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Sodium, volume and pressure control in haemodialysis patients for improved cardiovascular outcomes

Chronic volume overload is pervasive in patients on chronic haemodialysis and substantially increases the risk of cardiovascular death. The rediscovery of the three-compartment model in sodium metabolism revolutionizes our understanding of sodium (patho-)physiology and is an effect modifier that sti...

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Autores principales: Pinter, Jule, Chazot, Charles, Stuard, Stefano, Moissl, Ulrich, Canaud, Bernard
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7066545/
https://www.ncbi.nlm.nih.gov/pubmed/32162668
http://dx.doi.org/10.1093/ndt/gfaa017
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author Pinter, Jule
Chazot, Charles
Stuard, Stefano
Moissl, Ulrich
Canaud, Bernard
author_facet Pinter, Jule
Chazot, Charles
Stuard, Stefano
Moissl, Ulrich
Canaud, Bernard
author_sort Pinter, Jule
collection PubMed
description Chronic volume overload is pervasive in patients on chronic haemodialysis and substantially increases the risk of cardiovascular death. The rediscovery of the three-compartment model in sodium metabolism revolutionizes our understanding of sodium (patho-)physiology and is an effect modifier that still needs to be understood in the context of hypertension and end-stage kidney disease. Assessment of fluid overload in haemodialysis patients is central yet difficult to achieve, because traditional clinical signs of volume overload lack sensitivity and specificity. The highest all-cause mortality risk may be found in haemodialysis patients presenting with high fluid overload but low blood pressure before haemodialysis treatment. The second highest risk may be found in patients with both high blood pressure and fluid overload, while high blood pressure but normal fluid overload may only relate to moderate risk. Optimization of fluid overload in haemodialysis patients should be guided by combining the traditional clinical evaluation with objective measurements such as bioimpedance spectroscopy in assessing the risk of fluid overload. To overcome the tide of extracellular fluid, the concept of time-averaged fluid overload during the interdialytic period has been established and requires possible readjustment of a negative target post-dialysis weight. (23)Na-magnetic resonance imaging studies will help to quantitate sodium accumulation and keep prescribed haemodialytic sodium mass balance on the radar. Cluster-randomization trials (e.g. on sodium removal) are underway to improve our therapeutic approach to cardioprotective haemodialysis management.
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spelling pubmed-70665452020-03-18 Sodium, volume and pressure control in haemodialysis patients for improved cardiovascular outcomes Pinter, Jule Chazot, Charles Stuard, Stefano Moissl, Ulrich Canaud, Bernard Nephrol Dial Transplant Reviews Chronic volume overload is pervasive in patients on chronic haemodialysis and substantially increases the risk of cardiovascular death. The rediscovery of the three-compartment model in sodium metabolism revolutionizes our understanding of sodium (patho-)physiology and is an effect modifier that still needs to be understood in the context of hypertension and end-stage kidney disease. Assessment of fluid overload in haemodialysis patients is central yet difficult to achieve, because traditional clinical signs of volume overload lack sensitivity and specificity. The highest all-cause mortality risk may be found in haemodialysis patients presenting with high fluid overload but low blood pressure before haemodialysis treatment. The second highest risk may be found in patients with both high blood pressure and fluid overload, while high blood pressure but normal fluid overload may only relate to moderate risk. Optimization of fluid overload in haemodialysis patients should be guided by combining the traditional clinical evaluation with objective measurements such as bioimpedance spectroscopy in assessing the risk of fluid overload. To overcome the tide of extracellular fluid, the concept of time-averaged fluid overload during the interdialytic period has been established and requires possible readjustment of a negative target post-dialysis weight. (23)Na-magnetic resonance imaging studies will help to quantitate sodium accumulation and keep prescribed haemodialytic sodium mass balance on the radar. Cluster-randomization trials (e.g. on sodium removal) are underway to improve our therapeutic approach to cardioprotective haemodialysis management. Oxford University Press 2020-03 2020-03-12 /pmc/articles/PMC7066545/ /pubmed/32162668 http://dx.doi.org/10.1093/ndt/gfaa017 Text en © The Author(s) 2020. Published by Oxford University Press on behalf of ERA-EDTA. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Reviews
Pinter, Jule
Chazot, Charles
Stuard, Stefano
Moissl, Ulrich
Canaud, Bernard
Sodium, volume and pressure control in haemodialysis patients for improved cardiovascular outcomes
title Sodium, volume and pressure control in haemodialysis patients for improved cardiovascular outcomes
title_full Sodium, volume and pressure control in haemodialysis patients for improved cardiovascular outcomes
title_fullStr Sodium, volume and pressure control in haemodialysis patients for improved cardiovascular outcomes
title_full_unstemmed Sodium, volume and pressure control in haemodialysis patients for improved cardiovascular outcomes
title_short Sodium, volume and pressure control in haemodialysis patients for improved cardiovascular outcomes
title_sort sodium, volume and pressure control in haemodialysis patients for improved cardiovascular outcomes
topic Reviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7066545/
https://www.ncbi.nlm.nih.gov/pubmed/32162668
http://dx.doi.org/10.1093/ndt/gfaa017
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