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Interactions between the volume effects of hydroxyethyl starch 130/0.4 and Ringer´s acetate
INTRODUCTION: The turnover of Ringer´s solutions is greatly dependent on the physiological situation, such as the presence of dehydration or anaesthesia. The present study evaluates whether the kinetics is affected by previous infusion of colloid fluid. METHODS: Ten male volunteers with a mean age o...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4057308/ https://www.ncbi.nlm.nih.gov/pubmed/23718743 http://dx.doi.org/10.1186/cc12749 |
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author | Hahn, Robert G Bergek, Christian Gebäck, Tobias Zdolsek, Joachim |
author_facet | Hahn, Robert G Bergek, Christian Gebäck, Tobias Zdolsek, Joachim |
author_sort | Hahn, Robert G |
collection | PubMed |
description | INTRODUCTION: The turnover of Ringer´s solutions is greatly dependent on the physiological situation, such as the presence of dehydration or anaesthesia. The present study evaluates whether the kinetics is affected by previous infusion of colloid fluid. METHODS: Ten male volunteers with a mean age of 22 years underwent three infusion experiments, on separate days and in random order. The experiments included 10 mL/kg of 6% hydroxyethyl starch 130/0.4 (Voluven™), 20 mL/kg of Ringer's acetate, and a combination of both, where Ringer´s was administered 75 minutes after the starch infusion ended. The kinetics of the volume expansion was analysed by non-linear least- squares regression, based on urinary excretion and serial measurement of blood haemoglobin concentration for up to 420 minutes. RESULTS: The mean volume of distribution of the starch was 3.12 L which agreed well with the plasma volume (3.14 L) estimated by anthropometry. The volume expansion following the infusion of starch showed monoexponential elimination kinetics with a half-life of two hours. Two interaction effects were found when Ringer´s acetate was infused after the starch. First, there was a higher tendency for Ringer´s acetate to distribute to a peripheral compartment at the expense of the plasma volume expansion. The translocated amount of Ringer´s was 70% higher when HES had been infused earlier. Second, the elimination half-life of Ringer´s acetate was five times longer when administered after the starch (88 versus 497 minutes, P <0.02). CONCLUSIONS: Starch promoted peripheral accumulation of the later infused Ringer´s acetate solution and markedly prolonged the elimination half-life. TRIAL REGISTRATION: ClinicalTrials.gov: NCT01195025 |
format | Online Article Text |
id | pubmed-4057308 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-40573082014-10-23 Interactions between the volume effects of hydroxyethyl starch 130/0.4 and Ringer´s acetate Hahn, Robert G Bergek, Christian Gebäck, Tobias Zdolsek, Joachim Crit Care Research INTRODUCTION: The turnover of Ringer´s solutions is greatly dependent on the physiological situation, such as the presence of dehydration or anaesthesia. The present study evaluates whether the kinetics is affected by previous infusion of colloid fluid. METHODS: Ten male volunteers with a mean age of 22 years underwent three infusion experiments, on separate days and in random order. The experiments included 10 mL/kg of 6% hydroxyethyl starch 130/0.4 (Voluven™), 20 mL/kg of Ringer's acetate, and a combination of both, where Ringer´s was administered 75 minutes after the starch infusion ended. The kinetics of the volume expansion was analysed by non-linear least- squares regression, based on urinary excretion and serial measurement of blood haemoglobin concentration for up to 420 minutes. RESULTS: The mean volume of distribution of the starch was 3.12 L which agreed well with the plasma volume (3.14 L) estimated by anthropometry. The volume expansion following the infusion of starch showed monoexponential elimination kinetics with a half-life of two hours. Two interaction effects were found when Ringer´s acetate was infused after the starch. First, there was a higher tendency for Ringer´s acetate to distribute to a peripheral compartment at the expense of the plasma volume expansion. The translocated amount of Ringer´s was 70% higher when HES had been infused earlier. Second, the elimination half-life of Ringer´s acetate was five times longer when administered after the starch (88 versus 497 minutes, P <0.02). CONCLUSIONS: Starch promoted peripheral accumulation of the later infused Ringer´s acetate solution and markedly prolonged the elimination half-life. TRIAL REGISTRATION: ClinicalTrials.gov: NCT01195025 BioMed Central 2013 2013-05-29 /pmc/articles/PMC4057308/ /pubmed/23718743 http://dx.doi.org/10.1186/cc12749 Text en Copyright © 2013 Hahn et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Hahn, Robert G Bergek, Christian Gebäck, Tobias Zdolsek, Joachim Interactions between the volume effects of hydroxyethyl starch 130/0.4 and Ringer´s acetate |
title | Interactions between the volume effects of hydroxyethyl starch 130/0.4 and Ringer´s acetate |
title_full | Interactions between the volume effects of hydroxyethyl starch 130/0.4 and Ringer´s acetate |
title_fullStr | Interactions between the volume effects of hydroxyethyl starch 130/0.4 and Ringer´s acetate |
title_full_unstemmed | Interactions between the volume effects of hydroxyethyl starch 130/0.4 and Ringer´s acetate |
title_short | Interactions between the volume effects of hydroxyethyl starch 130/0.4 and Ringer´s acetate |
title_sort | interactions between the volume effects of hydroxyethyl starch 130/0.4 and ringer´s acetate |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4057308/ https://www.ncbi.nlm.nih.gov/pubmed/23718743 http://dx.doi.org/10.1186/cc12749 |
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