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Comparison of block characteristics of spinal anesthesia following intravenous dexmedetomidine and clonidine

BACKGROUND AND AIMS: Different routes of administration of α2 adrenergic receptor agonists have been found to prolong the duration of spinal block. MATERIAL AND METHODS: One hundred and twenty patients, aged 18-60 years, of ASA physical status I or II posted for elective fixation of fractures of low...

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Autores principales: Agrawal, Akansha, Agrawal, Sanjay, Payal, Yashwant S
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/PMC5009840/
https://www.ncbi.nlm.nih.gov/pubmed/27625482
http://dx.doi.org/10.4103/0970-9185.188830
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author Agrawal, Akansha
Agrawal, Sanjay
Payal, Yashwant S
author_facet Agrawal, Akansha
Agrawal, Sanjay
Payal, Yashwant S
author_sort Agrawal, Akansha
collection PubMed
description BACKGROUND AND AIMS: Different routes of administration of α2 adrenergic receptor agonists have been found to prolong the duration of spinal block. MATERIAL AND METHODS: One hundred and twenty patients, aged 18-60 years, of ASA physical status I or II posted for elective fixation of fractures of lower limb under spinal anesthesia were selected. Spinal anesthesia was administered with 2.5 ml of 0.5% bupivacaine mixed with 10 μg fentanyl. The patients were randomized to receive intravenous (IV) dexmedetomidine 1 μg/kg/h for 15 min followed by infusion of 0.3 μg/kg/h (Group I), IV Clonidine 2 μg/kg/h for 15 min followed by infusion of 0.5 μg kg/h (Group II) or 15 ml of normal saline for 15 min followed by infusion at 50 ml/h (Group III). Motor and sensory blockade was evaluated using bromage score and pin prick method respectively. RESULTS: The median block height in all groups was T8. Time to achieve block height was fastest in Group I. Time of regression of sensory block to T12/L1 dermatome was 230.75 ± 21.25 min (Group I), 196.25 ± 20.27 min (Group II) and 163.88 ± 15.46 min (Group III) respectively. Regression of motor blocks to Bromage 0/1 was 274 ± 21.25 min, 234.25 ± 32.41 min and 130.12 ± 20.70 min in Groups I, II and III respectively. Bradycardia was seen in one patient in Group I and two patients in Group II. Hypotension was seen in five patients in Group I and seven patients in Group II. First requirement for postoperative analgesic was after 353.13 ± 39.60 min, 314.38 ± 30.64 min and 193.25 ± 17.74 min in Groups I, II and III respectively. CONCLUSION: IV α2 agonists are useful adjuvants for prolongation of the duration of spinal block. IV dexmedetomidine produces a better clinical profile compared to clonidine.
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spelling pubmed-50098402016-09-13 Comparison of block characteristics of spinal anesthesia following intravenous dexmedetomidine and clonidine Agrawal, Akansha Agrawal, Sanjay Payal, Yashwant S J Anaesthesiol Clin Pharmacol Original Article BACKGROUND AND AIMS: Different routes of administration of α2 adrenergic receptor agonists have been found to prolong the duration of spinal block. MATERIAL AND METHODS: One hundred and twenty patients, aged 18-60 years, of ASA physical status I or II posted for elective fixation of fractures of lower limb under spinal anesthesia were selected. Spinal anesthesia was administered with 2.5 ml of 0.5% bupivacaine mixed with 10 μg fentanyl. The patients were randomized to receive intravenous (IV) dexmedetomidine 1 μg/kg/h for 15 min followed by infusion of 0.3 μg/kg/h (Group I), IV Clonidine 2 μg/kg/h for 15 min followed by infusion of 0.5 μg kg/h (Group II) or 15 ml of normal saline for 15 min followed by infusion at 50 ml/h (Group III). Motor and sensory blockade was evaluated using bromage score and pin prick method respectively. RESULTS: The median block height in all groups was T8. Time to achieve block height was fastest in Group I. Time of regression of sensory block to T12/L1 dermatome was 230.75 ± 21.25 min (Group I), 196.25 ± 20.27 min (Group II) and 163.88 ± 15.46 min (Group III) respectively. Regression of motor blocks to Bromage 0/1 was 274 ± 21.25 min, 234.25 ± 32.41 min and 130.12 ± 20.70 min in Groups I, II and III respectively. Bradycardia was seen in one patient in Group I and two patients in Group II. Hypotension was seen in five patients in Group I and seven patients in Group II. First requirement for postoperative analgesic was after 353.13 ± 39.60 min, 314.38 ± 30.64 min and 193.25 ± 17.74 min in Groups I, II and III respectively. CONCLUSION: IV α2 agonists are useful adjuvants for prolongation of the duration of spinal block. IV dexmedetomidine produces a better clinical profile compared to clonidine. Medknow Publications & Media Pvt Ltd 2016 /pmc/articles/PMC5009840/ /pubmed/27625482 http://dx.doi.org/10.4103/0970-9185.188830 Text en Copyright: © Journal of Anaesthesiology Clinical Pharmacology 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
Agrawal, Akansha
Agrawal, Sanjay
Payal, Yashwant S
Comparison of block characteristics of spinal anesthesia following intravenous dexmedetomidine and clonidine
title Comparison of block characteristics of spinal anesthesia following intravenous dexmedetomidine and clonidine
title_full Comparison of block characteristics of spinal anesthesia following intravenous dexmedetomidine and clonidine
title_fullStr Comparison of block characteristics of spinal anesthesia following intravenous dexmedetomidine and clonidine
title_full_unstemmed Comparison of block characteristics of spinal anesthesia following intravenous dexmedetomidine and clonidine
title_short Comparison of block characteristics of spinal anesthesia following intravenous dexmedetomidine and clonidine
title_sort comparison of block characteristics of spinal anesthesia following intravenous dexmedetomidine and clonidine
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5009840/
https://www.ncbi.nlm.nih.gov/pubmed/27625482
http://dx.doi.org/10.4103/0970-9185.188830
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