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Use of machine learning models to predict in‐hospital mortality in patients with acute coronary syndrome
BACKGROUND: Cardiovascular diseases are a significant health burden with the prevalence increasing worldwide. Thus, a highly accurate assessment and prediction of death risk are crucial to meet the clinical demand. This study sought to develop and validate a model to predict in‐hospital mortality am...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9933107/ https://www.ncbi.nlm.nih.gov/pubmed/36479714 http://dx.doi.org/10.1002/clc.23957 |
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author | Li, Rong Shen, Lan Ma, Wenyan Yan, Bo Chen, Wenchang Zhu, Jie Li, Linfeng Yuan, Junyi Pan, Changqing |
author_facet | Li, Rong Shen, Lan Ma, Wenyan Yan, Bo Chen, Wenchang Zhu, Jie Li, Linfeng Yuan, Junyi Pan, Changqing |
author_sort | Li, Rong |
collection | PubMed |
description | BACKGROUND: Cardiovascular diseases are a significant health burden with the prevalence increasing worldwide. Thus, a highly accurate assessment and prediction of death risk are crucial to meet the clinical demand. This study sought to develop and validate a model to predict in‐hospital mortality among patients with the acute coronary syndrome (ACS) using nonlinear algorithms. METHODS: A total of 2414 ACS patients were enrolled in this study. All samples were divided into five groups for cross‐validation. The logistic regression (LR) model and XGboost model were applied to predict in‐hospital mortality. The results of two models were compared between the variable set by the global registry of acute coronary events (GRACE) score and the selected variable set. RESULTS: The in‐hospital mortality rate was 3.5% in the dataset. Model performance on the selected variable set was better than that on GRACE variables: a 3% increase in area under the receiver operating characteristic (ROC) curve (AUC) for LR and 1.3% for XGBoost. The AUC of XGBoost is 0.913 (95% confidence interval [CI]: 0.910–0.916), demonstrating a better discrimination ability than LR (AUC = 0.904, 95% CI: 0.902–0.905) on the selected variable set. Almost perfect calibration was found in XGBoost (slope of predicted to observed events, 1.08; intercept, −0.103; p < .001). CONCLUSIONS: XGboost modeling, an advanced machine learning algorithm, identifies new variables and provides high accuracy for the prediction of in‐hospital mortality in ACS patients. |
format | Online Article Text |
id | pubmed-9933107 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-99331072023-02-17 Use of machine learning models to predict in‐hospital mortality in patients with acute coronary syndrome Li, Rong Shen, Lan Ma, Wenyan Yan, Bo Chen, Wenchang Zhu, Jie Li, Linfeng Yuan, Junyi Pan, Changqing Clin Cardiol Clinical Investigations BACKGROUND: Cardiovascular diseases are a significant health burden with the prevalence increasing worldwide. Thus, a highly accurate assessment and prediction of death risk are crucial to meet the clinical demand. This study sought to develop and validate a model to predict in‐hospital mortality among patients with the acute coronary syndrome (ACS) using nonlinear algorithms. METHODS: A total of 2414 ACS patients were enrolled in this study. All samples were divided into five groups for cross‐validation. The logistic regression (LR) model and XGboost model were applied to predict in‐hospital mortality. The results of two models were compared between the variable set by the global registry of acute coronary events (GRACE) score and the selected variable set. RESULTS: The in‐hospital mortality rate was 3.5% in the dataset. Model performance on the selected variable set was better than that on GRACE variables: a 3% increase in area under the receiver operating characteristic (ROC) curve (AUC) for LR and 1.3% for XGBoost. The AUC of XGBoost is 0.913 (95% confidence interval [CI]: 0.910–0.916), demonstrating a better discrimination ability than LR (AUC = 0.904, 95% CI: 0.902–0.905) on the selected variable set. Almost perfect calibration was found in XGBoost (slope of predicted to observed events, 1.08; intercept, −0.103; p < .001). CONCLUSIONS: XGboost modeling, an advanced machine learning algorithm, identifies new variables and provides high accuracy for the prediction of in‐hospital mortality in ACS patients. John Wiley and Sons Inc. 2022-12-07 /pmc/articles/PMC9933107/ /pubmed/36479714 http://dx.doi.org/10.1002/clc.23957 Text en © 2022 The Authors. Clinical Cardiology published by Wiley Periodicals, LLC. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Clinical Investigations Li, Rong Shen, Lan Ma, Wenyan Yan, Bo Chen, Wenchang Zhu, Jie Li, Linfeng Yuan, Junyi Pan, Changqing Use of machine learning models to predict in‐hospital mortality in patients with acute coronary syndrome |
title | Use of machine learning models to predict in‐hospital mortality in patients with acute coronary syndrome |
title_full | Use of machine learning models to predict in‐hospital mortality in patients with acute coronary syndrome |
title_fullStr | Use of machine learning models to predict in‐hospital mortality in patients with acute coronary syndrome |
title_full_unstemmed | Use of machine learning models to predict in‐hospital mortality in patients with acute coronary syndrome |
title_short | Use of machine learning models to predict in‐hospital mortality in patients with acute coronary syndrome |
title_sort | use of machine learning models to predict in‐hospital mortality in patients with acute coronary syndrome |
topic | Clinical Investigations |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9933107/ https://www.ncbi.nlm.nih.gov/pubmed/36479714 http://dx.doi.org/10.1002/clc.23957 |
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