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Individual mortality risk predictive system of patients with acute-on-chronic liver failure based on a random survival forest model

BACKGROUND: The basis of individualized treatment should be individualized mortality risk predictive information. The present study aimed to develop an online individual mortality risk predictive tool for acute-on-chronic liver failure (ACLF) patients based on a random survival forest (RSF) algorith...

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Autores principales: Zhang, Zhi-Qiao, He, Gang, Luo, Zhao-Wen, Cheng, Can-Chang, Wang, Peng, Li, Jing, Zhu, Ming-Gu, Ming, Lang, He, Ting-Shan, Ouyang, Yan-Ling, Huang, Yi-Yan, Wu, Xing-Liu, Ye, Yi-Nong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8318661/
https://www.ncbi.nlm.nih.gov/pubmed/34133353
http://dx.doi.org/10.1097/CM9.0000000000001539
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author Zhang, Zhi-Qiao
He, Gang
Luo, Zhao-Wen
Cheng, Can-Chang
Wang, Peng
Li, Jing
Zhu, Ming-Gu
Ming, Lang
He, Ting-Shan
Ouyang, Yan-Ling
Huang, Yi-Yan
Wu, Xing-Liu
Ye, Yi-Nong
author_facet Zhang, Zhi-Qiao
He, Gang
Luo, Zhao-Wen
Cheng, Can-Chang
Wang, Peng
Li, Jing
Zhu, Ming-Gu
Ming, Lang
He, Ting-Shan
Ouyang, Yan-Ling
Huang, Yi-Yan
Wu, Xing-Liu
Ye, Yi-Nong
author_sort Zhang, Zhi-Qiao
collection PubMed
description BACKGROUND: The basis of individualized treatment should be individualized mortality risk predictive information. The present study aimed to develop an online individual mortality risk predictive tool for acute-on-chronic liver failure (ACLF) patients based on a random survival forest (RSF) algorithm. METHODS: The current study retrospectively enrolled ACLF patients from the Department of Infectious Diseases of The First People's Hospital of Foshan, Shunde Hospital of Southern Medical University, and Jiangmen Central Hospital. Two hundred seventy-six consecutive ACLF patients were included in the present study as a model cohort (n = 276). Then the current study constructed a validation cohort by drawing patients from the model dataset based on the resampling method (n = 276). The RSF algorithm was used to develop an individual prognostic model for ACLF patients. The Brier score was used to evaluate the diagnostic accuracy of prognostic models. The weighted mean rank estimation method was used to compare the differences between the areas under the time-dependent ROC curves (AUROCs) of prognostic models. RESULTS: Multivariate Cox regression identified hepatic encephalopathy (HE), age, serum sodium level, acute kidney injury (AKI), red cell distribution width (RDW), and international normalization index (INR) as independent risk factors for ACLF patients. A simplified RSF model was developed based on these previous risk factors. The AUROCs for predicting 3-, 6-, and 12-month mortality were 0.916, 0.916, and 0.905 for the RSF model and 0.872, 0.866, and 0.848 for the Cox model in the model cohort, respectively. The Brier scores were 0.119, 0.119, and 0.128 for the RSF model and 0.138, 0.146, and 0.156 for the Cox model, respectively. The nonparametric comparison suggested that the RSF model was superior to the Cox model for predicting the prognosis of ACLF patients. CONCLUSIONS: The current study developed a novel online individual mortality risk predictive tool that could predict individual mortality risk predictive curves for individual patients. Additionally, the current online individual mortality risk predictive tool could further provide predicted mortality percentages and 95% confidence intervals at user-defined time points.
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spelling pubmed-83186612021-07-30 Individual mortality risk predictive system of patients with acute-on-chronic liver failure based on a random survival forest model Zhang, Zhi-Qiao He, Gang Luo, Zhao-Wen Cheng, Can-Chang Wang, Peng Li, Jing Zhu, Ming-Gu Ming, Lang He, Ting-Shan Ouyang, Yan-Ling Huang, Yi-Yan Wu, Xing-Liu Ye, Yi-Nong Chin Med J (Engl) Original Articles BACKGROUND: The basis of individualized treatment should be individualized mortality risk predictive information. The present study aimed to develop an online individual mortality risk predictive tool for acute-on-chronic liver failure (ACLF) patients based on a random survival forest (RSF) algorithm. METHODS: The current study retrospectively enrolled ACLF patients from the Department of Infectious Diseases of The First People's Hospital of Foshan, Shunde Hospital of Southern Medical University, and Jiangmen Central Hospital. Two hundred seventy-six consecutive ACLF patients were included in the present study as a model cohort (n = 276). Then the current study constructed a validation cohort by drawing patients from the model dataset based on the resampling method (n = 276). The RSF algorithm was used to develop an individual prognostic model for ACLF patients. The Brier score was used to evaluate the diagnostic accuracy of prognostic models. The weighted mean rank estimation method was used to compare the differences between the areas under the time-dependent ROC curves (AUROCs) of prognostic models. RESULTS: Multivariate Cox regression identified hepatic encephalopathy (HE), age, serum sodium level, acute kidney injury (AKI), red cell distribution width (RDW), and international normalization index (INR) as independent risk factors for ACLF patients. A simplified RSF model was developed based on these previous risk factors. The AUROCs for predicting 3-, 6-, and 12-month mortality were 0.916, 0.916, and 0.905 for the RSF model and 0.872, 0.866, and 0.848 for the Cox model in the model cohort, respectively. The Brier scores were 0.119, 0.119, and 0.128 for the RSF model and 0.138, 0.146, and 0.156 for the Cox model, respectively. The nonparametric comparison suggested that the RSF model was superior to the Cox model for predicting the prognosis of ACLF patients. CONCLUSIONS: The current study developed a novel online individual mortality risk predictive tool that could predict individual mortality risk predictive curves for individual patients. Additionally, the current online individual mortality risk predictive tool could further provide predicted mortality percentages and 95% confidence intervals at user-defined time points. Lippincott Williams & Wilkins 2021-07-20 2021-06-16 /pmc/articles/PMC8318661/ /pubmed/34133353 http://dx.doi.org/10.1097/CM9.0000000000001539 Text en Copyright © 2021 The Chinese Medical Association, produced by Wolters Kluwer, Inc. under the CC-BY-NC-ND license. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND), where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal. http://creativecommons.org/licenses/by-nc-nd/4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/)
spellingShingle Original Articles
Zhang, Zhi-Qiao
He, Gang
Luo, Zhao-Wen
Cheng, Can-Chang
Wang, Peng
Li, Jing
Zhu, Ming-Gu
Ming, Lang
He, Ting-Shan
Ouyang, Yan-Ling
Huang, Yi-Yan
Wu, Xing-Liu
Ye, Yi-Nong
Individual mortality risk predictive system of patients with acute-on-chronic liver failure based on a random survival forest model
title Individual mortality risk predictive system of patients with acute-on-chronic liver failure based on a random survival forest model
title_full Individual mortality risk predictive system of patients with acute-on-chronic liver failure based on a random survival forest model
title_fullStr Individual mortality risk predictive system of patients with acute-on-chronic liver failure based on a random survival forest model
title_full_unstemmed Individual mortality risk predictive system of patients with acute-on-chronic liver failure based on a random survival forest model
title_short Individual mortality risk predictive system of patients with acute-on-chronic liver failure based on a random survival forest model
title_sort individual mortality risk predictive system of patients with acute-on-chronic liver failure based on a random survival forest model
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8318661/
https://www.ncbi.nlm.nih.gov/pubmed/34133353
http://dx.doi.org/10.1097/CM9.0000000000001539
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