首页> 外文期刊>EuroIntervention: journal of EuroPCR in collaboration with the Working Group on Interventional Cardiology of the European Society of Cardiology >First clinical experience with the GARDEX EPD: A novel embolic protection device for Carotid artery stenting
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First clinical experience with the GARDEX EPD: A novel embolic protection device for Carotid artery stenting

机译:Gardex EPD的首先临床经验:一种用于颈动脉抵抗的新型栓塞保护装置

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Aims: Carotid artery stenting (CAS) has become an alternative to carotid endarterectomy in the treatment of carotid artery disease. The use of an embolic protection device (EPD) can reduce the frequency of embolic events during CAS. Difficult vascular anatomy may complicate current generation EPD placement. This problem is addressed by a new EPD, the GARDEX System. The aim of this study was to assess the safety and performance of the GARDEX EPD during CAS. Methods and results: Thirty-eight patients underwent CAS with the GARDEX EPD in two medical centres. All patients were prospectively followed up for 30 days. Device performance and procedural details were collected and analysed prospectively. Vessel anatomy and lesion morphology were evaluated and stratified into a scoring system for anatomic difficulty. More than a third of the patients were considered to have difficult vascular anatomy for CAS. All enrolled patients were successfully treated. There was one (2.6%) minor periprocedural stroke and there were two (5.3%) periprocedural TIAs which resolved within 24 hours. No additional complications were noted during the 30-day follow-up period. Conclusions: In this first experience, CAS under cerebral protection with the GARDEX EPD was safe and feasible. Our data suggest that the use of the GARDEX EPD is simple and shows high success rates even in challenging anatomies. The role of this new device in CAS needs to be further confirmed in a larger patient population.
机译:目的:颈动脉支架(CAS)已成为治疗颈动脉疾病的颈动脉切除术的替代品。使用栓塞保护装置(EPD)可以减少CA期间的栓塞事件的频率。困难的血管解剖可能会使当前的EPD安置复杂化。这个问题是通过Gardex系统的新EPD解决的。本研究的目的是评估CAS期间Gardex EPD的安全性和性能。方法和结果:三十八名患者接受了两种医疗中心的Gardex EPD。所有患者均均持续30天。设备性能和程序细节已预期收集和分析。评估血管解剖和病变形态,并分层成评分系统以用于解剖难度。超过三分之一的患者被认为对CAS具有困难的血管解剖学。所有注册的患者都已成功治疗。有一种(2.6%)次要的百倍细胞中风,有两种(5.3%)的霸权Tias,在24小时内解决。在30天的随访期间没有注意到任何额外的并发症。结论:在这第一次经验中,CAS下的CAS在Gardex EPD下的脑保护下是安全可行的。我们的数据表明,使用Gardex EPD的使用简单,即使在具有挑战性的解剖中也表现出高的成功率。在较大的患者人口中需要进一步证实CAS中的这种新设备的作用。

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