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对两种用于脂质分析的紧凑型分析仪的评估。

An evaluation of two compact analyzers used for lipid analysis.

作者信息

McKenney J M, Fary D F, Miller G, Proctor J D, Chinchili V M

机构信息

School of Pharmacy, Medical College of Virginia, Virginia Commonwealth University, Richmond 23298.

出版信息

J Fam Pract. 1993 May;36(5):526-33.

PMID:8482937
Abstract

BACKGROUND

A number of relatively inexpensive compact analyzers are available for use in physician offices and outpatient clinics to measure total cholesterol and, more recently, high-density lipoprotein (HDL) cholesterol and triglycerides. This study was designed to document the analytical performance of two of them, the Abbott Vision and the Kodak Ektachem DT60, for assays of total cholesterol, HDL cholesterol, triglycerides, and calculated low-density lipoprotein (LDL) cholesterol.

METHODS

Lipid profiles were measured from venous blood samples of 70 subjects with each test device, and results were compared with those from a laboratory standardized to the Centers for Disease Control. Coefficient of variation (CV) of multiple measurements from three pools of human serum (ie, precision), mean percent difference between device and standard laboratory results (ie, accuracy or bias), and 95% tolerance intervals (total error) were determined. The correct classification of patients into risk categories with device results was compared with the standardized laboratory results.

RESULTS

The average CVs for total cholesterol, triglycerides, and HDL cholesterol with the Vision analyzer were 3.6%, 4.4%, and 10.5%, respectively, and with the DT60, 5.0%, 4.1%, and 6.8%, respectively. The average percent biases for the same analytes with the Vision analyzer were 0.2%, 4.0%, and -2.3%, respectively, and with the DT60, -2.1%, 12.1%, and 0.1%, respectively. Total error assessments indicated that total and HDL cholesterol measurements in individual patients met the guidelines of the National Cholesterol Education Program with both devices, but that triglycerides and LDL cholesterol measurements did not. Classification of subjects into risk groups based on total or LDL cholesterol gave clinically satisfactory results with either device.

CONCLUSIONS

More precise measurement technology for LDL cholesterol is needed. Physicians and others who rely on compact analyzer results for diagnosis and treatment decisions should consider the degree of inaccuracy and imprecision in these values.

摘要

背景

有多种相对便宜的紧凑型分析仪可用于医生办公室和门诊诊所,以测量总胆固醇,最近还可测量高密度脂蛋白(HDL)胆固醇和甘油三酯。本研究旨在记录其中两款分析仪——雅培Vision和柯达Ektachem DT60——在总胆固醇、HDL胆固醇、甘油三酯以及计算得出的低密度脂蛋白(LDL)胆固醇检测中的分析性能。

方法

使用每个检测设备对70名受试者的静脉血样本进行血脂谱测量,并将结果与一个符合疾病控制中心标准的实验室的结果进行比较。确定了来自三个人血清池的多次测量的变异系数(CV)(即精密度)、设备结果与标准实验室结果之间的平均百分比差异(即准确度或偏差)以及95%的容许区间(总误差)。将根据设备结果对患者进行风险分类的正确情况与标准化实验室结果进行比较。

结果

Vision分析仪对总胆固醇、甘油三酯和HDL胆固醇的平均CV分别为3.6%、4.4%和10.5%;DT60对这些指标的平均CV分别为5.0%、4.1%和6.8%。Vision分析仪对相同分析物的平均百分比偏差分别为0.2%、4.0%和 -2.3%;DT60的分别为 -2.1%、12.1%和0.1%。总误差评估表明,两款设备对个体患者的总胆固醇和HDL胆固醇测量均符合国家胆固醇教育计划的指南,但甘油三酯和LDL胆固醇测量不符合。基于总胆固醇或LDL胆固醇将受试者分类到风险组,两款设备都给出了临床满意的结果。

结论

需要更精确的LDL胆固醇测量技术。依赖紧凑型分析仪结果进行诊断和治疗决策的医生及其他人员应考虑这些值中的不准确和不精确程度。

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