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A Computational Approach to Identify Interfering Medications on Urine Drug Screening Assays without Data from Confirmatory Testing

Urine drug screening (UDS) assays can rapidly and sensitively detect drugs of abuse but can also produce spurious results due to interfering substances. We previously developed an approach to identify interfering medications using electronic health record (EHR) data, but the approach was limited to...

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Autores principales: Ayala-Lopez, Nadia, Aref, Layla, Colby, Jennifer M, Hughey, Jacob J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8040373/
https://www.ncbi.nlm.nih.gov/pubmed/32991692
http://dx.doi.org/10.1093/jat/bkaa140
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author Ayala-Lopez, Nadia
Aref, Layla
Colby, Jennifer M
Hughey, Jacob J
author_facet Ayala-Lopez, Nadia
Aref, Layla
Colby, Jennifer M
Hughey, Jacob J
author_sort Ayala-Lopez, Nadia
collection PubMed
description Urine drug screening (UDS) assays can rapidly and sensitively detect drugs of abuse but can also produce spurious results due to interfering substances. We previously developed an approach to identify interfering medications using electronic health record (EHR) data, but the approach was limited to UDS assays for which presumptive positives were confirmed using more specific methods. Here we adapted the approach to search for medications that cause false positives on UDS assays lacking confirmation data. From our institution’s EHR data, we used our previous dataset of 698,651 UDS and confirmation results. We also collected 211,108 UDS results for acetaminophen, ethanol and salicylates. Both datasets included individuals’ prior medication exposures. We hypothesized that the odds of a presumptive positive would increase following exposure to an interfering medication independently of exposure to the assay’s target drug(s). For a given assay–medication pair, we quantified potential interference as an odds ratio from logistic regression. We evaluated interference of selected compounds in spiking experiments. Compared to the approach requiring confirmation data, our adapted approach showed only modestly diminished ability to detect interfering medications. Applying our approach to the new data, we discovered and validated multiple compounds that can cause presumptive positives on the UDS assay for acetaminophen. Our approach can reveal interfering medications using EHR data from institutions at which UDS results are not routinely confirmed.
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spelling pubmed-80403732021-04-15 A Computational Approach to Identify Interfering Medications on Urine Drug Screening Assays without Data from Confirmatory Testing Ayala-Lopez, Nadia Aref, Layla Colby, Jennifer M Hughey, Jacob J J Anal Toxicol Article Urine drug screening (UDS) assays can rapidly and sensitively detect drugs of abuse but can also produce spurious results due to interfering substances. We previously developed an approach to identify interfering medications using electronic health record (EHR) data, but the approach was limited to UDS assays for which presumptive positives were confirmed using more specific methods. Here we adapted the approach to search for medications that cause false positives on UDS assays lacking confirmation data. From our institution’s EHR data, we used our previous dataset of 698,651 UDS and confirmation results. We also collected 211,108 UDS results for acetaminophen, ethanol and salicylates. Both datasets included individuals’ prior medication exposures. We hypothesized that the odds of a presumptive positive would increase following exposure to an interfering medication independently of exposure to the assay’s target drug(s). For a given assay–medication pair, we quantified potential interference as an odds ratio from logistic regression. We evaluated interference of selected compounds in spiking experiments. Compared to the approach requiring confirmation data, our adapted approach showed only modestly diminished ability to detect interfering medications. Applying our approach to the new data, we discovered and validated multiple compounds that can cause presumptive positives on the UDS assay for acetaminophen. Our approach can reveal interfering medications using EHR data from institutions at which UDS results are not routinely confirmed. Oxford University Press 2020-11-30 /pmc/articles/PMC8040373/ /pubmed/32991692 http://dx.doi.org/10.1093/jat/bkaa140 Text en © The Author(s) 2020. Published by Oxford University Press. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Article
Ayala-Lopez, Nadia
Aref, Layla
Colby, Jennifer M
Hughey, Jacob J
A Computational Approach to Identify Interfering Medications on Urine Drug Screening Assays without Data from Confirmatory Testing
title A Computational Approach to Identify Interfering Medications on Urine Drug Screening Assays without Data from Confirmatory Testing
title_full A Computational Approach to Identify Interfering Medications on Urine Drug Screening Assays without Data from Confirmatory Testing
title_fullStr A Computational Approach to Identify Interfering Medications on Urine Drug Screening Assays without Data from Confirmatory Testing
title_full_unstemmed A Computational Approach to Identify Interfering Medications on Urine Drug Screening Assays without Data from Confirmatory Testing
title_short A Computational Approach to Identify Interfering Medications on Urine Drug Screening Assays without Data from Confirmatory Testing
title_sort computational approach to identify interfering medications on urine drug screening assays without data from confirmatory testing
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8040373/
https://www.ncbi.nlm.nih.gov/pubmed/32991692
http://dx.doi.org/10.1093/jat/bkaa140
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