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Development and validation of early death risk score model for emergency status prediction in very severe aplastic anemia

This study developed and validated the Early Death Risk Score Model for early identification of emergency patients with very severe aplastic anemia (VSAA). All 377 patients with VSAA receiving first-line immunosuppressive therapy (IST) were categorized into training (n=252) and validation (n=125) co...

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Autores principales: Liu, Xu, Yang, Wenrui, Zhang, Li, Jing, Liping, Ye, Lei, Zhou, Kang, Li, Yuan, Li, Jianping, Fan, Huihui, Yang, Yang, Xiong, Youzhen, Zhao, Xin, Zhang, Fengkui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10158980/
https://www.ncbi.nlm.nih.gov/pubmed/37153568
http://dx.doi.org/10.3389/fimmu.2023.1175048
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author Liu, Xu
Yang, Wenrui
Zhang, Li
Jing, Liping
Ye, Lei
Zhou, Kang
Li, Yuan
Li, Jianping
Fan, Huihui
Yang, Yang
Xiong, Youzhen
Zhao, Xin
Zhang, Fengkui
author_facet Liu, Xu
Yang, Wenrui
Zhang, Li
Jing, Liping
Ye, Lei
Zhou, Kang
Li, Yuan
Li, Jianping
Fan, Huihui
Yang, Yang
Xiong, Youzhen
Zhao, Xin
Zhang, Fengkui
author_sort Liu, Xu
collection PubMed
description This study developed and validated the Early Death Risk Score Model for early identification of emergency patients with very severe aplastic anemia (VSAA). All 377 patients with VSAA receiving first-line immunosuppressive therapy (IST) were categorized into training (n=252) and validation (n=125) cohorts. In the training cohort, age >24 years, absolute neutrophil count ≤0.015×10(9)/L, serum ferritin >900ng/mL and times of fever before IST >1 time were significantly associated with early death. Covariates were assigned scores and categorized as: low (score 0-4), medium (score 5-7) and high (score ≥8) risk. Early death rate was significantly different between risk groups and the validation cohort results were consistent with those of the training cohort. The area under the receiver operating characteristic curve for the model was 0.835 (0.734,0.936) in the training cohort and 0.862 (0.730,0.994) in the validation cohort. The calibration plots showed high agreement, and decision curve analysis showed good benefit in clinical applications. The VSAA Early Death Risk Score Model can help with early identification of emergency VSAA and optimize treatment strategies. Emergency VSAA with high risk is associated with high early death rate, and alternative donor hematopoietic stem cell transplantation could be a better treatment than IST even without HLA-matching.
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spelling pubmed-101589802023-05-05 Development and validation of early death risk score model for emergency status prediction in very severe aplastic anemia Liu, Xu Yang, Wenrui Zhang, Li Jing, Liping Ye, Lei Zhou, Kang Li, Yuan Li, Jianping Fan, Huihui Yang, Yang Xiong, Youzhen Zhao, Xin Zhang, Fengkui Front Immunol Immunology This study developed and validated the Early Death Risk Score Model for early identification of emergency patients with very severe aplastic anemia (VSAA). All 377 patients with VSAA receiving first-line immunosuppressive therapy (IST) were categorized into training (n=252) and validation (n=125) cohorts. In the training cohort, age >24 years, absolute neutrophil count ≤0.015×10(9)/L, serum ferritin >900ng/mL and times of fever before IST >1 time were significantly associated with early death. Covariates were assigned scores and categorized as: low (score 0-4), medium (score 5-7) and high (score ≥8) risk. Early death rate was significantly different between risk groups and the validation cohort results were consistent with those of the training cohort. The area under the receiver operating characteristic curve for the model was 0.835 (0.734,0.936) in the training cohort and 0.862 (0.730,0.994) in the validation cohort. The calibration plots showed high agreement, and decision curve analysis showed good benefit in clinical applications. The VSAA Early Death Risk Score Model can help with early identification of emergency VSAA and optimize treatment strategies. Emergency VSAA with high risk is associated with high early death rate, and alternative donor hematopoietic stem cell transplantation could be a better treatment than IST even without HLA-matching. Frontiers Media S.A. 2023-04-20 /pmc/articles/PMC10158980/ /pubmed/37153568 http://dx.doi.org/10.3389/fimmu.2023.1175048 Text en Copyright © 2023 Liu, Yang, Zhang, Jing, Ye, Zhou, Li, Li, Fan, Yang, Xiong, Zhao and Zhang 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
Liu, Xu
Yang, Wenrui
Zhang, Li
Jing, Liping
Ye, Lei
Zhou, Kang
Li, Yuan
Li, Jianping
Fan, Huihui
Yang, Yang
Xiong, Youzhen
Zhao, Xin
Zhang, Fengkui
Development and validation of early death risk score model for emergency status prediction in very severe aplastic anemia
title Development and validation of early death risk score model for emergency status prediction in very severe aplastic anemia
title_full Development and validation of early death risk score model for emergency status prediction in very severe aplastic anemia
title_fullStr Development and validation of early death risk score model for emergency status prediction in very severe aplastic anemia
title_full_unstemmed Development and validation of early death risk score model for emergency status prediction in very severe aplastic anemia
title_short Development and validation of early death risk score model for emergency status prediction in very severe aplastic anemia
title_sort development and validation of early death risk score model for emergency status prediction in very severe aplastic anemia
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10158980/
https://www.ncbi.nlm.nih.gov/pubmed/37153568
http://dx.doi.org/10.3389/fimmu.2023.1175048
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