Mesh for pelvic floor repair
    1.
    发明授权
    Mesh for pelvic floor repair 有权
    骨盆修补网

    公开(公告)号:US07087065B2

    公开(公告)日:2006-08-08

    申请号:US10263933

    申请日:2002-10-03

    IPC分类号: A61B17/04 A61F13/00

    摘要: A woven mesh is provided for supporting tissue or an organ within a female patient's pelvis, and a method for using the same. The mesh includes a central portion having a width, a length, first and second ends, and first and second side edges, and first and second wing portions extending from the first and second ends of the central portion respectively. The first and second wing portions each have a width, a length, and first and second peripheral edges. The width of the wing portions are each greater than the width of the central portion, and when positioned within the female patient, the central portion is positioned below and supports the tissue or organ. A mesh is also provided having woven fibers with voids therebetween, and having a central portion and first and second ends. The average size of the voids at least in the central portion is at least 25–50 mm2, and when positioned within the patient, the central portion is positioned below and supports the tissue or organ.

    摘要翻译: 提供用于支撑女性患者骨盆内的组织或器官的编织网及其使用方法。 网格包括具有宽度,长度,第一和第二端以及第一和第二侧边缘的中心部分,以及分别从中心部分的第一端和第二端延伸的第一和第二翼部分。 第一和第二翼部各自具有宽度,长度以及第一和第二周边边缘。 翼部的宽度各自大于中心部分的宽度,并且当定位在雌性患者体内时,中心部分位于下方并支撑组织或器官。 还提供了一种网格,其具有在其间具有空隙的编织纤维,并且具有中心部分和第一和第二端部。 至少在中心部分的空隙的平均尺寸至少为25-50mm 2,并且当位于患者体内时,中心部分位于下方并支撑组织或器官。

    Vaginal pessary
    2.
    发明授权
    Vaginal pessary 有权
    阴道子宫托

    公开(公告)号:US06645137B2

    公开(公告)日:2003-11-11

    申请号:US10180726

    申请日:2002-06-27

    IPC分类号: A61F200

    CPC分类号: A61F2/005 Y10S128/25

    摘要: A vaginal insert has a flexible body either in the form of a belt or a split cylinder. In either case, the insert may be coiled into a coiled state. The body has a reduced diameter when coiled and exhibits a resilient bias toward uncoiling and expanding in diameter from the coiled state. When the insert is inserted into the vagina of a patient, it expands and presses against the vaginal wall. This pressure in itself may be therapeutic, e.g., in treating cystocele and incontinence. A medicament may be conjoined with the insert that is introduced to the patient through contact with the insert. The insert can have a simultaneous mechanical and pharmacological effect, e.g., in the instance of treating incontinence with a drug and pressure. The belt-type body may incorporate mating ridges and grooves to keep the insert in a cylindrical configuration. Latch elements may be incorporated on the insert to support the insert in an expanded, partially uncoiled state.

    摘要翻译: 阴道插入物具有柔性体,其形式为带或分裂圆筒。 在任一情况下,插入件可以卷绕成卷绕状态。 当卷绕时主体具有减小的直径,并且呈现出从卷绕状态开始直径扩展的弹性偏压。 当插入物插入患者的阴道时,它会膨胀并压靠阴道壁。 该压力本身可以是治疗性的,例如在治疗膀胱癌和失禁中。 药物可以与通过与插入物接触引入患者的插入物结合。 插入物可以具有同时的机械和药理作用,例如在用药物和压力治疗失禁的情况下。 带式主体可以包括配合脊和凹槽以​​将插入件保持在圆柱形构型中。 闩锁元件可以结合在插入件上以将扩展的部分未卷曲的状态支撑在插入件上。

    System and method for assessing urinary function

    公开(公告)号:US07052452B2

    公开(公告)日:2006-05-30

    申请号:US10183790

    申请日:2002-06-27

    IPC分类号: A61F2/00 A61M29/00

    摘要: A medical system is provided for assessing urinary function. The system includes a control device and at least one test module capable of being removably coupled to the control device such that, when coupled, the system is capable of performing a test to assess urinary function. The control device may include a processor and memory having stored therein a plurality of software subroutine, at least one of which directs a test to assess urinary function. The test module may include a module identification device, and the control device selects the software subroutine based upon information obtained from the module identification device. The test module may further include a tubing assembly forming a first fluid conduit between a first fluid inlet and a first fluid outlet and an insert member dimensioned for at least partial insertion into a patient's urinary tract and coupled to the first fluid outlet so that fluid infused through the first fluid conduit flows through the insert member.

