Packard C J, Bell M A, Eaton R H, Dagen M M, Cassidy M, Shepherd J
Institute of Biochemistry, Royal Infirmary, Glasgow, UK.
Ann Clin Biochem. 1993 Jul;30 ( Pt 4):387-93. doi: 10.1177/000456329303000407.
The measurement of plasma cholesterol is subject to particularly stringent requirements of bias and imprecision because clinically important action limits lie within the bulk of the population distribution. A pilot scheme was conducted with the aim of improving the accuracy of the assay of cholesterol in 26 laboratories in Scotland and Northern Ireland. This involved the distribution of three sets of authentic human sera with varying cholesterol concentrations assigned by the reference Abell-Kendall method which was established and validated in a central laboratory. The precision (coefficient of variation) of cholesterol testing was 1.71% across all laboratories at the first distribution and this did not alter subsequently. Mean bias was initially 4.07% (median 4.14%) relative to the Abell-Kendall assigned values and this figure had fallen to 1.12% (median 0.92%) by the third distribution. We conclude that through a standardization scheme it is possible in a relatively short time to improve bias significantly and meet the criterion of < 2-3% bias required for optimum cholesterol measurement.
血浆胆固醇的测量对偏差和不精密度有着特别严格的要求,因为具有临床意义的行动界限处于总体人群分布范围内。在苏格兰和北爱尔兰的26个实验室开展了一项试点计划,旨在提高胆固醇检测的准确性。这涉及分发三组由参考阿贝尔-肯德尔方法指定的、胆固醇浓度各异的真实人类血清,该方法在一个中央实验室建立并经过验证。在首次分发时,所有实验室胆固醇检测的精密度(变异系数)为1.71%,随后并未改变。相对于阿贝尔-肯德尔指定值,平均偏差最初为4.07%(中位数为4.14%),到第三次分发时,这一数字已降至1.12%(中位数为0.92%)。我们得出结论,通过标准化方案,有可能在相对较短的时间内显著改善偏差,并达到最佳胆固醇测量所需的<2-3%偏差标准。