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    • 1. 发明申请
    • Method for estimating cardiac pumping capacity
    • 估计心脏抽吸能力的方法
    • US20080281214A1
    • 2008-11-13
    • US12149400
    • 2008-04-30
    • Ole Jakob ElleErik FossePer Steinar Halvorsen
    • Ole Jakob ElleErik FossePer Steinar Halvorsen
    • A61B5/02
    • A61B5/029A61B5/1107A61B2562/0219A61N1/36578
    • The present invention provides a system and a method for estimating changes in cardiac pumping capacity in response to an intervention from data recorded by an accelerometer positioned on an outer surface of the heart. Interventions such as intravenous administration of nitroprusside, betablocker, epinephrine (adrenaline), or changes in the intravascular volume such as by fluid filling, are considered. It is shown that it is possible to directly correlate changes in cardiac pumping capacity to changes in parameters or graphical representation derived from signals characteristic to the acceleration an outer surface of the heart. In particular, it is shown how the effect of the interventions can be directly read from these parameters or graphical representations, and can thereby assist in decisions regarding the treatment of a cardiac surgery patient. The invention is preferably used in a post-surgery monitoring unit for surveillance of cardiac surgery patients.
    • 本发明提供了一种系统和方法,用于响应于由位于心脏外表面上的加速度计记录的数据的干预来估计心脏泵送能力的变化。 考虑静脉内施用硝普钠,betablocker,肾上腺素(肾上腺素)或血管内体积变化(例如通过液体灌注)的干预措施。 显示了可以直接将心脏抽吸能力的变化与参考的变化或从心脏的外表面加速度特征的信号导出的图形表示相关联。 特别地,示出了如何从这些参数或图形表示直接阅读干预的效果,从而可以帮助关于心脏手术患者的治疗的决定。 本发明优选用于手术后监测单元,用于监控心脏手术患者。
    • 2. 发明授权
    • Method for estimating cardiac pumping capacity
    • 估计心脏抽吸能力的方法
    • US08282568B2
    • 2012-10-09
    • US12149400
    • 2008-04-30
    • Ole Jakob ElleErik FossePer Steinar Halvorsen
    • Ole Jakob ElleErik FossePer Steinar Halvorsen
    • A61B5/0402
    • A61B5/029A61B5/1107A61B2562/0219A61N1/36578
    • A system and a method for estimating changes in cardiac pumping capacity in response to an intervention from data recorded by an accelerometer positioned on an outer surface of the heart. Interventions such as intravenous administration of nitroprusside, betablocker, epinephrine (adrenaline), or changes in the intravascular volume such as by fluid filling, are considered. It is shown that it is possible to directly correlate changes in cardiac pumping capacity to changes in parameters or graphical representation derived from signals characteristic to the acceleration an outer surface of the heart. In particular, it is shown how the effect of the interventions can be directly read from these parameters or graphical representations, and can thereby assist in decisions regarding the treatment of a cardiac surgery patient. The invention is preferably used in a post-surgery monitoring unit for surveillance of cardiac surgery patients.
    • 一种系统和方法,用于根据位于心脏外表面上的加速度计记录的数据进行干预,来估计心脏泵送能力的变化。 考虑静脉内施用硝普钠,betablocker,肾上腺素(肾上腺素)或血管内体积变化(如通过液体灌注)等干预措施。 显示了可以直接将心脏抽吸能力的变化与参考的变化或从心脏的外表面加速度特征的信号导出的图形表示相关联。 特别地,示出了如何从这些参数或图形表示直接阅读干预的效果,从而可以帮助关于心脏手术患者的治疗的决定。 本发明优选用于手术后监测单元,用于监控心脏手术患者。
    • 3. 发明授权
    • Method and device for interconnection of two tubular organs
    • 两个管状器官相互连接的方法和装置
    • US08545524B2
    • 2013-10-01
    • US10522815
    • 2003-07-25
    • Sumit RoyErik FosseOle Jakob Elle
    • Sumit RoyErik FosseOle Jakob Elle
    • A61B17/11
    • A61F2/064A61B17/0644A61B17/11A61F2002/061A61F2002/821
    • A method for interconnection of two tubular organs via an opening at one end of an end portion of a first organ and an aperture in a side wall of a second organ. The end portion is initially passed through a first passage of a first element until the end portion projects past an end edge of the element, whereupon the end portion is everted round the end edge. Gripping parts of a second element with a second passage are then inserted in the second organ via the aperture. Finally, the first element with the everted portion of the first organ is inserted in the second passage, whereby the gripping parts are influenced in such a manner that they come into engagement with the inside of an edge portion of the aperture. A device for implementation of the method.
