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System and method for determining sigma of a clinical diagnostic process

机译:用于确定临床诊断过程的西格玛的系统和方法

摘要

A system and method for determining a sigma of a clinical diagnostic process are disclosed. Specimen data are collected from a plurality of laboratory instruments. The specimen data are evaluated to determine a concentration and an analytical standard deviation for each data point. A clinical diagnostic process is run and patient analyte values are acquired, and a standard deviation is assigned to each patient analyte value based on the standard deviation of specimen data having a corresponding concentration. A single sigma-metric is computed based on the patient analyte assigned standard deviations, the sigma- metric representing the sigma of the clinical diagnostic process. The computed sigma-metric is reported to a user or laboratory manager.
机译:公开了一种用于确定临床诊断过程的西格玛的系统和方法。从多个实验室仪器收集标本数据。评估样本数据以确定每个数据点的浓度和分析标准偏差。运行临床诊断过程并获取患者分析物值,并基于具有相应浓度的样本数据的标准偏差将标准偏差分配给每个患者分析物值。基于分配给患者分析物的标准偏差计算单个sigma-metric,该sigma-metric代表临床诊断过程的sigma。计算出的西格玛度量值会报告给用户或实验室管理员。

著录项

  • 公开/公告号AU2010274948B2

    专利类型

  • 公开/公告日2015-08-20

    原文格式PDF

  • 申请/专利权人 BIO-RAD LABORATORIES INC.;

    申请/专利号AU20100274948

  • 发明设计人 YUNDT-PACHECO JOHN;PARVIN CURTIS;

    申请日2010-04-12

  • 分类号G01N33/50;

  • 国家 AU

  • 入库时间 2022-08-21 15:10:46

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