Apparatus and method for inducing fibrillation
    31.
    发明授权
    Apparatus and method for inducing fibrillation 失效
    用于诱发纤颤的装置和方法

    公开(公告)号:US5649971A

    公开(公告)日:1997-07-22

    申请号:US568044

    申请日:1995-12-06

    IPC分类号: A61N1/38 A61N1/39 A61N1/362

    CPC分类号: A61N1/385 A61N1/3943

    摘要: A method and apparatus for inducing fibrillation in a patient's heart by delivering a direct current stimulus to the heart from a DC-to-DC converter. The hardware of a conventional implantable cardioverter/defibrillator (ICD) is utilized with a modification to the control algorithms. Particularly, when it is desired to induce fibrillation in a patient's heart, typically during ICD implant defibrillation threshold (DFT) testing, a command is delivered from an external instrument to the ICD to deliver the fibrillation shock. The DC-to-DC converter which is normally used to charge the ICD high voltage capacitors is activated and immediately thereafter or following a short period to allow the high voltage capacitors to charge, the high voltage output switches of the output stage are closed. This delivers the output current from the DC-to-DC converter to the defibrillation electrodes and through the patient's heart. This stimulus is continued for a predetermined time of between about 30 milliseconds to 5 seconds. At that point the output switches are opened and the converter is shut off. This DC stimulus delivered directly to the patient's heart induces fibrillation.

    摘要翻译: 一种用于通过从DC-DC转换器向心脏递送直流刺激来诱导患者心脏颤动的方法和装置。 传统的植入式心律转复除颤器(ICD)的硬件被用于控制算法的修改。 特别地,当期望在患者心脏中诱发纤维颤动时,通常在ICD植入物除颤阈值(DFT)测试期间,将命令从外部仪器传送至ICD以递送原纤维颤动。 通常用于对ICD高电压电容器充电的DC-DC转换器被激活并且紧接其后或在短时间之后,以允许高压电容器充电,输出级的高电压输出开关闭合。 这将输出电流从DC-DC转换器提供给除颤电极并通过患者的心脏。 该刺激持续约30毫秒至5秒的预定时间。 此时,输出开关打开,转换器关闭。 直接传递给患者心脏的直流刺激会导致纤维颤动。

    Pulse generator with case that can be active or inactive
    32.
    发明授权
    Pulse generator with case that can be active or inactive 失效
    脉冲发生器,可以处于活动或非活动状态

    公开(公告)号:US5620477A

    公开(公告)日:1997-04-15

    申请号:US455824

    申请日:1995-05-31

    IPC分类号: A61N1/375

    CPC分类号: A61N1/3752

    摘要: A pulse generator having a housing for enclosing and containing pulse generator defibrillation circuitry, particularly adapted to allow for ease of manufacture and use, is disclosed. At least one surface of the housing is electrically conductive and connected to the pulse generator circuitry for delivering defibrillating energy to the heart. The defibrillator is provided with a case activating lead connector cavity having two connector blocks. By plugging in a lead with a pin long enough to contact the only first connector block, the lead becomes active. Using a plug with a longer pin to contact both blocks activates the can. To use neither a lead in the case activating port, nor an active can, a plug with a short or nonconductive pin may be used to plug the cavity without activating the can. By using this system, various electrode configurations can be used as required to provide the optimum system for a given patient. The pulse generator housing is preferably implanted in the left pectoral region proximate the heart with the conductive surface facing the heart. Other implantable electrodes are discharged against the pulse generator housing electrode.

    摘要翻译: 公开了一种脉冲发生器,其具有用于封闭和容纳脉冲发生器除颤电路的壳体,特别适于容易制造和使用。 壳体的至少一个表面是导电的并且连接到脉冲发生器电路,用于将去纤维化能量递送到心脏。 除颤器设置有具有两个连接器块的壳体启动引线连接器腔。 通过插入一根引脚,引脚长度足以接触唯一的第一个连接器块,引线将变为活动状态。 使用较长针脚的插头接触两个块可激活罐头。 为了在启动端口的情况下既不使用引线,也不使用活动端子,可以使用具有短导体或非导通插头的插头来插入腔体而不激活罐体。 通过使用该系统,可以根据需要使用各种电极配置来为给定的患者提供最佳的系统。 脉冲发生器壳体优选地植入靠近心脏的左胸部区域,导电表面面向心脏。 其他可植入电极被排出脉冲发生器壳体电极。