    • 一种用于经由第一器官的端部的一端处的开口和第二器官的侧壁中的孔的两个管状器官互连的方法。 端部最初通过第一元件的第一通道,直到端部突出超过元件的端边缘,于是端部围绕端部边缘。 然后通过孔将具有第二通道的第二元件的夹持部件插入第二器官。 最后,将具有第一器官的转弯部分的第一元件插入第二通道中,由此夹持部件以与孔的边缘部分的内侧接合的方式受到影响。 一种实现该方法的设备。
    • 4. 发明申请
    • AUTOMATED MONITORING OF MYOCARDIAL FUNCTION BY ULTRASONIC TRANSDUCERS POSITIONED ON THE HEART
    • 通过位于心脏上的超声波传感器自动监测心肌功能
    • US20110046488A1
    • 2011-02-24
    • US12672569
    • 2008-08-29
    • Ole Jakob ElleErik FosseHalfdan IhlenAndreas EspinozaLars Hoff
    • Ole Jakob ElleErik FosseHalfdan IhlenAndreas EspinozaLars Hoff
    • A61B8/00
    • A61B8/485A61B8/0883A61B8/12A61B8/42A61B8/4488A61B8/488
    • The invention relates to a method and a post-operative care unit for analysing and quantifying an ultrasound tissue Doppler imaging (TDI) signal from a transducer fastened on the myocardium to obtain a parameter indicating regional cardiac ischaemia or correlates with global hypokinetic heart function. This has the advantage over manually operated probes that it can be automated and used continuously over long time. According to the method, a TDI signal trace corresponding to at least one of tissue velocity, strain or strain rate is extracted and correlated with an electrocardiogram to define subsections within a cardiac cycle in the extracted trace corresponding to the early systolic phase and the post-systolic phase. Then, a velocity, strain or strain rate is read in at least the post-systolic phase of the extracted trace, and a parameter which is a function of one of these readings and which indicates ischaemia or global hypokinetic function is generated.
    • 本发明涉及一种用于分析和量化来自紧固在心肌上的传感器的超声组织多普勒成像(TDI)信号以获得指示区域性心脏缺血或与全身低动力心脏功能相关的参数的方法和术后护理单元。 这具有超过手动操作的探头的优点,可以自动化并长时间连续使用。 根据该方法,提取对应于组织速度,应变或应变速率中的至少一个的TDI信号迹线,并将其与心电图相关联,以在对应于早期收缩期和后期收缩期的提取迹线中定义心脏周期内的子部分, 收缩期。 然后,至少在提取的迹线的收缩期后读取速度,应变或应变速率,并且产生作为这些读数中的一个的函数并且表示缺血或全身低动力学功能的参数。
    • 7. 发明授权
    • Percutaneous abdominal implant
    • 经皮腹部植入
    • US08821462B2
    • 2014-09-02
    • US12674666
    • 2008-08-19
    • Robert AxelssonMartin JohanssonBjørn EdwinErik Fosse
    • Robert AxelssonMartin JohanssonBjørn EdwinErik Fosse
    • A61F5/44A61M39/02A61F5/445
    • A61F5/445A61F2005/4455A61M39/0247A61M2039/0261
    • An implant for percutaneous implantation through the abdominal wall for encircling and engaging an externalized length of a body duct of a human or animal patient. The implant has an exterior tubular section defined by an circumferential exterior wall at least a part of which is adapted to protrude outwardly from the abdominal wall with a free end for mounting of a detachable device, an interior section defined by an circumferential interior wall adapted to extend through the abdominal wall and inside the patient for internal fixation of the implant, wherein the exterior tubular section and the interior section have a common axis A. The circumferential exterior wall of the exterior tubular section and the circumferential interior wall of the interior section are arranged axially spaced apart at a distance D from each other to provide an axial gap between opposing free ends of the exterior tubular section and the interior section, with the exterior tubular section and interior section being connected inside the sections.
