首页> 外国专利> Tubular stent-type endoprosthesis for use in cardiovascular surgery is cut out from stainless steel tube and has radial force slightly greater than the elastic retraction of blood vessel in which it is implanted

Tubular stent-type endoprosthesis for use in cardiovascular surgery is cut out from stainless steel tube and has radial force slightly greater than the elastic retraction of blood vessel in which it is implanted

机译:从不锈钢管上切下用于心血管外科的管状支架式内置假体,其径向力略大于植入其的血管的弹性回缩

摘要

Vascular stent made from stainless steel tube has crushing resistance 1.2-2 times the elastic retraction force of the vascular vessel. The stent is formed from a succession of annular segments articulated by curved sections. Stent for implanting in vascular vessel in its deployed state, aided by balloon expansion, is made by cutting stainless steel tube and, once implanted and deployed, it has crushing resistance from 1.2 times to 2 times of elastic retraction force of this vascular vessel. In case (I) of implanting the stent in coronary artery its crushing resistance in deployed state is 0.2 * 105 Pa, and in case (II) of implantation in periphery artery the crushing resistance is 0.5 * 105 Pa. The stent comprises a succession of annular segments composed of sections articulated by one or two curved connections between each two annular segments. In case (I) the length L1 of annular segment is approximately 1.4 mm, the number of connections is 1 and each segment consists of 7 sections. In case (II) the length L1 of annular segment is approximately 3.9 mm, the number of connections is 1 and each segment consists of 6 sections. Preferably each segment has the form of a coil composed of a succession of arms linked two to two by articulation zones, with each two arms linked with articulation zone forming one section, and with each arm of a segment disposed obliquely in relation to longitudinal axis, at an angle alpha above 20 deg , preferably 20-30 deg . Successive connections are preferably angularly shifted in relation to longitudinal axis of stent, forming helix path. The length L2 of each connection is preferably 1/4 of the length L1 of annular segment. The arms of two successive annular segments are preferably at the inverse alpha angle to each other, and the articulation zones of two adjacent annular segments are shifted in such way as to ensure oblique general direction of correspondent connection. The stent preferably has radio-opaque marker at each of its extremities, in form of curved piece closed around such extremity. The marker preferably has protective coating, to diminish its electric potential, or the stent extremity (or at least its part) destined to receive the marker comprise such protective coating.
机译:由不锈钢管制成的血管支架的抗压碎性是血管弹性回缩力的1.2-2倍。支架由弯曲部分铰接的一系列环形段形成。处于扩张状态的植入血管的支架,借助于球囊扩张,是通过切割不锈钢管制成的,一旦植入和部署,其抗压强度是该血管的弹性收缩力的1.2到2倍。在(I)将支架植入冠状动脉的情况下,其在展开状态下的抗压阻为0.2 * 10 5 Pa,在(II)植入周边动脉的情况下,抗压性为0.5 * 10 5 Pa Pa。该支架包括一系列环形段,该环形段由通过每两个环形段之间的一个或两个弯曲连接而铰接的段组成。在情况(I)中,环形段的长度L1约为1.4 mm,连接数为1,每个段由7个部分组成。在情况(II)中,环形段的长度L1约为3.9 mm,连接数为1,每个段由6个部分组成。优选地,每个段具有线圈的形式,该线圈由通过关节运动区域连接成两个的连续臂组成,其中每两个臂与关节运动区域连接形成一个部分,并且段的每个臂相对于纵轴倾斜地设置,以20度以上的α角,最好是20-30度。连续的连接优选地相对于支架的纵轴成角度地移位,从而形成螺旋路径。每个连接的长度L2优选为环形段的长度L1的1/4。两个连续的环形段的臂优选彼此成反α角,并且两个相邻的环形段的铰接区以确保相应连接的倾斜大体方向的方式移动。支架优选在其每个末端具有不透射线的标记,其形式是围绕该末端闭合的弯曲件。标记物优选具有保护涂层,以减小其电势,或预定接收标记物的支架末端(或至少其一部分)包括这种保护涂层。

著录项

  • 公开/公告号FR2793673A1

    专利类型

  • 公开/公告日2000-11-24

    原文格式PDF

  • 申请/专利权人 LEFEBVRE JEAN MARIE;

    申请/专利号FR19990006538

  • 发明设计人 LEFEBVRE JEAN MARIE;

    申请日1999-05-18

  • 分类号A61F2/06;

  • 国家 FR

  • 入库时间 2022-08-22 01:07:55

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