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    • 3. 发明申请
    • SYSTEM AND METHOD FOR DETERMINING INSULIN BOLUS QUANTITIES
    • 用于确定胰岛素凝块数量的系统和方法
    • WO2006066926A1
    • 2006-06-29
    • PCT/EP2005/013891
    • 2005-12-22
    • ROCHE DIAGNOSTICS GMBHF.HOFFMANN-LA ROCHE AG
    • HELLWIG, RobertWEINERT, Stefan
    • G06F19/00
    • G01N33/66A61M5/1413A61M2005/1405A61M2005/14208G01N33/74G01N2333/4745G01N2800/042G06F19/00G06F19/3468G16H50/50
    • A method of computing an insulin bolus quantity when a measured glucose value in a current time interval exceeds a target glucose value for the current time interval and when a time duration of glucose lowering action of the bolus to be administered spans the current and a number of the next adjacent time intervals, may comprise determining a corresponding number of percentages of insulin action of the recommended bolus quantity that will each be used lowering the glucose level during a respective one of the number of time intervals, and computing the recommended bolus quantity as a function of the measured glucose value, the target blood glucose level for a last one of the number of next adjacent time intervals, the insulin sensitivities for the current and each of the number of next adjacent time intervals, and the corresponding number of percentages.
    • 当当前时间间隔内的测量葡萄糖值超过当前时间间隔的目标葡萄糖值时,以及当要施用的推注的葡萄糖降低作用的持续时间跨越当前时间间隔和当前时间间隔的多个时,计算胰岛素推注量的方法 下一个相邻的时间间隔可以包括确定推荐的推注剂量的胰岛素作用百分比的相应数量,其将在每个时间间隔的相应时间段内分别使用降低葡萄糖水平,并将推荐的推注量计算为 测量的葡萄糖值的功能,下一个相邻时间间隔数量的最后一个的目标血糖水平,当前和下一个相邻时间间隔的数量的胰岛素敏感性以及相应的百分比数。
    • 4. 发明申请
    • STRUCTURED TESTING METHOD FOR DIAGNOSTIC OR THERAPY SUPPORT OF A PATIENT WITH A CHRONIC DISEASE AND DEVICES THEREOF
    • 具有慢性疾病的患者的诊断或治疗支持的结构化测试方法及其装置
    • WO2010072386A2
    • 2010-07-01
    • PCT/EP2009/009170
    • 2009-12-21
    • ROCHE DIAGNOSTICS GMBHF.HOFFMANN-LA ROCHE AG
    • WALLING, P., DouglasSONI, Abhishek, S.RASCH-MENGES, JuergenWEINERT, StefanBOUSAMRA, StevenEISENHARDT, Christoph
    • G06F19/00
    • G06F17/30289G01N33/49G01N33/66G06F19/00G06F19/3418G16H10/20G16H40/63
    • A structured testing method (200, 300, 388) for diagnostic or therapy support of a patient (12) with a chronic disease and devices (18) thereof are disclosed, devices (18) implement the structured collection procedure (70) based on a medical use case and/or question which provides at least one or more parameters (220, 222, 224, 226, 228, 230, 232, 237, 238, 240) defining at least one entry criterion (226), a schedule of events (222), at least one adherence criterion (224), and at least one exit criterion (228). The entry criterion (226) establish conditions needed to be met prior to obtaining biomarker data (256) from the patient (12). Each event (237) in the schedule of events (222) can include at least one or more of a performance time (238), guidance (230) to perform the event (237), a request (240) for information from the patient (12), a request (240) for patient action, and a request (240) for collection of at least one type of biomarker data (256) from the patient (12). The adherence criterion (224) is used to assess qualitatively whether an event (237) performed according to the schedule of events (222) provided data (256, 170, 145) which is acceptable to addressing the medical use case and/or question, and the exit criterion (228) establishes conditions needed to be met prior to exiting the structured collection procedure (70).
    • 公开了一种用于具有慢性疾病的患者(12)及其装置(18)的诊断或治疗支持的结构化测试方法(200,300,388),装置(18)基于 提供定义至少一个入口标准(226)的至少一个或多个参数(220,222,224,226,228,230,232,237,238,240)的医疗用例和/或问题,事件调度 (222),至少一个遵守标准(224)和至少一个退出标准(228)。 进入标准(226)建立在从患者(12)获得生物标志物数据(256)之前需要满足的条件。 事件调度表(222)中的每个事件(237)可以包括执行事件(237)的执行时间(238),指导(230),来自患者的信息的请求(240))中的至少一个或多个 (12),用于患者动作的请求(240)以及用于从患者(12)收集至少一种类型的生物标志物数据(256)的请求(240)。 遵守标准(224)用于定性地评估根据事件调度表(222)执行的事件(237)是否提供了解决医疗用例和/或问题可接受的数据(256,170,145) 并且退出标准(228)建立在退出结构化收集过程(70)之前需要满足的条件。