    • 用于通过腹壁进行经皮植入的植入物,用于环绕和接合人或动物患者的身体导管的外部长度。 所述植入物具有由周向外壁限定的外部管状部分,所述外部管状部分的至少一部分适于从所述腹壁向外突出,具有用于安装可拆卸装置的自由端,由周向内壁限定的内部部分, 延伸通过腹壁和患者内部,用于植入物的内部固定,其中外部管状部分和内部部分具有公共轴线A.外部管状部分的周向外壁和内部部分的圆周内壁是 以彼此间隔开的距离D轴向间隔开,以在外部管状部分和内部部分的相对的自由端之间提供轴向间隙,外部管状部分和内部部分连接在部分内部。
    • 9. 发明授权
    • Light system for use especially by operating theatre
    • 特别是手术室使用的轻系统
    • US06803727B2
    • 2004-10-12
    • US10221362
    • 2003-02-04
    • Frode LaerumErik FosseOle Jacob Elle
    • Frode LaerumErik FosseOle Jacob Elle
    • H01J160
    • A61B90/35A61B34/20A61B90/30F21V14/04F21V19/02F21V21/30F21V23/04F21W2131/205H05B33/0803H05B33/086
    • A lighting system, preferably for use in operating theatres, in which at least one light source is mounted to be movable an adjustable in a single ceiling and/or wall element in the form of a prefabricated module element (4). The light sources in each module element may be controlled singly or in clusters by means of a control device designed to direct the source or sources to focus at a point defined by an optical, ultrasound or magnetic, radio frequency pointer that is seen by an appropriate sensor/camera system or receiver in the room, and which, via control means, moves the light source to the desired position. The light source consists of light-emitting diodes, halogen bulbs or the end of one or several fiber-optical cables, fixed ion a holder shaped as one half of a cup or a sphere, the holder being arranges to be movable about two perpendicular axes in the xy-plane (the ceiling plane) of the ceiling module (4). The holder is attached to the ceiling element by means of a gyroscopic suspension system or a ball joint suspension system. On the top of the holder, which is at the back of the ceiling module (4), there is provided two attachment points (16, 17) offset by 90° with respect to each other but parallel to the plane of the ceiling when the light beam is directed downwards normal to the ceiling plane (xy-plane), respective linear actuators being articulated to the attachment points for reciprocating movement, so as to rotate the holder about the x-axis and the y-axis, respectively. This can also be done by use of rotary actuators, possibly mounted in combination with a gear unit, which rotate the suspension ball/holder directly about the axis of rotation.
    • 一种优选用于操作剧院的照明系统,其中安装有至少一个光源可移动,以预制模块元件(4)的形式在单个天花板和/或壁元件中可调节。 每个模块元件中的光源可以通过设计成将源或源聚焦在由适当的光学,超声或磁性的无线电频率指示器定义的点处的控制装置而被单独或成簇地控制 传感器/相机系统或接收器,并且通过控制装置将光源移动到期望的位置。 光源由发光二极管,卤素灯泡或一根或几根光纤光缆的端部组成,固定离子形成为杯子或球体的一半,保持器布置成可绕两个垂直轴线移动 在天花板模块(4)的xy平面(天花板平面)中。 支架通过陀螺悬挂系统或球窝悬挂系统连接到天花板上。 在天花板模块(4)的背面的支架的顶部,设有两个附接点(16,17),它们相对于彼此偏移90°,但平行于天花板的平面 光束垂直于天花板平面(xy平面)向下引导,相应的线性致动器铰接到连接点用于往复运动,从而分别围绕x轴和y轴旋转保持器。 这也可以通过使用可能与减速器组合安装的旋转致动器来完成,该减速器直接围绕旋转轴线旋转悬挂球/支架。
    • 10. 发明申请
    • Implant
    • 注入
    • US20060052759A1
    • 2006-03-09
    • US11218905
    • 2005-09-02
    • Martin JohanssonRobert AxelssonAnette JohnssonBjorn EdwinErik Fosse
    • Martin JohanssonRobert AxelssonAnette JohnssonBjorn EdwinErik Fosse
    • A61M31/00
    • A61M25/02A61M2025/0286A61M2025/0293
    • A percutaneous implant serves for implantation into an animal or a human body. The implant is of the kind that has an axial interior section for fixation inside the body, an axial exterior section in communication with the interior section and extending outwards from the body with a free end. The free end of the exterior section serves for mounting of a detachable device. A distal end of the interior section opposite the exterior section is provided with an anchoring section, extending radially from the distal end of the interior section. The anchoring section comprises an inner anchoring ring extending from or integral with the interior section, an outer anchoring ring, and at least one connection member for connecting the inner anchoring ring with the outer anchoring ring. Since a first connection point between a first end of the at least one connection member and the inner anchoring ring is angularly offset from a second connection point between a second end of the connection member and the outer anchoring ring, the anchoring section constitutes a resilient spring means, which adapts to the movements of the body. The implant is especially designed for use without externalization of the vessel to be brought into communication with the exterior.
    • 经皮植入物用于植入动物或人体。 植入物是具有用于固定在体内的轴向内部部分的类型的植入物,与内部部分连通并从身体向外向外延伸的自由端的轴向外部部分。 外部部分的自由端用于安装可拆卸装置。 内部部分的与外部部分相对的远端设置有从内部部分的远端径向延伸的锚固部分。 锚定部分包括从内部部分延伸或与内部部分一体的内部固定环,外部锚定环以及用于将内部锚固环与外部锚定环连接的至少一个连接构件。 由于至少一个连接构件的第一端和内部固定环之间的第一连接点与连接构件的第二端和外部固定环之间的第二连接点成角度地偏移,所以锚定区段构成弹性弹簧 意味着适应身体的运动。 植入物特别设计用于不外部化的容器以与外部连通。