    Endocardial lead system with defibrillation electrode fixation
    33.
    发明授权
    Endocardial lead system with defibrillation electrode fixation 失效
    心肌引导系统除颤电极固定

    公开(公告)号:US5476500A

    公开(公告)日:1995-12-19

    申请号:US170133

    申请日:1993-12-20

    IPC分类号: A61N1/04 A61N1/05

    CPC分类号: A61N1/0573 A61N1/0563

    摘要: A lead system for use with an implantable cardioverter/defibrillator is disclosed. The lead system includes a fixation hook positioned approximately half-way between the distal tip of the lead and the tricuspid valve. The distal tip of the lead is positioned at the apex of the right ventricle and may or may not be secured there by a second fixation means such as a screw tip or tines. The fixation hook allows the defibrillation electrode to be accurately positioned by the patient's surgeon and maintained in contact with the septum wall of the patient's heart. By providing such intimate contact between the defibrillation electrode and the septum wall, defibrillation thresholds are reduced.

    摘要翻译: 公开了一种与植入式心律转复除颤器一起使用的引导系统。 引导系统包括定位在引线的远端和三尖瓣之间大致中途的固定钩。 引线的远端位于右心室的顶点处,并且可以通过第二固定装置(例如螺钉尖端或尖齿)固定或不固定。 固定钩允许除颤电极被患者的外科医生精确地定位并保持与患者心脏的隔膜壁接触。 通过在除颤电极和隔膜壁之间提供这种紧密接触,降低了除颤阈值。

    Method for manufacturing implantable cardiac defibrillation leads
utilizing a material removal process
    34.
    发明授权
    Method for manufacturing implantable cardiac defibrillation leads utilizing a material removal process 失效
    使用材料去除工艺制造植入式心脏除颤线的方法

    公开(公告)号:US5226260A

    公开(公告)日:1993-07-13

    申请号:US819106

    申请日:1992-01-09

    IPC分类号: A61N1/05 B24C1/00 B24C3/32

    CPC分类号: B24C1/003 A61N1/05 B24C3/322

    摘要: A method of manufacturing a medical electronic lead portion having an elastomeric mass and typically having a conductive metal member embedded in the elastomeric mass. The method includes the step of eroding elastomer of the mass from around the conductive metal member to form a predetermined shape by exposing the lead portion to a jet of gas containing entrained, particulate abrasive. Preferably, the particulate abrasive is softer than the conductive metal member to avoid scratching thereof. For example, soluble particulate abrasive such as sodium bicarbonate can be used.

    摘要翻译: 一种制造具有弹性质量并且通常具有嵌入在弹性体中的导电金属构件的医疗电子引线部分的方法。 该方法包括通过将引线部分暴露于含有夹带的颗粒磨料的气体射流,来侵蚀质量的弹性体从导电金属构件周围形成预定形状的步骤。 优选地,颗粒磨料比导电金属构件更软,以避免其刮擦。 例如,可以使用可溶性颗粒磨料如碳酸氢钠。

    Pacemaker for detecting and terminating a tachycardia

    公开(公告)号:US4880005A

    公开(公告)日:1989-11-14

    申请号:US198614

    申请日:1988-05-23

    IPC分类号: A61N1/362

    CPC分类号: A61N1/3621

    摘要: A heart pacemaker detects pace-terminable tachycardia conditions in the atrium of the heart in accordance with selected high rate, rate stability, sudden onset and sustained high rate criteria. When a pace-terminable tachycardia is detected, programmed treatment modalities are applied to attempt to terminate the tachycardia. The tachycardia is treated by applying timed bursts of electrical pulses in formats defined by programmed primary and secondary treatment modalities. The primary and secondary treatments may be applied in an order which is dependent upon the prior successful treatment of similar tachycardias. The pacemaker may also utilize remembered treatment values which were successfully applied to treat similar tachycardias. The pacemaker may be programmed to restart the primary and secondary modes of treatment in the event that the modes initially failed to terminate a tachycardia. The pacemaker may also be programmed to limit the rate of burst pulses to avoid overstimulating the heart.

