Transcatheter Options for Treatment of Mitral Regurgitation

Schaefer Schaefer, H. Treede, H. Reichenspurner, L. Conradi
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引用次数: 1

Abstract

Transcatheter therapy for valvular heart disease (VHD) as an alternative for surgery, as the standard of care, has emerged rapidly over the last 10 years. Since the first transcatheter heart valve (THV) implantation in pulmonary position, in 2000, and in aortic position, in 2002, an enormous number of high-risk patients have undergone percutaneous aortic valve implantation and a wide variety of commercially available THVs have emerged within the medical sector. Interventional mitral valve repair (MVR) and implantation started with a variety of devices developed by industry, but few are available at the moment. In this article percutaneous systems for the treatment of mitral regurgitation (MR) in high-risk patients are introduced and discussed. Technologies currently under development can be classified by their anatomical approach. To date, only the percutaneous edge-to-edge approach is applied on a larger scale in clinical routine with the MitraClip device. Several other technologies for percutaneous MVR have achieved first-in-man results. For comparable results of transcatheter MVR to surgical MVR a combination of these technologies may be required. The field of transcatheter mitral valve implantation is evolving quickly as well. With half a dozen devices under development right now and a few entering the clinical test stage it may be just a matter of time until a THV for the mitral position will become commercially available. Considering that MR is among the most frequent entities in VHD and, furthermore, that life expectancy will continue to increase, it can be anticipated that in the near future there will be percutaneous strategies needed for the treatment of MR in high-risk patients. At present, all devices have to be restricted to inoperable patients or to compassionate use settings. However, once clinical proof of safety and efficacy have been demonstrated, extension to a broader patient spectrum seems likely. To ensure cautious and safe clinical introduction of these novel therapeutic options, guidance by interdisciplinary dedicated heart teams is of paramount importance.
经导管治疗二尖瓣返流的选择
经导管治疗瓣膜性心脏病(VHD)作为外科手术的一种替代方法,作为治疗标准,在过去十年中迅速兴起。自2000年首次在肺动脉位植入经导管心脏瓣膜(THV), 2002年在主动脉位植入经导管心脏瓣膜以来,大量高危患者接受了经皮主动脉瓣植入术,医疗领域出现了各种各样的商用THV。介入二尖瓣修复(MVR)和植入术开始于工业上开发的各种设备,但目前可用的设备很少。在本文中,经皮系统治疗二尖瓣反流(MR)在高危患者的介绍和讨论。目前正在开发的技术可以根据其解剖方法进行分类。迄今为止,只有经皮边缘对边缘入路在MitraClip设备的临床常规中大规模应用。其他几种经皮MVR技术已经取得了首次在人体中的效果。为了比较经导管MVR和外科MVR的结果,可能需要这些技术的组合。经导管二尖瓣植入术领域也在迅速发展。目前有六种设备正在开发中,其中一些进入临床测试阶段,用于二尖瓣位置的THV商业化可能只是时间问题。考虑到MR是VHD中最常见的实体之一,而且预期寿命将继续增加,可以预见,在不久的将来,将需要经皮策略来治疗高风险患者的MR。目前,所有的设备都必须被限制在不能手术的病人或同情使用的环境中。然而,一旦临床证明安全性和有效性得到证实,扩展到更广泛的患者范围似乎是可能的。为了确保谨慎和安全的临床引入这些新的治疗方案,跨学科的专业心脏团队的指导是至关重要的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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