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    • 3. 发明申请
    • IMPLANTABLE MEDICAL DEVICE LEAD CONNECTION ASSEMBLY
    • 可植入医疗设备引线连接总成
    • WO2010051495A1
    • 2010-05-06
    • PCT/US2009/062857
    • 2009-10-30
    • MEDTRONIC, INC.DONOFRIO, William, T.BURNES, John, E.KRAUSE, Paul, G.
    • DONOFRIO, William, T.BURNES, John, E.KRAUSE, Paul, G.
    • A61N1/375
    • A61N1/3752H01R13/5224H01R24/58H01R2107/00H01R2201/12Y10S439/909
    • A lead connection assembly of an implantable medical device (IMD) may include at least two different types of electrical connectors. In some examples, the lead connection assembly may include first and second electrical connectors that have at least one of a different electrical contact arrangement, a different lead connection receptacle geometry or a different size than the first electrical connector. The first electrical connector may be electrically connected to a first therapy module that generates cardiac rhythm therapy that is delivered to a heart of a patient, and the second electrical connector may be electrically connected to a second therapy module that generates electrical stimulation that is delivered to a tissue site within the patient. The second electrical connector may be configured to be incompatible with a lead that delivers the cardiac rhythm therapy to the patient.
    • 可植入医疗装置(IMD)的引线连接组件可以包括至少两种不同类型的电连接器。 在一些示例中,引线连接组件可以包括具有与第一电连接器不同的电接触布置,不同引线连接插座几何形状或不同尺寸中的至少一个的第一和第二电连接器。 第一电连接器可以电连接到第一治疗模块,该第一治疗模块产生被递送到患者的心脏的心律疗法,并且第二电连接器可以电连接到产生电刺激的第二治疗模块,该电刺激被递送到 患者内的组织部位。 第二电连接器可以被配置为与将心律治疗递送给患者的引线不相容。
    • 7. 发明申请
    • EXTRA-CARDIAC IMPLANTABLE DEVICE WITH FUSION PACING CAPABILITY
    • 具有融合能力的外部可植入装置
    • WO2009134960A3
    • 2010-04-08
    • PCT/US2009042217
    • 2009-04-30
    • MEDTRONIC INCBURNES JOHN EDOLAN BECKY L
    • BURNES JOHN EDOLAN BECKY L
    • A61N1/368
    • A61N1/368A61N1/0587A61N1/3682
    • According to this disclosure, a non-transvenous pacing and, optionally defibrillation, therapy device is implanted subcutaneously and oriented to provide cardiac sensing from electrodes spaced from a heart and deliver pacing and/or defibrillation from 0.one or more non-transvenous electrodes (e.g., an epicardial or pericardial electrode or electrode patch). A subject receiving a device according to this disclosure is monitored to confirm a relatively stable bundle branch block (i.e., delayed activation) of one ventricle. The subcutaneous device has electrodes disposed on the housing and/or having an electrode on a subcutaneous medical lead is oriented so that the pacing (and sensing) vector impinges mainly upon the one ventricle, and/or optionally an epicardial or pericardial lead is deployed to a last-to-depolarize ventricle (e.g., a left ventricle) so that single-ventricular pacing is delivered to achieve fusion depolarization of both ventricles.
    • 根据本公开,非静脉起搏和(可选地除颤)疗法装置被植入皮下并定向以提供来自与心脏间隔开的电极的心脏感测,并且从一个或多个非经静脉电极输送起搏和/或除颤 例如,心外膜或心包电极或电极贴片)。 监测接收根据本公开的装置的受试者以确认一个心室的相对稳定的束支传导阻滞(即,延迟激活)。 皮下装置具有设置在壳体上和/或具有皮下医疗引线上的电极的电极被定向成使得起搏(和感测)载体主要照射在一个心室上,和/或可选地将心外膜或心包引线部署到 最终到去极化的心室(例如,左心室),以便输送单心室起搏以实现两个心室的融合去极化。