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    • 78. 发明授权
    • Single pass telescoping cardiac lead for the left heart
    • 单通伸缩心脏线为左心
    • US06988007B1
    • 2006-01-17
    • US10218353
    • 2002-08-13
    • Kevin L. MorganGene A. BornzinJoseph J. FlorioJohn R. Helland
    • Kevin L. MorganGene A. BornzinJoseph J. FlorioJohn R. Helland
    • A61N1/05
    • A61N1/056A61N1/057A61N2001/0585
    • An implantable single-pass cardiac stimulation lead provides for placement of electrodes into electrical contact with two chambers of a patient's heart. The lead includes an inner lead body having at least one electrode at its distal end and an outer lead body having at least one electrode at its distal end. The outer lead body has an internal lumen that slidingly receives the inner lead body. The inner lead body is extendable from the outer lead body at a point proximal to the distal end of the outer lead body. The sliding of the inner lead body relative to the outer lead body enables the inner lead body distal electrode to have a varying distance from the outer lead body distal electrode and enables the inner lead body to extend into the coronary sinus region of the heart to place the inner lead body electrode into electrical contact with the left ventricle.
    • 可植入的单程心脏刺激引线提供将电极放置在与患者心脏的两个腔室电接触的位置。 引线包括在其远端具有至少一个电极的内引线体和在其远端具有至少一个电极的外引线体。 外引线体具有滑动地接收内引线体的内腔。 内引线体可以在外引线体的远离外引线体的远端的位置处延伸。 内引线体相对于外引线体的滑动能够使内引线体远端电极与外引线体远端电极间距离变化,能够使内引线体延伸到心脏的冠状窦区域 内部引线体电极与左心室电接触。
    • 79. 发明授权
    • Method and apparatus for using a rest mode indicator to automatically adjust control parameters of an implantable cardiac stimulation device
    • 用于使用静止模式指示器自动调节可植入心脏刺激装置的控制参数的方法和装置
    • US06968232B2
    • 2005-11-22
    • US10093225
    • 2002-03-06
    • Joseph J. FlorioGene A. BornzinPeter BoileauEric FalkenbergJanice Barstad
    • Joseph J. FlorioGene A. BornzinPeter BoileauEric FalkenbergJanice Barstad
    • A61N1/362A61N1/368A61N1/18
    • A61N1/3622A61N1/3682
    • An implantable cardiac stimulation device is described wherein a controller of the cardiac stimulation device controls selected functions of the device based on whether the patient is at rest and further based on whether the patient is prone to vagally-mediated arrhythmias. Functions of the device that may be controlled include, for example, a pacing base rate, an AV/PV delay, and a refractory period as well as overdrive pacing parameters and diagnostic data gathering parameters. In one example, if the patient is not prone to vagally-mediated arrhythmias, the base rate is lowered while the patient is at rest. Also, overdrive pacing parameters are set to be less aggressive. As such, the operation of the cardiac stimulation device is controlled to make it easier for the patient to rest while also reducing power consumption. However, if the patient is prone to vagally-mediated arrhythmias, the base rate is not lowered while the patient is at rest. Overdrive pacing parameters are instead set to be more aggressive, rather than less aggressive. In this manner, the cardiac stimulation device attempts to compensate for any increased risk of arrhythmia that may occur while the patient, who is prone to vagally-mediated arrhythmias, is at rest. Numerous other parameters may be adjusted dependent upon whether the patient is at rest or dependent upon whether the patient is prone to vagally-mediated arrhythmias.
    • 描述了可植入心脏刺激装置,其中心脏刺激装置的控制器基于患者是否处于静止状态并且还基于患者是否易于经历迷走神经介导的心律失常来控制装置的选定功能。 可以被控制的设备的功能包括例如起搏基准速率,AV / PV延迟和不应期,以及过速起搏参数和诊断数据采集参数。 在一个示例中,如果患者不易于经历迷走神经介导的心律失常,则在患者静止时基础速率降低。 此外,过度起搏参数设置为较不积极。 因此,控制心脏刺激装置的操作以使患者更容易休息,同时也降低功率消耗。 然而,如果患者容易出现迷走神经介导的心律失常,则在患者休息时基础速率不降低。 相反,超速起搏参数设置为更具侵略性,而不是较不积极。 以这种方式,心脏刺激装置试图补偿在容易发生迷走神经介导的心律失常的患者处于静止状态时可能出现的任何增加的心律失常风险。 可以根据患者是否休息或依赖于患者是否易于经历迷走神经介导的心律失常而调整许多其他参数。
    • 80. 发明授权
    • System and method of identifying fusion for dual-chamber automatic capture stimulation device
    • 识别双室自动捕获刺激装置融合的系统和方法
    • US06904321B1
    • 2005-06-07
    • US10208169
    • 2002-07-29
    • Gene A. BornzinJoseph J. FlorioLaurence S. Sloman
    • Gene A. BornzinJoseph J. FlorioLaurence S. Sloman
    • A61N1/37A61N1/36
    • A61N1/3712
    • A multi-chamber stimulation device and associated method reliably and automatically distinguish fusion from loss of capture during ventricular stimulation. The stimulation device provides immediate and accurate fusion detection when a loss of capture is suspected in the ventricles without delivering back-up stimulation pulses. To achieve this objective, the far-field signal present in the atrial channel is examined for evidence of a far-field R-wave whenever the ventricular channel detects a loss of capture. If a far-field R-wave is present, fusion is confirmed, and a far-field R-wave is absent, loss of capture is confirmed. Additionally, the stimulation device inhibits unnecessary back-up stimulation and threshold tests when fusion occurs, and provides appropriate adjustment of stimulation parameters based on confirmed fusion detection such that fusion re-occurrence is minimized.
    • 多室刺激装置和相关方法可靠和自动地将融合与心室刺激期间的捕获损失区分开来。 刺激装置提供即时和准确的融合检测,当脑袋怀疑丢失而不输送备用刺激脉冲时。 为了达到这个目的,每当心室通道检测到捕获的丢失时,都会检查存在于心房通道中的远场信号以获得远场R波的证据。 如果存在远场R波,则确认融合,并且不存在远场R波,确认捕获损失。 此外,当融合发生时,刺激装置抑制不必要的后备刺激和阈值测试,并且基于确认的融合检测提供刺激参数的适当调整,使得融合再现最小化。