Department of Neurology, Beijing Tiantan Hospital, Capital Medical University, Beijing, China.
Department of Interventional Neuroradiology, Beijing Tiantan Hospital, Capital Medical University, Beijing, China.
J Neurointerv Surg. 2020 Nov;12(11):1094-1098. doi: 10.1136/neurintsurg-2019-015607. Epub 2020 Feb 7.
In-stent restenosis (ISR) is one of the long-term adverse outcomes of endovascular angioplasty and stenting for symptomatic intracranial arterial stenosis. In this study, we try to evaluate the safety and efficacy of endovascular treatment for intracranial ISR.
We retrospectively collected patients with intracranial ISR who underwent endovascular treatment from June 2012 to August 2019 at a high-volume stroke center. Successful recanalization was defined as ≤30% residual stenosis. Stroke, myocardial infarction, and death after stenting within 30 days were used to evaluate periprocedural safety. Recurrent stroke in the territory of the culprit vessel and re-ISR in patients with clinical and vascular imaging follow-up data were used to evaluate the long-term outcome.
32 patients (59.6±7.2 years old) with ISR were recruited, including 22 patients (68.8%) treated with balloon dilatation, 8 patients (25%) with stenting, and 2 patients (6.3%) with failed procedures. Successful recanalization was achieved in 71.9% (23/32) of patients. There was no stroke, myocardial infarction or death within 30 days after the procedure. Recurrent stroke was found in 10.7% (3/28) of the patients, and re-ISR was found in 42.1% (8/19) of the patients. The re-ISR rate was lower in patients with stenting than in those with balloon dilatation (0% vs 57.1%, p=0.090), and in patients with successful recanalization than in those with unsuccessful recanalization (33.3% vs 75.0%, p=0.352), but with no statistically significant difference.
The periprocedural safety of endovascular treatment for intracranial ISR may be acceptable, but the long-term rates of recurrent stroke and re-ISR remain at high levels.
血管内成形术和支架置入术治疗症状性颅内动脉狭窄后,支架内再狭窄(ISR)是其长期不良转归之一。本研究旨在评估血管内治疗颅内 ISR 的安全性和有效性。
我们回顾性收集了 2012 年 6 月至 2019 年 8 月在一家高容量卒中中心接受血管内治疗的颅内 ISR 患者。成功再通定义为残余狭窄≤30%。30 天内支架置入术后发生的卒中、心肌梗死和死亡用于评估围手术期安全性。有临床和血管影像学随访资料的患者,以靶血管区域再发卒中和再 ISR 评估长期预后。
共纳入 32 例(59.6±7.2 岁)ISR 患者,其中 22 例(68.8%)接受球囊扩张治疗,8 例(25%)接受支架置入治疗,2 例(6.3%)治疗失败。71.9%(23/32)的患者实现了再通。术后 30 天内无卒中、心肌梗死或死亡。28 例患者中有 10.7%(3/28)出现再发卒中,19 例患者中有 42.1%(8/19)出现再 ISR。支架置入组的再 ISR 发生率低于球囊扩张组(0% vs 57.1%,p=0.090),而在再通成功组的发生率低于再通失败组(33.3% vs 75.0%,p=0.352),但差异均无统计学意义。
血管内治疗颅内 ISR 的围手术期安全性可能可以接受,但长期再发卒中率和再 ISR 率仍居高不下。