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    • 4. 发明申请
    • Vein Occlusion Devices and Methods for Catheter-Based Ablation
    • 静脉闭塞装置及基于导管消融的方法
    • US20110144637A1
    • 2011-06-16
    • US12635821
    • 2009-12-11
    • Jean-Luc PageardTeresa A. Mihalik
    • Jean-Luc PageardTeresa A. Mihalik
    • A61B18/14
    • A61B5/02158A61B5/026A61B5/04085A61B5/6853A61B5/6869A61B5/6885A61B18/14A61B2017/00039A61B2017/00084A61B2017/00243A61B2017/22067A61B2018/00011A61B2018/0022A61B2018/0212A61B2018/0262A61M2025/1052A61M2025/1086
    • Medical devices and methods for deriving an indication of occlusion of a blood vessel from one or more physiologic sensor are disclosed. The physiological parameters contemplated for implementation in accordance with embodiments of the disclosure may include pressure, flow, force, temperature, or tension.An exemplary device comprises a catheter having an expandable chamber coupled to a distal end portion of the catheter shaft. In various embodiments, one or more physiologic sensors may be disposed on the catheter shaft and electrically coupled to control electronics that may be provided in a console for measurement of a physiologic signal. Alternatively, an external sensor may be disposed in fluid communication with a lumen of the catheter to derive a physiological parameter such as pressure via mechanical coupling of pressure distal to the expandable chamber to the fluid in the lumen.The parameters measured by the physiologic sensor(s) provide a measure of the physiological parameters in at least a first region. The physiological parameter measured in the first region is evaluated to obtain an indication of occlusion distal to the expandable chamber. In other embodiments, measurements of the physiological parameters may be performed in the first region and a second region to derive differential measurements that are evaluated to obtain an indication of occlusion.
    • 公开了用于从一个或多个生理传感器导出血管闭塞指示的医疗装置和方法。 根据本公开的实施例预期实施的生理参数可以包括压力,流量,力,温度或张力。 示例性装置包括具有联接到导管轴的远端部分的可扩张腔的导管。 在各种实施例中,一个或多个生理传感器可以设置在导管轴上并且电耦合到可以设置在控制台中用于测量生理信号的控制电子装置。 或者,可以将外部传感器设置成与导管的内腔流体连通,从而通过机械耦合到可扩张腔的压力到腔内的流体而获得生理参数,例如压力。 由生理传感器测量的参数提供至少第一区域中的生理参数的度量。 评估在第一区域中测量的生理参数以获得在可扩展腔室远端的闭塞指示。 在其他实施例中,生理参数的测量可以在第一区域和第二区域中进行,以得到被评估以获得闭塞指示的差异测量值。
    • 7. 发明授权
    • Triple balloon catheter
    • 三重气囊导管
    • US08926602B2
    • 2015-01-06
    • US12695423
    • 2010-01-28
    • Jean-Luc Pageard
    • Jean-Luc Pageard
    • A61B18/02A61B18/00
    • A61B18/02A61B2018/0022A61B2018/00255A61B2018/00261A61B2018/00375A61B2018/00577A61B2018/0212
    • The present invention advantageously provides a method and system for cryogenically ablating large areas of tissue within the left atrium. In an exemplary embodiment a cryotherapy device includes a catheter body, a proximal end and a distal end; a first lumen; a second lumen; and an ablation element expandable from a first diameter to a second diameter, the ablation element having a surface portion that conforms to the uneven surface topography of the cardiac tissue. The ablation element can include one or more deformable balloon and/or flexible elements. The surface of the balloon can further be shaped by regulation of pressure within the one or more balloons. In an exemplary method, a tissue ablation device is provided and tissue in the left atrium is ablated with the device, whereby the ablation is created by freezing tissue.
    • 本发明有利地提供了用于低温切除左心房内的大面积组织的方法和系统。 在示例性实施例中,冷冻治疗装置包括导管主体,近端和远端; 第一个管腔 第二个管腔 以及可从第一直径扩展到第二直径的消融元件,所述消融元件具有与心脏组织的不平坦表面形貌一致的表面部分。 消融元件可以包括一个或多个可变形的球囊和/或柔性元件。 球囊的表面可以通过调节一个或多个气囊内的压力而进一步成形。 在一种示例性方法中,提供组织消融装置,并且使用该装置消除左心房中的组织,由此通过冷冻组织产生消融。
    • 8. 发明授权
    • Compliant balloon catheter
    • 符合气囊导管
    • US07727191B2
    • 2010-06-01
    • US11129210
    • 2005-05-13
    • Teresa Ann MihalikJean-Luc PageardJohn W. Lehmann
    • Teresa Ann MihalikJean-Luc PageardJohn W. Lehmann
    • A61M29/00A61F7/12
    • A61B18/02A61B2017/22051A61B2018/0022A61B2018/0212A61B2018/0262A61M25/1011A61M2025/1013
    • A catheter includes a first expandable membrane having a first pressurization limit and a second expandable membrane, having a second pressurization limit, wherein the second pressurization limit is greater than the first pressurization limit, the first expandable membrane defines a cooling chamber, the second expandable membrane being disposed around the first expandable membrane to define an junction therebetween. The catheter includes a coolant injection lumen in fluid communication with the at least one fluid inlet port and the cooling chamber, and a primary coolant return lumen in fluid communication with the at least one fluid outlet port and the cooling chamber. The coolant injection tube, the cooling chamber, and the primary coolant return lumen define a first fluid pathway. The catheter further includes a secondary coolant return lumen in fluid communication with the at least one fluid outlet port and the junction. The junction and the secondary coolant return lumen define a second fluid pathway. The catheter provides a fail-safe feature by selecting the appropriate first and second pressurization limits for the first and second expandable membranes.
    • 导管包括具有第一加压极限的第一可膨胀膜和具有第二加压极限的第二可膨胀膜,其中所述第二加压极限大于所述第一加压极限,所述第一可膨胀膜限定冷却室,所述第二可膨胀膜 被布置在第一可膨胀膜周围以限定它们之间的接合部。 所述导管包括与所述至少一个流体入口和所述冷却室流体连通的冷却剂注入腔,以及与所述至少一个流体出口和所述冷却室流体连通的主冷却剂返回内腔。 冷却剂注入管,冷却室和主冷却剂回流腔限定第一流体通路。 导管还包括与至少一个流体出口和接合部流体连通的二次冷却剂返回内腔。 连接点和二次冷却剂回流腔限定第二流体通路。 该导管通过为第一和第二可膨胀膜选择适当的第一和第二加压限制来提供故障安全特征。