Cardiorespiratory and antinociceptive effects of two different doses of lidocaine administered to horses during a constant intravenous infusion of xylazine and ketamine
Autor(a) principal: | |
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Data de Publicação: | 2013 |
Outros Autores: | , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNESP |
Texto Completo: | http://dx.doi.org/10.1186/1746-6148-9-199 http://hdl.handle.net/11449/111524 |
Resumo: | Background: This study investigated the antinociceptive effects of a constant rate infusion (CRI) of lidocaine during xylazine and ketamine anesthesia in horses and aimed to correlate these effects with cardiorespiratory variables, bispectral index (BIS) and plasma lidocaine concentrations. Six adult crossbred mares weighing 320-400 kg were anesthetized on three different occasions. Sedation was performed with xylazine (0.75 mg/kg IV) and anesthetic induction with guaifenesin (75 mg/kg IV) and ketamine (2 mg/kg IV). Anesthesia was maintained with 37.5 mu g/kg/min of xylazine and 87.5 mu g/kg/min of ketamine both administered intravenously for 75 min. The three treatments consisted of: lidocaine (loading dose: 5 mg/kg, CRI: 100 mu g/kg/min; THL); lidocaine (loading dose: 2.5 mg/kg; CRI: 50 mu g/kg/min: TLL); and saline (TS); all given 15 min after induction and maintained for 1 h. Antinociception was measured by response to electrical stimulation and bispectral index (BIS) was recorded during anesthesia. Parametric and non-parametric data were compared using ANOVA followed by Student-Newman-Keuls and Friedman tests, respectively.Results: Plasma lidocaine concentrations peaked at the end of lidocaine loading dose and was greater in THL (9.61 +/- 2.75 mu g/mL) vs TLL (4.50 +/- 3.34 mu g/mL). Electrical noxious stimulation caused purposeful movement in all horses from TS, but no response in THL. The BIS was decreased in THL only and was less when compared to the other treatments throughout anesthesia. Blood pressure, PaO2 and PaCO2 increased and heart rate (HR), respiratory rate (RR), pH, total plasma protein and temperature decreased during anesthesia in all treatments. PaCO2 and HR were greater and RR and pH less in THL compared to TLL and TS at 30 min during anesthesia. All recoveries were considered excellent. Time to standing was longer after THL (60 +/- 20 min) than following TLL and TS (32 +/- 17 and 30 +/- 15 min, respectively).Conclusions: At the highest dose administered (THL) lidocaine CRI during xylazine/ketamine anesthesia decreased BIS and motor response to noxious stimulation, and prolonged recovery time without significant added cardiorespiratory depression. |
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Cardiorespiratory and antinociceptive effects of two different doses of lidocaine administered to horses during a constant intravenous infusion of xylazine and ketamineAnesthesiaIntravenousBispectral indexElectroencephalographyAntinociceptionAnalgesiaBackground: This study investigated the antinociceptive effects of a constant rate infusion (CRI) of lidocaine during xylazine and ketamine anesthesia in horses and aimed to correlate these effects with cardiorespiratory variables, bispectral index (BIS) and plasma lidocaine concentrations. Six adult crossbred mares weighing 320-400 kg were anesthetized on three different occasions. Sedation was performed with xylazine (0.75 mg/kg IV) and anesthetic induction with guaifenesin (75 mg/kg IV) and ketamine (2 mg/kg IV). Anesthesia was maintained with 37.5 mu g/kg/min of xylazine and 87.5 mu g/kg/min of ketamine both administered intravenously for 75 min. The three treatments consisted of: lidocaine (loading dose: 5 mg/kg, CRI: 100 mu g/kg/min; THL); lidocaine (loading dose: 2.5 mg/kg; CRI: 50 mu g/kg/min: TLL); and saline (TS); all given 15 min after induction and maintained for 1 h. Antinociception was measured by response to electrical stimulation and bispectral index (BIS) was recorded during anesthesia. Parametric and non-parametric data were compared using ANOVA followed by Student-Newman-Keuls and Friedman tests, respectively.Results: Plasma lidocaine concentrations peaked at the end of lidocaine loading dose and was greater in THL (9.61 +/- 2.75 mu g/mL) vs TLL (4.50 +/- 3.34 mu g/mL). Electrical noxious stimulation caused purposeful movement in all horses from TS, but no response in THL. The BIS was