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Sevoflurane concentration for cannulation in developmental disabilities
OBJECTIVE: The goal of this study was to compare the end-tidal sevoflurane concentration and time for intravenous cannulation at induction of anesthesia using sevoflurane with or without nitrous oxide in healthy children and in those with developmental disabilities. METHODS: Normal and developmental...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9109363/ https://www.ncbi.nlm.nih.gov/pubmed/35578184 http://dx.doi.org/10.1186/s12871-022-01695-5 |
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author | Kunihiro, Naou Tsukamoto, Masanori Taura, Shiori Hitosugi, Takashi Miki, Yoichiro Yokoyama, Takeshi |
author_facet | Kunihiro, Naou Tsukamoto, Masanori Taura, Shiori Hitosugi, Takashi Miki, Yoichiro Yokoyama, Takeshi |
author_sort | Kunihiro, Naou |
collection | PubMed |
description | OBJECTIVE: The goal of this study was to compare the end-tidal sevoflurane concentration and time for intravenous cannulation at induction of anesthesia using sevoflurane with or without nitrous oxide in healthy children and in those with developmental disabilities. METHODS: Normal and developmentally disabled children were anesthetized by inhalation of sevoflurane with nitrous oxide or with nitrous oxide-free oxygen, and intravenous cannulae were introduced. Nitrous oxide was stopped after loss of consciousness. The following parameters were recorded for each patient: age, gender, height, weight, BMI, duration of intravenous cannulation, end-tidal concentration of sevoflurane at the completion of intravenous cannulation, and use of nitrous oxide. For each parameter except gender, p-value were calculated by one-way analysis of variance (ANOVA). For gender, p-value were calculated using the Fisher method. Two-way ANOVA was performed to evaluate the effect of patient health status and nitrous oxide use on the end-tidal concentrations of sevoflurane and the time required for intravenous cannulation. RESULTS: The end-tidal sevoflurane concentrations at the completion of the intravenous cannulation had received a significant main effect of the factor "the use of nitrous oxide" (F(1,166) = 25.8, p < 0.001, η(2) = 0.13) and a small effect of the factor "the patient health status" (F(1,166) = 0.259, p = 0.611, η(2) = 0.001). However, the time required for intravenous cannulation was not significantly affected by either of the two factors, "the use of nitrous oxide" (F(1,166) = 0.454, p = 0.501, η(2) = 0.003) and "the patient health status" (F(1,166) = 0.308, p = 0.579, η(2) = 0.002). CONCLUSIONS: Between the healthy children and the children with developmental disabilities, no significant differences in the time required for the intravenous cannulation from the beginning of anesthetic induction. However, the end-tidal sevoflurane concentrations at the completion of the intravenous cannulation was significantly different. Sevoflurane in alveoli might be diluted by nitrous oxide. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12871-022-01695-5. |
format | Online Article Text |
id | pubmed-9109363 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-91093632022-05-17 Sevoflurane concentration for cannulation in developmental disabilities Kunihiro, Naou Tsukamoto, Masanori Taura, Shiori Hitosugi, Takashi Miki, Yoichiro Yokoyama, Takeshi BMC Anesthesiol Research OBJECTIVE: The goal of this study was to compare the end-tidal sevoflurane concentration and time for intravenous cannulation at induction of anesthesia using sevoflurane with or without nitrous oxide in healthy children and in those with developmental disabilities. METHODS: Normal and developmentally disabled children were anesthetized by inhalation of sevoflurane with nitrous oxide or with nitrous oxide-free oxygen, and intravenous cannulae were introduced. Nitrous oxide was stopped after loss of consciousness. The following parameters were recorded for each patient: age, gender, height, weight, BMI, duration of intravenous cannulation, end-tidal concentration of sevoflurane at the completion of intravenous cannulation, and use of nitrous oxide. For each parameter except gender, p-value were calculated by one-way analysis of variance (ANOVA). For gender, p-value were calculated using the Fisher method. Two-way ANOVA was performed to evaluate the effect of patient health status and nitrous oxide use on the end-tidal concentrations of sevoflurane and the time required for intravenous cannulation. RESULTS: The end-tidal sevoflurane concentrations at the completion of the intravenous cannulation had received a significant main effect of the factor "the use of nitrous oxide" (F(1,166) = 25.8, p < 0.001, η(2) = 0.13) and a small effect of the factor "the patient health status" (F(1,166) = 0.259, p = 0.611, η(2) = 0.001). However, the time required for intravenous cannulation was not significantly affected by either of the two factors, "the use of nitrous oxide" (F(1,166) = 0.454, p = 0.501, η(2) = 0.003) and "the patient health status" (F(1,166) = 0.308, p = 0.579, η(2) = 0.002). CONCLUSIONS: Between the healthy children and the children with developmental disabilities, no significant differences in the time required for the intravenous cannulation from the beginning of anesthetic induction. However, the end-tidal sevoflurane concentrations at the completion of the intravenous cannulation was significantly different. Sevoflurane in alveoli might be diluted by nitrous oxide. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12871-022-01695-5. BioMed Central 2022-05-16 /pmc/articles/PMC9109363/ /pubmed/35578184 http://dx.doi.org/10.1186/s12871-022-01695-5 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Kunihiro, Naou Tsukamoto, Masanori Taura, Shiori Hitosugi, Takashi Miki, Yoichiro Yokoyama, Takeshi Sevoflurane concentration for cannulation in developmental disabilities |
title | Sevoflurane concentration for cannulation in developmental disabilities |
title_full | Sevoflurane concentration for cannulation in developmental disabilities |
title_fullStr | Sevoflurane concentration for cannulation in developmental disabilities |
title_full_unstemmed | Sevoflurane concentration for cannulation in developmental disabilities |
title_short | Sevoflurane concentration for cannulation in developmental disabilities |
title_sort | sevoflurane concentration for cannulation in developmental disabilities |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9109363/ https://www.ncbi.nlm.nih.gov/pubmed/35578184 http://dx.doi.org/10.1186/s12871-022-01695-5 |
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