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    • 5. 发明授权
    • Ventricular connector
    • US06732501B2
    • 2004-05-11
    • US10184481
    • 2002-06-26
    • Long Sheng YuPeter PiferiSteven M. Parnis
    • Long Sheng YuPeter PiferiSteven M. Parnis
    • A61N1362
    • A61M1/10A61M1/1008A61M1/101A61M1/1025A61M1/122A61M1/3659
    • A ventricular apex connector for quick connection and disconnection of an inflow tube of a ventricular assist device, comprising a sewing ring, a cylindrical ring, gripping pins, a spring ring and a sealing O-ring is provided. The cylindrical ring defines two openings, diametrically opposed to each other, in its walls. Gripping pins, comprising rods with gripping pads, are placed in the openings in the cylindrical ring so that the gripping pads are at rest within the inner circumference of the cylindrical ring. The spring ring is placed around the cylindrical ring and the rods of the gripping pads, which extend out of the outer wall of the cylindrical ring, are welded to the spring ring. The gripping pins are thus biased towards each other by the force of the spring ring. When the spring ring is squeezed, at points away from the gripping pin connection points, the deformation of the spring ring causes the gripping pads to be pulled out towards the inner wall of the cylindrical ring. An inflow tube of a heart pump may then be inserted into the ventricular apex connector, and upon the release of the spring ring, the inflow tube is sealedly held within the ventricle of the heart. In an embodiment an adapter sleeve may be attached to the inflow tube. In a further embodiment, the inflow tube may include an inner sleeve that is slidably and rotatably mounted therein. The inflow tube may have a bend at an end.
    • 6. 发明授权
    • Method and circuit for detecting cardiac rhythm abnormalities using a differential signal from a lead with a multi-electrode tip
    • 使用来自具有多电极尖端的引线的差分信号来检测心律异常的方法和电路
    • US06728575B2
    • 2004-04-27
    • US09999131
    • 2001-11-30
    • Sven-Erik Hedberg
    • Sven-Erik Hedberg
    • A61N1362
    • A61N1/3956
    • A cardiac lead has an end adapted for contact with cardiac tissue that has a number of dot-like electrodes which are separated from each other by electrically insulating material, and which are positioned at respective locations adapted for simultaneous contact with the cardiac tissue. The dot-like electrodes produce respective unipolar signals. At least one difference signal from the unipolar signals of a pair of the dot-like electrodes. The difference signal is edited in circuitry of a cardiac assist device and is compared to a threshold. If the threshold is exceeded, a signal indicating a cardiac rhythm abnormality, such as fibrillation, is generated for triggering electrical therapy delivered to the cardiac tissue by the cardiac assist device.
    • 心脏引线具有适于与具有多个点状电极的心脏组织接触的端部,其通过电绝缘材料彼此分离,并且位于适于与心脏组织同时接触的各个位置处。 点状电极产生相应的单极信号。 来自一对点状电极的单极信号的至少一个差分信号。 差分信号在心脏辅助装置的电路中编辑并与阈值进行比较。 如果超过阈值,则产生指示心律失常(例如原纤维化)的信号,用于触发由心脏辅助装置递送至心脏组织的电疗。
    • 7. 发明授权
    • Evoked response variability as an indicator of autonomic tone and surrogate for patient condition
    • 诱发反应变异性作为患者状况的自主神经和代谢指标
    • US06711439B1
    • 2004-03-23
    • US10077663
    • 2002-02-14
    • Kerry BradleyEuljoon ParkLaurence S. Sloman
    • Kerry BradleyEuljoon ParkLaurence S. Sloman
    • A61N1362
    • A61N1/371A61B5/4035
    • Modern implantable cardiac stimulation devices include processing and data storage capabilities that may be exploited to track myocardial condition and autonomic tone. Implantable devices have a capability to measure and store electrogram information over a period of time in a relatively large capacity memory, with advances in technology allowing increases in memory size. The evoked response varies in amplitude and morphology with changes in autonomic tone, ventricular filling, paced rate, and other parameters. The implantable cardiac device can be configured to sense and accurately quantify the evoked response, derive parameters from the quantified evoked response, store the parameters over long time periods, and derive variability statistics from the parameters to assist in tracking the patient's condition over time, and guiding the patient's therapy.
