Division of Hematology and Central Hematology Laboratory, Luzerner Kantonsspital, Lucerne 16 CH-6000, Switzerland.
Thromb J. 2013 Mar 7;11(1):6. doi: 10.1186/1477-9560-11-6.
While the assessment of analytical precision within medical laboratories has received much attention in scientific enquiry, the degree of as well as the sources causing variation between them remains incompletely understood. In this study, we quantified the variance components when performing coagulation tests with identical analytical platforms in different laboratories and computed intraclass correlations coefficients (ICC) for each coagulation test.
Data from eight laboratories measuring fibrinogen twice in twenty healthy subjects with one out of 3 different platforms and single measurements of prothrombin time (PT), and coagulation factors II, V, VII, VIII, IX, X, XI and XIII were analysed. By platform, the variance components of (i) the subjects, (ii) the laboratory and the technician and (iii) the total variance were obtained for fibrinogen as well as (i) and (iii) for the remaining factors using ANOVA.
The variability for fibrinogen measurements within a laboratory ranged from 0.02 to 0.04, the variability between laboratories ranged from 0.006 to 0.097. The ICC for fibrinogen ranged from 0.37 to 0.66 and from 0.19 to 0.80 for PT between the platforms. For the remaining factors the ICC's ranged from 0.04 (FII) to 0.93 (FVIII).
Variance components that could be attributed to technicians or laboratory procedures were substantial, led to disappointingly low intraclass correlation coefficients for several factors and were pronounced for some of the platforms. Our findings call for sustained efforts to raise the level of standardization of structures and procedures involved in the quantification of coagulation factors.
虽然医学实验室的分析精密度评估在科学研究中受到了广泛关注,但它们之间的变异性程度及其来源仍不完全清楚。在这项研究中,我们量化了在不同实验室使用相同分析平台进行凝血测试时的变异分量,并计算了每个凝血测试的组内相关系数(ICC)。
我们分析了来自 8 个实验室的数据,这些实验室使用 3 种不同平台中的 1 种对 20 名健康受试者的纤维蛋白原进行了两次测量,以及对凝血酶原时间(PT)和凝血因子 II、V、VII、VIII、IX、X、XI 和 XIII 进行了单次测量。按平台,我们使用 ANOVA 分别获得了纤维蛋白原的(i)个体、(ii)实验室和技术人员以及(iii)总方差的变异分量,以及其余因子的(i)和(iii)变异分量。
实验室内部纤维蛋白原测量的变异性范围为 0.02 至 0.04,实验室之间的变异性范围为 0.006 至 0.097。纤维蛋白原的 ICC 范围为 0.37 至 0.66,PT 之间的 ICC 范围为 0.19 至 0.80。对于其余因子,ICC 范围为 0.04(FII)至 0.93(FVIII)。
可归因于技术人员或实验室程序的变异分量很大,导致一些因子的组内相关系数令人失望地低,并且在一些平台上表现明显。我们的研究结果呼吁持续努力提高凝血因子定量所涉及的结构和程序的标准化水平。