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A machine-learning based model for automated recommendation of individualized treatment of rifampicin-resistant tuberculosis

BACKGROUND: Rifampicin resistant tuberculosis remains a global health problem with almost half a million new cases annually. In high-income countries patients empirically start a standardized treatment regimen, followed by an individualized regimen guided by drug susceptibility test (DST) results. I...

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Autores principales: Verboven, Lennert, Callens, Steven, Black, John, Maartens, Gary, Dooley, Kelly E., Potgieter, Samantha, Cartuyvels, Ruben, Laukens, Kris, Warren, Robin M., Van Rie, Annelies
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Journal Experts 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9949242/
https://www.ncbi.nlm.nih.gov/pubmed/36824956
http://dx.doi.org/10.21203/rs.3.rs-2525765/v1
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author Verboven, Lennert
Callens, Steven
Black, John
Maartens, Gary
Dooley, Kelly E.
Potgieter, Samantha
Cartuyvels, Ruben
Laukens, Kris
Warren, Robin M.
Van Rie, Annelies
author_facet Verboven, Lennert
Callens, Steven
Black, John
Maartens, Gary
Dooley, Kelly E.
Potgieter, Samantha
Cartuyvels, Ruben
Laukens, Kris
Warren, Robin M.
Van Rie, Annelies
author_sort Verboven, Lennert
collection PubMed
description BACKGROUND: Rifampicin resistant tuberculosis remains a global health problem with almost half a million new cases annually. In high-income countries patients empirically start a standardized treatment regimen, followed by an individualized regimen guided by drug susceptibility test (DST) results. In most settings, DST information is not available or is limited to isoniazid and fluoroquinolones. Whole genome sequencing could more accurately guide individualized treatment as the full drug resistance profile is obtained with a single test. Whole genome sequencing has not reached its full potential for patient care, in part due to the complexity of translating a resistance profile into the most effective individualized regimen. METHODS: We developed a treatment recommender clinical decision support system (CDSS) and an accompanying web application for user-friendly recommendation of the optimal individualized treatment regimen to a clinician. RESULTS: Following expert stakeholder meetings and literature review, nine drug features and 14 treatment regimen features were identified and quantified. Using machine learning, a model was developed to predict the optimal treatment regimen based on a training set of 3895 treatment regimen-expert feedback pairs. The acceptability of the treatment recommender CDSS was assessed as part of a clinical trial and in a routine care setting. Within the clinical trial setting, all patients received the CDSS recommended treatment. In 8 of 20 cases, the initial recommendation was recomputed because of stock out, clinical contra-indication or toxicity. In routine care setting, physicians rejected the treatment recommendation in 7 out of 15 cases because it deviated from the national TB treatment guidelines. A survey indicated that the treatment recommender CDSS is easy to use and useful in clinical practice but requires digital infrastructure support and training. CONCLUSIONS: Our findings suggest that global implementation of the novel treatment recommender CDSS holds the potential to improve treatment outcomes of rifampicin resistant tuberculosis.
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spelling pubmed-99492422023-02-24 A machine-learning based model for automated recommendation of individualized treatment of rifampicin-resistant tuberculosis Verboven, Lennert Callens, Steven Black, John Maartens, Gary Dooley, Kelly E. Potgieter, Samantha Cartuyvels, Ruben Laukens, Kris Warren, Robin M. Van Rie, Annelies Res Sq Article BACKGROUND: Rifampicin resistant tuberculosis remains a global health problem with almost half a million new cases annually. In high-income countries patients empirically start a standardized treatment regimen, followed by an individualized regimen guided by drug susceptibility test (DST) results. In most settings, DST information is not available or is limited to isoniazid and fluoroquinolones. Whole genome sequencing could more accurately guide individualized treatment as the full drug resistance profile is obtained with a single test. Whole genome sequencing has not reached its full potential for patient care, in part due to the complexity of translating a resistance profile into the most effective individualized regimen. METHODS: We developed a treatment recommender clinical decision support system (CDSS) and an accompanying web application for user-friendly recommendation of the optimal individualized treatment regimen to a clinician. RESULTS: Following expert stakeholder meetings and literature review, nine drug features and 14 treatment regimen features were identified and quantified. Using machine learning, a model was developed to predict the optimal treatment regimen based on a training set of 3895 treatment regimen-expert feedback pairs. The acceptability of the treatment recommender CDSS was assessed as part of a clinical trial and in a routine care setting. Within the clinical trial setting, all patients received the CDSS recommended treatment. In 8 of 20 cases, the initial recommendation was recomputed because of stock out, clinical contra-indication or toxicity. In routine care setting, physicians rejected the treatment recommendation in 7 out of 15 cases because it deviated from the national TB treatment guidelines. A survey indicated that the treatment recommender CDSS is easy to use and useful in clinical practice but requires digital infrastructure support and training. CONCLUSIONS: Our findings suggest that global implementation of the novel treatment recommender CDSS holds the potential to improve treatment outcomes of rifampicin resistant tuberculosis. American Journal Experts 2023-02-16 /pmc/articles/PMC9949242/ /pubmed/36824956 http://dx.doi.org/10.21203/rs.3.rs-2525765/v1 Text en https://creativecommons.org/licenses/by/4.0/This work is licensed under a Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by/4.0/) , which allows reusers to distribute, remix, adapt, and build upon the material in any medium or format, so long as attribution is given to the creator. The license allows for commercial use. https://creativecommons.org/licenses/by/4.0/License: This work is licensed under a Creative Commons Attribution 4.0 International License. Read Full License (https://creativecommons.org/licenses/by/4.0/)
spellingShingle Article
Verboven, Lennert
Callens, Steven
Black, John
Maartens, Gary
Dooley, Kelly E.
Potgieter, Samantha
Cartuyvels, Ruben
Laukens, Kris
Warren, Robin M.
Van Rie, Annelies
A machine-learning based model for automated recommendation of individualized treatment of rifampicin-resistant tuberculosis
title A machine-learning based model for automated recommendation of individualized treatment of rifampicin-resistant tuberculosis
title_full A machine-learning based model for automated recommendation of individualized treatment of rifampicin-resistant tuberculosis
title_fullStr A machine-learning based model for automated recommendation of individualized treatment of rifampicin-resistant tuberculosis
title_full_unstemmed A machine-learning based model for automated recommendation of individualized treatment of rifampicin-resistant tuberculosis
title_short A machine-learning based model for automated recommendation of individualized treatment of rifampicin-resistant tuberculosis
title_sort machine-learning based model for automated recommendation of individualized treatment of rifampicin-resistant tuberculosis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9949242/
https://www.ncbi.nlm.nih.gov/pubmed/36824956
http://dx.doi.org/10.21203/rs.3.rs-2525765/v1
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