首页> 外文期刊>Journal of Korean Neurosurgical Society >The Evolution of Flow-Diverting Stents for Cerebral Aneurysms; Historical Review, Modern Application, Complications, and Future Direction
【24h】

The Evolution of Flow-Diverting Stents for Cerebral Aneurysms; Historical Review, Modern Application, Complications, and Future Direction

机译:脑动脉瘤流动转移支架的演变;历史评论,现代应用,并发症和未来方向

获取原文
           

摘要

In spite of the developing endovascular era, large (15–25 mm) and giant (25 mm) wide-neck cerebral aneurysms remained technically challenging. Intracranial flow-diverting stents (FDS) were developed to address these challenges by targeting aneurysm hemodynamics to promote aneurysm occlusion. In 2011, the first FDS approved for use in the United States market. Shortly thereafter, the Pipeline of Uncoilable or Failed Aneurysms (PUFS) study was published demonstrating high efficacy and a similar complication profile to other intracranial stents. The initial FDA instructions for use (IFU) limited its use to patients 22 years old or older with wide-necked large or giant aneurysms of the internal carotid artery (ICA) from the petrous segment to superior hypophyseal artery/ophthalmic segment. Expanded IFU was tested in the Prospective Study on Embolization of Intracranial Aneurysms with PipelineTM Embolization Device (PREMIER) trial. With further post-approval clinical data, the United States FDA expanded the IFU to include patients with small or medium, wide-necked saccular or fusiform aneurysms from the petrous ICA to the ICA terminus. However, IFU is more restrictive in South Korea than in United States. Several systematic reviews and meta-analyses have sought to evaluate the overall efficacy of FDS for the treatment of cerebral aneurysms and consistently identify FDS as an effective technique for the treatment of aneurysms broadly with complication rates similar to other traditional techniques. A growing body of literature has demonstrated high efficacy of FDS for small aneurysms; distal artery aneurysms; non-saccular aneurysms posterior circulation aneurysms and complication rates similar to traditional techniques. In the short interval since the Pipeline Embolization Device was first introduced, FDS has been firmly entrenched as a powerful tool in the endovascular armamentarium. As new FDS are developed, established FDS are refined, and delivery systems are improved the uses for FDS will only expand further. Researchers continue to work to optimize the mechanical characteristics of the FDS themselves, aiming to optimize deploy ability and efficacy. With expanded use for small to medium aneurysms and posterior circulation aneurysms, FDS technology is firmly entrenched as a powerful tool to treat challenging aneurysms, both primarily and as an adjunct to coil embolization. With the aforementioned advances, the ease of FDS deployment will improve and complication rates will be further minimized. This will only further establish FDS deployment as a key strategy in the treatment of cerebral aneurysms.
机译:尽管存在显影血管内时代,但大(15-25毫米)和巨大(> 25毫米)宽颈部脑动脉瘤仍然在技术上挑战。开发了颅内流动转移支架(FDS)以通过靶向动脉瘤血流动力学来解决这些挑战,以促进动脉瘤闭塞。 2011年,第一个FDS批准用于美国市场。此后不久,未加工或失败的动脉瘤(PUFS)研究的管道被公布展示高疗效和与其他颅上的同样的并发症曲线。使用的初始FDA指令(IFU)限制其对22岁或以上患者的患者,从岩石段的内部颈动脉(ICA)的宽颈部大或巨型动脉瘤(ICA)到高级衰落动脉/眼科段。在颅内动脉瘤与管道栓塞装置(总理)试验的前瞻性研究中进行了扩展的IFU。通过进一步的审批临床数据,美国FDA扩展了IFU,将患有来自岩石ICA的小型或中等,宽颈部或梭形动脉瘤的患者纳入ICA末端。然而,IFU在韩国比在美国更严格。若干系统的评价和荟萃分析要求评估FDS治疗脑动脉瘤的整体疗效,并一致地将FDS鉴定为广泛处理动脉瘤的有效技术,其并发症与其他传统技术相似的并发症率。越来越多的文学体现了FDS对小动脉瘤的高疗效;远端动脉瘤;非椎弓束后循环动脉瘤和类似于传统技术的并发率。在第一次引入流水线栓塞装置的情况下,FDS已被牢固地作为血管内的血管内的强大工具被牢固地侵入。由于开发了新的FD,所建立的FDS是精制的,交付系统改善了FDS的用途将仅扩展。研究人员继续努力优化FDS本身的机械特性,旨在优化部署能力和功效。随着中小型动脉瘤和后循环动脉瘤的扩展使用,FDS技术被牢固地作为一种强大的工具,以治疗挑战动脉瘤,主要是线圈栓塞的辅助动脉瘤。随着上述进步,FDS部署的易用性将提高,并将进一步最小化并发症率。这将仅进一步建立FDS部署作为治疗脑动脉瘤的关键策略。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号