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Monitoring people at risk of drinking by a rapid urinary ethyl glucuronide test
Alcohol and illicit drug abuse are major public health problems worldwide. Since alcohol is the predominant substance of choice in polydrug abusers, monitoring its use, along with urinary drug screening in patients in rehabilitation programs, appeared to be crucial in identifying patients at risk of...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Slovak Toxicology Society SETOX
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6102674/ https://www.ncbi.nlm.nih.gov/pubmed/30147423 http://dx.doi.org/10.1515/intox-2017-0022 |
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author | Fucci, Nadia Gili, Alessio Aroni, Kyriaki Bacci, Mauro Carletti, Paola Pascali, Vincenzo Lorenzo Gambelunghe, Cristiana |
author_facet | Fucci, Nadia Gili, Alessio Aroni, Kyriaki Bacci, Mauro Carletti, Paola Pascali, Vincenzo Lorenzo Gambelunghe, Cristiana |
author_sort | Fucci, Nadia |
collection | PubMed |
description | Alcohol and illicit drug abuse are major public health problems worldwide. Since alcohol is the predominant substance of choice in polydrug abusers, monitoring its use, along with urinary drug screening in patients in rehabilitation programs, appeared to be crucial in identifying patients at risk of alcohol disorders leading to impaired quality of life. Ethyl β-D-6-glucuronide, a non-oxidative, non-volatile, stable and minor direct ethanol metabolite, has a 6h to 4 day window of detection in urine after the last alcohol intake. Each of the 119 subjects (85 males, 34 females) registered with the Public Health Service for Drug Dependence Treatment provided a urine sample for ethylglucoronide (EtG) determination in an immunochemical test with a 500 ng/ml cutoff. All results were evaluated with confirmation criteria of a fully validated gas chromatography/mass spectrometry assay. The diagnostic performance of the EtG immunochemical test was assessed using Receiver Operating Characteristic Curve analysis. The immunochemical test specificity was 100% for EtG urinary values above 500 ng/ml. No false positive results were found. With levels below 500 ng/ml, 12% of the samples were classified as negative. The average consumption of the incorrectly classified subjects was 171 ng/ml, with a misclassification error of 6.5% to 18.5%. High agreement between EtG as determined in an immunochemical test and gas chromatography/mass spectrometry, suggests that the rapid EtG test is a reliable, cost-effective alcohol monitoring assay for patient management in many non-forensic settings, such as drug rehabilitation programs. |
format | Online Article Text |
id | pubmed-6102674 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Slovak Toxicology Society SETOX |
record_format | MEDLINE/PubMed |
spelling | pubmed-61026742018-08-24 Monitoring people at risk of drinking by a rapid urinary ethyl glucuronide test Fucci, Nadia Gili, Alessio Aroni, Kyriaki Bacci, Mauro Carletti, Paola Pascali, Vincenzo Lorenzo Gambelunghe, Cristiana Interdiscip Toxicol Original Article Alcohol and illicit drug abuse are major public health problems worldwide. Since alcohol is the predominant substance of choice in polydrug abusers, monitoring its use, along with urinary drug screening in patients in rehabilitation programs, appeared to be crucial in identifying patients at risk of alcohol disorders leading to impaired quality of life. Ethyl β-D-6-glucuronide, a non-oxidative, non-volatile, stable and minor direct ethanol metabolite, has a 6h to 4 day window of detection in urine after the last alcohol intake. Each of the 119 subjects (85 males, 34 females) registered with the Public Health Service for Drug Dependence Treatment provided a urine sample for ethylglucoronide (EtG) determination in an immunochemical test with a 500 ng/ml cutoff. All results were evaluated with confirmation criteria of a fully validated gas chromatography/mass spectrometry assay. The diagnostic performance of the EtG immunochemical test was assessed using Receiver Operating Characteristic Curve analysis. The immunochemical test specificity was 100% for EtG urinary values above 500 ng/ml. No false positive results were found. With levels below 500 ng/ml, 12% of the samples were classified as negative. The average consumption of the incorrectly classified subjects was 171 ng/ml, with a misclassification error of 6.5% to 18.5%. High agreement between EtG as determined in an immunochemical test and gas chromatography/mass spectrometry, suggests that the rapid EtG test is a reliable, cost-effective alcohol monitoring assay for patient management in many non-forensic settings, such as drug rehabilitation programs. Slovak Toxicology Society SETOX 2017-12 2018-03-01 /pmc/articles/PMC6102674/ /pubmed/30147423 http://dx.doi.org/10.1515/intox-2017-0022 Text en Copyright © 2017 SETOX & Institute of Experimental Pharmacology and Toxicology, SASc. https://creativecommons.org/licenses/by-nc-nd/4.0/ This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 License. (CC BY-NC-ND 4.0) |
spellingShingle | Original Article Fucci, Nadia Gili, Alessio Aroni, Kyriaki Bacci, Mauro Carletti, Paola Pascali, Vincenzo Lorenzo Gambelunghe, Cristiana Monitoring people at risk of drinking by a rapid urinary ethyl glucuronide test |
title | Monitoring people at risk of drinking by a rapid urinary ethyl glucuronide test |
title_full | Monitoring people at risk of drinking by a rapid urinary ethyl glucuronide test |
title_fullStr | Monitoring people at risk of drinking by a rapid urinary ethyl glucuronide test |
title_full_unstemmed | Monitoring people at risk of drinking by a rapid urinary ethyl glucuronide test |
title_short | Monitoring people at risk of drinking by a rapid urinary ethyl glucuronide test |
title_sort | monitoring people at risk of drinking by a rapid urinary ethyl glucuronide test |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6102674/ https://www.ncbi.nlm.nih.gov/pubmed/30147423 http://dx.doi.org/10.1515/intox-2017-0022 |
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