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Prognostic nomogram for 30-day mortality of deep vein thrombosis patients in intensive care unit

BACKGROUND: We aimed to use the Medical Information Mart for Intensive Care III database to build a nomogram to identify 30-day mortality risk of deep vein thrombosis (DVT) patients in intensive care unit (ICU). METHODS: Stepwise logistic regression and logistic regression with least absolute shrink...

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Autores principales: Shen, Runnan, Gao, Ming, Tao, Yangu, Chen, Qinchang, Wu, Guitao, Guo, Xushun, Xia, Zuqi, You, Guochang, Hong, Zilin, Huang, Kai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7788873/
https://www.ncbi.nlm.nih.gov/pubmed/33407152
http://dx.doi.org/10.1186/s12872-020-01823-4
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author Shen, Runnan
Gao, Ming
Tao, Yangu
Chen, Qinchang
Wu, Guitao
Guo, Xushun
Xia, Zuqi
You, Guochang
Hong, Zilin
Huang, Kai
author_facet Shen, Runnan
Gao, Ming
Tao, Yangu
Chen, Qinchang
Wu, Guitao
Guo, Xushun
Xia, Zuqi
You, Guochang
Hong, Zilin
Huang, Kai
author_sort Shen, Runnan
collection PubMed
description BACKGROUND: We aimed to use the Medical Information Mart for Intensive Care III database to build a nomogram to identify 30-day mortality risk of deep vein thrombosis (DVT) patients in intensive care unit (ICU). METHODS: Stepwise logistic regression and logistic regression with least absolute shrinkage and selection operator (LASSO) were used to fit two prediction models. Bootstrap method was used to perform internal validation. RESULTS: We obtained baseline data of 535 DVT patients, 91 (17%) of whom died within 30 days. The discriminations of two new models were better than traditional scores. Compared with simplified acute physiology score II (SAPSII), the predictive abilities of two new models were improved (Net reclassification improvement [NRI] > 0; Integrated discrimination improvement [IDI] > 0; P < 0.05). The Brier scores of two new models in training set were 0.091 and 0.108. After internal validation, corrected area under the curves for two models were 0.850 and 0.830, while corrected Brier scores were 0.108 and 0.114. The more concise model was chosen to make the nomogram. CONCLUSIONS: The nomogram developed by logistic regression with LASSO model can provide an accurate prognosis for DVT patients in ICU.
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spelling pubmed-77888732021-01-07 Prognostic nomogram for 30-day mortality of deep vein thrombosis patients in intensive care unit Shen, Runnan Gao, Ming Tao, Yangu Chen, Qinchang Wu, Guitao Guo, Xushun Xia, Zuqi You, Guochang Hong, Zilin Huang, Kai BMC Cardiovasc Disord Research Article BACKGROUND: We aimed to use the Medical Information Mart for Intensive Care III database to build a nomogram to identify 30-day mortality risk of deep vein thrombosis (DVT) patients in intensive care unit (ICU). METHODS: Stepwise logistic regression and logistic regression with least absolute shrinkage and selection operator (LASSO) were used to fit two prediction models. Bootstrap method was used to perform internal validation. RESULTS: We obtained baseline data of 535 DVT patients, 91 (17%) of whom died within 30 days. The discriminations of two new models were better than traditional scores. Compared with simplified acute physiology score II (SAPSII), the predictive abilities of two new models were improved (Net reclassification improvement [NRI] > 0; Integrated discrimination improvement [IDI] > 0; P < 0.05). The Brier scores of two new models in training set were 0.091 and 0.108. After internal validation, corrected area under the curves for two models were 0.850 and 0.830, while corrected Brier scores were 0.108 and 0.114. The more concise model was chosen to make the nomogram. CONCLUSIONS: The nomogram developed by logistic regression with LASSO model can provide an accurate prognosis for DVT patients in ICU. BioMed Central 2021-01-06 /pmc/articles/PMC7788873/ /pubmed/33407152 http://dx.doi.org/10.1186/s12872-020-01823-4 Text en © The Author(s) 2021 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/. The Creative Commons Public Domain Dedication waiver (http://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 Article
Shen, Runnan
Gao, Ming
Tao, Yangu
Chen, Qinchang
Wu, Guitao
Guo, Xushun
Xia, Zuqi
You, Guochang
Hong, Zilin
Huang, Kai
Prognostic nomogram for 30-day mortality of deep vein thrombosis patients in intensive care unit
title Prognostic nomogram for 30-day mortality of deep vein thrombosis patients in intensive care unit
title_full Prognostic nomogram for 30-day mortality of deep vein thrombosis patients in intensive care unit
title_fullStr Prognostic nomogram for 30-day mortality of deep vein thrombosis patients in intensive care unit
title_full_unstemmed Prognostic nomogram for 30-day mortality of deep vein thrombosis patients in intensive care unit
title_short Prognostic nomogram for 30-day mortality of deep vein thrombosis patients in intensive care unit
title_sort prognostic nomogram for 30-day mortality of deep vein thrombosis patients in intensive care unit
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7788873/
https://www.ncbi.nlm.nih.gov/pubmed/33407152
http://dx.doi.org/10.1186/s12872-020-01823-4
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