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Efficacy and Safety of Combination Antiplatelet Therapies in Patients With Symptomatic Intracranial Atherosclerotic Stenosis

Authors :
Dong-Wha Kang
Byung-Chul Lee
Moon Ku Han
Kyung Bok Lee
Hyun Wook Nah
Joung-Ho Rha
Jong-Moo Park
Yong-Jin Cho
Hee-Joon Bae
Gyeong Moon Kim
Yong-Seok Lee
Keun-Sik Hong
Ja Seong Koo
Nijasri C. Suwanwela
Sun U. Kwon
Sung Cheol Yun
K.S. Lawrence Wong
Hahn Young Kim
Sang Wook Jeong
Ju-Hun Lee
Jong S. Kim
Dong-Eog Kim
Vincent Mok
Seung-Hoon Lee
Kyung Ho Yu
Source :
Stroke. 42:2883-2890
Publication Year :
2011
Publisher :
Ovid Technologies (Wolters Kluwer Health), 2011.

Abstract

Background and Purpose— An optimal strategy for management of symptomatic intracranial atherosclerotic stenosis (ICAS) has not yet been established. We compared the efficacy of 2 combinations of antiplatelets, aspirin plus cilostazol (cilostazol group) verus aspirin plus clopidogrel (clopidogrel group), on the progression of ICAS, which is known to be associated with clinical stroke recurrence. Methods— In this investigator-initiated double-blind trial, 457 patients with acute symptomatic stenosis in the M1 segment of the middle cerebral artery or the basilar artery were randomly allocated into either a cilostazol group or a clopidogrel group. After 7 months of treatment, follow-up MR angiogram and MRI were performed. The primary end point was the progression of ICAS in comparison with stenosis on the baseline MR angiogram. Secondary end points included the occurrence of new ischemic lesions on MRI, composite of cardiovascular events, and major bleeding complications. Results— Cardiovascular events occurred in 15 of 232 patients (6.4%) in the cilostazol group and 10 of 225 (4.4%) in the clopidogrel group ( P =0.312). Cilostazol did not reduce the progression of symptomatic ICAS (20 of 202) compared to clopidogrel (32 of 207) (odds ratio, 0.61; P =0.092), although favorable changes in serum lipoproteins were observed in the cilostazol group. There were no significant differences between the 2 groups with respect to new ischemic lesions (18.7% versus 12.0%; P =0.078) and major hemorrhagic complications (0.9% versus 2.6%; P =0.163). Conclusions— This trial failed to show significant difference in preventing progression of ICAS and new ischemic lesions between the 2 combination antiplatelet therapies in the patients with symptomatic ICAS. Clinical Trial Registration— URL: http://www.clinicaltrials.gov . Unique identifier: NCT00130039.

Details

ISSN :
15244628 and 00392499
Volume :
42
Database :
OpenAIRE
Journal :
Stroke
Accession number :
edsair.doi.dedup.....13fc62fa6447a6cb7492906f49d2d3a3
Full Text :
https://doi.org/10.1161/strokeaha.110.609370