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Intraosseous and intravenous administration of antibiotics yields comparable plasma concentrations during experimental septic shock

BACKGROUND: We aimed to investigate whether comparable antibiotic concentrations could be reached with intraosseous and intravenous administration during septic shock. METHODS: In this randomized, prospective experimental study conducted at an animal research laboratory at the University Hospital of...

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Autores principales: Strandberg, G, Larsson, A, Lipcsey, M, Michalek, J, Eriksson, M
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4338763/
https://www.ncbi.nlm.nih.gov/pubmed/25557933
http://dx.doi.org/10.1111/aas.12454
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author Strandberg, G
Larsson, A
Lipcsey, M
Michalek, J
Eriksson, M
author_facet Strandberg, G
Larsson, A
Lipcsey, M
Michalek, J
Eriksson, M
author_sort Strandberg, G
collection PubMed
description BACKGROUND: We aimed to investigate whether comparable antibiotic concentrations could be reached with intraosseous and intravenous administration during septic shock. METHODS: In this randomized, prospective experimental study conducted at an animal research laboratory at the University Hospital of Uppsala, eight anesthetized pigs, weighing 21.2 to 29.1 kg (mean: 25.2 ± 2.3 kg), received endotoxin infusion at 4 μg/kg/h for 6 h. At the onset of clinical shock, alternatively after 3 h of endotoxemia, they received 75 mg/kg of cefotaxime and 7 mg/kg of gentamicin either in a proximal tibial intraosseous catheter or in a peripheral intravenous catheter. Mixed venous samples were taken after 5, 15, 30, 60, 120 and 180 min and analyzed for antibiotic concentrations. RESULTS: For both antibiotics, plasma concentrations after intraosseous and intravenous administration followed similar curves throughout the observation period, and peak concentrations were comparable. Mean concentration area under the curve (AUC mg × h/l) for cefotaxime was 108.1 ± 19.5 after intraosseous and 116.5 ± 11.1 after intravenous administration; ratio 0.93, (95% CI 0.71–1.19). Mean AUC for gentamicin was 28.1 ± 6.8 for intraosseous and 32.2 ± 3.5 for intravenous administration; ratio 0.87 (95% CI 0.62–1.19). CONCLUSIONS: In this porcine septic shock model, intraosseous and intravenous administration of gentamicin and cefotaxime yielded comparable concentrations. In an emergency, intraosseous administration of these antibiotics may be considered in severe infections when venous access is difficult.
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spelling pubmed-43387632015-03-04 Intraosseous and intravenous administration of antibiotics yields comparable plasma concentrations during experimental septic shock Strandberg, G Larsson, A Lipcsey, M Michalek, J Eriksson, M Acta Anaesthesiol Scand Intensive Care and Physiology BACKGROUND: We aimed to investigate whether comparable antibiotic concentrations could be reached with intraosseous and intravenous administration during septic shock. METHODS: In this randomized, prospective experimental study conducted at an animal research laboratory at the University Hospital of Uppsala, eight anesthetized pigs, weighing 21.2 to 29.1 kg (mean: 25.2 ± 2.3 kg), received endotoxin infusion at 4 μg/kg/h for 6 h. At the onset of clinical shock, alternatively after 3 h of endotoxemia, they received 75 mg/kg of cefotaxime and 7 mg/kg of gentamicin either in a proximal tibial intraosseous catheter or in a peripheral intravenous catheter. Mixed venous samples were taken after 5, 15, 30, 60, 120 and 180 min and analyzed for antibiotic concentrations. RESULTS: For both antibiotics, plasma concentrations after intraosseous and intravenous administration followed similar curves throughout the observation period, and peak concentrations were comparable. Mean concentration area under the curve (AUC mg × h/l) for cefotaxime was 108.1 ± 19.5 after intraosseous and 116.5 ± 11.1 after intravenous administration; ratio 0.93, (95% CI 0.71–1.19). Mean AUC for gentamicin was 28.1 ± 6.8 for intraosseous and 32.2 ± 3.5 for intravenous administration; ratio 0.87 (95% CI 0.62–1.19). CONCLUSIONS: In this porcine septic shock model, intraosseous and intravenous administration of gentamicin and cefotaxime yielded comparable concentrations. In an emergency, intraosseous administration of these antibiotics may be considered in severe infections when venous access is difficult. Blackwell Publishing Ltd 2015-03 2015-01-05 /pmc/articles/PMC4338763/ /pubmed/25557933 http://dx.doi.org/10.1111/aas.12454 Text en © 2015 The Authors. The Acta Anaesthesiologica Scandinavica Foundation. Published by John Wiley & Sons Ltd. http://creativecommons.org/licenses/by-nc/4.0/ This is an open access article under the terms of the Creative Commons Attribution-NonCommercial License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Intensive Care and Physiology
Strandberg, G
Larsson, A
Lipcsey, M
Michalek, J
Eriksson, M
Intraosseous and intravenous administration of antibiotics yields comparable plasma concentrations during experimental septic shock
title Intraosseous and intravenous administration of antibiotics yields comparable plasma concentrations during experimental septic shock
title_full Intraosseous and intravenous administration of antibiotics yields comparable plasma concentrations during experimental septic shock
title_fullStr Intraosseous and intravenous administration of antibiotics yields comparable plasma concentrations during experimental septic shock
title_full_unstemmed Intraosseous and intravenous administration of antibiotics yields comparable plasma concentrations during experimental septic shock
title_short Intraosseous and intravenous administration of antibiotics yields comparable plasma concentrations during experimental septic shock
title_sort intraosseous and intravenous administration of antibiotics yields comparable plasma concentrations during experimental septic shock
topic Intensive Care and Physiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4338763/
https://www.ncbi.nlm.nih.gov/pubmed/25557933
http://dx.doi.org/10.1111/aas.12454
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