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    • 131. 发明授权
    • PAC therapy
    • PAC疗法
    • US07801607B1
    • 2010-09-21
    • US11735872
    • 2007-04-16
    • Gene A. BornzinPeter Boileau
    • Gene A. BornzinPeter Boileau
    • A61N1/37
    • A61N1/3627A61N1/3624A61N1/3712A61N1/3714
    • An implantable cardiac device is programmed to detect and classify premature atrial contractions (PACs) and administer responsive pacing therapy. The responsive pacing therapy is in the form of an atrial extrastimulus, which is intended to preempt initiation of a reentrant tachycardia. The atrial extrastimulus is timed to occur late enough after a PAC to ensure atrial capture, but early enough that the resulting atrial depolarization does not conduct through the AV node to the ventricles if the PAC has already done so. If both of these criteria cannot be met, the device may be configured to inhibit the atrial extrastimulus.
    • 可植入心脏装置被编程以检测和分类早产性心房收缩(PAC)并进行响应性起搏治疗。 响应性起搏治疗是以心房超激发的形式,其旨在抢先引发折返性心动过速。 房间超激发定时发生在PAC后足够晚,以确保心房捕获,但足够早,如果PAC已经这样做,所产生的心房去极化不会通过AV节点进入心室。 如果这两个标准都不能满足,则可以将该装置配置成抑制心房再刺激。
    • 132. 发明申请
    • System and Method for Setting Atrioventricular Pacing Delays Based on Far-Field Atrial Signals
    • 基于远场心房信号设置房室起搏延迟的系统和方法
    • US20100121395A1
    • 2010-05-13
    • US12267483
    • 2008-11-07
    • Jong GillGene A. Bornzin
    • Jong GillGene A. Bornzin
    • A61N1/368
    • A61N1/368A61B5/0452A61N1/3704
    • An intrinsic inter-atrial conduction delay is determined by a pacemaker or implantable cardioverter-defibrillator based, at least in part, on far-field atrial events sensed using ventricular pacing/sensing leads. An atrioventricular pacing delay is then set based on the inter-atrial conduction delay. By detecting atrial events using ventricular leads, rather than using atrial leads, a more useful measurement of the intrinsic inter-atrial conduction delay can be obtained. In this regard, since atrial electrodes detect atrial activity locally around the electrodes, a near-field atrial event sensed using an atrial electrode might not properly represent the actual timing of the atrial event across both the right and left atria. Far-field atrial events sensed using ventricular leads thus allow for a more useful measurement of inter-atrial conduction delays for use in setting atrioventricular pacing delays. The delivery of individual V-pulses to the heart of the patient may be timed relative to the ends of individual far-field atrial events.
    • 至少部分地基于使用心室起搏/感测引线感测的远场心房事件,起搏器或植入式心律转复除颤器确定内在的心房间传导延迟。 然后基于心房间传导延迟来设置房室起搏延迟。 通过使用心室导联检测心房事件,而不是使用心房线,可以获得更有用的内在心房传导延迟的测量。 在这方面,由于心房电极在电极周围局部地检测心房活动,使用心房电极感测到的近场心房事件可能不能正确地表示在右心房和左心房两侧的心房事件的实际时间。 使用心室引线检测的远场心房事件因此允许更有用的测量心房间传导延迟,用于设置房室起搏延迟。 单个V脉冲到患者心脏的传送可以相对于单个远场心房事件的结束而定时。
    • 133. 发明申请
    • HYBRID BATTERY SYSTEM WITH BIOELECTRIC CELL FOR IMPLANTABLE CARDIAC THERAPY DEVICE
    • 具有用于可植入心脏治疗装置的生物电池的混合电池系统
    • US20100114236A1
    • 2010-05-06
    • US12263348
    • 2008-10-31
    • Naixiong JiangGene A. BornzinJohn W. Poore
    • Naixiong JiangGene A. BornzinJohn W. Poore
    • A61N1/362H01M10/36
    • A61N1/378A61N1/3956A61N1/3981H01M8/16H01M10/0525H01M10/425H01M10/44H01M16/006H02J7/0054H02J7/0063Y02E60/527
    • A system and method for powering an implantable cardiac therapy device (ICTD) via a hybrid battery system. The hybrid battery is comprised of a low voltage and low current bioelectric cell, a high voltage and high current rechargeable cell, and a charging means. Via the charging means, the bioelectric cell maintains the rechargeable cell at or near full power. The rechargeable cell is configured to power some or all operations of the ICTD. Some ICTD operations may be powered directly by the bioelectric cell. The rechargeable cell is further configured to be charged via a continuous charging process, reducing the complexity of the charging circuitry. In an embodiment, at least the bioelectric cell is external to the ICTD, enabling easy replacement of this power source. In an embodiment, a consumable anode of the bioelectric cell is external to the ICTD, enabling replacement of the power source by replacing only the anode.
