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    • 82. 发明申请
    • IMPLANTABLE HEART STIMULATOR
    • 可植入心脏刺激器
    • WO2002068048A1
    • 2002-09-06
    • PCT/SE2002/000344
    • 2002-02-26
    • ST. JUDE MEDICAL ABECKERDAL, JohanOBEL, MartinMICSKI, Eva
    • ECKERDAL, JohanOBEL, MartinMICSKI, Eva
    • A61N1/375
    • A61N1/056A61N1/205A61N1/375
    • An implantable heart stimulator comprises a pulse generator for delivering electric stimulation pulses to a patient's heart through a lead (14), connectable to said pulse generator, possibly through a connector top (12) on a pulse generator housing (10). The pulse generator housing is electrically conductive. In an infection control apparatus for such a heart stimulator the exterior surfaces of the possible connector top (12) and of a proximal part (16) of the lead (14) are electrically conductive. The proximal part extends to a position, which after implantation of the lead is situated between a location beyond the entry into the venous system and the entry to vena cava superior. The generator housing (10) and the electrical conductive surfaces of the proximal lead part and of the possible connector top are adapted to form at last two separate electrodes and a current source is provided to supply an electric infection control current between these electrodes.
    • 可植入心脏刺激器包括脉冲发生器,脉冲发生器可通过引线(14)将电刺激脉冲传送到患者的心脏,该引线可连接到所述脉冲发生器,可能通过脉冲发生器壳体(10)上的连接器顶部(12)连接。 脉冲发生器壳体是导电的。 在用于这种心脏刺激器的感染控制装置中,可能的连接器顶部(12)和引线(14)的近侧部分(16)的外表面是导电的。 近端部分延伸到一个位置,该位置在引线的植入位于超过进入静脉系统的位置和进入腔静脉上方的位置之间。 发电机壳体(10)和近端引线部分和可能的连接器顶部的导电表面适于形成最后两个单独的电极,并且提供电流源以在这些电极之间提供电感应控制电流。
    • 83. 发明申请
    • IMPLANTABLE MEDICAL LEAD WITH BLOOD SEAL
    • 可植入医疗领域与血液密封
    • WO2013060372A1
    • 2013-05-02
    • PCT/EP2011/068857
    • 2011-10-27
    • ST. JUDE MEDICAL ABECKERDAL, Johan
    • ECKERDAL, Johan
    • A61N1/05
    • A61N1/0573
    • An implantable medical lead (1) comprises an insulating tubing (41) with a channel (42) housing a conductor (72) electrically connected to a shaft (60) present in a lumen (51) of a bearing (50). The shaft (60) is also connected to a fixation helix (22) present in a lumen (23) of a lead header (21). A clot-inducing structure (80, 82, 84, 86) of a thrombogenic material is present in a distal portion (44) of the channel (42) and/or in the lumen (51) of the bearing (50) to trigger formation of a clot when blood enters the implantable medical lead (1) and thereby inhibit blood from entering further into the channel (42).
    • 可植入医疗引线(1)包括绝缘管(41),其具有通道(42),该通道(42)容纳与轴承(50)的内腔(51)中存在的轴(60)电连接的导体(72)。 轴(60)还连接到存在于引线头(21)的内腔(23)中的固定螺旋(22)。 血栓形成材料的凝块诱导结构(80,82,84,86)存在于通道(42)的远端部分(44)和/或轴承(50)的内腔(51)中以触发 当血液进入可植入医疗引线(1)时,凝块形成,从而抑制血液进一步进入通道(42)。
    • 89. 发明申请
    • METHOD AND DEVICE FOR DETECTING INCIPIENT A-V NODE MALFUNCTION
    • 用于检测致命的A-V节点故障的方法和装置
    • WO2011076264A1
    • 2011-06-30
    • PCT/EP2009/067787
    • 2009-12-22
    • ST. JUDE MEDICAL ABLINDGREN, Anders
    • LINDGREN, Anders
    • A61B5/0456A61N1/368
    • A61N1/3702A61B5/02438A61B5/0402A61B5/686A61B5/6869A61N1/365A61N1/3682A61N1/37258
    • The present invention generally relates to implantable stimulation devices, such as pacemakers, defibrillators, and cardioverters, and, in particular, to implantable medical devices using atrial based pacing such as an AAI pacing mode and methods for such implantable medical devices for detecting early stages of incipient A-V node malfunction as well as presence of A-V node malfunction. An AV conduction capacity is detected, wherein a sensed ventricular event following an intrinsic or paced atrial event during a predetermined period of time indicates good AV conduction capacity and wherein absence of a ventricular event within the predetermined period of time indicates poor AV conduction capacity. At least one A- V node function parameter indicating a function of the A-V node is determined, wherein the A-V node function parameter includes whether a status of the AV conduction capacity is good or poor. Incipient A-V node malfunction is detected where poor AV conduction capacity indicates incipient A-V node malfunction.
    • 本发明一般涉及可植入的刺激装置,例如起搏器,除颤器和心律转换器,特别是涉及使用基于心房的起搏(例如AAI起搏模式)的可植入医疗装置以及用于这种可植入医疗装置的方法来检测早期阶段 初始AV节点故障以及AV节点故障的存在。 检测到AV传导容量,其中在预定时间段内的本征或起搏心房事件之后的感测到的心室事件表示良好的AV传导能力,并且其中在预定时间段内不存在心室事件表示差的AV传导能力。 确定表示A-V节点的功能的至少一个A- V节点功能参数,其中,所述A-V节点功能参数包括AV传导容量的状态是好还是差。 检测到初始的A-V节点故障,其中差的AV传导容量指示初始的A-V节点故障。
    • 90. 发明申请
    • IMPLANTABLE MEDICAL DEVICE AND METHOD FOR MONITORING SYNCHRONICITY OF THE VENTRICLES OF A HEART
    • 用于监测心脏通气道的同步性的可植入医疗装置和方法
    • WO2010074611A1
    • 2010-07-01
    • PCT/SE2008/000742
    • 2008-12-22
    • ST. JUDE MEDICAL ABJÄRVERUD, Karin
    • JÄRVERUD, Karin
    • A61N1/365A61B5/053
    • A61N1/3622A61B5/053A61B5/7239A61N1/36521A61N1/36585
    • The present invention generally relates to the field of implantable heart stimulation devices, such as pacemakers, and similar cardiac stimulation devices that also are capable of monitoring and detecting electrical activities and events within the heart. More specifically, the present invention relates to an implantable medical device and a method for monitoring ventricular synchronicity of a heart. In particular, impedance signals are measured and an occurrence of a notch is detected in the impedance signal coincident with a period including a change from rapid to slow filling of a ventricle. The notch is indicated by a first positive slope change in a negative slope in a predetermined time window during a diastolic phase of a cardiac cycle. A degree of synchronicity is determined based on the notch feature, wherein a decreasing notch feature indicates an increased degree of synchronicity in the filling phase of the ventricles.
    • 本发明一般涉及可植入的心脏刺激装置领域,例如起搏器和类似的心脏刺激装置,其也能够监测和检测心脏内的电活动和事件。 更具体地,本发明涉及可植入医疗装置和用于监测心脏的心室同步性的方法。 特别地,测量阻抗信号,并且在阻抗信号中检测到陷波的发生,该阻抗信号与包括从心室的快速到慢速填充的变化的周期一致。 在心脏周期的舒张期期间,在预定时间窗中的负斜率的第一正斜率变化来表示凹口。 基于凹口特征确定同步度,其中减小的切口特征表示在心室的填充阶段中增加的同步度。