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    • 1. 发明授权
    • Device for indicator dilution measurements
    • 指示剂稀释测量装置
    • US09375159B2
    • 2016-06-28
    • US12738073
    • 2008-10-15
    • Ulf BorgReinhold KnollFrederic MichardUlrich Pfeiffer
    • Ulf BorgReinhold KnollFrederic MichardUlrich Pfeiffer
    • A61B5/02A61B5/029A61B5/028A61B5/0275
    • A61B5/029A61B5/02755A61B5/028
    • The invention relates to indicator dilution measurements of a central volume (V1) with a first site of injection (S1) upstream of the central volume (V1) a second site of detection (S2) of the diluted indicator downstream of the central volume (V1), wherein a first additional volume (V2) is defined between the first site (S1) and the central volume (V1) and a first additional branch (B2) is defined between the first site (S1) and the central volume (V1) and wherein a second additional volume (V3) is defined between the central volume (V1) and the second site (S2) and a second additional branch (B3) is defined between the central volume (V1) and the second site (S2) wherein a result of central volumetric parameters are corrected for the first and second additional volumes (V2, V3) and/or for the first and second additional branches (B2, B3).
    • 本发明涉及具有中心体积(V1)上游的第一注射部位(S1)的中心体积(V1)的指示剂稀释测量,第二中心体积(V1)下游的稀释指示的检测位置(S2) ),其中在所述第一部位(S1)和所述中心体积(V1)之间限定第一附加体积(V2),并且在所述第一部位(S1)和所述中心体积(V1)之间限定第一附加分支(B2) 并且其中在所述中心体积(V1)和所述第二部位(S2)之间限定第二附加体积(V3),并且在所述中心体积(V1)和所述第二部位(S2)之间限定第二附加分支(B3),其中 针对第一和第二附加体积(V2,V3)和/或第一和第二附加分支(B2,B3)校正中心体积参数的结果。
    • 2. 发明申请
    • Device for Indicator Dilution Measurements
    • 指示剂稀释测量装置
    • US20110105911A1
    • 2011-05-05
    • US12738073
    • 2008-10-15
    • Ulf BorgReinhold KnollFrederic MichardUlrich Pfeiffer
    • Ulf BorgReinhold KnollFrederic MichardUlrich Pfeiffer
    • A61B5/02
    • A61B5/029A61B5/02755A61B5/028
    • The invention relates to indicator dilution measurements of a central volume (V1) with a first site of injection (S1) upstream of the central volume (V1) a second site of detection (S2) of the diluted indicator downstream of the central volume (V1), wherein a first additional volume (V2) is defined between the first site (S1) and the central volume (V1) and a first additional branch (B2) is defined between the first site (S1) and the central volume (V1) and wherein a second additional volume (V3) is defined between the central volume (V1) and the second site (S2) and a second additional branch (B3) is defined between the central volume (V1) and the second site (S2) wherein a result of central volumetric parameters are corrected for the first and second additional volumes (V2, V3) and/or for the first and second additional branches (B2, B3).
