Zhang Jinming, Chen Xingtong, Wu Jiaming, Feng Penghui, Wang Wei, Zhong Kun, Yuan Shuai, Du Yuxuan, Zhang Chuanbao, He Falin
National Center for Clinical Laboratories, Institute of Geriatric Medicine, Chinese Academy of Medical Sciences, Beijing Hospital/ National Center of Gerontology, Beijing, PR China.
Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, PR China.
Pract Lab Med. 2024 Jul 23;41:e00422. doi: 10.1016/j.plabm.2024.e00422. eCollection 2024 Aug.
We aimed to evaluate the analytical performance of second-trimester maternal serum screening in China, and to compare if there are differences in sigma levels across different methods and months.
A retrospective study was conducted to assess the analytical quality levels of laboratories by calculating the Sigma metrics with prenatal screening biomarkers: AFP, Total β-hCG, free β-hCG, uE3. Data from 591 laboratories were selected. Sigma metrics were computed using the formula: Sigma metrics(σ) = (%TEa - |%Bias|)/%CV. The Friedman test and Mann-Whitney test were used to compare differences across various methods and different months. The Hodges-Lehmann was used for determining 95 % confidence intervals of pseudo-medians.
Only uE3 showed significant monthly variations in sigma calculations. However, around 8 % of laboratories across all four analytes demonstrated sigma levels both above 6 and below 3 in different months. Laboratories utilizing time-resolved fluorescence methods significantly outperformed those using chemiluminescence in sigma level. For AFP, the pseudo-median difference between these methods lies within a 95 % confidence interval of (-3.22, -1.93), while for uE3, it is at (-2.30, -1.40). Notably, the median sigma levels for all analytes reached the 4-sigma threshold, with free β-hCG even attaining the 6-sigma level.
With current standards, China's second-trimester maternal serum screening is of relatively high analytical quality, and variations in sigma levels exist across different months and methods.
我们旨在评估中国孕中期母血清筛查的分析性能,并比较不同方法和月份间西格玛水平是否存在差异。
开展一项回顾性研究,通过计算产前筛查生物标志物(甲胎蛋白、总β人绒毛膜促性腺激素、游离β人绒毛膜促性腺激素、雌三醇)的西格玛指标来评估实验室的分析质量水平。选取了591家实验室的数据。西格玛指标使用公式计算:西格玛指标(σ)=(%TEa - |%偏差|)/%CV。采用弗里德曼检验和曼-惠特尼检验比较不同方法和不同月份间的差异。使用霍奇斯-莱曼方法确定伪中位数的95%置信区间。
仅雌三醇在西格玛计算中显示出显著的月度变化。然而,在所有四种分析物中,约8%的实验室在不同月份的西格玛水平既高于6又低于3。采用时间分辨荧光法的实验室在西格玛水平上显著优于使用化学发光法的实验室。对于甲胎蛋白,这些方法之间的伪中位数差异在95%置信区间(-3.22, -1.93)内,而对于雌三醇,为(-2.30, -1.40)。值得注意的是,所有分析物的中位数西格玛水平均达到4西格玛阈值,游离β人绒毛膜促性腺激素甚至达到了6西格玛水平。
按照当前标准,中国孕中期母血清筛查具有较高的分析质量,且西格玛水平在不同月份和方法间存在差异。