-eluting stent
Citation
Journal of the American College of Cardiology, v.57, no.11, pp 1264 - 1270
Pages
7
Journal Title
Journal of the American College of Cardiology
Volume
57
Number
11
Start Page
1264
End Page
1270
URI
https://scholarworks.bwise.kr/sch/handle/2021.sw.sch/16641
DOI
10.1016/j.jacc.2010.10.035
ISSN
0735-1097
1558-3597
Abstract
Objectives The purpose of this study was to determine whether cilostazol reduces intimal hyperplasia in patients undergoing long zotarolimus-eluting stent implantation (stent length: >= 30 mm) for native long coronary lesions (length: >= 25 mm). Background Restenosis after drug-eluting stent implantation remains a significant clinical problem in long coronary lesions. Methods Patients (n = 499) were assigned randomly to triple (aspirin, clopidogrel, and cilostazol, triple group: n = 250) or dual antiplatelet therapy (aspirin and clopidogrel and placebo, dual group: n = 249) for 8 months after long zotarolimus-eluting stent implantation. The primary end point was in-stent late loss at the 8-month angiography according to the intention-to-treat principle. Results The 2 groups had similar baseline characteristics. The in-stent (0.56 +/- 0.55 mm vs. 0.68 +/- 0.59 mm, p = 0.045) and in-segment (0.32 +/- 0.54 mm vs. 0.47 +/- 0.54 mm, p = 0.006) late loss were significantly lower in the triple versus dual group, as were 8-month in-stent restenosis (10.8% vs. 19.1%, p = 0.016), in-segment restenosis (12.2% vs. 20.0%, p = 0.028), and 12-month ischemic-driven target lesion revascularization (5.2% vs. 10.0%, p = 0.042) rates. At 12 months, major adverse cardiac events including death, myocardial infarction, and ischemic-driven target lesion revascularization tended to be lower in the triple group than the dual group (7.2% vs. 12.0%, p = 0.07). Percent intimal hyperplasia volume by volumetric intravascular ultrasound analysis was reduced from 27.1 +/- 13.2% for the dual group to 22.1 +/- 9.9% for the triple group (p = 0.017). Conclusions Patients receiving triple antiplatelet therapy after long zotarolimus-eluting stent implantation had decreased extent of late luminal loss, percent intimal hyperplasia volume, and angiographic restenosis, resulting in a reduced risk of 12-month target lesion revascularization compared with patients receiving dual antiplatelet therapy. (Triple Versus Dual Antiplatelet Therapy after ABT578-Eluting Stent; NCT00589927) (J Am Coll Cardiol 2011; 57: 1264-70) (C) 2011 by the American College of Cardiology Foundation
Files in This Item
There are no files associated with this item.
Appears in
Collections
College of Medicine > Department of Internal Medicine > 1. Journal Articles
College of Medicine > Department of Internal Medicine > 1. Journal Articles
College of Medicine > Department of Internal Medicine > 1. Journal Articles

qrcode

Items in ScholarWorks are protected by copyright, with all rights reserved, unless otherwise indicated.

Related Researcher

Researcher cho, yoon haeng photo

cho, yoon haeng
College of Medicine (Department of Internal Medicine)
Read more

Altmetrics

Total Views & Downloads

BROWSE