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Clinically unrecognized plasma volume expansion predicts long‐term all‐cause‐mortality in chronic heart failure

INTRODUCTION: Chronic heart failure (CHF) is associated with elevated total blood volume (BV) and distinct phenotypes of total red cell volume (RCV) and plasma volume (PV) elevations. Especially PV expansion during clinical decompensation is linked with adverse clinical outcomes. The role of PV expa...

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Autores principales: Ahlgrim, Christoph, Seiler, Florian, Birkner, Philipp, Schoechlin, Simon, Grundmann, Sebastian, Bode, Christoph, Pottgiesser, Torben
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9574737/
https://www.ncbi.nlm.nih.gov/pubmed/35920821
http://dx.doi.org/10.1002/clc.23893
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author Ahlgrim, Christoph
Seiler, Florian
Birkner, Philipp
Schoechlin, Simon
Grundmann, Sebastian
Bode, Christoph
Pottgiesser, Torben
author_facet Ahlgrim, Christoph
Seiler, Florian
Birkner, Philipp
Schoechlin, Simon
Grundmann, Sebastian
Bode, Christoph
Pottgiesser, Torben
author_sort Ahlgrim, Christoph
collection PubMed
description INTRODUCTION: Chronic heart failure (CHF) is associated with elevated total blood volume (BV) and distinct phenotypes of total red cell volume (RCV) and plasma volume (PV) elevations. Especially PV expansion during clinical decompensation is linked with adverse clinical outcomes. The role of PV expansion in compensated CHF patients is less clear. Aim of the present study is to investigate the impact of BV parameters on long‐term mortality in CHF patients investigated at a compensated state. METHODS AND RESULTS: BV, PV and RCV were determined in 44 (9 female) compensated CHF patients using an abbreviated carbon monoxide method, who were followed up for 6.0 years, (range: 3.7–6.5 years) for all‐cause mortality. In univariate analysis PV expansion but not BV and RCV predicted all‐cause mortality (p = .021). A cutoff of 1800 ml PV/m² body‐surface area allows stratification for all‐cause mortality (p = .044). PV expansion but not RCV reduction explains the significantly lower hematocrit values of nonsurvivors. DISCUSSION: In this pilot study, PV expansion, which was unnoticed from a clinician's perspective, but is indicated by significantly lower hematocrit, appears to be a relevant predictor of long‐term all‐cause mortality. Whether PV expansion constitutes an adverse CHF phenotype and can be targeted by diuretic therapy is currently unclear.
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spelling pubmed-95747372022-10-17 Clinically unrecognized plasma volume expansion predicts long‐term all‐cause‐mortality in chronic heart failure Ahlgrim, Christoph Seiler, Florian Birkner, Philipp Schoechlin, Simon Grundmann, Sebastian Bode, Christoph Pottgiesser, Torben Clin Cardiol Clinical Investigations INTRODUCTION: Chronic heart failure (CHF) is associated with elevated total blood volume (BV) and distinct phenotypes of total red cell volume (RCV) and plasma volume (PV) elevations. Especially PV expansion during clinical decompensation is linked with adverse clinical outcomes. The role of PV expansion in compensated CHF patients is less clear. Aim of the present study is to investigate the impact of BV parameters on long‐term mortality in CHF patients investigated at a compensated state. METHODS AND RESULTS: BV, PV and RCV were determined in 44 (9 female) compensated CHF patients using an abbreviated carbon monoxide method, who were followed up for 6.0 years, (range: 3.7–6.5 years) for all‐cause mortality. In univariate analysis PV expansion but not BV and RCV predicted all‐cause mortality (p = .021). A cutoff of 1800 ml PV/m² body‐surface area allows stratification for all‐cause mortality (p = .044). PV expansion but not RCV reduction explains the significantly lower hematocrit values of nonsurvivors. DISCUSSION: In this pilot study, PV expansion, which was unnoticed from a clinician's perspective, but is indicated by significantly lower hematocrit, appears to be a relevant predictor of long‐term all‐cause mortality. Whether PV expansion constitutes an adverse CHF phenotype and can be targeted by diuretic therapy is currently unclear. John Wiley and Sons Inc. 2022-08-03 /pmc/articles/PMC9574737/ /pubmed/35920821 http://dx.doi.org/10.1002/clc.23893 Text en © 2022 The Authors. Clinical Cardiology published by Wiley Periodicals LLC. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Clinical Investigations
Ahlgrim, Christoph
Seiler, Florian
Birkner, Philipp
Schoechlin, Simon
Grundmann, Sebastian
Bode, Christoph
Pottgiesser, Torben
Clinically unrecognized plasma volume expansion predicts long‐term all‐cause‐mortality in chronic heart failure
title Clinically unrecognized plasma volume expansion predicts long‐term all‐cause‐mortality in chronic heart failure
title_full Clinically unrecognized plasma volume expansion predicts long‐term all‐cause‐mortality in chronic heart failure
title_fullStr Clinically unrecognized plasma volume expansion predicts long‐term all‐cause‐mortality in chronic heart failure
title_full_unstemmed Clinically unrecognized plasma volume expansion predicts long‐term all‐cause‐mortality in chronic heart failure
title_short Clinically unrecognized plasma volume expansion predicts long‐term all‐cause‐mortality in chronic heart failure
title_sort clinically unrecognized plasma volume expansion predicts long‐term all‐cause‐mortality in chronic heart failure
topic Clinical Investigations
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9574737/
https://www.ncbi.nlm.nih.gov/pubmed/35920821
http://dx.doi.org/10.1002/clc.23893
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