Literature DB >> 26140955

Elevation of red blood cell distribution width during hospitalization predicts mortality in patients with acute decompensated heart failure.

Yusuke Uemura1, Rei Shibata2, Kenji Takemoto3, Tomohiro Uchikawa3, Masayoshi Koyasu3, Hiroki Watanabe3, Takayuki Mitsuda3, Ayako Miura3, Ryo Imai3, Masato Watarai3, Toyoaki Murohara2.   

Abstract

BACKGROUND: Increased red blood cell distribution width (RDW) is associated with adverse outcomes in heart failure. In the present study, we assessed the association between changes in RDW values during hospitalization and long-term prognosis in patients with acute decompensated heart failure (ADHF).
METHODS: We measured the RDW value in 229 consecutive patients with ADHF. Blood samples were obtained at the time of hospital admission and at discharge. Changes in RDW were calculated as the mean difference between RDW values on admission and those at the time of hospital discharge.
RESULTS: Patients were followed up for a median of 692 days. A Kaplan-Meier survival analysis demonstrated that patients whose RDW levels increased during hospitalization had significantly higher all-cause and cardiac-based mortality following heart failure than did patients whose RDW levels decreased during hospitalization. A multivariate Cox regression analysis revealed that change in RDW values during hospitalization, but not the values of RDW and hemoglobin on admission, was independently correlated with all-cause and cardiac-based mortality after adjusting for other risk factors in patients with ADHF.
CONCLUSIONS: These data document that the change in RDW values during hospitalization independently predicts poor outcomes in patients with ADHF. Continuous follow-up of RDW values could provide useful information for long-term prognosis after heart failure.
Copyright © 2015 Japanese College of Cardiology. Published by Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  Acute decompensated heart failure; Mortality; Red blood cell distribution width

Mesh:

Substances:

Year:  2015        PMID: 26140955     DOI: 10.1016/j.jjcc.2015.05.011

Source DB:  PubMed          Journal:  J Cardiol        ISSN: 0914-5087            Impact factor:   3.159


  20 in total

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