decreased in THL only and was less when compared to the other treatments throughout anesthesia. Blood pressure, PaO2 and PaCO2 increased and heart rate (HR), respiratory rate (RR), pH, total plasma protein and temperature decreased during anesthesia in all treatments. PaCO2 and HR were greater and RR and pH less in THL compared to TLL and TS at 30 min during anesthesia. All recoveries were considered excellent. Time to standing was longer after THL (60 +/- 20 min) than following TLL and TS (32 +/- 17 and 30 +/- 15 min, respectively).Conclusions: At the highest dose administered (THL) lidocaine CRI during xylazine/ketamine anesthesia decreased BIS and motor response to noxious stimulation, and prolonged recovery time without significant added cardiorespiratory depression.Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Campina Grande Fed Univ HRTC CGFU, Hlth & Rural Technol Ctr, Acad Unit Vet Med, Patos de Minas, Paraiba, BrazilUNESP Univ Estadual Paulista, Sch Vet Med & Anim Sci, Dept Vet Surg & Anesthesiol, BR-18618970 Sao Paulo, BrazilLouisiana State Univ, Sch Vet Med, Dept Vet Clin Sci, Baton Rouge, LA 70803 USAColorado State Univ, Coll Vet Med & Biomed Sci, Dept Clin Sci, Ft Collins, CO 80523 USAUniv Calif Davis, Dept Surg & Radiol Sci, Davis, CA 95616 USAUniv Sao Paulo, Dept Vet Med, BR-13635900 Pirassununga, SP, BrazilUNESP Univ Estadual Paulista, Sch Vet Med & Anim Sci, Dept Vet Surg & Anesthesiol, BR-18618970 Sao Paulo, BrazilBiomed Central Ltd.Campina Grande Fed Univ HRTC CGFUUniversidade Estadual Paulista (Unesp)Louisiana State UnivColorado State UnivUniv Calif DavisUniversidade de São Paulo (USP)Nobrega Neto, Pedro I.Luna, Stélio Pacca Loureiro [UNESP]Queiroz-Williams, PatriciaMama, Khursheed R.Steffey, Eugene P.Carregaro, Adriano B.2014-12-03T13:08:44Z2014-12-03T13:08:44Z2013-10-09info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article9application/pdfhttp://dx.doi.org/10.1186/1746-6148-9-199Bmc Veterinary Research. London: Biomed Central Ltd, v. 9, 9 p., 2013.1746-6148http://hdl.handle.net/11449/11152410.1186/1746-6148-9-199WOS:000326635500001WOS000326635500001.pdf44732604100996230000-0001-5312-9076Web of Sciencereponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengBMC Veterinary Research1.9580,934info:eu-repo/semantics/openAccess2023-11-02T06:12:19Zoai:repositorio.unesp.br:11449/111524Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-05T16:44:47.120313Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false |
dc.title.none.fl_str_mv |
Cardiorespiratory and antinociceptive effects of two different doses of lidocaine administered to horses during a constant intravenous infusion of xylazine and ketamine |
title |
Cardiorespiratory and antinociceptive effects of two different doses of lidocaine administered to horses during a constant intravenous infusion of xylazine and ketamine |
spellingShingle |
Cardiorespiratory and antinociceptive effects of two different doses of lidocaine administered to horses during a constant intravenous infusion of xylazine and ketamine Nobrega Neto, Pedro I. Anesthesia Intravenous Bispectral index Electroencephalography Antinociception Analgesia |
title_short |
Cardiorespiratory and antinociceptive effects of two different doses of lidocaine administered to horses during a constant intravenous infusion of xylazine and ketamine |
title_full |
Cardiorespiratory and antinociceptive effects of two different doses of lidocaine administered to horses during a constant intravenous infusion of xylazine and ketamine |
title_fullStr |
Cardiorespiratory and antinociceptive effects of two different doses of lidocaine administered to horses during a constant intravenous infusion of xylazine and ketamine |
title_full_unstemmed |
Cardiorespiratory and antinociceptive effects of two different doses of lidocaine administered to horses during a constant intravenous infusion of xylazine and ketamine |
title_sort |
Cardiorespiratory and antinociceptive effects of two different doses of lidocaine administered to horses during a constant intravenous infusion of xylazine and ketamine |
author |
Nobrega Neto, Pedro I. |
author_facet |
Nobrega Neto, Pedro I. Luna, Stélio Pacca Loureiro [UNESP] Queiroz-Williams, Patricia Mama, Khursheed R. Steffey, Eugene P. Carregaro, Adriano B. |
author_role |
author |
author2 |
Luna, Stélio Pacca Loureiro [UNESP] Queiroz-Williams, Patricia Mama, Khursheed R. Steffey, Eugene P. Carregaro, Adriano B. |