    • 通过混合电池系统为植入式心脏治疗装置(ICTD)供电的系统和方法。 混合电池包括低电压和低电流生物电池,高电压和高电流可再充电电池以及充电装置。 通过充电装置,生物电池将可再充电电池维持在或接近全功率。 可充电电池被配置为为ICTD的一些或所有操作供电。 一些ICTD操作可以由生物电池直接供电。 可再充电电池还被配置为经由连续充电过程进行充电,从而降低充电电路的复杂性。 在一个实施例中,至少生物电池在ICTD的外部,使得能够容易地更换该电源。 在一个实施例中,生物电池的消耗性阳极在ICTD的外部,能够通过仅替换阳极来替换电源。
    • 134. 发明授权
    • Calibrating implantable optical sensors
    • 校准植入光学传感器
    • US07630078B1
    • 2009-12-08
    • US11683521
    • 2007-03-08
    • Yelena NabutovskyGene A. BornzinTaraneh Ghaffari FaraziJohn W. Poore
    • Yelena NabutovskyGene A. BornzinTaraneh Ghaffari FaraziJohn W. Poore
    • G01B9/08
    • A61B5/14542A61B5/02028A61B5/14535A61B5/1459A61B2560/0223A61N1/36557
    • A measurement light detector detects light transmitted by a light source of an implantable system that is scattered back into an implantable housing, and produces a measurement signal indicative of the intensity of the light detected by the measurement light detector. A calibration light detector detects a portion of the transmitted light that has not exited the housing, and produces a calibration signal that is indicative of the intensity of the light detected by the calibration light detector, which is indicative of the intensity of the light transmitted by the light source. Changes in the intensity of the transmitted light are compensated for based on the calibration signal produced by the calibration light detector. This description is not intended to be a complete description of, or limit the scope of, the invention. Other features, aspects, and objects of the invention can be obtained from a review of the specification, the figures, and the claims.
    • 测量光检测器检测由可植入系统的光源透射的光,其被散射回到可植入的壳体中,并且产生指示由测量光检测器检测到的光的强度的测量信号。 校准光检测器检测未离开壳体的透射光的一部分,并且产生指示由校准光检测器检测的光的强度的校准信号,该校准信号指示由光学器件发射的光的强度 光源。 基于由校准光检测器产生的校准信号来补偿透射光强度的变化。 本说明书不是对本发明的完整描述或限制本发明的范围。 本发明的其它特征,方面和目的可以通过对说明书,附图和权利要求的评述来获得。
    • 136. 发明授权
    • Detection of renal failure by cardiac implantable medical device
    • 通过心脏植入式医疗器械检测肾功能衰竭
    • US07529580B2
    • 2009-05-05
    • US11202534
    • 2005-08-11
    • Jong GillGene A. Bornzin
    • Jong GillGene A. Bornzin
    • A61B5/02
    • A61B5/0452A61B5/201A61N1/3702
    • Morphological features within electrical cardiac signals are tracked and feature changes are monitored to detect renal failure. The morphological feature may be an interval between corresponding polarization events such as the interval between QRS-complexes and peaks of corresponding T-waves (QTmax interval); the interval between QRS-complexes and ends of corresponding T-waves (QTend interval); or the interval between P-waves and corresponding QRS-complexes (PR interval). The feature may also be the elevation of a cardiac signal segment between corresponding polarization events, such as QRS-complexes and corresponding T-waves (ST segment); a duration of a polarization event, such as a QRS-complex (QRS width); or an amplitude of a polarization event, such as a T-wave (T-wave amplitude). The change in the feature may comprise a decrease in QTmax intervals, a decrease in QTend intervals, a deviation in ST segment elevation, an increase in QRS width, an increase in PR interval or a deviation in T-wave amplitude.
    • 跟踪电心脏信号中的形态特征,并监测特征变化以检测肾衰竭。 形态特征可以是相应的极化事件之间的间隔,例如QRS-复合物之间的间隔和对应的T波的峰值(QTmax间隔); QRS复合体与相应T波结束之间的间隔(QTend间隔); 或P波与相应的QRS复合体之间的间隔(PR间隔)。 该特征还可以是对应的极化事件之间的心脏信号段的升高,例如QRS复合物和相应的T波(ST段); 极化事件的持续时间,例如QRS复合(QRS宽度); 或极化事件的振幅,例如T波(T波振幅)。 特征的变化可以包括QTmax间隔的减小,QTend间隔的减小,ST段抬高的偏差,QRS宽度的增加,PR间期的增加或T波幅度的偏差。
    • 139. 发明授权
    • Detection of renal failure by cardiac implantable medical device
    • 通过心脏植入式医疗器械检测肾功能衰竭
    • US07400920B1
    • 2008-07-15
    • US11202553
    • 2005-08-11
    • Jong GillGene A. Bornzin
    • Jong GillGene A. Bornzin
    • A61B5/04
    • A61B5/0468A61B5/201
    • Morphological features within electrical cardiac signals are tracked and changes in features are monitored to detect renal failure. The morphological feature may be an interval between corresponding polarization events such as the interval between QRS-complexes and peaks of corresponding T-waves (QTmax interval); the interval between QRS-complexes and ends of corresponding T-waves (QTend interval); or the interval between P-waves and corresponding QRS-complexes (PR interval). The feature may also be the elevation of a cardiac signal segment between corresponding polarization events, such as QRS-complexes and corresponding T-waves (ST segment); a duration of a polarization event, such as a QRS-complex (QRS width); or an amplitude of a polarization event, such as a T-wave (T-wave amplitude). The change in the feature may comprise a decrease in QTmax intervals, a decrease in QTend intervals, a deviation in ST segment elevation, an increase in QRS width, an increase in PR interval or a deviation in T-wave amplitude.
    • 跟踪电心电信号中的形态学特征,监测特征变化以检测肾功能衰竭。 形态特征可以是相应的极化事件之间的间隔,例如QRS-复合物之间的间隔和对应的T波的峰值(QTmax间隔); QRS复合体与相应T波结束之间的间隔(QTend间隔); 或P波与相应的QRS复合体之间的间隔(PR间隔)。 该特征还可以是对应的极化事件之间的心脏信号段的升高,例如QRS复合物和相应的T波(ST段); 极化事件的持续时间,例如QRS复合(QRS宽度); 或极化事件的振幅,例如T波(T波振幅)。 特征的变化可以包括QTmax间隔的减小,QTend间隔的减小,ST段抬高的偏差,QRS宽度的增加,PR间期的增加或T波幅度的偏差。