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所有筛查免疫测定呈阳性的丁丙诺啡样本都需要进行确认吗?

Do all screening immunoassay positive buprenorphine samples need to be confirmed?

作者信息

Saleem Mohamed, Martin Helen, Tolya Anne, Coates Penny

机构信息

Chemical Pathology Directorate, South Australia Pathology, Adelaide, Australia.

出版信息

Ann Clin Biochem. 2017 Nov;54(6):707-711. doi: 10.1177/0004563216688489. Epub 2017 May 15.

Abstract

Background Interference from opiates in the Microgenics CEDIA® Buprenorphine assay is known to produce false-positive buprenorphine screening immunoassay results necessitating confirmatory buprenorphine testing by chromatography/mass spectrometry methods. Method We reviewed data on falsely positive buprenorphine immunoassay screen (cut-off ≥ 5  µg/L) but negative for buprenorphine by gas chromatography mass spectrometry (cut-off ≥ 5  µg/L) and had a positive opiate immunoassay result (cut-off ≥ 300  µg/L). The results were collected over three months, and the data were evaluated to determine whether there is an opiate immunoassay screen concentration below which a false-positive buprenorphine result will not occur. Results We found that cross-reactivity in the CEDIA® buprenorphine immunoassay by opiates at concentrations <2000  µg/L will not cause a false-positive buprenorphine result. After changing our practice to not proceed with confirmatory buprenorphine gas chromatography mass spectrometry assay when the opiate screening concentration is below an even more conservative cut-off of <1500  µg/L, we estimate a potential cost-saving of AU$ 17,810 per year without compromising clinical care. Conclusion Samples with CEDIA® opiate immunoassay result <2000  µg/L and a positive CEDIA® buprenorphine immunoassay screen do not require confirmatory testing for buprenorphine.

摘要

背景

已知在Microgenics CEDIA®丁丙诺啡检测中,阿片类药物的干扰会产生丁丙诺啡筛查免疫分析假阳性结果,因此需要通过色谱/质谱法进行丁丙诺啡确证检测。方法:我们回顾了丁丙诺啡免疫分析筛查假阳性(临界值≥5 μg/L)但气相色谱质谱法检测丁丙诺啡为阴性(临界值≥5 μg/L)且阿片类药物免疫分析结果为阳性(临界值≥300 μg/L)的数据。结果收集了三个月,对数据进行评估以确定是否存在一个阿片类药物免疫分析筛查浓度,低于该浓度不会出现丁丙诺啡假阳性结果。结果:我们发现,浓度<2000 μg/L的阿片类药物在CEDIA®丁丙诺啡免疫分析中的交叉反应不会导致丁丙诺啡假阳性结果。在将我们的做法改为当阿片类药物筛查浓度低于更保守的临界值<1500 μg/L时不进行丁丙诺啡气相色谱质谱确证检测后,我们估计每年可节省潜在成本17,810澳元,且不影响临床护理。结论:CEDIA®阿片类药物免疫分析结果<2000 μg/L且CEDIA®丁丙诺啡免疫分析筛查为阳性的样本不需要进行丁丙诺啡确证检测。

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