Evaluation of Immunoassay Performance for the Detection of Opioids in Urine.

IF 1.9 Q3 MEDICAL LABORATORY TECHNOLOGY Journal of Applied Laboratory Medicine Pub Date : 2025-05-02 DOI:10.1093/jalm/jfae169
Michael E Walsh, Michael T Kelliher, Jacqueline A Hubbard, Mark A Cervinski
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Abstract

Background: Immunoassay drug screens provide rapid analysis of urine for the presence of therapeutics and drugs of abuse. Compared to definitive (confirmatory) methods, immunoassays are prone to false-positive and -negative results. Laboratories generally rely on manufacturers' claims regarding method sensitivity and specificity; few have the resources to independently verify performance. In this study, we review the performance of our opioid immunoassay drug screens in comparison to a definitive method.

Methods: Results of 859 urine samples tested via opioid immunoassay screens for buprenorphine, fentanyl, methadone metabolite (2-ethylidene-1,5-dimethyl-3,3-diphenylpyrrolidine; EDDP), opiates, and oxycodone were compared to definitive results obtained via liquid chromatography-tandem mass spectrometry (LC-MS/MS). The data examined here included multiple samples from individual patients. Our quantitative LC-MS/MS method includes 19 opioid compounds (parent drugs plus metabolites).

Results: Immunoassay sensitivity and specificity ranged from 96% to 100% and 84% to 99%, respectively. The sensitivity and specificity of these screens were similar to manufacturers' claims with some exceptions. The opiates immunoassay had poor performance when limiting the comparison to its target compound, morphine, but improved when including all compounds listed in the manufacturer's instructions for use (IFU). While demonstrating good sensitivity, the buprenorphine immunoassay demonstrated lower specificity than stated in the IFU.

Conclusions: The opioid immunoassay screens in use at our facility compared favorably to a definitive LC-MS/MS method. The urine fentanyl screen had the lowest sensitivity (96%) and had a specificity of 97%. The urine buprenorphine assay was the least specific (84%) and had a sensitivity of 99%.

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尿中阿片类药物的免疫检测性能评价。
背景:免疫分析药物筛选提供快速分析尿液治疗药物和滥用药物的存在。与确定(确认)方法相比,免疫测定法容易产生假阳性和阴性结果。实验室通常依赖于制造商关于方法敏感性和特异性的声明;很少有公司拥有独立验证性能的资源。在这项研究中,我们回顾了我们的阿片类免疫测定药物筛选的性能,与确定的方法进行比较。方法:对859份尿样进行阿片免疫筛选,检测丁丙诺啡、芬太尼、美沙酮代谢物(2-乙基-1,5-二甲基-3,3-二苯基吡咯烷);将EDDP)、阿片类药物和羟考酮与液相色谱-串联质谱(LC-MS/MS)获得的明确结果进行比较。这里检查的数据包括来自个体患者的多个样本。我们的定量LC-MS/MS方法包括19种阿片类化合物(母体药物加上代谢物)。结果:免疫测定的敏感性为96% ~ 100%,特异性为84% ~ 99%。除了一些例外,这些筛查的敏感性和特异性与制造商的声明相似。阿片类药物免疫测定在限制其目标化合物吗啡的比较时表现不佳,但在包括制造商使用说明书(IFU)中列出的所有化合物时则有所改善。虽然丁丙诺啡免疫分析法显示出良好的敏感性,但其特异性低于IFU。结论:在我们的设施中使用的阿片类免疫分析筛选优于确定的LC-MS/MS方法。尿芬太尼筛查的灵敏度最低(96%),特异性为97%。尿丁丙诺啡试验的特异性最低(84%),敏感性为99%。
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来源期刊
Journal of Applied Laboratory Medicine
Journal of Applied Laboratory Medicine MEDICAL LABORATORY TECHNOLOGY-
CiteScore
3.70
自引率
5.00%
发文量
137
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