首页> 外文期刊>Journal of neurosurgery. >Multicenter clinical trial of the NexStent coiled sheet stent in the treatment of extracranial carotid artery stenosis: immediate results and late clinical outcomes.
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Multicenter clinical trial of the NexStent coiled sheet stent in the treatment of extracranial carotid artery stenosis: immediate results and late clinical outcomes.

机译:NexStent螺旋片状支架在颅外颈动脉狭窄治疗中的多中心临床试验:即刻效果和晚期临床效果。

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OBJECT: Carotid angioplasty with stent placement has been proposed as an alternative method for revascularization of carotid artery (CA) stenosis. A novel stent with a coiled sheet design (NexStent; EndoTex Interventional Systems, Inc., Cupertino, CA) has been introduced because it provides improved flexibility over conventional tubular designs during navigation through tortuous arterial segments. The authors report the results of a multicenter study in which they evaluated the safety, feasibility, and effectiveness of this stent in the treatment of CA stenosis. METHODS: Enrollment was limited to patients with 70% or more symptomatic or asymptomatic stenosis of the internal CA. The primary end point was a technically successful implantation procedure (delivery of the stent to the target siteand retrieval of the delivery device) resulting in less than 30% residual stenosis on angiograms obtained immediately postprocedure and no death or ipsilateral stroke immediately after or within 30 days following the procedure. The secondary effectiveness end point was prevention of an ipsilateral stroke within 31 days to 1 year postprocedure. The tertiary effectiveness end point was less than 70% residual stenosis demonstrated on CA Doppler ultrasonography performed at 6 and 12 months. Forty-four patients (mean age 71 years, range 51-89 years; 30 patients were men and 18 [41%] had symptomatic stenotic lesions) were treated using 45 NexStents (two stents were placed in one patient). Residual stenosis on postprocedure angiograms was less than 30% in all patients. The 1-month primary end point was achieved in 41 patients (93%). The three major adverse events that occurred within 30 days were one death related to congestive heart failure and two ipsilateral strokes, one of which resulted in death. No ipsilateral stroke occurred between 1 and 12 months postprocedure among 35 patients who completed the follow-up evaluation. Asymptomatic recurrent stenosis was identified in one patient at 6 months postprocedure, requiring the performance of repeated angioplasty. CONCLUSIONS: Placement of the NexStent was feasible and resulted in the effective treatment of patients with CA stenosis, with promising long-term results.
机译:目的:颈动脉血管成形术与支架置入术已被提议作为颈动脉狭窄的再血管化方法。已经引入了一种具有卷曲片状设计的新型支架(NexStent; EndoTex Interventional Systems,Inc.,Cupertino,CA),因为它在通过曲折的动脉节段期间提供了优于传统管状设计的灵活性。作者报告了一项多中心研究的结果,他们在其中评估了该支架在治疗CA狭窄中的安全性,可行性和有效性。方法:入组仅限于内部CA有症状或无症状狭窄的70%或更高的患者。主要终点是技术上成功的植入程序(将支架输送到目标部位并收回输送装置),使得术后立即获得的血管造影照片上的残余狭窄少于30%,并且在30天内或之后立即无死亡或同侧中风遵循以下步骤。次要疗效终点是术后31天到1年内预防同侧中风。在6和12个月时进行的CA多普勒超声检查显示,三级有效性终点小于70%的残余狭窄。使用45个NexStents治疗了44例患者(平均年龄71岁,范围51-89岁;男性30例,有症状性狭窄病变的18例[41%])(两名患者放置了两个支架)。在所有患者中,术后血管造影的残余狭窄少于30%。 41例患者(93%)达到了1个月的主要终点。 30天之内发生的三个主要不良事件是:1例与充血性心力衰竭相关的死亡和2例同侧中风,其中1例导致死亡。在完成随访评估的35例患者中,术后1至12个月内未发生同侧中风。术后6个月,在一名患者中发现无症状的复发性狭窄,需要进行重复的血管成形术。结论:NexStent的置入是可行的,并能有效治疗CA狭窄患者,并有望获得长期效果。

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