Haeckel Rainer, Wosniok Werner
Institut für Laboratoriumsmedizin, Zentralkrankenhaus Sankt-Juergen-Strasse, Bremen, Germany.
Clin Chem Lab Med. 2004 Feb;42(2):198-203. doi: 10.1515/CCLM.2004.036.
A novel statistical approach has recently been described to estimate diagnostic "errors" in method comparison studies. This procedure requires a population-based probability, pp, which describes the spread of values within the population under study, and an analytical probability, Pa, quantifying the risk of errors at a decision limit due to replacing one method by the other. The population probability was derived from 207 subjects who were submitted to an oral glucose tolerance test due to suspicion of type 2 diabetes. The new concept was then applied in a reverse mode by determining the analytical variability of glucose concentrations for a fixed discordance rate diagnosing type 2 diabetes. If a combined discordance rate (sum of positive and negative discordances) of 5% is allowed, a maximal imprecision of 3.7% can be tolerated in the absence of bias. In the presence of a 3.0% bias, the allowable imprecision must be reduced to 2.8%. The relationship between bias and imprecision followed a complex function and not a simple linear model. These allowable limits were achieved with venous plasma in the fasting state. The allowable analytical specifications were slightly more stringent with capillary blood. After a 2 h glucose challenge, higher error rates could be tolerated, indicating that post-load glucose concentrations have a higher diagnostic efficiency than fasting levels. The new concept has the advantage that it is derived from patient's samples in relation to diagnostic requirements.
最近描述了一种新的统计方法,用于估计方法比较研究中的诊断“误差”。该程序需要一个基于总体的概率pp,它描述了所研究总体内值的分布,以及一个分析概率Pa,用于量化在决策限处由于用一种方法替代另一种方法而产生误差的风险。总体概率来自207名因怀疑患有2型糖尿病而接受口服葡萄糖耐量试验的受试者。然后,通过确定诊断2型糖尿病的固定不一致率下葡萄糖浓度的分析变异性,以反向模式应用这一新概念。如果允许5%的综合不一致率(阳性和阴性不一致的总和),在无偏差的情况下可容忍的最大不精密度为3.7%。在存在3.0%偏差的情况下,允许的不精密度必须降至2.8%。偏差与不精密度之间的关系遵循复杂函数,而非简单线性模型。这些允许限度是在空腹状态下的静脉血浆中实现的。对于毛细血管血,允许的分析规范略为严格。在进行2小时葡萄糖激发试验后,可以容忍更高的误差率,这表明负荷后血糖浓度比空腹水平具有更高的诊断效率。这一新概念的优点在于它是根据患者样本与诊断要求得出的。