Caudill S P, Cooper G R, Smith S J, Myers G L
Environmental Health Laboratory Sciences Division, National Center for Environmental Health, National Centers for Disease Control and Prevention, Atlanta, GA 30341-3724, USA.
Clin Chem. 1998 Aug;44(8 Pt 1):1650-8.
We examine the effect of systematic bias and random error, quality control, and intraperson biological variation on the National Cholesterol Education Program (NCEP) clinical classifications for reported lipid measurements. We consider misclassification to occur if a true lipid homeostatic set point is within a desirable range but the reported lipid value is in a high-risk range, or if a true lipid homeostatic set point is in a high-risk range but the reported lipid value is in a desirable range. To evaluate the overall adequacy of the NCEP guidelines to ensure correct patient classification, we construct operating characteristic curves for total cholesterol, triglycerides, high-density lipoprotein cholesterol, and low-density lipoprotein cholesterol. We demonstrate that if laboratories are meeting the NCEP guidelines for inherent bias and analytic precision and are using standard quality-control (QC) procedures incorporating at least two QC samples per analytical run from each of two QC pools (for a total of 4 QC samples), the current NCEP guidelines are adequate to ensure (probability >0.90) correct patient classifications regardless of the size of the systematic bias of the laboratory or increased random analytic error. Thus we suggest that at least two concentrations of QC material be included in the QC scheme to ensure that the measurement system is operating within desired specifications across the entire range of desirable and high-risk lipid concentrations and to ensure with high probability that patients are correctly classified.
我们研究了系统偏差、随机误差、质量控制以及个体内生物学变异对美国国家胆固醇教育计划(NCEP)报告的血脂测量临床分类的影响。如果真实的血脂稳态设定点处于理想范围内,但报告的血脂值处于高风险范围内,或者如果真实的血脂稳态设定点处于高风险范围内,但报告的血脂值处于理想范围内,我们认为发生了错误分类。为了评估NCEP指南确保正确患者分类的总体充分性,我们构建了总胆固醇、甘油三酯、高密度脂蛋白胆固醇和低密度脂蛋白胆固醇的操作特征曲线。我们证明,如果实验室符合NCEP关于固有偏差和分析精密度的指南,并且使用的标准质量控制(QC)程序在每次分析运行中从两个QC池中的每一个至少纳入两个QC样本(总共4个QC样本),那么当前的NCEP指南足以确保(概率>0.90)正确的患者分类,而不管实验室系统偏差的大小或随机分析误差的增加。因此,我们建议在QC方案中至少包含两种浓度的QC材料,以确保测量系统在理想和高风险血脂浓度的整个范围内按照期望的规格运行,并以高概率确保患者得到正确分类。