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Defining Delayed Perihematomal Edema Expansion in Intracerebral Hemorrhage: Segmentation, Time Course, Risk Factors and Clinical Outcome

We attempt to generate a definition of delayed perihematomal edema expansion (DPE) and analyze its time course, risk factors, and clinical outcomes. A multi-cohort data was derived from the Chinese Intracranial Hemorrhage Image Database (CICHID). A non-contrast computed tomography (NCCT) -based deep...

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Autores principales: Chen, Yihao, Qin, Chenchen, Chang, Jianbo, Liu, Yixun, Zhang, Qinghua, Ye, Zeju, Li, Zhaojian, Tian, Fengxuan, Ma, Wenbin, Wei, Junji, Feng, Ming, Chen, Shengpan, Yao, Jianhua, Wang, Renzhi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9125313/
https://www.ncbi.nlm.nih.gov/pubmed/35615357
http://dx.doi.org/10.3389/fimmu.2022.911207
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author Chen, Yihao
Qin, Chenchen
Chang, Jianbo
Liu, Yixun
Zhang, Qinghua
Ye, Zeju
Li, Zhaojian
Tian, Fengxuan
Ma, Wenbin
Wei, Junji
Feng, Ming
Chen, Shengpan
Yao, Jianhua
Wang, Renzhi
author_facet Chen, Yihao
Qin, Chenchen
Chang, Jianbo
Liu, Yixun
Zhang, Qinghua
Ye, Zeju
Li, Zhaojian
Tian, Fengxuan
Ma, Wenbin
Wei, Junji
Feng, Ming
Chen, Shengpan
Yao, Jianhua
Wang, Renzhi
author_sort Chen, Yihao
collection PubMed
description We attempt to generate a definition of delayed perihematomal edema expansion (DPE) and analyze its time course, risk factors, and clinical outcomes. A multi-cohort data was derived from the Chinese Intracranial Hemorrhage Image Database (CICHID). A non-contrast computed tomography (NCCT) -based deep learning model was constructed for fully automated segmentation hematoma and perihematomal edema (PHE). Time course of hematoma and PHE evolution correlated to initial hematoma volume was volumetrically assessed. Predictive values for DPE were calculated through receiver operating characteristic curve analysis and were tested in an independent cohort. Logistic regression analysis was utilized to identify risk factors for DPE formation and poor outcomes. The test cohort’s Dice scores of lesion segmentation were 0.877 and 0.642 for hematoma and PHE, respectively. Overall, 1201 patients were enrolled for time-course analysis of ICH evolution. A total of 312 patients were further selected for DPE analysis. Time course analysis showed the growth peak of PHE approximately concentrates in 14 days after onset. The best cutoff for DPE to predict poor outcome was 3.34 mL of absolute PHE expansion from 4-7 days to 8-14 days (AUC=0.784, sensitivity=72.2%, specificity=81.2%), and 3.78 mL of absolute PHE expansion from 8-14 days to 15-21 days (AUC=0.682, sensitivity=59.3%, specificity=92.1%) in the derivation sample. Patients with DPE was associated with worse outcome (OR: 12.340, 95%CI: 6.378-23.873, P<0.01), and the larger initial hematoma volume (OR: 1.021, 95%CI: 1.000-1.043, P=0.049) was the significant risk factor for DPE formation. This study constructed a well-performance deep learning model for automatic segmentations of hematoma and PHE. A new definition of DPE was generated and is confirmed to be related to poor outcomes in ICH. Patients with larger initial hematoma volume have a higher risk of developing DPE formation.