    Device for staunching uterus bleeding
    5.
    发明授权
    Device for staunching uterus bleeding 有权
    用于猝死子宫出血的装置

    公开(公告)号:US6024753A

    公开(公告)日:2000-02-15

    申请号:US117757

    申请日:1998-12-24

    摘要: A device for staunching uterine bleeding comprising an expandable balloon and a tubular handle connected therewith for the insertion of the balloon into the uterine cavity, which can be connected to a fluid source for pressurizing the balloon to effecting and maintain the expansion thereof. The balloon is dimensioned to fill the uterine cavity at expansion and to exert pressure against the bounding wall thereof over substantially the total surface of the wall. The device further includes a pump and control unit and a hose connected to one end thereof with the handle at the other end thereof with a connection element for connecting to a fluid source. The hose can be detachable mounted to the pump and control unit in operative co-operation therewith and forms together with the balloon and the handle a separate unit for one-way use.

    摘要翻译: PCT No.PCT / SE97 / 00162 Sec。 371日期1998年12月24日第 102(e)日期1998年12月24日PCT提交1997年2月4日PCT公布。 第WO97 / 27810号公报 日期1997年8月7日一种用于猝死子宫出血的装置,包括可膨胀气囊和与之连接的管状手柄,用于将气囊插入子宫腔,所述子宫腔可连接到流体源以对气囊进行加压并保持膨胀 其中。 气囊的尺寸被设计成在膨胀时填充子宫腔,并在壁的整个总表面上施加压力以抵抗其边界壁。 该装置还包括泵和控制单元以及与其一端连接的软管,其另一端具有用于连接到流体源的连接元件。 软管可以可拆卸地安装到泵和控制单元,与之配合,并与气囊和手柄一起形成用于单向使用的单独单元。

    Method for localizing a region in the human body, in particular venous
thrombi, by the uptake of a radioactive substance, particularly .sup.125 I
-
    6.
    发明授权
    Method for localizing a region in the human body, in particular venous thrombi, by the uptake of a radioactive substance, particularly .sup.125 I - 失效
    通过摄取放射性物质,特别是125I-纤维蛋白原来定位人体中的区域,特别是静脉血栓的方法

    公开(公告)号:US4453075A

    公开(公告)日:1984-06-05

    申请号:US481977

    申请日:1983-04-04

    摘要: An apparatus for determining the depth position of venous thrombi in the lower extremities utilizes a unique property in .sup.125 I. This resides in the fact that in approximately half of all disintegrations, two photons are emitted simultaneously. These two coincident photons have, like separately emitted photons, an energy of approximately 28 keV. A scintillation detector perceives the coincidently emitted photons as one photon of an energy of 56 keV. The quotient between the number of separately emitted photons and the number of coincident photons may thus be determined. This quotient constitutes a parameter which is greatly dependent on the distance between the detector and the source of radiation, whereby there is obtained a possibility of determining the depth of the thrombus.

    摘要翻译: 用于确定下肢静脉血栓的深度位置的装置利用125I中的独特性质。 这归因于在大约一半的崩解中,两个光子同时发射。 这两个重合的光子像独立发射的光子一样具有约28keV的能量。 闪烁探测器将同时发射的光子感知为56 keV能量的一个光子。 因此可以确定分开发射的光子的数量与重合的光子的数量之间的商。 该商构成了很大程度上取决于检测器与辐射源之间的距离的参数,从而获得了确定血栓深度的可能性。

    System and method for assessing urinary function
    7.
    发明授权
    System and method for assessing urinary function 有权
    泌尿功能评估系统及方法

    公开(公告)号:US07255673B2

    公开(公告)日:2007-08-14

    申请号:US10183656

    申请日:2002-06-27

    IPC分类号: A61F2/00 A61B5/00

    摘要: A method is provided for assessing urinary function including removably coupling a first test module to a portable control device, selecting from a plurality of different tests a first test to assess urinary function, the selection being made based on first module identification information obtained by the control device from the test module, and performing the first test. The method may also include one or more of the steps of inserting an insert member coupled to the first test module at least partially into a patient's urinary tract, infusing fluid through the insert member into the urinary tract, and measuring pressure within the urinary tract as fluid is infused therein. The method may further include uncoupling the first test module from the portable control device, coupling a second test module to the portable control device, selecting a second test to assess urinary function based on second module identification information obtained by the control device from the second test module, and performing the second test.

