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首例经导管植入新型球囊扩张式 Myval 心脏瓣膜治疗失败的无缝线 Perceval 生物瓣中瓣。

First-in-man Valve-in-Valve with the new balloon-expandable Myval transcatheter heart valve in a failed sutureless Perceval bioprosthesis.

机构信息

Department of Cardiac Surgery, IRCCS San Raffaele Hospital, Vita-Salute San Raffaele University, Milan, Italy.

Department of Interventional Cardiology, IRCCS San Raffaele Hospital, Vita-Salute San Raffaele University, Milan, Italy.

出版信息

J Card Surg. 2021 Jul;36(7):2546-2548. doi: 10.1111/jocs.15533. Epub 2021 Apr 2.

Abstract

Sutureless aortic bioprostheses were introduced more than ten years ago, with the aim of decreasing cross-clamp time and thus becoming the first choice in older patients for many surgeons. However, published data are limited to a 5-year follow-up, and some cases of deterioration have already been described. High-risk patients who once have benefitted from a fast sutureless aortic replacement and now are experiencing a prosthesis dysfunction, could take advantage of a percutaneous Valve-in-Sutureless technique. Furthermore, thanks to technological improvement, new transcatheter prostheses have been designed, allowing a more precise positioning. In this report, we described the first Myval-in-Perceval case, which resulted in a safe and effective procedure.

摘要

无缝线主动脉生物瓣假体在十多年前被引入,目的是减少阻断时间,从而成为许多外科医生为老年患者的首选。然而,已发表的数据仅限于 5 年的随访,并且已经描述了一些假体恶化的情况。曾经受益于快速无缝线主动脉置换术且现在面临假体功能障碍的高危患者,可以采用经皮瓣中瓣技术。此外,得益于技术的改进,新的经导管假体已经设计出来,能够实现更精确的定位。在本报告中,我们描述了首例 Myval-in-Perceval 病例,该病例结果安全有效。

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