Comparison of carotid endarterectomy and repeated carotid angioplasty and stenting for in-stent restenosis (CERCAS trial): a randomised study.

IF 4.4 1区 医学 Q1 CLINICAL NEUROLOGY Stroke and Vascular Neurology Pub Date : 2023-10-01 Epub Date: 2023-03-27 DOI:10.1136/svn-2022-002075
Tomáš Hrbáč, Jiří Fiedler, Václav Procházka, Tomáš Jonszta, Martin Roubec, David Pakizer, Daniel Václavík, David Netuka, Tomáš Heryán, David Školoudík
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引用次数: 1

Abstract

Background and aim: In-stent restenosis (ISR) belongs to an infrequent but potentially serious complication after carotid angioplasty and stenting in patients with severe carotid stenosis. Some of these patients might be contraindicated to repeat percutaneous transluminal angioplasty with or without stenting (rePTA/S). The purpose of the study is to compare the safety and effectiveness of carotid endarterectomy with stent removal (CEASR) and rePTA/S in patients with carotid ISR.

Methods: Consecutive patients with carotid ISR (≥80%) were randomly allocated to the CEASR or rePTA/S group. The incidence of restenosis after intervention, stroke, transient ischaemic attack myocardial infarction and death 30 days and 1 year after intervention and restenosis 1 year after intervention between patients in CEASR and rePTA/S groups were statistically evaluated.

Results: A total of 31 patients were included in the study; 14 patients (9 males; mean age 66.3±6.6 years) were allocated to CEASR and 17 patients (10 males; mean age 68.8±5.6 years) to the rePTA/S group. The implanted stent in carotid restenosis was successfully removed in all patients in the CEASR group. No clinical vascular event was recorded periproceduraly, 30 days and 1 year after intervention in both groups. Only one patient in the CEASR group had asymptomatic occlusion of the intervened carotid artery within 30 days and one patient died in the rePTA/S group within 1 year after intervention. Restenosis after intervention was significantly greater in the rePTA/S group (mean 20.9%) than in the CEASR group (mean 0%, p=0.04), but all stenoses were <50%. Incidence of 1-year restenosis that was ≥70% did not differ between the rePTA/S and CEASR groups (4 vs 1 patient; p=0.233).

Conclusion: CEASR seems to be effective and save procedures for patients with carotid ISR and might be considered as a treatment option.

Trial registration number: NCT05390983.

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颈动脉内膜切除术与重复颈动脉血管成形术及支架置入术治疗支架内再狭窄的比较(CERCAS试验):一项随机研究。
背景和目的:支架内再狭窄(ISR)是严重颈动脉狭窄患者颈动脉血管成形术和支架置入术后一种罕见但潜在的严重并发症。其中一些患者可能被禁止重复进行经皮腔内血管成形术,无论是否进行支架植入(rePTA/S)。本研究的目的是比较颈动脉ISR患者行颈动脉内膜剥脱术并支架移除(CEASR)和rePTA/S的安全性和有效性。方法:将连续的颈动脉ISR(≥80%)患者随机分为CEASR组或rePTA/S组。介入治疗后再狭窄的发生率、中风、短暂性缺血性发作心肌梗死和死亡30天和1 介入治疗后一年和再狭窄1 对CEASR和rePTA/S组患者干预后一年的情况进行统计评估。结果:本研究共纳入31例患者;14名患者(9名男性;平均年龄66.3±6.6岁)被分配到CEASR组,17名患者(10名男性,平均年龄68.8±5.6岁)被分到rePTA/S组。CEASR组的所有患者均成功移除了颈动脉再狭窄的植入支架。术前30天和术后1天均未记录到临床血管事件 两组干预后一年。CEASR组中只有一名患者在30天内出现介入颈动脉无症状闭塞,rePTA/S组中有一名患者于1天内死亡 干预后一年。rePTA/S组干预后再狭窄(平均20.9%)明显大于CEASR组(平均0%,p=0.04),但所有狭窄均为。试验注册号:NCT05390983。
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来源期刊
Stroke and Vascular Neurology
Stroke and Vascular Neurology Medicine-Cardiology and Cardiovascular Medicine
CiteScore
11.20
自引率
1.70%
发文量
63
审稿时长
15 weeks
期刊介绍: Stroke and Vascular Neurology (SVN) is the official journal of the Chinese Stroke Association. Supported by a team of renowned Editors, and fully Open Access, the journal encourages debate on controversial techniques, issues on health policy and social medicine.
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