    摘要翻译: 提供了一种用于评估尿功能的方法,包括将第一测试模块可移除地耦合到便携式控制设备,从多个不同测试中选择第一测试来评估尿功能,所述选择是基于通过控制获得的第一模块识别信息 设备,并执行第一次测试。 该方法还可以包括一个或多个步骤:将连接到第一测试模块的插入构件至少部分地插入到患者的尿道中,将流体通过插入构件输入尿道,并且测量尿道内的压力作为 流体注入其中。 该方法还可以包括将第一测试模块与便携式控制设备解耦,将第二测试模块耦合到便携式控制设备,基于由第二测试由控制设备获得的第二模块识别信息,选择第二测试来评估尿功能 模块,并执行第二个测试。

    Surgical instrument for treating female urinary incontinence
    9.
    发明申请
    Surgical instrument for treating female urinary incontinence 有权
    用于治疗女性尿失禁的手术器械

    公开(公告)号:US20050148813A1

    公开(公告)日:2005-07-07

    申请号:US11049507

    申请日:2005-02-02

    摘要: A surgical assembly and method for treating female urinary incontinence. The assembly includes a substantially flat, flexible tape having first and second ends, wherein at least a portion of the tape is adapted to be permanently implanted into a female patient's body as a loop beneath the urethra. The assembly further includes a flexible sheath having a first portion covering a first length of the tape and a second portion covering a second length of the tape. The first and second portions substantially cover the entire length of the implant portion of the tape prior to implantation of the tape and sheath combination into the patient's body. Following implantation into the patient's body, the first and second portions of the sheath are removable from the first and second ends of the tape respectively.

    摘要翻译: 一种用于治疗女性尿失禁的手术组件和方法。 组件包括具有第一和第二端的基本平坦的柔性带,其中至少一部分带适于作为尿道下方的环永久地植入女性患者体内。 组件还包括柔性护套,其具有覆盖带的第一长度的第一部分和覆盖带的第二长度的第二部分。 在将带和组合植入患者体内之前,第一部分和第二部分基本上覆盖胶带的植入部分的整个长度。 在植入患者身体之后,护套的第一和第二部分分别从带的第一和第二端移除。

    Surgical instrument for treating female urinary incontinence
    10.
    发明授权
    Surgical instrument for treating female urinary incontinence 失效
    用于治疗女性尿失禁的手术器械

    公开(公告)号:US5899909A

    公开(公告)日:1999-05-04

    申请号:US804680

    申请日:1997-02-25

    摘要: A surgical instrument and a method for treating female urinary incontinence. The instrument comprises a shank having a handle at one end thereof, and two curved needle-like elements which are connected at one end thereof each with one end of a tape intended to be implanted into the body. These elements can be connected one at a time with the shank at the other end thereof to form a curved end portion of the shank and are intended to be passed into the body via the vagina, each element being dimensioned to extend from the inside of the vaginal wall over the back of the pubic bone to the outside of the abdominal wall. When practicing the method the tape is passed into the body via the vagina first at one end and then at the other end at one side and the other, respectively, of the urethra to form a loop around the urethra, located between urethra and the vaginal wall. The tape is extended over the pubis and through the abdominal wall and is tightened. Then, the tape ends are cut at the abdominal wall, and the tape is left implanted in the body.

    摘要翻译: 一种手术器械和一种治疗女性尿失禁的方法。 仪器包括在其一端具有手柄的柄,以及两个弯曲的针状元件,其一端连接,每个具有旨在植入身体的带的一端。 这些元件可以在其另一端与柄同时连接一个,以形成柄的弯曲端部,并且旨在经由阴道进入身体,每个元件的尺寸被设计成从内侧延伸 阴道壁在耻骨后面到腹壁外侧。 当实施该方法时,胶带首先在阴道的一端通过阴道,然后在另一端分别在尿道的一侧和另一端进入身体,以在尿道周围形成环,位于尿道和阴道之间 壁。 胶带延伸到耻骨上并穿过腹壁并收紧。 然后,将带末端在腹壁处切割,并将带子植入体内。