Evaluation of hemodynamic effects of xenon in dogs undergoing hemorrhagic shock

Detalhes bibliográficos
Autor(a) principal: Franceschi, Ruben C.
Data de Publicação: 2013
Outros Autores: Malbouisson, Luiz, Yoshinaga, Eduardo, Auler Jr., Jose Otavio Costa, Figueiredo, Luiz Francisco Poli de, Carmona, Maria Jose C.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Clinics
Texto Completo: https://www.revistas.usp.br/clinics/article/view/53164
Resumo: OBJECTIVES: The anesthetic gas xenon is reported to preserve hemodynamic stability during general anesthesia. However, the effects of the gas during shock are unclear. The objective of this study was to evaluate the effect of Xe on hemodynamic stability and tissue perfusion in a canine model of hemorrhagic shock. METHOD: Twenty-six dogs, mechanically ventilated with a fraction of inspired oxygen of 21% and anesthetized with etomidate and vecuronium, were randomized into Xenon (Xe; n = 13) or Control (C; n = 13) groups. Following hemodynamic monitoring, a pressure-driven shock was induced to reach an arterial pressure of 40 mmHg. Hemodynamic data and blood samples were collected prior to bleeding, immediately after bleeding and 5, 20 and 40 minutes following shock. The Xe group was treated with 79% Xe diluted in ambient air, inhaled for 20 minutes after shock. RESULT: The mean bleeding volume was 44 mL.kg-1 in the C group and 40 mL.kg-1 in the Xe group. Hemorrhage promoted a decrease in both the cardiac index (p
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spelling Evaluation of hemodynamic effects of xenon in dogs undergoing hemorrhagic shock XenonHemorrhagic ShockGeneral Anesthesia OBJECTIVES: The anesthetic gas xenon is reported to preserve hemodynamic stability during general anesthesia. However, the effects of the gas during shock are unclear. The objective of this study was to evaluate the effect of Xe on hemodynamic stability and tissue perfusion in a canine model of hemorrhagic shock. METHOD: Twenty-six dogs, mechanically ventilated with a fraction of inspired oxygen of 21% and anesthetized with etomidate and vecuronium, were randomized into Xenon (Xe; n = 13) or Control (C; n = 13) groups. Following hemodynamic monitoring, a pressure-driven shock was induced to reach an arterial pressure of 40 mmHg. Hemodynamic data and blood samples were collected prior to bleeding, immediately after bleeding and 5, 20 and 40 minutes following shock. The Xe group was treated with 79% Xe diluted in ambient air, inhaled for 20 minutes after shock. RESULT: The mean bleeding volume was 44 mL.kg-1 in the C group and 40 mL.kg-1 in the Xe group. Hemorrhage promoted a decrease in both the cardiac index (pHospital das Clínicas, Faculdade de Medicina, Universidade de São Paulo2013-01-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfhttps://www.revistas.usp.br/clinics/article/view/5316410.6061/CLINICS/2013(02)OA18Clinics; Vol. 68 No. 2 (2013); 231-238 Clinics; v. 68 n. 2 (2013); 231-238 Clinics; Vol. 68 Núm. 2 (2013); 231-238 1980-53221807-5932reponame:Clinicsinstname:Universidade de São Paulo (USP)instacron:USPenghttps://www.revistas.usp.br/clinics/article/view/53164/57225Franceschi, Ruben C.Malbouisson, LuizYoshinaga, EduardoAuler Jr., Jose Otavio CostaFigueiredo, Luiz Francisco Poli deCarmona, Maria Jose C.info:eu-repo/semantics/openAccess2013-04-08T20:40:36Zoai:revistas.usp.br:article/53164Revistahttps://www.revistas.usp.br/clinicsPUBhttps://www.revistas.usp.br/clinics/oai||clinics@hc.fm.usp.br1980-53221807-5932opendoar:2013-04-08T20:40:36Clinics - Universidade de São Paulo (USP)false
dc.title.none.fl_str_mv Evaluation of hemodynamic effects of xenon in dogs undergoing hemorrhagic shock
title Evaluation of hemodynamic effects of xenon in dogs undergoing hemorrhagic shock
spellingShingle Evaluation of hemodynamic effects of xenon in dogs undergoing hemorrhagic shock
Franceschi, Ruben C.