    • 现代可植入心脏刺激装置包括可被利用来追踪心肌状况和自主神经紧张的处理和数据存储能力。 可移植设备具有在相对大容量存储器中在一段时间内测量和存储电描记图信息的能力,技术的进步允许存储器大小增加。 诱发反应的幅度和形态随着自主神经调节,心室充盈,起搏率和其他参数的变化而变化。 可植入心脏装置可被配置为感测并准确量化诱发反应,从量化的诱发反应导出参数,在长时间段内存储参数,并从参数中导出可变性统计数据,以帮助随时间跟踪患者的状况,以及 指导患者的治疗。
    • 8. 发明授权
    • Pacemaker having adaptive arrhythmia detection windows
    • 起搏器具有适应性心律失常检测窗口
    • US06708062B2
    • 2004-03-16
    • US10003935
    • 2001-10-30
    • James H. EricksenMartin A. RossingFareed Assad
    • James H. EricksenMartin A. RossingFareed Assad
    • A61N1362
    • A61N1/3622
    • Methods for improving detection of arrhythmias by adaptively increasing arrhythmia detection intervals. One method includes increasing the V2V, the overall cardiac cycle length, thereby decreasing the pacing rate in the presence of ventricular safety paces (VSPs). Another method includes shortening the trigger interval following the atrial pace event, during which time the pacemaker will detect V-sense events, while leaving the A2V VSP interval unchanged, at the end of which any required VSP will be generated. In yet another method, the interval from A-pace to V-pace, the PAV interval, is shortened, while leaving the overall V2V cycle interval unchanged. This increases the ventricular to artial V2A interval, increasing the detection window for arthythmias. The PAV interval can be shortened in response to a recent history of VSP events.
    • 通过自适应地增加心律失常检测间隔来改善心律失常检测的方法。 一种方法包括增加V2V,整个心脏周期长度,从而降低在心室安全步伐(VSP)存在的起搏速率。 另一种方法包括缩短心房起搏事件之后的触发间隔,在此期间,起搏器将检测V感测事件,同时保持A2V VSP间隔不变,在其结束时将生成任何所需的VSP。 在另一种方法中,缩短了从A速到V步的间隔,PAV间隔,同时保持V2V周期的整体间隔不变。 这将心室增加到术语V2A间隔,增加了心律失常的检测窗口。 可以根据最近的VSP事件历史来缩短PAV间隔。
    • 9. 发明授权
    • Cardiac rhythm management system with user interface indicating energy of pacing pulses
    • 具有指示起搏脉冲能量的用户界面的心律管理系统
    • US06671551B2
    • 2003-12-30
    • US10021861
    • 2001-12-17
    • Vickie L. ConleyAllan T. Koshiol
    • Vickie L. ConleyAllan T. Koshiol
    • A61N1362
    • A61N1/37247A61N1/371G06F19/00G06F19/3418
    • An implantable cardiac rhythm management system includes a user interface, such as an external programmer, for performing therapy energy threshold tests. The threshold tests allow the caregiver to determine the threshold energy at which paces capture the heart, i.e., cause a resulting contraction of the heart chamber to which the paces are delivered. The programmer provides recorded indications of the energy corresponding to each paced event, so that the caregiver can easily determine the point at which capture was lost. This recorded representation of pacing energy makes it easy for the caregiver to determine proper pacing thresholds to be used to ensure adequate pacing, while minimizing energy drain to prolong the useful life of the implanted device.
    • 植入式心律管理系统包括用于执行治疗能量阈值测试的诸如外部编程器的用户界面。 阈值测试允许护理人员确定步态捕获心脏的阈值能量,即导致心脏腔室的递送收缩。 程序员提供与每个节奏对应的能量的记录指示,使得看护者可以容易地确定捕获丢失的点。 记录起搏能量的表现使护理人员能够轻松地确定适当的起搏阈值,以确保充分起搏,同时最大限度地减少能量消耗以延长植入器械的使用寿命。