author2_role |
author author author author author |
dc.contributor.none.fl_str_mv |
Campina Grande Fed Univ HRTC CGFU Universidade Estadual Paulista (Unesp) Louisiana State Univ Colorado State Univ Univ Calif Davis Universidade de São Paulo (USP) |
dc.contributor.author.fl_str_mv |
Nobrega Neto, Pedro I. Luna, Stélio Pacca Loureiro [UNESP] Queiroz-Williams, Patricia Mama, Khursheed R. Steffey, Eugene P. Carregaro, Adriano B. |
dc.subject.por.fl_str_mv |
Anesthesia Intravenous Bispectral index Electroencephalography Antinociception Analgesia |
topic |
Anesthesia Intravenous Bispectral index Electroencephalography Antinociception Analgesia |
description |
Background: This study investigated the antinociceptive effects of a constant rate infusion (CRI) of lidocaine during xylazine and ketamine anesthesia in horses and aimed to correlate these effects with cardiorespiratory variables, bispectral index (BIS) and plasma lidocaine concentrations. Six adult crossbred mares weighing 320-400 kg were anesthetized on three different occasions. Sedation was performed with xylazine (0.75 mg/kg IV) and anesthetic induction with guaifenesin (75 mg/kg IV) and ketamine (2 mg/kg IV). Anesthesia was maintained with 37.5 mu g/kg/min of xylazine and 87.5 mu g/kg/min of ketamine both administered intravenously for 75 min. The three treatments consisted of: lidocaine (loading dose: 5 mg/kg, CRI: 100 mu g/kg/min; THL); lidocaine (loading dose: 2.5 mg/kg; CRI: 50 mu g/kg/min: TLL); and saline (TS); all given 15 min after induction and maintained for 1 h. Antinociception was measured by response to electrical stimulation and bispectral index (BIS) was recorded during anesthesia. Parametric and non-parametric data were compared using ANOVA followed by Student-Newman-Keuls and Friedman tests, respectively.Results: Plasma lidocaine concentrations peaked at the end of lidocaine loading dose and was greater in THL (9.61 +/- 2.75 mu g/mL) vs TLL (4.50 +/- 3.34 mu g/mL). Electrical noxious stimulation caused purposeful movement in all horses from TS, but no response in THL. The BIS was decreased in THL only and was less when compared to the other treatments throughout anesthesia. Blood pressure, PaO2 and PaCO2 increased and heart rate (HR), respiratory rate (RR), pH, total plasma protein and temperature decreased during anesthesia in all treatments. PaCO2 and HR were greater and RR and pH less in THL compared to TLL and TS at 30 min during anesthesia. All recoveries were considered excellent. Time to standing was longer after THL (60 +/- 20 min) than following TLL and TS (32 +/- 17 and 30 +/- 15 min, respectively).Conclusions: At the highest dose administered (THL) lidocaine CRI during xylazine/ketamine anesthesia decreased BIS and motor response to noxious stimulation, and prolonged recovery time without significant added cardiorespiratory depression. |
publishDate |
2013 |
dc.date.none.fl_str_mv |
2013-10-09 2014-12-03T13:08:44Z 2014-12-03T13:08:44Z |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://dx.doi.org/10.1186/1746-6148-9-199 Bmc Veterinary Research. London: Biomed Central Ltd, v. 9, 9 p., 2013. 1746-6148 http://hdl.handle.net/11449/111524 10.1186/1746-6148-9-199 WOS:000326635500001 WOS000326635500001.pdf 4473260410099623 0000-0001-5312-9076 |
url |
http://dx.doi.org/10.1186/1746-6148-9-199 http://hdl.handle.net/11449/111524 |
identifier_str_mv |
Bmc Veterinary Research. London: Biomed Central Ltd, v. 9, 9 p., 2013. 1746-6148 10.1186/1746-6148-9-199 WOS:000326635500001 WOS000326635500001.pdf 4473260410099623 0000-0001-5312-9076 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
BMC Veterinary Research 1.958 0,934 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
9 application/pdf |
dc.publisher.none.fl_str_mv |
Biomed Central Ltd. |
publisher.none.fl_str_mv |
Biomed Central Ltd. |
dc.source.none.fl_str_mv |
Web of Science reponame:Repositório Institucional da UNESP instname:Universidade Estadual Paulista (UNESP) instacron:UNESP |
instname_str |
Universidade Estadual Paulista (UNESP) |
instacron_str |
UNESP |
institution |
UNESP |
reponame_str |
Repositório Institucional da UNESP |
collection |
Repositório Institucional da UNESP |
repository.name.fl_str_mv |
Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP) |
repository.mail.fl_str_mv |
|
_version_ |
1808128695378903040 |