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Advancing polytrauma care: developing and validating machine learning models for early mortality prediction

BACKGROUND: Rapid identification of high-risk polytrauma patients is crucial for early intervention and improved outcomes. This study aimed to develop and validate machine learning models for predicting 72 h mortality in adult polytrauma patients using readily available clinical parameters. METHODS:...

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Autores principales: He, Wen, Fu, Xianghong, Chen, Song
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10518974/
https://www.ncbi.nlm.nih.gov/pubmed/37743498
http://dx.doi.org/10.1186/s12967-023-04487-8
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author He, Wen
Fu, Xianghong
Chen, Song
author_facet He, Wen
Fu, Xianghong
Chen, Song
author_sort He, Wen
collection PubMed
description BACKGROUND: Rapid identification of high-risk polytrauma patients is crucial for early intervention and improved outcomes. This study aimed to develop and validate machine learning models for predicting 72 h mortality in adult polytrauma patients using readily available clinical parameters. METHODS: A retrospective analysis was conducted on polytrauma patients from the Dryad database and our institution. Missing values pertinent to eligible individuals within the Dryad database were compensated for through the k-nearest neighbor algorithm, subsequently randomizing them into training and internal validation factions on a 7:3 ratio. The patients of our institution functioned as external validation cohorts. The predictive efficacy of random forest (RF), neural network, and XGBoost models was assessed through an exhaustive suite of performance indicators. The SHapley Additive exPlanations (SHAP) and Local Interpretable Model-Agnostic Explanations (LIME) methods were engaged to explain the supreme-performing model. Conclusively, restricted cubic spline analysis and multivariate logistic regression were employed as sensitivity analyses to verify the robustness of the findings. RESULTS: Parameters including age, body mass index, Glasgow Coma Scale, Injury Severity Score, pH, base excess, and lactate emerged as pivotal predictors of 72 h mortality. The RF model exhibited unparalleled performance, boasting an area under the receiver operating characteristic curve (AUROC) of 0.87 (95% confidence interval [CI] 0.84–0.89), an area under the precision-recall curve (AUPRC) of 0.67 (95% CI 0.61–0.73), and an accuracy of 0.83 (95% CI 0.81–0.86) in the internal validation cohort, paralleled by an AUROC of 0.98 (95% CI 0.97–0.99), an AUPRC of 0.88 (95% CI 0.83–0.93), and an accuracy of 0.97 (95% CI 0.96–0.98) in the external validation cohort. It provided the highest net benefit in the decision curve analysis in relation to the other models. The outcomes of the sensitivity examinations were congruent with those inferred from SHAP and LIME. CONCLUSIONS: The RF model exhibited the best performance in predicting 72 h mortality in adult polytrauma patients and has the potential to aid clinicians in identifying high-risk patients and guiding clinical decision-making. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12967-023-04487-8.
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spelling pubmed-105189742023-09-26 Advancing polytrauma care: developing and validating machine learning models for early mortality prediction He, Wen Fu, Xianghong Chen, Song J Transl Med Research BACKGROUND: Rapid identification of high-risk polytrauma patients is crucial for early intervention and improved outcomes. This study aimed to develop and validate machine learning models for predicting 72 h mortality in adult polytrauma patients using readily available clinical parameters. METHODS: A retrospective analysis was conducted on polytrauma patients from the Dryad database and our institution. Missing values pertinent to eligible individuals within the Dryad database were compensated for through the k-nearest neighbor algorithm, subsequently randomizing them into training and internal validation factions on a 7:3 ratio. The patients of our institution functioned as external validation cohorts. The predictive efficacy of random forest (RF), neural network, and XGBoost models was assessed through an exhaustive suite of performance indicators. The SHapley Additive exPlanations (SHAP) and Local Interpretable Model-Agnostic Explanations (LIME) methods were engaged to explain the supreme-performing model. Conclusively, restricted cubic spline analysis and multivariate logistic regression were employed as sensitivity analyses to verify the robustness of the findings. RESULTS: Parameters including age, body mass index, Glasgow Coma Scale, Injury Severity Score, pH, base excess, and lactate emerged as pivotal predictors of 72 h mortality. The RF model exhibited unparalleled performance, boasting an area under the receiver operating characteristic curve (AUROC) of 0.87 (95% confidence interval [CI] 0.84–0.89), an area under the precision-recall curve (AUPRC) of 0.67 (95% CI 0.61–0.73), and an accuracy of 0.83 (95% CI 0.81–0.86) in the internal validation cohort, paralleled by an AUROC of 0.98 (95% CI 0.97–0.99), an AUPRC of 0.88 (95% CI 0.83–0.93), and an accuracy of 0.97 (95% CI 0.96–0.98) in the external validation cohort. It provided the highest net benefit in the decision curve analysis in relation to the other models. The outcomes of the sensitivity examinations were congruent with those inferred from SHAP and LIME. CONCLUSIONS: The RF model exhibited the best performance in predicting 72 h mortality in adult polytrauma patients and has the potential to aid clinicians in identifying high-risk patients and guiding clinical decision-making. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12967-023-04487-8. BioMed Central 2023-09-25 /pmc/articles/PMC10518974/ /pubmed/37743498 http://dx.doi.org/10.1186/s12967-023-04487-8 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
He, Wen
Fu, Xianghong
Chen, Song
Advancing polytrauma care: developing and validating machine learning models for early mortality prediction
title Advancing polytrauma care: developing and validating machine learning models for early mortality prediction
title_full Advancing polytrauma care: developing and validating machine learning models for early mortality prediction
title_fullStr Advancing polytrauma care: developing and validating machine learning models for early mortality prediction
title_full_unstemmed Advancing polytrauma care: developing and validating machine learning models for early mortality prediction
title_short Advancing polytrauma care: developing and validating machine learning models for early mortality prediction
title_sort advancing polytrauma care: developing and validating machine learning models for early mortality prediction
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10518974/
https://www.ncbi.nlm.nih.gov/pubmed/37743498
http://dx.doi.org/10.1186/s12967-023-04487-8
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