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Comparison of different regimens of intravenous dexmedetomidine on duration of subarachnoid block

BACKGROUND AND AIMS: Many studies have studied the effect of intravenous dexmedetomidine on the prolongation of the duration of the subarachnoid block (SAB). These studies had administered dexmedetomidine using different regimens. This study was designed to find out the suitable regimen with maximum...

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Autores principales: Thomas, Anil, Satyaprakash, M. V. S., Elakkumanan, Lenin Babu, Bidkar, Prasanna Udupi, Mishra, Sandeep Kumar
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/PMC5187616/
https://www.ncbi.nlm.nih.gov/pubmed/28096582
http://dx.doi.org/10.4103/0970-9185.194777
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author Thomas, Anil
Satyaprakash, M. V. S.
Elakkumanan, Lenin Babu
Bidkar, Prasanna Udupi
Mishra, Sandeep Kumar
author_facet Thomas, Anil
Satyaprakash, M. V. S.
Elakkumanan, Lenin Babu
Bidkar, Prasanna Udupi
Mishra, Sandeep Kumar
author_sort Thomas, Anil
collection PubMed
description BACKGROUND AND AIMS: Many studies have studied the effect of intravenous dexmedetomidine on the prolongation of the duration of the subarachnoid block (SAB). These studies had administered dexmedetomidine using different regimens. This study was designed to find out the suitable regimen with maximum advantages and minimum disadvantages. MATERIAL AND METHODS: Ninety-three ASA 1 and 2 patients scheduled to undergo surgeries under SAB were randomly allocated into three groups namely B, M, and BM. After SAB, Group B received 0.5 μg/kg of dexmedetomidine bolus over 15 min, Group M received 0.5 μg/kg/h of dexmedetomidine infusion until the end of surgery, Group BM received both bolus and infusion. RESULTS: The time to achieve T10 sensory level (SL) was significantly faster in the Groups B and BM than in the Group M. Maximum block height achieved was T4 and was same in all the groups. The Time to achieve maximum SL and Bromage 3 was comparable in all groups. The two-segment regression time and time to reach Bromage 0 was significantly higher in Groups M and BM than Group B. The time for a first request of analgesia was similar in Groups M and BM. The maximum sedation attained in all groups was Ramsay Sedation Score of 3. Side effects such as bradycardia, hypotension, and desaturation were comparable between the groups. CONCLUSION: We conclude that the continuous infusion of dexmedetomidine results in more advantages than just a bolus dose. Therefore, we suggest using only the maintenance dose of intravenous dexmedetomidine after subarachnoid blockade for prolonging the duration and achieving sedation.
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spelling pubmed-51876162017-01-17 Comparison of different regimens of intravenous dexmedetomidine on duration of subarachnoid block Thomas, Anil Satyaprakash, M. V. S. Elakkumanan, Lenin Babu Bidkar, Prasanna Udupi Mishra, Sandeep Kumar J Anaesthesiol Clin Pharmacol Original Article BACKGROUND AND AIMS: Many studies have studied the effect of intravenous dexmedetomidine on the prolongation of the duration of the subarachnoid block (SAB). These studies had administered dexmedetomidine using different regimens. This study was designed to find out the suitable regimen with maximum advantages and minimum disadvantages. MATERIAL AND METHODS: Ninety-three ASA 1 and 2 patients scheduled to undergo surgeries under SAB were randomly allocated into three groups namely B, M, and BM. After SAB, Group B received 0.5 μg/kg of dexmedetomidine bolus over 15 min, Group M received 0.5 μg/kg/h of dexmedetomidine infusion until the end of surgery, Group BM received both bolus and infusion. RESULTS: The time to achieve T10 sensory level (SL) was significantly faster in the Groups B and BM than in the Group M. Maximum block height achieved was T4 and was same in all the groups. The Time to achieve maximum SL and Bromage 3 was comparable in all groups. The two-segment regression time and time to reach Bromage 0 was significantly higher in Groups M and BM than Group B. The time for a first request of analgesia was similar in Groups M and BM. The maximum sedation attained in all groups was Ramsay Sedation Score of 3. Side effects such as bradycardia, hypotension, and desaturation were comparable between the groups. CONCLUSION: We conclude that the continuous infusion of dexmedetomidine results in more advantages than just a bolus dose. Therefore, we suggest using only the maintenance dose of intravenous dexmedetomidine after subarachnoid blockade for prolonging the duration and achieving sedation. Medknow Publications & Media Pvt Ltd 2016 /pmc/articles/PMC5187616/ /pubmed/28096582 http://dx.doi.org/10.4103/0970-9185.194777 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
Thomas, Anil
Satyaprakash, M. V. S.
Elakkumanan, Lenin Babu
Bidkar, Prasanna Udupi
Mishra, Sandeep Kumar
Comparison of different regimens of intravenous dexmedetomidine on duration of subarachnoid block
title Comparison of different regimens of intravenous dexmedetomidine on duration of subarachnoid block
title_full Comparison of different regimens of intravenous dexmedetomidine on duration of subarachnoid block
title_fullStr Comparison of different regimens of intravenous dexmedetomidine on duration of subarachnoid block
title_full_unstemmed Comparison of different regimens of intravenous dexmedetomidine on duration of subarachnoid block
title_short Comparison of different regimens of intravenous dexmedetomidine on duration of subarachnoid block
title_sort comparison of different regimens of intravenous dexmedetomidine on duration of subarachnoid block
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5187616/
https://www.ncbi.nlm.nih.gov/pubmed/28096582
http://dx.doi.org/10.4103/0970-9185.194777
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