Efficacy and safety of combination antiplatelet therapies in patients with symptomatic intracranial atherosclerotic stenosis.

نویسندگان

  • Sun U Kwon
  • Keun-Sik Hong
  • Dong-Wha Kang
  • Jong-Moo Park
  • Ju-Hun Lee
  • Yong-Jin Cho
  • Kyung-Ho Yu
  • Ja-Seong Koo
  • K S Lawrence Wong
  • Seung-Hoon Lee
  • Kyung Bok Lee
  • Dong-Eog Kim
  • Sang-Wook Jeong
  • Hee-Joon Bae
  • Byung-Chul Lee
  • Moon-Ku Han
  • Joung-Ho Rha
  • Hahn Young Kim
  • Vincent C Mok
  • Yong-Seok Lee
  • Gyeong-Moon Kim
  • Nijasri Charnnarong Suwanwela
  • Sung-Cheol Yun
  • Hyun-Wook Nah
  • Jong S Kim
چکیده

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.

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عنوان ژورنال:
  • Stroke

دوره 42 10  شماره 

صفحات  -

تاریخ انتشار 2011