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Theoretical effect of hyperventilation on speed of recovery and risk of rehypnotization following recovery - a GasMan(®) simulation
BACKGROUND: Hyperventilation may be used to hasten recovery from general anesthesia with potent inhaled anesthetics. However, its effect may be less pronounced with the newer, less soluble agents, and it may result in rehypnotization if subsequent hypoventilation occurs because more residual anesthe...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3502091/ https://www.ncbi.nlm.nih.gov/pubmed/22989260 http://dx.doi.org/10.1186/1471-2253-12-22 |
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author | De Wolf, Andre M Van Zundert, Tom C De Cooman, Sofie Hendrickx, Jan F |
author_facet | De Wolf, Andre M Van Zundert, Tom C De Cooman, Sofie Hendrickx, Jan F |
author_sort | De Wolf, Andre M |
collection | PubMed |
description | BACKGROUND: Hyperventilation may be used to hasten recovery from general anesthesia with potent inhaled anesthetics. However, its effect may be less pronounced with the newer, less soluble agents, and it may result in rehypnotization if subsequent hypoventilation occurs because more residual anesthetic will be available in the body for redistribution to the central nervous system. We used GasMan(®) simulations to examine these issues. METHODS: One MAC of isoflurane, sevoflurane, or desflurane was administered to a fictitious 70 kg patient for 8 h with normoventilation (alveolar minute ventilation [V(A)] 5 L.min(-1)), resulting in full saturation of the vessel rich group (VRG) and >95% saturation of the muscle group. After 8 h, agent administration was stopped, and fresh gas flow was increased to 10 L.min(-1) to avoid rebreathing. At that same time, we continued with one simulation where normoventilation was maintained, while in a second simulation hyperventilation was instituted (10 L.min(-1)). We determined the time needed for the partial pressure in the VRG (F(VRG); representing the central nervous system) to reach 0.3 MAC (MACawake). After reaching MACawake in the VRG, several degrees of hypoventilation were instituted (V(A) of 2.5, 1.5, 1, and 0.5 L.min(-1)) to determine whether F(VRG) would increase above 0.3 MAC(= rehypnotization). RESULTS: Time to reach 0.3 MAC in the VRG with normoventilation was 14 min 42 s with isoflurane, 9 min 12 s with sevoflurane, and 6 min 12 s with desflurane. Hyperventilation reduced these recovery times by 30, 18, and 13% for isoflurane, sevoflurane, and desflurane, respectively. Rehypnotization was observed with V(A) of 0.5 L.min(-1) with desflurane, 0.5 and 1 L.min(-1) with sevoflurane, and 0.5, 1, 1.5, and 2.5 L.min(-1) with isoflurane. Only with isoflurane did initial hyperventilation slightly increase the risk of rehypnotization. CONCLUSIONS: These GasMan(®) simulations confirm that the use of hyperventilation to hasten recovery is marginally beneficial with the newer, less soluble agents. In addition, subsequent hypoventilation results in rehypnotization only with more soluble agents, unless hypoventilation is severe. Also, initial hyperventilation does not increase the risk of rehypnotization with less soluble agents when subsequent hypoventilation occurs. Well-controlled clinical studies are required to validate these simulations. |
format | Online Article Text |
id | pubmed-3502091 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-35020912012-11-21 Theoretical effect of hyperventilation on speed of recovery and risk of rehypnotization following recovery - a GasMan(®) simulation De Wolf, Andre M Van Zundert, Tom C De Cooman, Sofie Hendrickx, Jan F BMC Anesthesiol Research Article BACKGROUND: Hyperventilation may be used to hasten recovery from general anesthesia with potent inhaled anesthetics. However, its effect may be less pronounced with the newer, less soluble agents, and it may result in rehypnotization if subsequent hypoventilation occurs because more residual anesthetic will be available in the body for redistribution to the central nervous system. We used GasMan(®) simulations to examine these issues. METHODS: One MAC of isoflurane, sevoflurane, or desflurane was administered to a fictitious 70 kg patient for 8 h with normoventilation (alveolar minute ventilation [V(A)] 5 L.min(-1)), resulting in full saturation of the vessel rich group (VRG) and >95% saturation of the muscle group. After 8 h, agent administration was stopped, and fresh gas flow was increased to 10 L.min(-1) to avoid rebreathing. At that same time, we continued with one simulation where normoventilation was maintained, while in a second simulation hyperventilation was instituted (10 L.min(-1)). We determined the time needed for the partial pressure in the VRG (F(VRG); representing the central nervous system) to reach 0.3 MAC (MACawake). After reaching MACawake in the VRG, several degrees of hypoventilation were instituted (V(A) of 2.5, 1.5, 1, and 0.5 L.min(-1)) to determine whether F(VRG) would increase above 0.3 MAC(= rehypnotization). RESULTS: Time to reach 0.3 MAC in the VRG with normoventilation was 14 min 42 s with isoflurane, 9 min 12 s with sevoflurane, and 6 min 12 s with desflurane. Hyperventilation reduced these recovery times by 30, 18, and 13% for isoflurane, sevoflurane, and desflurane, respectively. Rehypnotization was observed with V(A) of 0.5 L.min(-1) with desflurane, 0.5 and 1 L.min(-1) with sevoflurane, and 0.5, 1, 1.5, and 2.5 L.min(-1) with isoflurane. Only with isoflurane did initial hyperventilation slightly increase the risk of rehypnotization. CONCLUSIONS: These GasMan(®) simulations confirm that the use of hyperventilation to hasten recovery is marginally beneficial with the newer, less soluble agents. In addition, subsequent hypoventilation results in rehypnotization only with more soluble agents, unless hypoventilation is severe. Also, initial hyperventilation does not increase the risk of rehypnotization with less soluble agents when subsequent hypoventilation occurs. Well-controlled clinical studies are required to validate these simulations. BioMed Central 2012-09-18 /pmc/articles/PMC3502091/ /pubmed/22989260 http://dx.doi.org/10.1186/1471-2253-12-22 Text en Copyright ©2012 De Wolf 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 Article De Wolf, Andre M Van Zundert, Tom C De Cooman, Sofie Hendrickx, Jan F Theoretical effect of hyperventilation on speed of recovery and risk of rehypnotization following recovery - a GasMan(®) simulation |
title | Theoretical effect of hyperventilation on speed of recovery and risk of rehypnotization following recovery - a GasMan(®) simulation |
title_full | Theoretical effect of hyperventilation on speed of recovery and risk of rehypnotization following recovery - a GasMan(®) simulation |
title_fullStr | Theoretical effect of hyperventilation on speed of recovery and risk of rehypnotization following recovery - a GasMan(®) simulation |
title_full_unstemmed | Theoretical effect of hyperventilation on speed of recovery and risk of rehypnotization following recovery - a GasMan(®) simulation |
title_short | Theoretical effect of hyperventilation on speed of recovery and risk of rehypnotization following recovery - a GasMan(®) simulation |
title_sort | theoretical effect of hyperventilation on speed of recovery and risk of rehypnotization following recovery - a gasman(®) simulation |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3502091/ https://www.ncbi.nlm.nih.gov/pubmed/22989260 http://dx.doi.org/10.1186/1471-2253-12-22 |
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