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ADEQUACY ASSESSMENT METHOD AND SYSTEM

机译:适当性评估方法和系统

摘要

The present application relates to an adequacy assessment method and system. The method comprises: obtaining biochemical detection data, and extracting latest assay data of a periodic assay record; calculating a body fluid volume according to the latest assay data; calculating a urea clearance index according to the calculated body fluid volume and a specified parameter; and displaying and outputting the urea clearance index of an adequacy assessment. Compared with the prior art, in the present application, biochemical detection data of a patient before dialysis is collected by one time, automatic assessment of each dialysis is achieved, multiple biochemical detections before and after dialysis do not rely on blood collection, the burden of multiple blood collections and blood losses of the patient is not aggravated, and dialysis adequacy is monitored and therapeutic schemes are adjusted in real time in a dialysis process; moreover, the method and the system do not rely on dialysis machines and peripheral auxiliary equipment.
机译:本申请涉及一种充足性评估方法和系统。该方法包括:获取生化检测数据,提取周期性检测记录的最新检测数据。根据最新的测定数据计算体液量;根据计算出的体液量和指定参数计算尿素清除指数;显示并输出充分性评价的尿素清除率指标。与现有技术相比,在本申请中,一次收集患者透析前的生化检测数据,实现每次透析的自动评估,透析前后的多次生化检测不依赖于血液采集,负担较大。不会增加患者的多次采血和失血量,并且在透析过程中监控透析的充分性并实时调整治疗方案;而且,该方法和系统不依赖于透析机和外围辅助设备。

著录项

  • 公开/公告号WO2020052433A1

    专利类型

  • 公开/公告日2020-03-19

    原文格式PDF

  • 申请/专利权人 BEIJING IFMSOFT INFORMATION TECHNOLOGY CO. LTD.;

    申请/专利号WO2019CN102947

  • 发明设计人 WANG WEI;CHEN JIA;

    申请日2019-08-28

  • 分类号G16H10/40;G16H20/40;G16H50/30;A61M1/14;

  • 国家 WO

  • 入库时间 2022-08-21 11:12:49

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