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Dexmedetomidine ameliorates monitored anaesthesia care

BACKGROUND AND AIMS: Monitored anaesthesia care (MAC) is meant for procedures under local anaesthesia. Various drugs have been used for this purpose. The recently introduced alpha2 agonist, dexmedetomidine provides “conscious sedation” with adequate analgesia and minimal respiratory depression. Henc...

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Autores principales: Gupta, Priyamvada, Joshi, Samrat, Jethava, Durga, Kumar, Ankit
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4050931/
https://www.ncbi.nlm.nih.gov/pubmed/24963179
http://dx.doi.org/10.4103/0019-5049.130816
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author Gupta, Priyamvada
Joshi, Samrat
Jethava, Durga
Kumar, Ankit
author_facet Gupta, Priyamvada
Joshi, Samrat
Jethava, Durga
Kumar, Ankit
author_sort Gupta, Priyamvada
collection PubMed
description BACKGROUND AND AIMS: Monitored anaesthesia care (MAC) is meant for procedures under local anaesthesia. Various drugs have been used for this purpose. The recently introduced alpha2 agonist, dexmedetomidine provides “conscious sedation” with adequate analgesia and minimal respiratory depression. Hence, the safety and efficacy of two doses of dexmedetomidine for sedation and analgesia were evaluated. METHODS: A total of 90 patients were distributed in three groups of 30 each: Dexmedetomidine 0.5 μg/kg (DL), dexmedetomidine 1.0 μg/kg (DH) and normal saline (C). The initial loading dose was followed by maintenance infusion of 0.2-0.7 μg/kg/h of dexmedetomidine or equivalent volume of saline. Study drug was started at least 15 min before placement of local anaesthesia. Drugs were titrated to a target level of sedation (=3 on Ramsay sedation scale [RSS]). Midazolam 0.02 mg/kg for RSS < 3 and fentanyl 0.5 μg/kg were supplemented as required. The statistical analysis was performed using Chi-square test and mean and anova analysis. RESULTS: In groups DL and DH fewer patients required supplemental midazolam, 56.7% (17/30) and 40% (12/30), compared with control, where 86.7% (26/30)needed midazolam supplements. P = 0.000. Both groups DL and DH required significantly less fentanyl (84.8 and 83.9 μg) versus control (144.2 μg). There was significantly increased ease of achieving and maintaining targeted sedation and analgesia in both dexmedetomidine groups when compared with placebo (P = 0.001). Adverse events observed with dexmedetomidine were bradycardia and hypotension. CONCLUSIONS: Dexmedetomidine in the doses studied was considered safe and effective sedative and analgesic for patients undergoing procedures under MAC.
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spelling pubmed-40509312014-06-24 Dexmedetomidine ameliorates monitored anaesthesia care Gupta, Priyamvada Joshi, Samrat Jethava, Durga Kumar, Ankit Indian J Anaesth Clinical Investigation BACKGROUND AND AIMS: Monitored anaesthesia care (MAC) is meant for procedures under local anaesthesia. Various drugs have been used for this purpose. The recently introduced alpha2 agonist, dexmedetomidine provides “conscious sedation” with adequate analgesia and minimal respiratory depression. Hence, the safety and efficacy of two doses of dexmedetomidine for sedation and analgesia were evaluated. METHODS: A total of 90 patients were distributed in three groups of 30 each: Dexmedetomidine 0.5 μg/kg (DL), dexmedetomidine 1.0 μg/kg (DH) and normal saline (C). The initial loading dose was followed by maintenance infusion of 0.2-0.7 μg/kg/h of dexmedetomidine or equivalent volume of saline. Study drug was started at least 15 min before placement of local anaesthesia. Drugs were titrated to a target level of sedation (=3 on Ramsay sedation scale [RSS]). Midazolam 0.02 mg/kg for RSS < 3 and fentanyl 0.5 μg/kg were supplemented as required. The statistical analysis was performed using Chi-square test and mean and anova analysis. RESULTS: In groups DL and DH fewer patients required supplemental midazolam, 56.7% (17/30) and 40% (12/30), compared with control, where 86.7% (26/30)needed midazolam supplements. P = 0.000. Both groups DL and DH required significantly less fentanyl (84.8 and 83.9 μg) versus control (144.2 μg). There was significantly increased ease of achieving and maintaining targeted sedation and analgesia in both dexmedetomidine groups when compared with placebo (P = 0.001). Adverse events observed with dexmedetomidine were bradycardia and hypotension. CONCLUSIONS: Dexmedetomidine in the doses studied was considered safe and effective sedative and analgesic for patients undergoing procedures under MAC. Medknow Publications & Media Pvt Ltd 2014 /pmc/articles/PMC4050931/ /pubmed/24963179 http://dx.doi.org/10.4103/0019-5049.130816 Text en Copyright: © Indian 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-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Clinical Investigation
Gupta, Priyamvada
Joshi, Samrat
Jethava, Durga
Kumar, Ankit
Dexmedetomidine ameliorates monitored anaesthesia care
title Dexmedetomidine ameliorates monitored anaesthesia care
title_full Dexmedetomidine ameliorates monitored anaesthesia care
title_fullStr Dexmedetomidine ameliorates monitored anaesthesia care
title_full_unstemmed Dexmedetomidine ameliorates monitored anaesthesia care
title_short Dexmedetomidine ameliorates monitored anaesthesia care
title_sort dexmedetomidine ameliorates monitored anaesthesia care
topic Clinical Investigation
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4050931/
https://www.ncbi.nlm.nih.gov/pubmed/24963179
http://dx.doi.org/10.4103/0019-5049.130816
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