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Comparison of clonidine and dexmedetomidine as adjuncts to intravenous regional anaesthesia

BACKGROUND AND AIMS: Intravenous regional anaesthesia (IVRA) provides reliable and rapid analgesia with good muscular relaxation of the extremity distal to the tourniquet, but tourniquet pain and absence of post-operative analgesia are major drawbacks. α2 agonists, clonidine and dexmedetomidine are...

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Autores principales: Sardesai, Shalini Pravin, Patil, Kalyani Nilesh, Sarkar, Adnanali
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4697246/
https://www.ncbi.nlm.nih.gov/pubmed/26755839
http://dx.doi.org/10.4103/0019-5049.170034
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author Sardesai, Shalini Pravin
Patil, Kalyani Nilesh
Sarkar, Adnanali
author_facet Sardesai, Shalini Pravin
Patil, Kalyani Nilesh
Sarkar, Adnanali
author_sort Sardesai, Shalini Pravin
collection PubMed
description BACKGROUND AND AIMS: Intravenous regional anaesthesia (IVRA) provides reliable and rapid analgesia with good muscular relaxation of the extremity distal to the tourniquet, but tourniquet pain and absence of post-operative analgesia are major drawbacks. α2 agonists, clonidine and dexmedetomidine are known to potentiate peripheral nerve blocks. The aim of this study was to compare clonidine and dexmedetomidine as adjuvants to IVRA with respect to block characteristics, tourniquet pain and post-operative analgesia. METHODS: A prospective, randomised, double-blind study was conducted on 60 adult patients of American Society of Anesthesiologists physical status grades I and II, in two groups of 30 each, to receive either clonidine 1 μg/kg or dexmedetomidine 1 μg/kg added to 40 ml 0.5% preservative-free lignocaine. Independent samples t-test was used for analysing demographic data, haemodynamic data and block characteristics and Mann-Whitney U-test for skewed data. RESULTS: Sensorimotor block onset was significantly faster and recovery delayed with dexmedetomidine as compared to clonidine. Intra-operative visual analogue scale (VAS) at 10 min, 15 min and 40 min and post-operative VAS at 30 min and 2 h were significantly higher with clonidine. Fentanyl consumption and sedation were comparable. Duration of analgesia was significantly longer with dexmedetomidine. Haemodynamic parameters were comparable. CONCLUSIONS: Dexmedetomidine significantly facilitates onset, prolongs recovery of sensory as well as motor block and also prolongs duration of analgesia as compared to clonidine.   Both decrease tourniquet pain satisfactorily and have comparable intra-operative fentanyl requirement . Patient satisfaction is better with dexmedetomidine.
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spelling pubmed-46972462016-01-11 Comparison of clonidine and dexmedetomidine as adjuncts to intravenous regional anaesthesia Sardesai, Shalini Pravin Patil, Kalyani Nilesh Sarkar, Adnanali Indian J Anaesth Clinical Investigation BACKGROUND AND AIMS: Intravenous regional anaesthesia (IVRA) provides reliable and rapid analgesia with good muscular relaxation of the extremity distal to the tourniquet, but tourniquet pain and absence of post-operative analgesia are major drawbacks. α2 agonists, clonidine and dexmedetomidine are known to potentiate peripheral nerve blocks. The aim of this study was to compare clonidine and dexmedetomidine as adjuvants to IVRA with respect to block characteristics, tourniquet pain and post-operative analgesia. METHODS: A prospective, randomised, double-blind study was conducted on 60 adult patients of American Society of Anesthesiologists physical status grades I and II, in two groups of 30 each, to receive either clonidine 1 μg/kg or dexmedetomidine 1 μg/kg added to 40 ml 0.5% preservative-free lignocaine. Independent samples t-test was used for analysing demographic data, haemodynamic data and block characteristics and Mann-Whitney U-test for skewed data. RESULTS: Sensorimotor block onset was significantly faster and recovery delayed with dexmedetomidine as compared to clonidine. Intra-operative visual analogue scale (VAS) at 10 min, 15 min and 40 min and post-operative VAS at 30 min and 2 h were significantly higher with clonidine. Fentanyl consumption and sedation were comparable. Duration of analgesia was significantly longer with dexmedetomidine. Haemodynamic parameters were comparable. CONCLUSIONS: Dexmedetomidine significantly facilitates onset, prolongs recovery of sensory as well as motor block and also prolongs duration of analgesia as compared to clonidine.   Both decrease tourniquet pain satisfactorily and have comparable intra-operative fentanyl requirement . Patient satisfaction is better with dexmedetomidine. Medknow Publications & Media Pvt Ltd 2015-11 /pmc/articles/PMC4697246/ /pubmed/26755839 http://dx.doi.org/10.4103/0019-5049.170034 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 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 Clinical Investigation
Sardesai, Shalini Pravin
Patil, Kalyani Nilesh
Sarkar, Adnanali
Comparison of clonidine and dexmedetomidine as adjuncts to intravenous regional anaesthesia
title Comparison of clonidine and dexmedetomidine as adjuncts to intravenous regional anaesthesia
title_full Comparison of clonidine and dexmedetomidine as adjuncts to intravenous regional anaesthesia
title_fullStr Comparison of clonidine and dexmedetomidine as adjuncts to intravenous regional anaesthesia
title_full_unstemmed Comparison of clonidine and dexmedetomidine as adjuncts to intravenous regional anaesthesia
title_short Comparison of clonidine and dexmedetomidine as adjuncts to intravenous regional anaesthesia
title_sort comparison of clonidine and dexmedetomidine as adjuncts to intravenous regional anaesthesia
topic Clinical Investigation
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4697246/
https://www.ncbi.nlm.nih.gov/pubmed/26755839
http://dx.doi.org/10.4103/0019-5049.170034
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