Cardiorespiratory and antinociceptive effects of two different doses of lidocaine administered to horses during a constant intravenous infusion of xylazine and ketamine

Detalhes bibliográficos
Autor(a) principal: Nobrega Neto, Pedro I.
Data de Publicação: 2013
Outros Autores: Luna, Stélio Pacca Loureiro [UNESP], Queiroz-Williams, Patricia, Mama, Khursheed R., Steffey, Eugene P., Carregaro, Adriano B.
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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spelling 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
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0,934
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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)
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instname_str Universidade Estadual Paulista (UNESP)
instacron_str UNESP
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reponame_str Repositório Institucional da UNESP
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repository.name.fl_str_mv Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)
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