    • 本发明涉及具有中心体积(V1)上游的第一注射部位(S1)的中心体积(V1)的指示剂稀释测量,第二中心体积(V1)下游的稀释指示的检测位置(S2) ),其中在所述第一部位(S1)和所述中心体积(V1)之间限定第一附加体积(V2),并且在所述第一部位(S1)和所述中心体积(V1)之间限定第一附加分支(B2) 并且其中在所述中心体积(V1)和所述第二部位(S2)之间限定第二附加体积(V3),并且在所述中心体积(V1)和所述第二部位(S2)之间限定第二附加分支(B3),其中 针对第一和第二附加体积(V2,V3)和/或第一和第二附加分支(B2,B3)校正中心体积参数的结果。
    • 3. 发明授权
    • Method and apparatus to determine the end of the systolic part of a pressure curve
    • 确定压力曲线收缩部分末端的方法和装置
    • US08506496B2
    • 2013-08-13
    • US12744772
    • 2008-11-24
    • Reinhold KnollUlf BorgUlrich Pfeiffer
    • Reinhold KnollUlf BorgUlrich Pfeiffer
    • A61B5/02A61B5/04
    • A61B5/029A61B5/021
    • The invention relates to a method and an apparatus for determining the systolic phase interval (SP) of an arterial pressure curve with a starting point (t0) of the systolic phase interval (SP) and an end point (tN) of the systolic phase interval (SP) wherein a QT interval is defined as the start of the Q wave and the end of the T wave in the hearts electrical cycle and wherein the determination of the end point (tN) of the systolic phase interval (SP) is restricted to the measured points of arterial pressure which fulfill the condition that the difference in time between the end point (tN) to be determined of the systolic phase interval (SP) and the starting point (t0) of the systolic phase interval (SP) is smaller than the QT interval.
    • 本发明涉及用于确定动脉压曲线的收缩期间隔(SP)的方法和装置,其具有收缩期间隔(SP)的起始点(t0)和收缩相间期的终点(tN) (SP),其中QT间隔被定义为心脏电循环中Q波的开始和T波的结束,并且其中心脏收缩期间隔(SP)的终点(tN)的确定被限制为 满足如下条件的动脉压的测量点,其中确定收缩期间隔(SP)的终点(tN)与收缩相间隔(SP)的起始点(t0)之间的时间差在较小 比QT间隔。
    • 6. 发明申请
    • Dilution apparatus, method and computer program
    • 稀释装置,方法和计算机程序
    • US20070135716A1
    • 2007-06-14
    • US11637373
    • 2006-12-12
    • Ulrich PfeifferReinhold Knoll
    • Ulrich PfeifferReinhold Knoll
    • A61B5/02
    • A61B5/0275A61B5/028A61B5/029A61B5/0295A61B5/7225A61B5/7239A61B5/7278
    • An apparatus for determining a patient's circulatory fill status is adapted to provide a dilution curve and is capable to derive the ratio between the patient's global end-diastolic volume GEDV and the patient's intra thoracic thermo volume ITTV from the dilution curve. Further, a computer program for determining a patient's circulatory fill status has instructions adapted to carry out the steps of generating the dilution curve on basis of provided measurement data of dilution versus time, deriving the ratio between the patient's global end-diastolic volume GEDV and the patient's intra thoracic thermo volume ITTV from the dilution curve, and determining the patient's circulatory fill status on basis of the ratio between the patient's global end-diastolic volume GEDV and the patient's intra thoracic thermo volume ITTV, when the computer program is run on a computer. A method is also provided.
    • 用于确定患者的循环充盈状态的装置适于提供稀释曲线,并且能够从稀释曲线导出患者的全身舒张末期容积GEDV与患者的胸内热体积ITTV之间的比率。 此外,用于确定患者的循环填充状态的计算机程序具有适于执行基于所提供的稀释度与时间的测量数据产生稀释曲线的步骤的指令,导出患者的全身舒张末期容积GEDV与 患者的胸腔内热量ITTV从稀释曲线,并且当计算机程序在计算机上运行时,基于患者的全身舒张末期容积GEDV与患者的胸内热体积ITTV之间的比率确定患者的循环填充状态 。 还提供了一种方法。
    • 7. 发明授权
    • Process for determining a patient's circulatory fill status
    • 确定患者循环灌注状态的过程
    • US5526817A
    • 1996-06-18
    • US325347
    • 1994-10-31
    • Ulrich PfeifferReinhold Knoll
    • Ulrich PfeifferReinhold Knoll
    • A61B5/00A61B5/028
    • A61B5/411A61B5/028
    • A process and a device for determining a patient's circulatory fill status, particularly the global end-diastolic volume of the heart (GEDV), intrathoracic blood volume (ITBV), pulmonary blood volume (PBV), extravascular lung water volume (EVLW), and/or global cardiac function index (CFI) by means of thermo-dilution; with this process intrathoracic thermo-volume (ITTV) and pulmonary thermo-volume (PTV), for example, are obtained and the global end-diastolic volume of the heart (GEDV) is determined from the equationGEDV=ITTV-PTV.The other volumes can be calculated by means of this parameter, which is specific for the fill status of the heart, as well as other species-specific characteristics (a, a', b, b').
