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Development and Validation of a Risk Score in Chinese Patients With Chronic Heart Failure

BACKGROUND: Acute exacerbation of chronic heart failure contributes to substantial increases in major adverse cardiovascular events (MACE). The study developed a risk score to evaluate the severity of heart failure which was related to the risk of MACE. METHODS: This single-center retrospective obse...

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Autores principales: Lin, Maoning, Zhan, Jiachen, Luan, Yi, Li, Duanbin, Shan, Yu, Xu, Tian, Fu, Guosheng, Zhang, Wenbin, Wang, Min
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9130568/
https://www.ncbi.nlm.nih.gov/pubmed/35647038
http://dx.doi.org/10.3389/fcvm.2022.865843
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author Lin, Maoning
Zhan, Jiachen
Luan, Yi
Li, Duanbin
Shan, Yu
Xu, Tian
Fu, Guosheng
Zhang, Wenbin
Wang, Min
author_facet Lin, Maoning
Zhan, Jiachen
Luan, Yi
Li, Duanbin
Shan, Yu
Xu, Tian
Fu, Guosheng
Zhang, Wenbin
Wang, Min
author_sort Lin, Maoning
collection PubMed
description BACKGROUND: Acute exacerbation of chronic heart failure contributes to substantial increases in major adverse cardiovascular events (MACE). The study developed a risk score to evaluate the severity of heart failure which was related to the risk of MACE. METHODS: This single-center retrospective observational study included 5,777 patients with heart failure. A credible random split-sample method was used to divide data into training and validation dataset (split ratio = 0.7:0.3). Least absolute shrinkage and selection operator (Lasso) logistic regression was applied to select predictors and develop the risk score to predict the severity category of heart failure. Receiver operating characteristic (ROC) curves, and calibration curves were used to assess the model’s discrimination and accuracy. RESULTS: Body-mass index (BMI), ejection fraction (EF), serum creatinine, hemoglobin, C-reactive protein (CRP), and neutrophil lymphocyte ratio (NLR) were identified as predictors and assembled into the risk score (P < 0.05), which showed good discrimination with AUC in the training dataset (0.770, 95% CI:0.746–0.794) and validation dataset (0.756, 95% CI:0.717–0.795) and was well calibrated in both datasets (all P > 0.05). As the severity of heart failure worsened according to risk score, the incidence of MACE, length of hospital stay, and treatment cost increased (P < 0.001). CONCLUSION: A risk score incorporating BMI, EF, serum creatinine, hemoglobin, CRP, and NLR, was developed and validated. It effectively evaluated individuals’ severity classification of heart failure, closely related to MACE.
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spelling pubmed-91305682022-05-26 Development and Validation of a Risk Score in Chinese Patients With Chronic Heart Failure Lin, Maoning Zhan, Jiachen Luan, Yi Li, Duanbin Shan, Yu Xu, Tian Fu, Guosheng Zhang, Wenbin Wang, Min Front Cardiovasc Med Cardiovascular Medicine BACKGROUND: Acute exacerbation of chronic heart failure contributes to substantial increases in major adverse cardiovascular events (MACE). The study developed a risk score to evaluate the severity of heart failure which was related to the risk of MACE. METHODS: This single-center retrospective observational study included 5,777 patients with heart failure. A credible random split-sample method was used to divide data into training and validation dataset (split ratio = 0.7:0.3). Least absolute shrinkage and selection operator (Lasso) logistic regression was applied to select predictors and develop the risk score to predict the severity category of heart failure. Receiver operating characteristic (ROC) curves, and calibration curves were used to assess the model’s discrimination and accuracy. RESULTS: Body-mass index (BMI), ejection fraction (EF), serum creatinine, hemoglobin, C-reactive protein (CRP), and neutrophil lymphocyte ratio (NLR) were identified as predictors and assembled into the risk score (P < 0.05), which showed good discrimination with AUC in the training dataset (0.770, 95% CI:0.746–0.794) and validation dataset (0.756, 95% CI:0.717–0.795) and was well calibrated in both datasets (all P > 0.05). As the severity of heart failure worsened according to risk score, the incidence of MACE, length of hospital stay, and treatment cost increased (P < 0.001). CONCLUSION: A risk score incorporating BMI, EF, serum creatinine, hemoglobin, CRP, and NLR, was developed and validated. It effectively evaluated individuals’ severity classification of heart failure, closely related to MACE. Frontiers Media S.A. 2022-05-11 /pmc/articles/PMC9130568/ /pubmed/35647038 http://dx.doi.org/10.3389/fcvm.2022.865843 Text en Copyright © 2022 Lin, Zhan, Luan, Li, Shan, Xu, Fu, Zhang 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 Cardiovascular Medicine
Lin, Maoning
Zhan, Jiachen
Luan, Yi
Li, Duanbin
Shan, Yu
Xu, Tian
Fu, Guosheng
Zhang, Wenbin
Wang, Min
Development and Validation of a Risk Score in Chinese Patients With Chronic Heart Failure
title Development and Validation of a Risk Score in Chinese Patients With Chronic Heart Failure
title_full Development and Validation of a Risk Score in Chinese Patients With Chronic Heart Failure
title_fullStr Development and Validation of a Risk Score in Chinese Patients With Chronic Heart Failure
title_full_unstemmed Development and Validation of a Risk Score in Chinese Patients With Chronic Heart Failure
title_short Development and Validation of a Risk Score in Chinese Patients With Chronic Heart Failure
title_sort development and validation of a risk score in chinese patients with chronic heart failure
topic Cardiovascular Medicine
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9130568/
https://www.ncbi.nlm.nih.gov/pubmed/35647038
http://dx.doi.org/10.3389/fcvm.2022.865843
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