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Phosphate-containing dialysis solution prevents hypophosphatemia during continuous renal replacement therapy

BACKGROUND: Hypophosphatemia occurs in up to 80% of the patients during continuous renal replacement therapy (CRRT). Phosphate supplementation is time-consuming and the phosphate level might be dangerously low before normophosphatemia is re-established. This study evaluated the possibility to preven...

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Autores principales: BROMAN, M, CARLSSON, O, FRIBERG, H, WIESLANDER, A, GODALY, G
Formato: Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3015056/
https://www.ncbi.nlm.nih.gov/pubmed/21039362
http://dx.doi.org/10.1111/j.1399-6576.2010.02338.x
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author BROMAN, M
CARLSSON, O
FRIBERG, H
WIESLANDER, A
GODALY, G
author_facet BROMAN, M
CARLSSON, O
FRIBERG, H
WIESLANDER, A
GODALY, G
author_sort BROMAN, M
collection PubMed
description BACKGROUND: Hypophosphatemia occurs in up to 80% of the patients during continuous renal replacement therapy (CRRT). Phosphate supplementation is time-consuming and the phosphate level might be dangerously low before normophosphatemia is re-established. This study evaluated the possibility to prevent hypophosphatemia during CRRT treatment by using a new commercially available phosphate-containing dialysis fluid. METHODS: Forty-two heterogeneous intensive care unit patients, admitted between January 2007 and July 2008, undergoing hemodiafiltration, were treated with a new Gambro dialysis solution with 1.2 mM phosphate (Phoxilium) or with standard medical treatment (Hemosol B0). The patients were divided into three groups: group 1 (n=14) receiving standard medical treatment and intravenous phosphate supplementation as required, group 2 (n=14) receiving the phosphate solution as dialysate solution and Hemosol B0 as replacement solution and group 3 (n=14) receiving the phosphate-containing solution as both dialysate and replacement solutions. RESULTS: Standard medical treatment resulted in hypophosphatemia in 11 of 14 of the patients (group 1) compared with five of 14 in the patients receiving phosphate solution as the dialysate solution and Hemosol B0 as the replacement solution (group 2). Patients treated with the phosphate-containing dialysis solution (group 3) experienced stable serum phosphate levels throughout the study. Potassium, ionized calcium, magnesium, pH, pCO(2) and bicarbonate remained unchanged throughout the study. CONCLUSION: The new phosphate-containing replacement and dialysis solution reduces the variability of serum phosphate levels during CRRT and eliminates the incidence of hypophosphatemia.
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spelling pubmed-30150562011-01-08 Phosphate-containing dialysis solution prevents hypophosphatemia during continuous renal replacement therapy BROMAN, M CARLSSON, O FRIBERG, H WIESLANDER, A GODALY, G Acta Anaesthesiol Scand Intensive Care & Physiology BACKGROUND: Hypophosphatemia occurs in up to 80% of the patients during continuous renal replacement therapy (CRRT). Phosphate supplementation is time-consuming and the phosphate level might be dangerously low before normophosphatemia is re-established. This study evaluated the possibility to prevent hypophosphatemia during CRRT treatment by using a new commercially available phosphate-containing dialysis fluid. METHODS: Forty-two heterogeneous intensive care unit patients, admitted between January 2007 and July 2008, undergoing hemodiafiltration, were treated with a new Gambro dialysis solution with 1.2 mM phosphate (Phoxilium) or with standard medical treatment (Hemosol B0). The patients were divided into three groups: group 1 (n=14) receiving standard medical treatment and intravenous phosphate supplementation as required, group 2 (n=14) receiving the phosphate solution as dialysate solution and Hemosol B0 as replacement solution and group 3 (n=14) receiving the phosphate-containing solution as both dialysate and replacement solutions. RESULTS: Standard medical treatment resulted in hypophosphatemia in 11 of 14 of the patients (group 1) compared with five of 14 in the patients receiving phosphate solution as the dialysate solution and Hemosol B0 as the replacement solution (group 2). Patients treated with the phosphate-containing dialysis solution (group 3) experienced stable serum phosphate levels throughout the study. Potassium, ionized calcium, magnesium, pH, pCO(2) and bicarbonate remained unchanged throughout the study. CONCLUSION: The new phosphate-containing replacement and dialysis solution reduces the variability of serum phosphate levels during CRRT and eliminates the incidence of hypophosphatemia. Blackwell Publishing Ltd 2011-01 /pmc/articles/PMC3015056/ /pubmed/21039362 http://dx.doi.org/10.1111/j.1399-6576.2010.02338.x Text en Acta Anaesthesiologica Scandinavica © 2011 The Acta Anaesthesiologica Scandinavica Foundation http://creativecommons.org/licenses/by/2.5/ Re-use of this article is permitted in accordance with the Creative Commons Deed, Attribution 2.5, which does not permit commercial exploitation.
spellingShingle Intensive Care & Physiology
BROMAN, M
CARLSSON, O
FRIBERG, H
WIESLANDER, A
GODALY, G
Phosphate-containing dialysis solution prevents hypophosphatemia during continuous renal replacement therapy
title Phosphate-containing dialysis solution prevents hypophosphatemia during continuous renal replacement therapy
title_full Phosphate-containing dialysis solution prevents hypophosphatemia during continuous renal replacement therapy
title_fullStr Phosphate-containing dialysis solution prevents hypophosphatemia during continuous renal replacement therapy
title_full_unstemmed Phosphate-containing dialysis solution prevents hypophosphatemia during continuous renal replacement therapy
title_short Phosphate-containing dialysis solution prevents hypophosphatemia during continuous renal replacement therapy
title_sort phosphate-containing dialysis solution prevents hypophosphatemia during continuous renal replacement therapy
topic Intensive Care & Physiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3015056/
https://www.ncbi.nlm.nih.gov/pubmed/21039362
http://dx.doi.org/10.1111/j.1399-6576.2010.02338.x
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