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Machine Learning Classification of False-Positive Human Immunodeficiency Virus Screening Results

BACKGROUND: Human immunodeficiency virus (HIV) screening has improved significantly in the past decade as we have implemented tests that include antigen detection of p24. Incorporation of p24 detection narrows the window from 4 to 2 weeks between infection acquisition and ability to detect infection...

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Autores principales: Elkhadrawi, Mahmoud, Stevens, Bryan A, Wheeler, Bradley J, Akcakaya, Murat, Wheeler, Sarah
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8652341/
https://www.ncbi.nlm.nih.gov/pubmed/34934521
http://dx.doi.org/10.4103/jpi.jpi_7_21
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author Elkhadrawi, Mahmoud
Stevens, Bryan A
Wheeler, Bradley J
Akcakaya, Murat
Wheeler, Sarah
author_facet Elkhadrawi, Mahmoud
Stevens, Bryan A
Wheeler, Bradley J
Akcakaya, Murat
Wheeler, Sarah
author_sort Elkhadrawi, Mahmoud
collection PubMed
description BACKGROUND: Human immunodeficiency virus (HIV) screening has improved significantly in the past decade as we have implemented tests that include antigen detection of p24. Incorporation of p24 detection narrows the window from 4 to 2 weeks between infection acquisition and ability to detect infection, reducing unintentional spread of HIV. The fourth- and fifth-generation HIV (HIV5G) screening tests in low prevalence populations have high numbers of false-positive screens and it is unclear if orthogonal testing improves diagnostic and public health outcomes. METHODS: We used a cohort of 60,587 HIV5G screening tests with molecular and clinical correlates collected from 2016 to 2018 and applied machine learning to generate a classifier that could predict likely true and false positivity. RESULTS: The best classification was achieved by using support vector machines and transformation of results with principle component analysis. The final classifier had an accuracy of 94% for correct classification of false-positive screens and an accuracy of 92% for classification of true-positive screens. CONCLUSIONS: Implementation of this classifier as a screening method for all HIV5G reactive screens allows for improved workflow with likely true positives reported immediately to reduce infection spread and initiate follow-up testing and treatment and likely false positives undergoing orthogonal testing utilizing the same specimen already drawn to reduce distress and follow-up visits. Application of machine learning to the clinical laboratory allows for workflow improvement and decision support to provide improved patient care and public health.
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spelling pubmed-86523412021-12-20 Machine Learning Classification of False-Positive Human Immunodeficiency Virus Screening Results Elkhadrawi, Mahmoud Stevens, Bryan A Wheeler, Bradley J Akcakaya, Murat Wheeler, Sarah J Pathol Inform Research Article BACKGROUND: Human immunodeficiency virus (HIV) screening has improved significantly in the past decade as we have implemented tests that include antigen detection of p24. Incorporation of p24 detection narrows the window from 4 to 2 weeks between infection acquisition and ability to detect infection, reducing unintentional spread of HIV. The fourth- and fifth-generation HIV (HIV5G) screening tests in low prevalence populations have high numbers of false-positive screens and it is unclear if orthogonal testing improves diagnostic and public health outcomes. METHODS: We used a cohort of 60,587 HIV5G screening tests with molecular and clinical correlates collected from 2016 to 2018 and applied machine learning to generate a classifier that could predict likely true and false positivity. RESULTS: The best classification was achieved by using support vector machines and transformation of results with principle component analysis. The final classifier had an accuracy of 94% for correct classification of false-positive screens and an accuracy of 92% for classification of true-positive screens. CONCLUSIONS: Implementation of this classifier as a screening method for all HIV5G reactive screens allows for improved workflow with likely true positives reported immediately to reduce infection spread and initiate follow-up testing and treatment and likely false positives undergoing orthogonal testing utilizing the same specimen already drawn to reduce distress and follow-up visits. Application of machine learning to the clinical laboratory allows for workflow improvement and decision support to provide improved patient care and public health. Wolters Kluwer - Medknow 2021-11-20 /pmc/articles/PMC8652341/ /pubmed/34934521 http://dx.doi.org/10.4103/jpi.jpi_7_21 Text en Copyright: © 2021 Journal of Pathology Informatics https://creativecommons.org/licenses/by-nc-sa/4.0/This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Research Article
Elkhadrawi, Mahmoud
Stevens, Bryan A
Wheeler, Bradley J
Akcakaya, Murat
Wheeler, Sarah
Machine Learning Classification of False-Positive Human Immunodeficiency Virus Screening Results
title Machine Learning Classification of False-Positive Human Immunodeficiency Virus Screening Results
title_full Machine Learning Classification of False-Positive Human Immunodeficiency Virus Screening Results
title_fullStr Machine Learning Classification of False-Positive Human Immunodeficiency Virus Screening Results
title_full_unstemmed Machine Learning Classification of False-Positive Human Immunodeficiency Virus Screening Results
title_short Machine Learning Classification of False-Positive Human Immunodeficiency Virus Screening Results
title_sort machine learning classification of false-positive human immunodeficiency virus screening results
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8652341/
https://www.ncbi.nlm.nih.gov/pubmed/34934521
http://dx.doi.org/10.4103/jpi.jpi_7_21
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