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E-070 Endovascular treatment of the vertebral artery origin stenosis by using the closed-cell, self-expandable carotid wallstent
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  1. J KO1,
  2. T Lee2
  1. 1Neurosurgery, Pusan National University Hospital, Busan, Korea, Republic of
  2. 2Diagnostic Radiology, Pusan National University Hospital, Busan, Korea, Republic of

Abstract

Background Endovascular treatment has been considered a good alternative to surgery for symptomatic vertebral artery origin stenosis (VAOS) due to the high risk of morbidity associated with surgery. The purpose of this study was to evaluate the feasibility and efficacy of insertion of the closed-cell, self-expandable Carotid Wallstent for treatment of VAOS.

Methods The records of 72 patients with VAOS refractory to adequate medication who were treated by endovascular treatment with the Carotid Wallstent from December 2004 to November 2010 were retrospectively evaluated.

Results Of the 72 patients, 43 presented with transient ischemic attacks. Forty-seven patients (65.3%) manifested other brachiocephalic stenoses; of these, 40 patients had occlusion, hypoplasia, or stenosis of the contralateral vertebral artery. Overall technical success (defined as 20% or less residual stenosis) was 100%. Procedure-related complications (n=8, 11.1%) included sudden asystole (n=1), acute in-stent thrombosis (n=3), minor stroke (n=3), and stent shortening (n=1). All complications were resolved without permanent neurological deficit. Angiographic follow-up (mean, 13.0 months) was achieved in 49 patients and revealed in-stent restenosis in 1 patient (2.0%) and stent malposition by shortening in 2 patients (4.1%). No stent fracture occurred in any of the patients on follow-up angiography. All patients were neurologically stable at clinical follow-up.

Conclusions Endovascular treatment of symptomatic VAOS using the closed-cell, self-expandable Carotid Wallstent is technically feasible and effective in alleviating patient symptoms and for improving vertebrobasilar blood flow.

Disclosures J. Ko: None. T. Lee: None.

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