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Intraoperative effect of dexmedetomidine infusion during living donor liver transplantation: A randomized control trial

BACKGROUND: Dexmedetomidine hydrochloride (Dex) is a useful adjuvant for general anesthesia. The aim was to evaluate the effects of Dex infusion during living donors liver transplantation (LDLT) on the general anesthetic requirements, hemodynamics, oxygen consumption (VO(2)), and CO(2) production (V...

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Autores principales: Sayed, E, Yassen, KA
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4916812/
https://www.ncbi.nlm.nih.gov/pubmed/27375383
http://dx.doi.org/10.4103/1658-354X.174914
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author Sayed, E
Yassen, KA
author_facet Sayed, E
Yassen, KA
author_sort Sayed, E
collection PubMed
description BACKGROUND: Dexmedetomidine hydrochloride (Dex) is a useful adjuvant for general anesthesia. The aim was to evaluate the effects of Dex infusion during living donors liver transplantation (LDLT) on the general anesthetic requirements, hemodynamics, oxygen consumption (VO(2)), and CO(2) production (VCO(2)). MATERIALS AND METHODS: Forty LDLT recipients were allocated randomly to receive either Dex (0.2-0.7 μg/kg/h) or placebo (control [C]). Patient state index (PSI), SEDLine monitored anesthesia depth (25-50) with desflurane (Des) % and fentanyl altered accordingly. Transesophageal Doppler (TED), invasive mean arterial blood pressure (MAP) and heart rate (HR) were monitoring any Dex side effects and altering infusion rate accordingly; TED was used for fluid optimization. Metabolic gas monitoring (VO(2), VCO(2)) and Des consumption were recorded. RESULTS: Dex reduced Des and fentanyl consumption versus C (120.0 ± 30.2 vs. 248.0 ± 38.8) ml, (440.0 ± 195.74 vs. 1300.0 ± 32) μg, respectively (P < 0.01). Dex was delivered for 11.35 ± 2.45 h with comparable HR, MAP, and TED variables versus C and with similar mean noradrenaline support (5.63 ± 2.44 vs. 5.83 ± 2.57 mg, P = 0.81). VO(2) was reduced with Dex vs. C during anhepatic, 30 min postreperfusion and end of surgery (193.2 ± 26.78 vs. 239 ± 14.93) (172.1 ± 28.14 vs. 202.7 ± 18.03) and (199.7 ± 26.63 vs. 283.8 ± 14.83) ml/min/m(2) respectively (P < 0.01). VCO(2) was also reduced with Dex versus C during the same periods (195.2 ± 46.41 vs. 216.7 ± 29.90, P = 0.09), (210.6 ± 60.71 vs. 253.9 ± 32.51, P = 0.01), and (158.7 ± 49.96 vs. 209.7 ± 16.78, P < 0.01), ml/min/m(2) respectively. CONCLUSION: TED and PSI guided Dex infusion helped to reduce Des and fentanyl consumption as well as VO(2) and VCO(2) at a lower cost with no adverse effects on hemodynamics.
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spelling pubmed-49168122016-07-02 Intraoperative effect of dexmedetomidine infusion during living donor liver transplantation: A randomized control trial Sayed, E Yassen, KA Saudi J Anaesth Original Article BACKGROUND: Dexmedetomidine hydrochloride (Dex) is a useful adjuvant for general anesthesia. The aim was to evaluate the effects of Dex infusion during living donors liver transplantation (LDLT) on the general anesthetic requirements, hemodynamics, oxygen consumption (VO(2)), and CO(2) production (VCO(2)). MATERIALS AND METHODS: Forty LDLT recipients were allocated randomly to receive either Dex (0.2-0.7 μg/kg/h) or placebo (control [C]). Patient state index (PSI), SEDLine monitored anesthesia depth (25-50) with desflurane (Des) % and fentanyl altered accordingly. Transesophageal Doppler (TED), invasive mean arterial blood pressure (MAP) and heart rate (HR) were monitoring any Dex side effects and altering infusion rate accordingly; TED was used for fluid optimization. Metabolic gas monitoring (VO(2), VCO(2)) and Des consumption were recorded. RESULTS: Dex reduced Des and fentanyl consumption versus C (120.0 ± 30.2 vs. 248.0 ± 38.8) ml, (440.0 ± 195.74 vs. 1300.0 ± 32) μg, respectively (P < 0.01). Dex was delivered for 11.35 ± 2.45 h with comparable HR, MAP, and TED variables versus C and with similar mean noradrenaline support (5.63 ± 2.44 vs. 5.83 ± 2.57 mg, P = 0.81). VO(2) was reduced with Dex vs. C during anhepatic, 30 min postreperfusion and end of surgery (193.2 ± 26.78 vs. 239 ± 14.93) (172.1 ± 28.14 vs. 202.7 ± 18.03) and (199.7 ± 26.63 vs. 283.8 ± 14.83) ml/min/m(2) respectively (P < 0.01). VCO(2) was also reduced with Dex versus C during the same periods (195.2 ± 46.41 vs. 216.7 ± 29.90, P = 0.09), (210.6 ± 60.71 vs. 253.9 ± 32.51, P = 0.01), and (158.7 ± 49.96 vs. 209.7 ± 16.78, P < 0.01), ml/min/m(2) respectively. CONCLUSION: TED and PSI guided Dex infusion helped to reduce Des and fentanyl consumption as well as VO(2) and VCO(2) at a lower cost with no adverse effects on hemodynamics. Medknow Publications & Media Pvt Ltd 2016 /pmc/articles/PMC4916812/ /pubmed/27375383 http://dx.doi.org/10.4103/1658-354X.174914 Text en Copyright: © Saudi Journal of Anaesthesia http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution NonCommercial ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non commercially, as long as the author is credited and the new creations are licensed under the identical terms.
spellingShingle Original Article
Sayed, E
Yassen, KA
Intraoperative effect of dexmedetomidine infusion during living donor liver transplantation: A randomized control trial
title Intraoperative effect of dexmedetomidine infusion during living donor liver transplantation: A randomized control trial
title_full Intraoperative effect of dexmedetomidine infusion during living donor liver transplantation: A randomized control trial
title_fullStr Intraoperative effect of dexmedetomidine infusion during living donor liver transplantation: A randomized control trial
title_full_unstemmed Intraoperative effect of dexmedetomidine infusion during living donor liver transplantation: A randomized control trial
title_short Intraoperative effect of dexmedetomidine infusion during living donor liver transplantation: A randomized control trial
title_sort intraoperative effect of dexmedetomidine infusion during living donor liver transplantation: a randomized control trial
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4916812/
https://www.ncbi.nlm.nih.gov/pubmed/27375383
http://dx.doi.org/10.4103/1658-354X.174914
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