Department of Laboratory Medicine, Bucheon St. Mary's Hospital, College of Medicine, The Catholic University of Korea, Seoul, Korea.
Ann Lab Med. 2021 Sep 1;41(5):447-454. doi: 10.3343/alm.2021.41.5.447.
Urine reagent strip test (URST) results are semi-quantitative; therefore, the precision of URSTs is evaluated as the proportion of categorical results from repeated measurements of a sample that are concordant with an expected result. However, URSTs have quantitative readout values before ordinal results challenging statistical monitoring for internal quality control (IQC) with control rules. This study aimed to determine the sigma metric of URSTs and derive appropriate control rules for IQC.
The URiSCAN Super Plus fully automated urine analyzer (YD Diagnostics, Yongin, Korea) was used for URSTs. Change in reflectance rate (change %R) data from IQC for URSTs performed between November 2018 and May 2020 were analyzed. Red blood cells, bilirubin, urobilinogen, ketones, protein, glucose, leukocytes, and pH were measured from 2-3 levels of control materials. The total allowable error (TE) for a grade was the difference in midpoints of a predefined change %R range between two adjacent grades. The sigma metric was calculated as TE/SD. Sigma metric-based control rules were determined with Westgard EZ Rules 3 software (Westgard QC, Madison, WI, USA).
Seven out of the eight analytes had a sigma metric >4 in the control materials with a negative grade (-), which were closer to the cut-offs. Corresponding control rules ranged from 1 to 1.
Although the URST is a semi-quantitative test, statistical IQC can be performed using the readout values. According to the sigma metric, control rules recommended for URST IQC in routine clinical practice are 1 to 1.
尿液试剂带检测(URST)结果为半定量;因此,URST 的精密度通过对同一样本重复测量的分类结果与预期结果一致的比例进行评估。然而,URST 在出现有序结果之前具有定量读数,这对使用控制规则进行内部质量控制(IQC)的统计监测提出了挑战。本研究旨在确定 URST 的西格玛度量,并为 IQC 推导出适当的控制规则。
使用 YD 诊断公司(韩国龙仁)的 URiSCAN Super Plus 全自动尿液分析仪进行 URST。分析 2018 年 11 月至 2020 年 5 月之间进行的 URST 的 IQC 中反射率变化率(变化%R)数据。从 2-3 个水平的控制材料中测量红细胞、胆红素、尿胆原、酮体、蛋白质、葡萄糖、白细胞和 pH。等级的总允许误差(TE)是两个相邻等级之间预定变化%R 范围内中点之间的差异。西格玛度量是通过 Westgard EZ Rules 3 软件(Westgard QC,威斯康星州麦迪逊)计算得出的。
在具有负等级(-)的控制材料中,8 种分析物中有 7 种的西格玛度量>4,这更接近临界点。相应的控制规则范围从 1 到 1。
尽管 URST 是一种半定量测试,但可以使用读数进行统计 IQC。根据西格玛度量,推荐用于常规临床实践中的 URST IQC 的控制规则为 1 到 1。