,Enterprise stent for symptomatic complex intracranial atherosclerotic stenosis: safety and efficien

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Purpose: To evaluate the safety and efficacy of Enterprise stent in the treatment of symptomatic complex intracranial atherosclerotic stenosis.Methods and materials: 20 complex cases among 53 patients with symptomatic ischemic stroke who were treated with balloon angioplasty and enterprise stents in Department of Neuro-interventional Radiology,The First Affiliated Hospital of Zhengzhou University from Jan.2014 to Dec.2017 were retrospectively enrolled in this study.Diagnostic criteria for complex intracranial atherosclerotic stenosis were as follows: 1) intracranial atherosclerotic stenosis was ≥70% confirmed by digital subtraction angiography (DSA) using the formulas described by the Warfarin Aspirin Symptomatic Intracranial Disease (WASID) method;2) length of lesion was >10 mm.Basic characteristics of target lesions,technical success rate,perioperative safety,follow-up outcomes were investigated.Results: 20 patients were enrolled in this study,including 15 males and 5 females from 44 to 70 years old with an average age of 57.20 ± 9.25.20 lesions were treated with 20 enterprise stents.The average preoperative and postoperative residual stenosis was reduced from (77.45 ± 8.44)% to (24.89 ± 16.61)%.The successful rate of operation was 100%.Among the perioperative complications,only 1 case (5%) experienced perforating branch event.The average clinical follow-up period was 13.15 ± 11.33 months (time range: 5-38).There were no ischemic events,no bleeding events and no various causes of death during the follow-up period.8 lesions (40.0%) underwent DSA follow-up examinations and 12 lesions (60.0%) were checked by CT angiography during the follow-up period.3 lesions (15.0%) developed ISR without any cerebral ischemia symptoms.Conclusion: This retrospective,single-center study suggests that enterprise stent is effective in the treatment of symptomatic complex intracranial atherosclerotic stenosis with less perioperative complications.Prospective,multicenter,randomized controlled trials are expected.
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