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Early prediction of ventilator-associated pneumonia in critical care patients: a machine learning model
BACKGROUND: This study was performed to develop and validate machine learning models for early detection of ventilator-associated pneumonia (VAP) 24 h before diagnosis, so that VAP patients can receive early intervention and reduce the occurrence of complications. PATIENTS AND METHODS: This study wa...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9233772/ https://www.ncbi.nlm.nih.gov/pubmed/35752818 http://dx.doi.org/10.1186/s12890-022-02031-w |
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author | Liang, Yingjian Zhu, Chengrui Tian, Cong Lin, Qizhong Li, Zhiliang Li, Zhifei Ni, Dongshu Ma, Xiaochun |
author_facet | Liang, Yingjian Zhu, Chengrui Tian, Cong Lin, Qizhong Li, Zhiliang Li, Zhifei Ni, Dongshu Ma, Xiaochun |
author_sort | Liang, Yingjian |
collection | PubMed |
description | BACKGROUND: This study was performed to develop and validate machine learning models for early detection of ventilator-associated pneumonia (VAP) 24 h before diagnosis, so that VAP patients can receive early intervention and reduce the occurrence of complications. PATIENTS AND METHODS: This study was based on the MIMIC-III dataset, which was a retrospective cohort. The random forest algorithm was applied to construct a base classifier, and the area under the receiver operating characteristic curve (AUC), sensitivity and specificity of the prediction model were evaluated. Furthermore, We also compare the performance of Clinical Pulmonary Infection Score (CPIS)-based model (threshold value ≥ 3) using the same training and test data sets. RESULTS: In total, 38,515 ventilation sessions occurred in 61,532 ICU admissions. VAP occurred in 212 of these sessions. We incorporated 42 VAP risk factors at admission and routinely measured the vital characteristics and laboratory results. Five-fold cross-validation was performed to evaluate the model performance, and the model achieved an AUC of 84% in the validation, 74% sensitivity and 71% specificity 24 h after intubation. The AUC of our VAP machine learning model is nearly 25% higher than the CPIS model, and the sensitivity and specificity were also improved by almost 14% and 15%, respectively. CONCLUSIONS: We developed and internally validated an automated model for VAP prediction using the MIMIC-III cohort. The VAP prediction model achieved high performance based on its AUC, sensitivity and specificity, and its performance was superior to that of the CPIS model. External validation and prospective interventional or outcome studies using this prediction model are envisioned as future work. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12890-022-02031-w. |
format | Online Article Text |
id | pubmed-9233772 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-92337722022-06-27 Early prediction of ventilator-associated pneumonia in critical care patients: a machine learning model Liang, Yingjian Zhu, Chengrui Tian, Cong Lin, Qizhong Li, Zhiliang Li, Zhifei Ni, Dongshu Ma, Xiaochun BMC Pulm Med Research BACKGROUND: This study was performed to develop and validate machine learning models for early detection of ventilator-associated pneumonia (VAP) 24 h before diagnosis, so that VAP patients can receive early intervention and reduce the occurrence of complications. PATIENTS AND METHODS: This study was based on the MIMIC-III dataset, which was a retrospective cohort. The random forest algorithm was applied to construct a base classifier, and the area under the receiver operating characteristic curve (AUC), sensitivity and specificity of the prediction model were evaluated. Furthermore, We also compare the performance of Clinical Pulmonary Infection Score (CPIS)-based model (threshold value ≥ 3) using the same training and test data sets. RESULTS: In total, 38,515 ventilation sessions occurred in 61,532 ICU admissions. VAP occurred in 212 of these sessions. We incorporated 42 VAP risk factors at admission and routinely measured the vital characteristics and laboratory results. Five-fold cross-validation was performed to evaluate the model performance, and the model achieved an AUC of 84% in the validation, 74% sensitivity and 71% specificity 24 h after intubation. The AUC of our VAP machine learning model is nearly 25% higher than the CPIS model, and the sensitivity and specificity were also improved by almost 14% and 15%, respectively. CONCLUSIONS: We developed and internally validated an automated model for VAP prediction using the MIMIC-III cohort. The VAP prediction model achieved high performance based on its AUC, sensitivity and specificity, and its performance was superior to that of the CPIS model. External validation and prospective interventional or outcome studies using this prediction model are envisioned as future work. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12890-022-02031-w. BioMed Central 2022-06-25 /pmc/articles/PMC9233772/ /pubmed/35752818 http://dx.doi.org/10.1186/s12890-022-02031-w Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 Liang, Yingjian Zhu, Chengrui Tian, Cong Lin, Qizhong Li, Zhiliang Li, Zhifei Ni, Dongshu Ma, Xiaochun Early prediction of ventilator-associated pneumonia in critical care patients: a machine learning model |
title | Early prediction of ventilator-associated pneumonia in critical care patients: a machine learning model |
title_full | Early prediction of ventilator-associated pneumonia in critical care patients: a machine learning model |
title_fullStr | Early prediction of ventilator-associated pneumonia in critical care patients: a machine learning model |
title_full_unstemmed | Early prediction of ventilator-associated pneumonia in critical care patients: a machine learning model |
title_short | Early prediction of ventilator-associated pneumonia in critical care patients: a machine learning model |
title_sort | early prediction of ventilator-associated pneumonia in critical care patients: a machine learning model |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9233772/ https://www.ncbi.nlm.nih.gov/pubmed/35752818 http://dx.doi.org/10.1186/s12890-022-02031-w |
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