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Differences in the predictive value of red cell distribution width for the mortality of patients with heart failure due to various heart diseases

BACKGROUND: Increased red blood cell distribution width (RDW) is associated with adverse outcomes in patients with heart failure (HF). The objective of this study was to compare the differences in the predictive value of RDW in patients with HF due to different causes. METHODS: We retrospectively in...

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Autores principales: Zhang, Yang, Wang, Yan, Kang, Jin-Suo, Yu, Jin-Xing, Yin, Shi-Jie, Cong, Xiang-Feng, Chen, Xi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Science Press 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4712371/
https://www.ncbi.nlm.nih.gov/pubmed/26788042
http://dx.doi.org/10.11909/j.issn.1671-5411.2015.06.001
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author Zhang, Yang
Wang, Yan
Kang, Jin-Suo
Yu, Jin-Xing
Yin, Shi-Jie
Cong, Xiang-Feng
Chen, Xi
author_facet Zhang, Yang
Wang, Yan
Kang, Jin-Suo
Yu, Jin-Xing
Yin, Shi-Jie
Cong, Xiang-Feng
Chen, Xi
author_sort Zhang, Yang
collection PubMed
description BACKGROUND: Increased red blood cell distribution width (RDW) is associated with adverse outcomes in patients with heart failure (HF). The objective of this study was to compare the differences in the predictive value of RDW in patients with HF due to different causes. METHODS: We retrospectively investigated 1,021 HF patients from October 2009 to December 2011 at Fuwai Hospital (Beijing, China). HF in these patients was caused by three diseases; coronary heart disease (CHD), dilated cardiomyopathy (DCM) and valvular heart disease (VHD). Patients were followed-up for 21 ± 9 months. RESULTS: The RDW, mortality and survival duration were significantly different among the three groups. Kaplan–Meier analysis showed that the cumulative survival decreased significantly with increased RDW in patients with HF caused by CHD and DCM, but not in those with HF patients caused by VHD. In a multivariable model, RDW was identified as an independent predictor for the mortality of HF patients with CHD (P < 0.001, HR 1.315, 95% CI 1.122–1.543). The group with higher N-terminal pro-brain natriuretic peptide (NT-proBNP) and higher RDW than median had the lowest cumulative survival in patients with HF due to CHD, but not in patients with HF due to DCM. CONCLUSIONS: RDW is a prognostic indicator for patients with HF caused by CHD and DCM; thus, RDW adds important information to NT-proBNP in CHD caused HF patients.
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spelling pubmed-47123712016-01-19 Differences in the predictive value of red cell distribution width for the mortality of patients with heart failure due to various heart diseases Zhang, Yang Wang, Yan Kang, Jin-Suo Yu, Jin-Xing Yin, Shi-Jie Cong, Xiang-Feng Chen, Xi J Geriatr Cardiol Research Article BACKGROUND: Increased red blood cell distribution width (RDW) is associated with adverse outcomes in patients with heart failure (HF). The objective of this study was to compare the differences in the predictive value of RDW in patients with HF due to different causes. METHODS: We retrospectively investigated 1,021 HF patients from October 2009 to December 2011 at Fuwai Hospital (Beijing, China). HF in these patients was caused by three diseases; coronary heart disease (CHD), dilated cardiomyopathy (DCM) and valvular heart disease (VHD). Patients were followed-up for 21 ± 9 months. RESULTS: The RDW, mortality and survival duration were significantly different among the three groups. Kaplan–Meier analysis showed that the cumulative survival decreased significantly with increased RDW in patients with HF caused by CHD and DCM, but not in those with HF patients caused by VHD. In a multivariable model, RDW was identified as an independent predictor for the mortality of HF patients with CHD (P < 0.001, HR 1.315, 95% CI 1.122–1.543). The group with higher N-terminal pro-brain natriuretic peptide (NT-proBNP) and higher RDW than median had the lowest cumulative survival in patients with HF due to CHD, but not in patients with HF due to DCM. CONCLUSIONS: RDW is a prognostic indicator for patients with HF caused by CHD and DCM; thus, RDW adds important information to NT-proBNP in CHD caused HF patients. Science Press 2015-11 /pmc/articles/PMC4712371/ /pubmed/26788042 http://dx.doi.org/10.11909/j.issn.1671-5411.2015.06.001 Text en Institute of Geriatric Cardiology http://creativecommons.org/licenses/by-nc-sa/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 Unported License, which allows readers to alter, transform, or build upon the article and then distribute the resulting work under the same or similar license to this one. The work must be attributed back to the original author and commercial use is not permitted without specific permission.
spellingShingle Research Article
Zhang, Yang
Wang, Yan
Kang, Jin-Suo
Yu, Jin-Xing
Yin, Shi-Jie
Cong, Xiang-Feng
Chen, Xi
Differences in the predictive value of red cell distribution width for the mortality of patients with heart failure due to various heart diseases
title Differences in the predictive value of red cell distribution width for the mortality of patients with heart failure due to various heart diseases
title_full Differences in the predictive value of red cell distribution width for the mortality of patients with heart failure due to various heart diseases
title_fullStr Differences in the predictive value of red cell distribution width for the mortality of patients with heart failure due to various heart diseases
title_full_unstemmed Differences in the predictive value of red cell distribution width for the mortality of patients with heart failure due to various heart diseases
title_short Differences in the predictive value of red cell distribution width for the mortality of patients with heart failure due to various heart diseases
title_sort differences in the predictive value of red cell distribution width for the mortality of patients with heart failure due to various heart diseases
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4712371/
https://www.ncbi.nlm.nih.gov/pubmed/26788042
http://dx.doi.org/10.11909/j.issn.1671-5411.2015.06.001
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