    Method and System for Device Identification
    39.
    发明申请
    Method and System for Device Identification 有权
    设备识别方法与系统

    公开(公告)号:US20100073680A1

    公开(公告)日:2010-03-25

    申请号:US12626577

    申请日:2009-11-25

    申请人: Benjamin D. Pless

    发明人: Benjamin D. Pless

    IPC分类号: G01B9/02

    CPC分类号: G06K9/2036 G06K9/00577

    摘要: Disclosed are a method and system for performing device identification and a medical device susceptible to identification using interference patterns for performing device identification. A source signal may be directed from an energy source towards the surface of a device for reflection therefrom. An interference pattern may be detected from the surface of the device, such as by a sensor. A determination as to whether a match exists between the representation of the interference pattern and a stored representation of an interference pattern may be performed. If a match exists, the device may be identified based on the stored representation of the interference pattern. Otherwise, a representation of the interference pattern may be stored and a unique identifier may be assigned to the stored representation of the interference pattern.

    摘要翻译: 公开了用于执行设备识别的方法和系统以及易于使用用于执行设备识别的干扰图案的识别的医疗设备。 源信号可以从能量源朝向装置的表面引导以从其反射。 可以从设备的表面(例如通过传感器)检测干涉图案。 可以执行关于在干涉图案的表示和存储的干涉图案的表示之间是否存在匹配的确定。 如果存在匹配,则可以基于存储的干涉图案的表示来识别该设备。 否则,可以存储干扰图案的表示,并且可以将唯一标识符分配给所存储的干涉图案的表示。

    AUTO ADJUSTING SYSTEM FOR BRAIN TISSUE STIMULATOR
    40.
    发明申请
    AUTO ADJUSTING SYSTEM FOR BRAIN TISSUE STIMULATOR 有权
    用于脑组织刺激仪的自动调节系统

    公开(公告)号:US20080319511A1

    公开(公告)日:2008-12-25

    申请号:US11767432

    申请日:2007-06-22

    申请人: Benjamin D. Pless

    发明人: Benjamin D. Pless

    IPC分类号: A61N1/36 A61B5/04

    摘要: An implantable neurostimulator for treating disorders such as epilepsy, pain, movement disorders and depression includes a detection subsystem capable of detecting a physiological condition and a therapy subsystem capable of providing a course of therapy in response to the condition. The therapy subsystem includes an auto-adjust module for automatically adjusting one or more parameters of the therapy so that the therapy subsystem can provide an adjusted parameter to the patient and solicit the patient's feedback concerning the adjustment without requiring the presence of, or immediate involvement with, a clinician or physician. The patient feedback can be analyzed by computer, clinician or a combination of both to determine an optimal range of parameters for subsequent courses of therapy. In this manner, information useful in tuning the neurostimulator therapy parameters to optimize them for individual patient can be acquired automatically outside of the traditional clinical setting, saving time and minimizing patient fatigue that otherwise would be experience in marathon, in-clinic tuning sessions. The auto-adjust module also can be configured to prompt the patient to provide feedback even when parameters are not being adjusted, so as to acquire information for a baseline or about any placebo effect when the patient is otherwise expecting changes to the therapy to be made.

    摘要翻译: 用于治疗诸如癫痫,疼痛,运动障碍和抑郁症的疾病的可植入神经刺激器包括能够检测生理状况的检测子系统和能够响应于该病症提供治疗过程的治疗子系统。 治疗子系统包括用于自动调整治疗的一个或多个参数的自动调整模块,使得治疗子系统可以向患者提供经调整的参数,并征求患者关于调整的反馈,而不需要存在或立即参与 ,临床医生或医师。 患者反馈可以由计算机,临床医师或两者的组合进行分析,以确定后续治疗疗程的最佳参数范围。 以这种方式,可以在传统临床环境之外自动获取调整神经刺激器治疗参数以优化个体患者的信息的有用信息,节省时间并最大限度地减少患者疲劳,否则将在马拉松,临床内调整课程中体验。 自动调整模块还可以被配置为即使在参数未被调整的情况下也提示患者提供反馈,以便当患者以其他方式期望改变治疗时获得基线信息或约为任何安慰剂效应 。