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Enlarging Red Blood Cell Distribution Width During Hospitalization Identifies a Very High-Risk Subset of Acutely Decompensated Heart Failure Patients and Adds Valuable Prognostic Information on Top of Hemoconcentration

Red blood cell distribution width (RDW) may serve as an integrative marker of pathological processes that portend worse prognosis in heart failure (HF). The prognostic value of RDW variation (ΔRDW) during hospitalization for acute heart failure (AHF) has yet to be studied. We retrospectively analyze...

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Autores principales: Ferreira, João Pedro, Girerd, Nicolas, Arrigo, Mattia, Medeiros, Pedro Bettencourt, Ricardo, Miguel Bento, Almeida, Tiago, Rola, Alexandre, Tolpannen, Heli, Laribi, Said, Gayat, Etienne, Mebazaa, Alexandre, Mueller, Christian, Zannad, Faiez, Rossignol, Patrick, Aragão, Irene
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4998821/
https://www.ncbi.nlm.nih.gov/pubmed/27057905
http://dx.doi.org/10.1097/MD.0000000000003307
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author Ferreira, João Pedro
Girerd, Nicolas
Arrigo, Mattia
Medeiros, Pedro Bettencourt
Ricardo, Miguel Bento
Almeida, Tiago
Rola, Alexandre
Tolpannen, Heli
Laribi, Said
Gayat, Etienne
Mebazaa, Alexandre
Mueller, Christian
Zannad, Faiez
Rossignol, Patrick
Aragão, Irene
author_facet Ferreira, João Pedro
Girerd, Nicolas
Arrigo, Mattia
Medeiros, Pedro Bettencourt
Ricardo, Miguel Bento
Almeida, Tiago
Rola, Alexandre
Tolpannen, Heli
Laribi, Said
Gayat, Etienne
Mebazaa, Alexandre
Mueller, Christian
Zannad, Faiez
Rossignol, Patrick
Aragão, Irene
author_sort Ferreira, João Pedro
collection PubMed
description Red blood cell distribution width (RDW) may serve as an integrative marker of pathological processes that portend worse prognosis in heart failure (HF). The prognostic value of RDW variation (ΔRDW) during hospitalization for acute heart failure (AHF) has yet to be studied. We retrospectively analyzed 2 independent cohorts: Centro Hospitalar do Porto (derivation cohort) and Lariboisière hospital (validation cohort). In the derivation cohort a total of 170 patients (age 76.2 ± 10.3 years) were included and in the validation cohort 332 patients were included (age 76.4 ± 12.2 years). In the derivation cohort the primary composite outcome of HF admission and/or cardiovascular death occurred in 78 (45.9%) patients during the 180-day follow-up period. Discharge RDW and ΔRDW were both increased when hemoglobin levels were lower; peripheral edema was also associated with increased discharge RDW (all P < 0.05). Discharge RDW value was significantly associated with adverse events: RDW > 15% at discharge was associated with a 2-fold increase in event rate, HR = 1.95 (1.05–3.62), P = 0.04, while a ΔRDW >0 also had a strong association with outcome, HR = 2.47 (1.35–4.51), P = 0.003. The addition of both discharge RDW > 15% and ΔRDW > 0 to hemoconcentration was associated with a significant improvement in the net reclassification index, NRI = 18.3 (4.3–43.7), P = 0.012. Overlapping results were found in the validation cohort. As validated in 2 independent AHF cohorts, an in-hospital RDW enlargement and an elevated RDW at discharge are associated with increased rates of mid-term events. RDW variables improve the risk stratification of these patients on top of well-established prognostic markers.
