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评估URiSCAN 2 ACR试纸条以估算尿白蛋白/肌酐比值。

Evaluation of the URiSCAN 2 ACR Strip to estimate the urine albumin/creatinine ratios.

作者信息

Lim Sangeun, Yu Hui-Jin, Lee Seungjun, Park Hyosoon, Kwon Min-Jung, Woo Hee-Yeon

机构信息

Department of Laboratory Medicine, Kangbuk Samsung Hospital, Sungkyunkwan University School of Medicine, Seoul, Korea.

出版信息

J Clin Lab Anal. 2018 Mar;32(3). doi: 10.1002/jcla.22289. Epub 2017 Jun 26.

Abstract

BACKGROUND

The urine albumin/creatinine ratio (ACR) test is used to screen patients with chronic diseases, such as diabetes, hypertension and cardiovascular diseases that put them at an increased risk of developing kidney disease. Here, we evaluated the performance of the URiSCAN 2 ACR Strip (URiSCAN; YD diagnostics, Yongin, Korea), a semiquantitative point-of-care testing (POCT) assay, and we compared to an existing POCT assay and a quantitative assay.

MATERIALS AND METHODS

A total of 1,020 random urine specimens were analyzed using the semiquantitative URiSCAN 2 ACR Strip and semiquantitative CLINITEK Microalbumin 2 Strip (CLINITEK; Siemens, New York, USA). We evaluated the precision of the URiSCAN 2 ACR Strip and compared the results of the ACR obtained from URiSCAN to those of CLINITEK with the quantitative results of a quantitative assay as a reference.

RESULTS

The precision evaluation of the URiSCAN revealed a range between the cutoff (C )-20% and C +20% bounds, the C -C interval, with 85.8% confidence. URiSCAN and CLINITEK showed sensitivity and specificity of 87.7% and 72.2%, and 90.2% and 83.0%, respectively. The concordance rates of URiSCAN with CLINITEK and the quantitative assay were 75.6% and 79.1%, respectively. The concordance rate in the abnormal range (≥30 mg/g) between URiSCAN and the quantitative assay were higher than that between CLINITEK and the quantitative assay (78.8% vs 75.4%).

CONCLUSIONS

URiSCAN showed good precision and comparable sensitivity with lower specificity than those of CLINITEK.

摘要

背景

尿白蛋白/肌酐比值(ACR)检测用于筛查患有慢性疾病的患者,如糖尿病、高血压和心血管疾病患者,这些疾病会增加他们患肾病的风险。在此,我们评估了URiSCAN 2 ACR试纸条(URiSCAN;韩国龙仁市YD诊断公司)的性能,这是一种半定量即时检验(POCT)检测方法,并将其与现有的POCT检测方法和定量检测方法进行了比较。

材料与方法

使用半定量的URiSCAN 2 ACR试纸条和半定量的CLINITEK微量白蛋白2试纸条(CLINITEK;美国纽约西门子公司)对总共1020份随机尿液标本进行了分析。我们评估了URiSCAN 2 ACR试纸条的精密度,并将URiSCAN获得的ACR结果与CLINITEK的结果进行比较,以定量检测的定量结果作为参考。

结果

URiSCAN的精密度评估显示,在临界值(C)-20%至C+20%界限之间,即C-C区间,置信度为85.8%。URiSCAN和CLINITEK的敏感性和特异性分别为87.7%和72.2%,以及90.2%和83.0%。URiSCAN与CLINITEK以及定量检测的一致性率分别为75.6%和79.

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