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Insights about serum sodium behavior after 24 hours of continuous renal replacement therapy

OBJECTIVE: The aim of this study was to investigate the clinical and laboratorial factors associated with serum sodium variation during continuous renal replacement therapy and to assess whether the perfect admixture formula could predict 24-hour sodium variation. METHODS: Thirty-six continuous rena...

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Autores principales: Romano, Thiago Gomes, Martins, Cassia Pimenta Barufi, Mendes, Pedro Vitale, Besen, Bruno Adler Maccagnan Pinheiro, Zampieri, Fernando Godinho, Park, Marcelo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Associação de Medicina Intensiva Brasileira - AMIB 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4943049/
https://www.ncbi.nlm.nih.gov/pubmed/27410407
http://dx.doi.org/10.5935/0103-507X.20160026
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author Romano, Thiago Gomes
Martins, Cassia Pimenta Barufi
Mendes, Pedro Vitale
Besen, Bruno Adler Maccagnan Pinheiro
Zampieri, Fernando Godinho
Park, Marcelo
author_facet Romano, Thiago Gomes
Martins, Cassia Pimenta Barufi
Mendes, Pedro Vitale
Besen, Bruno Adler Maccagnan Pinheiro
Zampieri, Fernando Godinho
Park, Marcelo
author_sort Romano, Thiago Gomes
collection PubMed
description OBJECTIVE: The aim of this study was to investigate the clinical and laboratorial factors associated with serum sodium variation during continuous renal replacement therapy and to assess whether the perfect admixture formula could predict 24-hour sodium variation. METHODS: Thirty-six continuous renal replacement therapy sessions of 33 patients, in which the affluent prescription was unchanged during the first 24 hours, were retrieved from a prospective collected database and then analyzed. A mixed linear model was performed to investigate the factors associated with large serum sodium variations (≥ 8mEq/L), and a Bland-Altman plot was generated to assess the agreement between the predicted and observed variations. RESULTS: In continuous renal replacement therapy 24-hour sessions, SAPS 3 (p = 0.022) and baseline hypernatremia (p = 0.023) were statistically significant predictors of serum sodium variations ≥ 8mEq/L in univariate analysis, but only hypernatremia demonstrated an independent association (β = 0.429, p < 0.001). The perfect admixture formula for sodium prediction at 24 hours demonstrated poor agreement with the observed values. CONCLUSIONS: Hypernatremia at the time of continuous renal replacement therapy initiation is an important factor associated with clinically significant serum sodium variation. The use of 4% citrate or acid citrate dextrose - formula A 2.2% as anticoagulants was not associated with higher serum sodium variations. A mathematical prediction for the serum sodium concentration after 24 hours was not feasible.
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spelling pubmed-49430492016-07-14 Insights about serum sodium behavior after 24 hours of continuous renal replacement therapy Romano, Thiago Gomes Martins, Cassia Pimenta Barufi Mendes, Pedro Vitale Besen, Bruno Adler Maccagnan Pinheiro Zampieri, Fernando Godinho Park, Marcelo Rev Bras Ter Intensiva Original Article OBJECTIVE: The aim of this study was to investigate the clinical and laboratorial factors associated with serum sodium variation during continuous renal replacement therapy and to assess whether the perfect admixture formula could predict 24-hour sodium variation. METHODS: Thirty-six continuous renal replacement therapy sessions of 33 patients, in which the affluent prescription was unchanged during the first 24 hours, were retrieved from a prospective collected database and then analyzed. A mixed linear model was performed to investigate the factors associated with large serum sodium variations (≥ 8mEq/L), and a Bland-Altman plot was generated to assess the agreement between the predicted and observed variations. RESULTS: In continuous renal replacement therapy 24-hour sessions, SAPS 3 (p = 0.022) and baseline hypernatremia (p = 0.023) were statistically significant predictors of serum sodium variations ≥ 8mEq/L in univariate analysis, but only hypernatremia demonstrated an independent association (β = 0.429, p < 0.001). The perfect admixture formula for sodium prediction at 24 hours demonstrated poor agreement with the observed values. CONCLUSIONS: Hypernatremia at the time of continuous renal replacement therapy initiation is an important factor associated with clinically significant serum sodium variation. The use of 4% citrate or acid citrate dextrose - formula A 2.2% as anticoagulants was not associated with higher serum sodium variations. A mathematical prediction for the serum sodium concentration after 24 hours was not feasible. Associação de Medicina Intensiva Brasileira - AMIB 2016 /pmc/articles/PMC4943049/ /pubmed/27410407 http://dx.doi.org/10.5935/0103-507X.20160026 Text en http://creativecommons.org/licenses/by/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Romano, Thiago Gomes
Martins, Cassia Pimenta Barufi
Mendes, Pedro Vitale
Besen, Bruno Adler Maccagnan Pinheiro
Zampieri, Fernando Godinho
Park, Marcelo
Insights about serum sodium behavior after 24 hours of continuous renal replacement therapy
title Insights about serum sodium behavior after 24 hours of continuous renal replacement therapy
title_full Insights about serum sodium behavior after 24 hours of continuous renal replacement therapy
title_fullStr Insights about serum sodium behavior after 24 hours of continuous renal replacement therapy
title_full_unstemmed Insights about serum sodium behavior after 24 hours of continuous renal replacement therapy
title_short Insights about serum sodium behavior after 24 hours of continuous renal replacement therapy
title_sort insights about serum sodium behavior after 24 hours of continuous renal replacement therapy
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4943049/
https://www.ncbi.nlm.nih.gov/pubmed/27410407
http://dx.doi.org/10.5935/0103-507X.20160026
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