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Optimal doses of sevoflurane and propofol in rabbits

BACKGROUND: Although sevoflurane and propofol are commonly used anesthetics in rabbits, optimal doses of remain unclear. We thus assessed the optimal hypnotic doses of sevoflurane and propofol, and evaluated the influence of dexmedetomidine on sevoflurane and propofol requirements. METHODS: Twenty-e...

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Autores principales: Terada, Yoshihide, Ishiyama, Tadahiko, Asano, Nobumasa, Kotoda, Masakazu, Ikemoto, Kodai, Shintani, Noriyuki, Sessler, Daniel I, Matsukawa, Takashi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4289294/
https://www.ncbi.nlm.nih.gov/pubmed/25409660
http://dx.doi.org/10.1186/1756-0500-7-820
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author Terada, Yoshihide
Ishiyama, Tadahiko
Asano, Nobumasa
Kotoda, Masakazu
Ikemoto, Kodai
Shintani, Noriyuki
Sessler, Daniel I
Matsukawa, Takashi
author_facet Terada, Yoshihide
Ishiyama, Tadahiko
Asano, Nobumasa
Kotoda, Masakazu
Ikemoto, Kodai
Shintani, Noriyuki
Sessler, Daniel I
Matsukawa, Takashi
author_sort Terada, Yoshihide
collection PubMed
description BACKGROUND: Although sevoflurane and propofol are commonly used anesthetics in rabbits, optimal doses of remain unclear. We thus assessed the optimal hypnotic doses of sevoflurane and propofol, and evaluated the influence of dexmedetomidine on sevoflurane and propofol requirements. METHODS: Twenty-eight Japanese white rabbits were randomly assigned to one of four groups (n = 7 each). Rabbits were given either sevoflurane, propofol, sevoflurane + dexmedetomidine, or propofol + dexmedetomidine (injected 30 μg∙kg(-1)∙hr(-1) for 10 min followed by an infusion of 3.5 μg∙kg(-1)∙hr(-1)). Hypnotic level was evaluated with Bispectral Index (BIS), a well-validated electroenchalographic measure, with values between 40 and 60 representing optimal hypnosis. BIS measurements were made 10 minutes after the adjustment of target end-tidal sevoflurane concentration in the sevoflurane group and sevoflurane + dexmedetomidine group, and at 10 min after the change of infusion rate in the propofol group and propofol + dexmedetomidine group. RESULTS: BIS values were linearly related to sevoflurane concentration and propofol infusion rate, with or without dexmedetomidine. Sevoflurane concentration at BIS = 50 was 3.9 ± 0.2% in the sevoflurane group and 2.6 ± 0.3% in the sevoflurane + dexmedetomidine group. The propofol infusion rate to make BIS = 50 was 102 ± 5 mg∙kg(-1)∙hr(-1) in the propofol group, and 90 ± 10 mg∙kg(-1)∙hr(-1) in the propofol + dexmedetomidine group. CONCLUSIONS: The optimal end-tidal concentration of sevoflurane alone was thus 3.9%, and optimal infusion rate for propofol alone was 102 mg∙kg(-1)∙hr(-1). Dexmedetomidine reduced sevoflurane requirement by 33% and propofol requirement by 11%.
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spelling pubmed-42892942015-01-11 Optimal doses of sevoflurane and propofol in rabbits Terada, Yoshihide Ishiyama, Tadahiko Asano, Nobumasa Kotoda, Masakazu Ikemoto, Kodai Shintani, Noriyuki Sessler, Daniel I Matsukawa, Takashi BMC Res Notes Research Article BACKGROUND: Although sevoflurane and propofol are commonly used anesthetics in rabbits, optimal doses of remain unclear. We thus assessed the optimal hypnotic doses of sevoflurane and propofol, and evaluated the influence of dexmedetomidine on sevoflurane and propofol requirements. METHODS: Twenty-eight Japanese white rabbits were randomly assigned to one of four groups (n = 7 each). Rabbits were given either sevoflurane, propofol, sevoflurane + dexmedetomidine, or propofol + dexmedetomidine (injected 30 μg∙kg(-1)∙hr(-1) for 10 min followed by an infusion of 3.5 μg∙kg(-1)∙hr(-1)). Hypnotic level was evaluated with Bispectral Index (BIS), a well-validated electroenchalographic measure, with values between 40 and 60 representing optimal hypnosis. BIS measurements were made 10 minutes after the adjustment of target end-tidal sevoflurane concentration in the sevoflurane group and sevoflurane + dexmedetomidine group, and at 10 min after the change of infusion rate in the propofol group and propofol + dexmedetomidine group. RESULTS: BIS values were linearly related to sevoflurane concentration and propofol infusion rate, with or without dexmedetomidine. Sevoflurane concentration at BIS = 50 was 3.9 ± 0.2% in the sevoflurane group and 2.6 ± 0.3% in the sevoflurane + dexmedetomidine group. The propofol infusion rate to make BIS = 50 was 102 ± 5 mg∙kg(-1)∙hr(-1) in the propofol group, and 90 ± 10 mg∙kg(-1)∙hr(-1) in the propofol + dexmedetomidine group. CONCLUSIONS: The optimal end-tidal concentration of sevoflurane alone was thus 3.9%, and optimal infusion rate for propofol alone was 102 mg∙kg(-1)∙hr(-1). Dexmedetomidine reduced sevoflurane requirement by 33% and propofol requirement by 11%. BioMed Central 2014-11-19 /pmc/articles/PMC4289294/ /pubmed/25409660 http://dx.doi.org/10.1186/1756-0500-7-820 Text en © Terada et al.; licensee BioMed Central Ltd. 2014 This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Terada, Yoshihide
Ishiyama, Tadahiko
Asano, Nobumasa
Kotoda, Masakazu
Ikemoto, Kodai
Shintani, Noriyuki
Sessler, Daniel I
Matsukawa, Takashi
Optimal doses of sevoflurane and propofol in rabbits
title Optimal doses of sevoflurane and propofol in rabbits
title_full Optimal doses of sevoflurane and propofol in rabbits
title_fullStr Optimal doses of sevoflurane and propofol in rabbits
title_full_unstemmed Optimal doses of sevoflurane and propofol in rabbits
title_short Optimal doses of sevoflurane and propofol in rabbits
title_sort optimal doses of sevoflurane and propofol in rabbits
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4289294/
https://www.ncbi.nlm.nih.gov/pubmed/25409660
http://dx.doi.org/10.1186/1756-0500-7-820
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