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Development and validation of a predictive model for in-hospital mortality in patients with sepsis-associated liver injury
BACKGROUND: Sepsis is often accompanied by organ dysfunction and acute organ failure, among which the liver is commonly involved. Sepsis patients suffering from liver injury have a greater risk of mortality than patients suffering from general sepsis. As of now, there are no tools that are specifica...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
AME Publishing Company
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9577780/ https://www.ncbi.nlm.nih.gov/pubmed/36267798 http://dx.doi.org/10.21037/atm-22-4319 |
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author | Liu, Yousheng Sun, Run Jiang, Haiyan Liang, Guiwen Huang, Zhongwei Qi, Lei Lu, Juying |
author_facet | Liu, Yousheng Sun, Run Jiang, Haiyan Liang, Guiwen Huang, Zhongwei Qi, Lei Lu, Juying |
author_sort | Liu, Yousheng |
collection | PubMed |
description | BACKGROUND: Sepsis is often accompanied by organ dysfunction and acute organ failure, among which the liver is commonly involved. Sepsis patients suffering from liver injury have a greater risk of mortality than patients suffering from general sepsis. As of now, there are no tools that are specifically designed for assessing the prognosis of such patients. This study aimed to develop and validate a model to predict the risk of in-hospital mortality in patients with sepsis-associated liver injury (SALI). METHODS: Data were obtained from the Medical Information Mart for Intensive Care (MIMIC)-IV database. In the analysis, all patients with SALI who met the inclusion and exclusion criteria were included. A primary outcome was in-hospital mortality, and clinical data were extracted for these patients. In a ratio of 8:2, the data were divided into training and validation groups at random. Least absolute shrinkage and selection operator (LASSO) regression was used for data dimension reduction and feature selection, and independent factors related to prognosis were identified through multi-factor logistics analysis. A nomogram was developed to visualize the model, and the performance of the model was evaluated by the area under the curve (AUC) as well as calibration and decision curve analysis (DCA) through internal verification. RESULTS: A total of 616 and 154 patients with SALI were included in the training and validation cohorts, respectively. The LASSO regression and logistic multivariate analysis showed that nine factors were associated with in-hospital mortality in patients with SALI. Both the training and validation cohorts had higher AUCs than sequential organ failure assessment (SOFA) and simplified acute physiology score 2 (SAPS2): 0.753 (95% CI: 0.715–0.791) and 0.783 (95% CI: 0.749–0.817), respectively. Both the training and validation cohorts showed good calibration results for the prediction model. In terms of clinical practicability, DCA of the predictive model demonstrated greater net benefits than the SOFA and SAPS2 scores. CONCLUSIONS: We developed a predictive model that can effectively predict the in-hospital mortality of SALI patients, with satisfactory performance and clinical practicability. This model can assist clinicians in the early identification of high-risk patients and provide a reference for clinical treatment strategies. |
format | Online Article Text |
id | pubmed-9577780 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | AME Publishing Company |
record_format | MEDLINE/PubMed |
spelling | pubmed-95777802022-10-19 Development and validation of a predictive model for in-hospital mortality in patients with sepsis-associated liver injury Liu, Yousheng Sun, Run Jiang, Haiyan Liang, Guiwen Huang, Zhongwei Qi, Lei Lu, Juying Ann Transl Med Original Article BACKGROUND: Sepsis is often accompanied by organ dysfunction and acute organ failure, among which the liver is commonly involved. Sepsis patients suffering from liver injury have a greater risk of mortality than patients suffering from general sepsis. As of now, there are no tools that are specifically designed for assessing the prognosis of such patients. This study aimed to develop and validate a model to predict the risk of in-hospital mortality in patients with sepsis-associated liver injury (SALI). METHODS: Data were obtained from the Medical Information Mart for Intensive Care (MIMIC)-IV database. In the analysis, all patients with SALI who met the inclusion and exclusion criteria were included. A primary outcome was in-hospital mortality, and clinical data were extracted for these patients. In a ratio of 8:2, the data were divided into training and validation groups at random. Least absolute shrinkage and selection operator (LASSO) regression was used for data dimension reduction and feature selection, and independent factors related to prognosis were identified through multi-factor logistics analysis. A nomogram was developed to visualize the model, and the performance of the model was evaluated by the area under the curve (AUC) as well as calibration and decision curve analysis (DCA) through internal verification. RESULTS: A total of 616 and 154 patients with SALI were included in the training and validation cohorts, respectively. The LASSO regression and logistic multivariate analysis showed that nine factors were associated with in-hospital mortality in patients with SALI. Both the training and validation cohorts had higher AUCs than sequential organ failure assessment (SOFA) and simplified acute physiology score 2 (SAPS2): 0.753 (95% CI: 0.715–0.791) and 0.783 (95% CI: 0.749–0.817), respectively. Both the training and validation cohorts showed good calibration results for the prediction model. In terms of clinical practicability, DCA of the predictive model demonstrated greater net benefits than the SOFA and SAPS2 scores. CONCLUSIONS: We developed a predictive model that can effectively predict the in-hospital mortality of SALI patients, with satisfactory performance and clinical practicability. This model can assist clinicians in the early identification of high-risk patients and provide a reference for clinical treatment strategies. AME Publishing Company 2022-09 /pmc/articles/PMC9577780/ /pubmed/36267798 http://dx.doi.org/10.21037/atm-22-4319 Text en 2022 Annals of Translational Medicine. All rights reserved. https://creativecommons.org/licenses/by-nc-nd/4.0/Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) . |
spellingShingle | Original Article Liu, Yousheng Sun, Run Jiang, Haiyan Liang, Guiwen Huang, Zhongwei Qi, Lei Lu, Juying Development and validation of a predictive model for in-hospital mortality in patients with sepsis-associated liver injury |
title | Development and validation of a predictive model for in-hospital mortality in patients with sepsis-associated liver injury |
title_full | Development and validation of a predictive model for in-hospital mortality in patients with sepsis-associated liver injury |
title_fullStr | Development and validation of a predictive model for in-hospital mortality in patients with sepsis-associated liver injury |
title_full_unstemmed | Development and validation of a predictive model for in-hospital mortality in patients with sepsis-associated liver injury |
title_short | Development and validation of a predictive model for in-hospital mortality in patients with sepsis-associated liver injury |
title_sort | development and validation of a predictive model for in-hospital mortality in patients with sepsis-associated liver injury |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9577780/ https://www.ncbi.nlm.nih.gov/pubmed/36267798 http://dx.doi.org/10.21037/atm-22-4319 |
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