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spelling pubmed-49988212016-08-29 Enlarging Red Blood Cell Distribution Width During Hospitalization Identifies a Very High-Risk Subset of Acutely Decompensated Heart Failure Patients and Adds Valuable Prognostic Information on Top of Hemoconcentration Ferreira, João Pedro Girerd, Nicolas Arrigo, Mattia Medeiros, Pedro Bettencourt Ricardo, Miguel Bento Almeida, Tiago Rola, Alexandre Tolpannen, Heli Laribi, Said Gayat, Etienne Mebazaa, Alexandre Mueller, Christian Zannad, Faiez Rossignol, Patrick Aragão, Irene Medicine (Baltimore) 3400 Red blood cell distribution width (RDW) may serve as an integrative marker of pathological processes that portend worse prognosis in heart failure (HF). The prognostic value of RDW variation (ΔRDW) during hospitalization for acute heart failure (AHF) has yet to be studied. We retrospectively analyzed 2 independent cohorts: Centro Hospitalar do Porto (derivation cohort) and Lariboisière hospital (validation cohort). In the derivation cohort a total of 170 patients (age 76.2 ± 10.3 years) were included and in the validation cohort 332 patients were included (age 76.4 ± 12.2 years). In the derivation cohort the primary composite outcome of HF admission and/or cardiovascular death occurred in 78 (45.9%) patients during the 180-day follow-up period. Discharge RDW and ΔRDW were both increased when hemoglobin levels were lower; peripheral edema was also associated with increased discharge RDW (all P < 0.05). Discharge RDW value was significantly associated with adverse events: RDW > 15% at discharge was associated with a 2-fold increase in event rate, HR = 1.95 (1.05–3.62), P = 0.04, while a ΔRDW >0 also had a strong association with outcome, HR = 2.47 (1.35–4.51), P = 0.003. The addition of both discharge RDW > 15% and ΔRDW > 0 to hemoconcentration was associated with a significant improvement in the net reclassification index, NRI = 18.3 (4.3–43.7), P = 0.012. Overlapping results were found in the validation cohort. As validated in 2 independent AHF cohorts, an in-hospital RDW enlargement and an elevated RDW at discharge are associated with increased rates of mid-term events. RDW variables improve the risk stratification of these patients on top of well-established prognostic markers. Wolters Kluwer Health 2016-04-08 /pmc/articles/PMC4998821/ /pubmed/27057905 http://dx.doi.org/10.1097/MD.0000000000003307 Text en Copyright © 2016 Wolters Kluwer Health, Inc. All rights reserved. http://creativecommons.org/licenses/by/4.0 This is an open access article distributed under the Creative Commons Attribution License 4.0, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. http://creativecommons.org/licenses/by/4.0
spellingShingle 3400
Ferreira, João Pedro
Girerd, Nicolas
Arrigo, Mattia
Medeiros, Pedro Bettencourt
Ricardo, Miguel Bento
Almeida, Tiago
Rola, Alexandre
Tolpannen, Heli
Laribi, Said
Gayat, Etienne
Mebazaa, Alexandre
Mueller, Christian
Zannad, Faiez
Rossignol, Patrick
Aragão, Irene
Enlarging Red Blood Cell Distribution Width During Hospitalization Identifies a Very High-Risk Subset of Acutely Decompensated Heart Failure Patients and Adds Valuable Prognostic Information on Top of Hemoconcentration
title Enlarging Red Blood Cell Distribution Width During Hospitalization Identifies a Very High-Risk Subset of Acutely Decompensated Heart Failure Patients and Adds Valuable Prognostic Information on Top of Hemoconcentration
title_full Enlarging Red Blood Cell Distribution Width During Hospitalization Identifies a Very High-Risk Subset of Acutely Decompensated Heart Failure Patients and Adds Valuable Prognostic Information on Top of Hemoconcentration
title_fullStr Enlarging Red Blood Cell Distribution Width During Hospitalization Identifies a Very High-Risk Subset of Acutely Decompensated Heart Failure Patients and Adds Valuable Prognostic Information on Top of Hemoconcentration
title_full_unstemmed Enlarging Red Blood Cell Distribution Width During Hospitalization Identifies a Very High-Risk Subset of Acutely Decompensated Heart Failure Patients and Adds Valuable Prognostic Information on Top of Hemoconcentration
title_short Enlarging Red Blood Cell Distribution Width During Hospitalization Identifies a Very High-Risk Subset of Acutely Decompensated Heart Failure Patients and Adds Valuable Prognostic Information on Top of Hemoconcentration
title_sort enlarging red blood cell distribution width during hospitalization identifies a very high-risk subset of acutely decompensated heart failure patients and adds valuable prognostic information on top of hemoconcentration
topic 3400
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4998821/
https://www.ncbi.nlm.nih.gov/pubmed/27057905
http://dx.doi.org/10.1097/MD.0000000000003307
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