Salik Aysun Erbahceci, Selcuk Hatem H, Zalov Hasanagha, Kilinc Fatih, Cirak Musa, Kara Batuhan
Department of Radiology, University of Health Sciences, Dr Sadi Konuk Training and Research Hospital, Istanbul, Turkey.
Department of Neurosurgery, Dr Sadi Konuk Training and Research Hospital, Istanbul, Turkey.
Interv Neuroradiol. 2019 Oct;25(5):484-490. doi: 10.1177/1591019919832244. Epub 2019 Apr 16.
The aim of this retrospective study is to evaluate medium-term results of undersized balloon angioplasty and stenting for symptomatic high-grade (70-99%) stenosis of a major intracranial artery with Enterprise stent.
This study included 68 consecutive symptomatic (recurrent transient ischemic attack (TIA) or ischemic stroke under dual antiplatelet treatment) patients with high-grade (70-99%) stenosis of a major intracranial artery who were endovascularly treated with undersized balloon angioplasty and Enterprise stent deployment between July 2012 and December 2017. Primary outcomes were any stroke or death within 30 days after procedure. Secondary outcomes were technical success rates, stroke and restenosis during the follow-up period.
A total of 68 lesions in 68 patients (mean age: 62 ± 7 years) were treated with a technical success rate of 99%. The degree of pre-procedural stenosis was 92 ± 6% and dropped to 12 ± 10% after stent deployment. No patient developed any stroke or death during the periprocedural period. Intracranial hemorrhage was observed in 1 (1.5%) patient. In 60 (88%) patients with available imaging follow-up in-stent restenosis was observed in 2 patients. Mean follow-up period was 22 ± 17 months (range 6-72) and none of the patients experienced recurrent TIA or stroke during the follow-up period.
In this retrospective single-center study undersized balloon angioplasty and deployment of a self-expandable stent with relatively low radial force was safe and effective for endovascular treatment of high-grade intracranial arterial stenosis with high technical success rate, low periprocedural complication rates and favorable medium-term follow-up results.
本回顾性研究旨在评估使用Enterprise支架对症状性颅内主要动脉重度(70 - 99%)狭窄进行小号球囊血管成形术和支架置入术的中期结果。
本研究纳入了68例连续的症状性患者(在双重抗血小板治疗下出现复发性短暂性脑缺血发作(TIA)或缺血性卒中),这些患者颅内主要动脉存在重度(70 - 99%)狭窄,于2012年7月至2017年12月期间接受了小号球囊血管成形术和Enterprise支架置入的血管内治疗。主要结局是术后30天内发生的任何卒中或死亡。次要结局是技术成功率、随访期间的卒中及再狭窄情况。
68例患者共68处病变(平均年龄:62±7岁)接受了治疗,技术成功率为99%。术前狭窄程度为92±6%,支架置入后降至12±10%。围手术期无患者发生任何卒中或死亡。1例(1.5%)患者出现颅内出血。60例(88%)有可用影像随访的患者中,2例观察到支架内再狭窄。平均随访期为22±17个月(范围6 - 72个月),随访期间无患者经历复发性TIA或卒中。
在这项回顾性单中心研究中,小号球囊血管成形术和置入径向力相对较低的自膨式支架对颅内动脉重度狭窄的血管内治疗是安全有效的,技术成功率高,围手术期并发症发生率低,中期随访结果良好。