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Prediction of early prognosis after traumatic brain injury by multifactor model

AIMS: To design a model to predict the early prognosis of patients with traumatic brain injury (TBI) based on parameters that can be quickly obtained in emergency conditions from medical history, physical examination, and supplementary examinations. METHODS: The medical records of TBI patients who w...

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Autores principales: Yang, Bocheng, Sun, Xiaochuan, Shi, Quanhong, Dan, Wei, Zhan, Yan, Zheng, Dinghao, Xia, Yulong, Xie, Yanfeng, Jiang, Li
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9627380/
https://www.ncbi.nlm.nih.gov/pubmed/36017774
http://dx.doi.org/10.1111/cns.13935
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author Yang, Bocheng
Sun, Xiaochuan
Shi, Quanhong
Dan, Wei
Zhan, Yan
Zheng, Dinghao
Xia, Yulong
Xie, Yanfeng
Jiang, Li
author_facet Yang, Bocheng
Sun, Xiaochuan
Shi, Quanhong
Dan, Wei
Zhan, Yan
Zheng, Dinghao
Xia, Yulong
Xie, Yanfeng
Jiang, Li
author_sort Yang, Bocheng
collection PubMed
description AIMS: To design a model to predict the early prognosis of patients with traumatic brain injury (TBI) based on parameters that can be quickly obtained in emergency conditions from medical history, physical examination, and supplementary examinations. METHODS: The medical records of TBI patients who were hospitalized in two medical institutions between June 2015 and June 2021 were collected and analyzed. Patients were divided into the training set, validation set, and testing set. The possible predictive indicators were screened after analyzing the data of patients in the training set. Then prediction models were found based on the possible predictive indicators in the training set. Data of patients in the validation set and the testing set was provided to validate the predictive values of the models. RESULTS: Age, Glasgow coma scale score, Apolipoprotein E genotype, damage area, serum C‐reactive protein, and interleukin‐8 (IL‐8) levels, and Marshall computed tomography score were found associated with early prognosis of TBI patients. The accuracy of the early prognosis prediction model (EPPM) was 80%, and the sensitivity and specificity of the EPPM were 78.8% and 80.8% in the training set. The accuracy of the EPPM was 79%, and the sensitivity and specificity of the EPPM were 66.7% and 86.2% in the validation set. The accuracy of the early EPPM was 69.1%, and the sensitivity and specificity of the EPPM were 67.9% and 77.8% in the testing set. CONCLUSION: Prediction models integrating general information, clinical manifestations, and auxiliary examination results may provide a reliable and rapid method to evaluate and predict the early prognosis of TBI patients.
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spelling pubmed-96273802022-11-03 Prediction of early prognosis after traumatic brain injury by multifactor model Yang, Bocheng Sun, Xiaochuan Shi, Quanhong Dan, Wei Zhan, Yan Zheng, Dinghao Xia, Yulong Xie, Yanfeng Jiang, Li CNS Neurosci Ther Original Articles AIMS: To design a model to predict the early prognosis of patients with traumatic brain injury (TBI) based on parameters that can be quickly obtained in emergency conditions from medical history, physical examination, and supplementary examinations. METHODS: The medical records of TBI patients who were hospitalized in two medical institutions between June 2015 and June 2021 were collected and analyzed. Patients were divided into the training set, validation set, and testing set. The possible predictive indicators were screened after analyzing the data of patients in the training set. Then prediction models were found based on the possible predictive indicators in the training set. Data of patients in the validation set and the testing set was provided to validate the predictive values of the models. RESULTS: Age, Glasgow coma scale score, Apolipoprotein E genotype, damage area, serum C‐reactive protein, and interleukin‐8 (IL‐8) levels, and Marshall computed tomography score were found associated with early prognosis of TBI patients. The accuracy of the early prognosis prediction model (EPPM) was 80%, and the sensitivity and specificity of the EPPM were 78.8% and 80.8% in the training set. The accuracy of the EPPM was 79%, and the sensitivity and specificity of the EPPM were 66.7% and 86.2% in the validation set. The accuracy of the early EPPM was 69.1%, and the sensitivity and specificity of the EPPM were 67.9% and 77.8% in the testing set. CONCLUSION: Prediction models integrating general information, clinical manifestations, and auxiliary examination results may provide a reliable and rapid method to evaluate and predict the early prognosis of TBI patients. John Wiley and Sons Inc. 2022-08-26 /pmc/articles/PMC9627380/ /pubmed/36017774 http://dx.doi.org/10.1111/cns.13935 Text en © 2022 The Authors. CNS Neuroscience & Therapeutics published by John Wiley & Sons Ltd. 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 Original Articles
Yang, Bocheng
Sun, Xiaochuan
Shi, Quanhong
Dan, Wei
Zhan, Yan
Zheng, Dinghao
Xia, Yulong
Xie, Yanfeng
Jiang, Li
Prediction of early prognosis after traumatic brain injury by multifactor model
title Prediction of early prognosis after traumatic brain injury by multifactor model
title_full Prediction of early prognosis after traumatic brain injury by multifactor model
title_fullStr Prediction of early prognosis after traumatic brain injury by multifactor model
title_full_unstemmed Prediction of early prognosis after traumatic brain injury by multifactor model
title_short Prediction of early prognosis after traumatic brain injury by multifactor model
title_sort prediction of early prognosis after traumatic brain injury by multifactor model
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9627380/
https://www.ncbi.nlm.nih.gov/pubmed/36017774
http://dx.doi.org/10.1111/cns.13935
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