    • PCT No.PCT / EP93 / 01052 Sec。 371日期:1994年10月31日 102(e)日期1994年10月31日PCT 1993年4月30日PCT PCT。 公开号WO93 / 21823 日期:1993年11月11日。一种用于确定患者的循环充盈状态,特别是心脏的全身舒张末期容积(GEDV),胸内血容量(ITBV),肺血容量(PBV),血管外肺 水量(EVLW)和/或全身心脏功能指数(CFI); 通过该过程获得例如胸腔内热量(ITTV)和肺热容积(PTV),并且从GEDV = ITTV-PTV等式确定心脏的全身舒张末期容积(GEDV)。 其他体积可以通过该参数计算,该参数是针对心脏的填充状态,以及其他物种特异性特征(a,a',b,b')特有的。
    • 10. 发明授权
    • Disposable sensor device and monitoring system with trimming element
    • 一次性传感器装置和带修剪元件的监控系统
    • US08920329B2
    • 2014-12-30
    • US12529010
    • 2008-02-19
    • Reinhold KnollFrederic MichardMatthias FahleTobias ThomamüllerUlrich Pfeiffer
    • Reinhold KnollFrederic MichardMatthias FahleTobias ThomamüllerUlrich Pfeiffer
    • A61B5/02A61B5/0215A61B5/00
    • A61B5/02141A61B5/002A61B5/0215A61B2560/0214A61B2560/045A61B2562/227
    • The invention relates to a disposable sensor device (51) for patient monitoring comprising a sensor (52) for providing an electric quantity based on a quantity to be detected, a first signal terminal (54) for providing a tap for the electric quantity, a first supply terminal (53) for supplying the sensor with an electrical supply quantity, a first connector for accommodating the first signal terminal (54) and the first supply terminal (53), a second signal terminal (56) for providing a further tap for the electric quantity, and a second connector for accommodating at least the second signal terminal (56). The invention further relates to a disposable sensor device for patient monitoring comprising a sensor (7) for providing an electric quantity based on a quantity to be detected; a first signal terminal (22) for providing a tap for the electric quantity; a first connector (A) for accommodating the first signal terminal, wherein the first connector (A) is provided with a trimming element (R2) which simulates the influence of a selectively attachable first monitoring device (1) on a measuring of the electric quantity, wherein the trimming element (R2) is electrically effective depending on a connector structure of a corresponding further connector (B, C) to be coupled with the first connector (A).
    • 本发明涉及一种用于患者监测的一次性传感器装置(51),包括用于基于待检测的量提供电量的传感器(52),用于提供用于电量的抽头的第一信号端子(54) 用于向传感器提供电源的第一供应端子(53),用于容纳第一信号端子(54)和第一供应端子(53)的第一连接器,用于提供另一分接头的第二信号端子 以及用于容纳至少第二信号端子(56)的第二连接器。 本发明还涉及一种用于患者监测的一次性传感器装置,其包括用于基于待检测量提供电量的传感器(7) 用于为电量提供水龙头的第一信号端子(22) 用于容纳所述第一信号端子的第一连接器(A),其中所述第一连接器(A)设置有修整元件(R2),所述修整元件(R2)模拟可选择地附接的第一监视装置(1)对所述电量的测量的影响 ,其中根据要与第一连接器(A)耦合的相应的另外的连接器(B,C)的连接器结构,修整元件(R2)是电学上有效的。