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    • 21. 发明授权
    • Circumferential ablation device assembly
    • US6117101A
    • 2000-09-12
    • US199736
    • 1998-11-25
    • Chris J. DiederichMichael D. LeshJames C. Peacock, IIIMichael R. Ross
    • Chris J. DiederichMichael D. LeshJames C. Peacock, IIIMichael R. Ross
    • A61B17/00A61B18/00A61B18/14A61F2/958A61N7/02A61B17/20
    • A61B18/1492A61B18/00A61M25/1002A61N7/02A61B2017/00243A61B2018/00083A61B2018/00148A61B2018/00214A61M2210/125A61N7/022
    • This invention is a circumferential ablation device assembly which is adapted to forming a circumferential conduction block in a pulmonary vein. The assembly includes a circumferential ablation element which is adapted to ablate a circumferential region of tissue along a pulmonary vein wall which circumscribes the pulmonary vein lumen, thereby transecting the electrical conductivity of the pulmonary vein against conduction along its longitudinal axis and into the left atrium. The circumferential ablation element includes an expandable member with a working length that is adjustable from a radially collapsed position to a radially expanded position. An equatorial band circumscribes the outer surface of the working length and is adapted to ablate tissue adjacent thereto when actuated by an ablation actuator. The equatorial band has a length relative to the longitudinal axis of the expandable member that is narrow relative to the working length, and is also substantially shorter than its circumference when the working length is in the radially expanded position. A pattern of insulators may be included over an ablation element which otherwise spans the working length in order to form the equatorial band described. The expandable member is also adapted to conform to the pulmonary vein in the region of its ostium, such as by providing a great deal of radial compliance or by providing a taper along the working length which has a distally reducing outer diameter. A linear ablation element is provided adjacent to the circumferential ablation element in a combination assembly which is adapted for use in a less-invasive "maze"-type procedure in the region of the pulmonary vein ostia in the left ventricle. A cylindrical ultrasound transducer is provided on an inner member within the balloon and forms the circumferential ablation member by emitting a radial ultrasound signal which is circumferential to the transducer and highly collimated to the transducer's length. The circumferential ultrasound signal sonically couples to the balloon's outer skin to form the circumferential ablation element that is adapted to ablate a circumferential path of tissue engaged to the balloon.
    • 22. 发明申请
    • COAPTATION ENHANCEMENT IMPLANT, SYSTEM, AND METHOD
    • 加工植入,系统和方法
    • US20120197388A1
    • 2012-08-02
    • US13099532
    • 2011-05-03
    • Alex KhairkhahanMichael D. Lesh
    • Alex KhairkhahanMichael D. Lesh
    • A61F2/24
    • A61F2/246A61B17/0401A61B17/064A61B17/068A61B17/12122A61B17/12172A61B2017/00867A61B2017/0412A61B2017/0448A61B2017/0464A61B2017/048A61B2017/0649A61F2/2454A61F2/2457A61F2/2466A61F2250/0003
    • Implants, implant systems, and methods for treatment of mitral valve regurgitation and other valve diseases generally include a coaptation assist body which remains within the blood flow path as the leaflets of the valve move, the valve bodies often being relatively thin, elongate (along the blood flow path), and/or conformable structures which extend laterally from commissure to commissure, allowing the native leaflets to engage and seal against the large, opposed surfaces on either side of the valve body during the heart cycle phase when the ventricle contracts to empty that chamber of blood, and allows blood to pass around the valve body so that blood flows from the atrium to the ventricle during the filling phase of the heart cycle. Separate deployment of independent anchors near each of the commissures may facilitate positioning and support of an exemplary triangular valve body, with a third anchor being deployed in the ventricle. An outer surface of the valve body may accommodate tissue ingrowth or endothelialization, while a fluid-absorbing matrix can swell after introduction into the heart. The valve body shape may be selected after an anchor has been deployed, and catheter-based deployment systems may have a desirable low profile.
    • 植入物,植入物系统和治疗二尖瓣关闭不全的其它瓣膜疾病的方法通常包括接合辅助体,其保持在血流动路径内,因为瓣膜的小叶移动,瓣膜体通常相对较薄(沿着 血流路径)和/或适形结构,其从合缝延伸到合缝,允许天然小叶在心脏周期阶段期间在心脏周期阶段期间接合并密封在阀体两侧的大的相对表面上,当心室收缩为空 血液室,并允许血液在阀体周围通过,使得血液在心脏周期的充盈阶段期间从心房流向心室。 在每个连合处附近单独部署独立的锚杆可以促进示例性三角形阀体的定位和支撑,其中第三锚定部分在心室中。 阀体的外表面可以适应组织向内生长或内皮化,而吸入液体的基质可以在引入心脏后膨胀。 可以在锚定器部署之后选择阀体形状,并且基于导管的部署系统可以具有期望的低轮廓。