Luzzi Veronica I, Saunders Al N, Koenig John W, Turk John, Lo Stanley F, Garg Uttam C, Dietzen Dennis J
Department of Pediatrics, Washington University School of Medicine, St. Louis, MO, USA.
Clin Chem. 2004 Apr;50(4):717-22. doi: 10.1373/clinchem.2003.028878. Epub 2004 Feb 5.
The analytic performance and accuracy of drug detection below Substance Abuse and Mental Health Services Administration (SAMHSA) cutoffs is not well known. In some patient populations, clinically significant concentrations of abused drugs in urine may not be detected when current SAMHSA cutoffs are used. Our objectives were to define the precision profiles of three immunoassay systems for drugs of abuse and to evaluate the accuracy of testing at concentrations at which the CV was <20%.
Drug-free urine was supplemented with analytes to assess the precision in three commercial drugs-of-abuse immunoassay systems below the SAMHSA-dictated cutoffs for amphetamines, opiates, benzoylecgonine, phencyclidine, and cannabinoids. Consecutive urine samples with signals associated with a CV <20% by Emit immunoassay and below SAMHSA cutoffs were then subjected to confirmatory analysis.
The CV of all immunoassay systems tested remained <20% to drug concentrations well below SAMHSA cutoffs. The accuracy of urine drug-screening results between the SAMHSA-specified cutoffs and the precision-based cutoffs was less than accuracy for specimens above the SAMHSA cutoffs, but the use of the precision-based cutoff produced a 15.6% increase in the number of screen-positive specimens and a 7.8% increase in the detection of specimens that yielded positive results on confirmatory testing.
The precision of three commercial immunoassay systems for drugs-of-abuse screening is adequate to detect drugs below SAMHSA cutoffs. Knowledge of the positive predictive values of screening immunoassays at lower cutoff concentrations could enable efficient use of confirmatory testing resources and improved detection of illicit drug use.
低于美国药物滥用和精神健康服务管理局(SAMHSA)临界值的药物检测的分析性能和准确性尚不清楚。在一些患者群体中,当使用当前的SAMHSA临界值时,尿液中临床上显著浓度的滥用药物可能无法被检测到。我们的目标是确定三种滥用药物免疫分析系统的精密度概况,并评估在变异系数(CV)<20%的浓度下检测的准确性。
向无药物尿液中添加分析物,以评估三种商用滥用药物免疫分析系统在低于SAMHSA规定的苯丙胺、阿片类药物、苯甲酰芽子碱、苯环己哌啶和大麻素临界值时的精密度。然后,对通过Emit免疫分析显示变异系数<20%且低于SAMHSA临界值的连续尿液样本进行确证分析。
所有测试的免疫分析系统在远低于SAMHSA临界值的药物浓度下,变异系数均保持<20%。SAMHSA规定的临界值与基于精密度的临界值之间的尿液药物筛查结果的准确性低于高于SAMHSA临界值的标本,但使用基于精密度的临界值使筛查阳性标本数量增加了15.6%,确证检测呈阳性结果的标本检测率增加了7.8%。
三种商用滥用药物免疫分析系统用于筛查的精密度足以检测低于SAMHSA临界值的药物。了解较低临界浓度下筛查免疫分析的阳性预测值,有助于有效利用确证检测资源,并改善对非法药物使用的检测。