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spelling pubmed-91253132022-05-24 Defining Delayed Perihematomal Edema Expansion in Intracerebral Hemorrhage: Segmentation, Time Course, Risk Factors and Clinical Outcome Chen, Yihao Qin, Chenchen Chang, Jianbo Liu, Yixun Zhang, Qinghua Ye, Zeju Li, Zhaojian Tian, Fengxuan Ma, Wenbin Wei, Junji Feng, Ming Chen, Shengpan Yao, Jianhua Wang, Renzhi Front Immunol Immunology We attempt to generate a definition of delayed perihematomal edema expansion (DPE) and analyze its time course, risk factors, and clinical outcomes. A multi-cohort data was derived from the Chinese Intracranial Hemorrhage Image Database (CICHID). A non-contrast computed tomography (NCCT) -based deep learning model was constructed for fully automated segmentation hematoma and perihematomal edema (PHE). Time course of hematoma and PHE evolution correlated to initial hematoma volume was volumetrically assessed. Predictive values for DPE were calculated through receiver operating characteristic curve analysis and were tested in an independent cohort. Logistic regression analysis was utilized to identify risk factors for DPE formation and poor outcomes. The test cohort’s Dice scores of lesion segmentation were 0.877 and 0.642 for hematoma and PHE, respectively. Overall, 1201 patients were enrolled for time-course analysis of ICH evolution. A total of 312 patients were further selected for DPE analysis. Time course analysis showed the growth peak of PHE approximately concentrates in 14 days after onset. The best cutoff for DPE to predict poor outcome was 3.34 mL of absolute PHE expansion from 4-7 days to 8-14 days (AUC=0.784, sensitivity=72.2%, specificity=81.2%), and 3.78 mL of absolute PHE expansion from 8-14 days to 15-21 days (AUC=0.682, sensitivity=59.3%, specificity=92.1%) in the derivation sample. Patients with DPE was associated with worse outcome (OR: 12.340, 95%CI: 6.378-23.873, P<0.01), and the larger initial hematoma volume (OR: 1.021, 95%CI: 1.000-1.043, P=0.049) was the significant risk factor for DPE formation. This study constructed a well-performance deep learning model for automatic segmentations of hematoma and PHE. A new definition of DPE was generated and is confirmed to be related to poor outcomes in ICH. Patients with larger initial hematoma volume have a higher risk of developing DPE formation. Frontiers Media S.A. 2022-05-09 /pmc/articles/PMC9125313/ /pubmed/35615357 http://dx.doi.org/10.3389/fimmu.2022.911207 Text en Copyright © 2022 Chen, Qin, Chang, Liu, Zhang, Ye, Li, Tian, Ma, Wei, Feng, Chen, Yao and Wang https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Chen, Yihao
Qin, Chenchen
Chang, Jianbo
Liu, Yixun
Zhang, Qinghua
Ye, Zeju
Li, Zhaojian
Tian, Fengxuan
Ma, Wenbin
Wei, Junji
Feng, Ming
Chen, Shengpan
Yao, Jianhua
Wang, Renzhi
Defining Delayed Perihematomal Edema Expansion in Intracerebral Hemorrhage: Segmentation, Time Course, Risk Factors and Clinical Outcome
title Defining Delayed Perihematomal Edema Expansion in Intracerebral Hemorrhage: Segmentation, Time Course, Risk Factors and Clinical Outcome
title_full Defining Delayed Perihematomal Edema Expansion in Intracerebral Hemorrhage: Segmentation, Time Course, Risk Factors and Clinical Outcome
title_fullStr Defining Delayed Perihematomal Edema Expansion in Intracerebral Hemorrhage: Segmentation, Time Course, Risk Factors and Clinical Outcome
title_full_unstemmed Defining Delayed Perihematomal Edema Expansion in Intracerebral Hemorrhage: Segmentation, Time Course, Risk Factors and Clinical Outcome
title_short Defining Delayed Perihematomal Edema Expansion in Intracerebral Hemorrhage: Segmentation, Time Course, Risk Factors and Clinical Outcome
title_sort defining delayed perihematomal edema expansion in intracerebral hemorrhage: segmentation, time course, risk factors and clinical outcome
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9125313/
https://www.ncbi.nlm.nih.gov/pubmed/35615357
http://dx.doi.org/10.3389/fimmu.2022.911207
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