Xenon
Hemorrhagic Shock
General Anesthesia
title_short Evaluation of hemodynamic effects of xenon in dogs undergoing hemorrhagic shock
title_full Evaluation of hemodynamic effects of xenon in dogs undergoing hemorrhagic shock
title_fullStr Evaluation of hemodynamic effects of xenon in dogs undergoing hemorrhagic shock
title_full_unstemmed Evaluation of hemodynamic effects of xenon in dogs undergoing hemorrhagic shock
title_sort Evaluation of hemodynamic effects of xenon in dogs undergoing hemorrhagic shock
author Franceschi, Ruben C.
author_facet Franceschi, Ruben C.
Malbouisson, Luiz
Yoshinaga, Eduardo
Auler Jr., Jose Otavio Costa
Figueiredo, Luiz Francisco Poli de
Carmona, Maria Jose C.
author_role author
author2 Malbouisson, Luiz
Yoshinaga, Eduardo
Auler Jr., Jose Otavio Costa
Figueiredo, Luiz Francisco Poli de
Carmona, Maria Jose C.
author2_role author
author
author
author
author
dc.contributor.author.fl_str_mv Franceschi, Ruben C.
Malbouisson, Luiz
Yoshinaga, Eduardo
Auler Jr., Jose Otavio Costa
Figueiredo, Luiz Francisco Poli de
Carmona, Maria Jose C.
dc.subject.por.fl_str_mv Xenon
Hemorrhagic Shock
General Anesthesia
topic Xenon
Hemorrhagic Shock
General Anesthesia
description OBJECTIVES: The anesthetic gas xenon is reported to preserve hemodynamic stability during general anesthesia. However, the effects of the gas during shock are unclear. The objective of this study was to evaluate the effect of Xe on hemodynamic stability and tissue perfusion in a canine model of hemorrhagic shock. METHOD: Twenty-six dogs, mechanically ventilated with a fraction of inspired oxygen of 21% and anesthetized with etomidate and vecuronium, were randomized into Xenon (Xe; n = 13) or Control (C; n = 13) groups. Following hemodynamic monitoring, a pressure-driven shock was induced to reach an arterial pressure of 40 mmHg. Hemodynamic data and blood samples were collected prior to bleeding, immediately after bleeding and 5, 20 and 40 minutes following shock. The Xe group was treated with 79% Xe diluted in ambient air, inhaled for 20 minutes after shock. RESULT: The mean bleeding volume was 44 mL.kg-1 in the C group and 40 mL.kg-1 in the Xe group. Hemorrhage promoted a decrease in both the cardiac index (p
publishDate 2013
dc.date.none.fl_str_mv 2013-01-01
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv https://www.revistas.usp.br/clinics/article/view/53164
10.6061/CLINICS/2013(02)OA18
url https://www.revistas.usp.br/clinics/article/view/53164
identifier_str_mv 10.6061/CLINICS/2013(02)OA18
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv https://www.revistas.usp.br/clinics/article/view/53164/57225
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Hospital das Clínicas, Faculdade de Medicina, Universidade de São Paulo
publisher.none.fl_str_mv Hospital das Clínicas, Faculdade de Medicina, Universidade de São Paulo
dc.source.none.fl_str_mv Clinics; Vol. 68 No. 2 (2013); 231-238
Clinics; v. 68 n. 2 (2013); 231-238
Clinics; Vol. 68 Núm. 2 (2013); 231-238
1980-5322
1807-5932
reponame:Clinics
instname:Universidade de São Paulo (USP)
instacron:USP
instname_str Universidade de São Paulo (USP)
instacron_str USP
institution USP
reponame_str Clinics
collection Clinics
repository.name.fl_str_mv Clinics - Universidade de São Paulo (USP)
repository.mail.fl_str_mv ||clinics@hc.fm.usp.br
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