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Automated individualization of dialysate sodium concentration reduces intradialytic plasma sodium changes in hemodialysis
In standard care, hemodialysis patients are often treated with a center‐specific fixed dialysate sodium concentration, potentially resulting in diffusive sodium changes for patients with plasma sodium concentrations below or above this level. While diffusive sodium load may be associated with thirst...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6850400/ https://www.ncbi.nlm.nih.gov/pubmed/30939213 http://dx.doi.org/10.1111/aor.13463 |
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author | Ságová, Michaela Wojke, Ralf Maierhofer, Andreas Gross, Malte Canaud, Bernard Gauly, Adelheid |
author_facet | Ságová, Michaela Wojke, Ralf Maierhofer, Andreas Gross, Malte Canaud, Bernard Gauly, Adelheid |
author_sort | Ságová, Michaela |
collection | PubMed |
description | In standard care, hemodialysis patients are often treated with a center‐specific fixed dialysate sodium concentration, potentially resulting in diffusive sodium changes for patients with plasma sodium concentrations below or above this level. While diffusive sodium load may be associated with thirst and higher interdialytic weight gain, excessive diffusive sodium removal may cause intradialytic symptoms. In contrast, the new hemodialysis machine option “Na control” provides automated individualization of dialysate sodium during treatment with the aim to reduce such intradialytic sodium changes without the need to determine the plasma sodium concentration. This proof‐of‐principle study on sodium control was designed as a monocentric randomized controlled crossover trial: 32 patients with residual diuresis of ≤1000 mL/day were enrolled to be treated by high‐volume post‐dilution hemodiafiltration (HDF) for 2 weeks each with “Na control” (individually and automatically adjusted dialysate sodium concentration) versus “standard fixed Na” (fixed dialysate sodium 138 mmol/L), in randomized order. Pre‐ and post‐dialytic plasma sodium concentrations were determined at bedside by direct potentiometry. The study hypothesis consisted of 2 components: the mean plasma sodium change between the start and end of the treatment being within ±1.0 mmol/L for sodium‐controlled treatments, and a lower variability of the plasma sodium changes for “Na control” than for “standard fixed Na” treatments. Three hundred seventy‐two treatments of 31 adult chronic hemodialysis patients (intention‐to‐treat population) were analyzed. The estimate for the mean plasma sodium change was −0.53 mmol/L (95% confidence interval: [−1.04; −0.02] mmol/L) for “Na control” treatments and −0.95 mmol/L (95% CI: [−1.76; −0.15] mmol/L) for “standard fixed Na” treatments. The standard deviation of the plasma sodium changes was 1.39 mmol/L for “Na control” versus 2.19 mmol/L for “standard fixed Na” treatments (P = 0.0004). Whereas the 95% CI for the estimate for the mean plasma sodium change during “Na control” treatments marginally overlapped the lower border of the predefined margin ±1.0 mmol/L, the variability of intradialytic plasma sodium changes was lower during “Na control” versus “standard fixed Na” treatments. Thus, automated dialysate sodium individualization by “Na control” approaches isonatremic dialysis in the clinical setting. |
format | Online Article Text |
id | pubmed-6850400 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-68504002019-11-18 Automated individualization of dialysate sodium concentration reduces intradialytic plasma sodium changes in hemodialysis Ságová, Michaela Wojke, Ralf Maierhofer, Andreas Gross, Malte Canaud, Bernard Gauly, Adelheid Artif Organs Main Text Articles In standard care, hemodialysis patients are often treated with a center‐specific fixed dialysate sodium concentration, potentially resulting in diffusive sodium changes for patients with plasma sodium concentrations below or above this level. While diffusive sodium load may be associated with thirst and higher interdialytic weight gain, excessive diffusive sodium removal may cause intradialytic symptoms. In contrast, the new hemodialysis machine option “Na control” provides automated individualization of dialysate sodium during treatment with the aim to reduce such intradialytic sodium changes without the need to determine the plasma sodium concentration. This proof‐of‐principle study on sodium control was designed as a monocentric randomized controlled crossover trial: 32 patients with residual diuresis of ≤1000 mL/day were enrolled to be treated by high‐volume post‐dilution hemodiafiltration (HDF) for 2 weeks each with “Na control” (individually and automatically adjusted dialysate sodium concentration) versus “standard fixed Na” (fixed dialysate sodium 138 mmol/L), in randomized order. Pre‐ and post‐dialytic plasma sodium concentrations were determined at bedside by direct potentiometry. The study hypothesis consisted of 2 components: the mean plasma sodium change between the start and end of the treatment being within ±1.0 mmol/L for sodium‐controlled treatments, and a lower variability of the plasma sodium changes for “Na control” than for “standard fixed Na” treatments. Three hundred seventy‐two treatments of 31 adult chronic hemodialysis patients (intention‐to‐treat population) were analyzed. The estimate for the mean plasma sodium change was −0.53 mmol/L (95% confidence interval: [−1.04; −0.02] mmol/L) for “Na control” treatments and −0.95 mmol/L (95% CI: [−1.76; −0.15] mmol/L) for “standard fixed Na” treatments. The standard deviation of the plasma sodium changes was 1.39 mmol/L for “Na control” versus 2.19 mmol/L for “standard fixed Na” treatments (P = 0.0004). Whereas the 95% CI for the estimate for the mean plasma sodium change during “Na control” treatments marginally overlapped the lower border of the predefined margin ±1.0 mmol/L, the variability of intradialytic plasma sodium changes was lower during “Na control” versus “standard fixed Na” treatments. Thus, automated dialysate sodium individualization by “Na control” approaches isonatremic dialysis in the clinical setting. John Wiley and Sons Inc. 2019-04-29 2019-10 /pmc/articles/PMC6850400/ /pubmed/30939213 http://dx.doi.org/10.1111/aor.13463 Text en © 2019 The Authors. Artificial Organs published by Wiley Periodicals, Inc. on behalf of International Center for Artificial Organ and Transplantation (ICAOT) This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Main Text Articles Ságová, Michaela Wojke, Ralf Maierhofer, Andreas Gross, Malte Canaud, Bernard Gauly, Adelheid Automated individualization of dialysate sodium concentration reduces intradialytic plasma sodium changes in hemodialysis |
title | Automated individualization of dialysate sodium concentration reduces intradialytic plasma sodium changes in hemodialysis |
title_full | Automated individualization of dialysate sodium concentration reduces intradialytic plasma sodium changes in hemodialysis |
title_fullStr | Automated individualization of dialysate sodium concentration reduces intradialytic plasma sodium changes in hemodialysis |
title_full_unstemmed | Automated individualization of dialysate sodium concentration reduces intradialytic plasma sodium changes in hemodialysis |
title_short | Automated individualization of dialysate sodium concentration reduces intradialytic plasma sodium changes in hemodialysis |
title_sort | automated individualization of dialysate sodium concentration reduces intradialytic plasma sodium changes in hemodialysis |
topic | Main Text Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6850400/ https://www.ncbi.nlm.nih.gov/pubmed/30939213 http://dx.doi.org/10.1111/aor.13463 |
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