Evaluation of hemodynamic effects of xenon in dogs undergoing hemorrhagic shock
Autor(a) principal: | |
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Data de Publicação: | 2013 |
Outros Autores: | , , , , |
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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Clinics |
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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 |
_version_ |
1800222759741030400 |