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Randomised double-blind comparative study of dexmedetomidine and tramadol for post-spinal anaesthesia shivering
BACKGROUND AND AIMS: Dexmedetomidine (α(2) adrenergic agonist) has been used for prevention of post anaesthesia shivering. Its use for the treatment of post-spinal anaesthesia shivering has not been evaluated. The aim of this study was to evaluate and compare the efficacy, haemodynamic and adverse e...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4090989/ https://www.ncbi.nlm.nih.gov/pubmed/25024466 http://dx.doi.org/10.4103/0019-5049.135031 |
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author | Mittal, Geeta Gupta, Kanchan Katyal, Sunil Kaushal, Sandeep |
author_facet | Mittal, Geeta Gupta, Kanchan Katyal, Sunil Kaushal, Sandeep |
author_sort | Mittal, Geeta |
collection | PubMed |
description | BACKGROUND AND AIMS: Dexmedetomidine (α(2) adrenergic agonist) has been used for prevention of post anaesthesia shivering. Its use for the treatment of post-spinal anaesthesia shivering has not been evaluated. The aim of this study was to evaluate and compare the efficacy, haemodynamic and adverse effects of dexmedetomidine with those of tramadol, when used for control of post-spinal anaesthesia shivering. METHODS: A prospective, randomised, and double-blind study was conducted in 50 American Society of Anaesthesiologists Grade I and II patients of either gender, aged between 18 and 65 years, scheduled for various surgical procedures under spinal anaesthesia. The patients were randomised in two groups of 25 patients each to receive either dexmedetomidine 0.5 μg/kg or tramadol 0.5 mg/kg as a slow intravenous bolus. Grade of shivering, onset of shivering, time for cessation of shivering, recurrence, response rate, and adverse effects were observed at scheduled intervals. Unpaired t-test was used for analysing the data. RESULTS: Time taken for cessation of shivering was significantly less with dexmedetomidine when compared to tramadol. Nausea and vomiting was observed only in tramadol group (28% and; 20% respectively). There was not much difference in the sedation profile of both the drugs. CONCLUSION: We conclude that although both drugs are effective, the time taken for cessation of shivering is less with dexmedetomidine when compared to tramadol. Moreover, dexmedetomidine has negligible adverse effects, whereas tramadol is associated with significant nausea and vomiting. |
format | Online Article Text |
id | pubmed-4090989 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-40909892014-07-14 Randomised double-blind comparative study of dexmedetomidine and tramadol for post-spinal anaesthesia shivering Mittal, Geeta Gupta, Kanchan Katyal, Sunil Kaushal, Sandeep Indian J Anaesth Clinical Investigation BACKGROUND AND AIMS: Dexmedetomidine (α(2) adrenergic agonist) has been used for prevention of post anaesthesia shivering. Its use for the treatment of post-spinal anaesthesia shivering has not been evaluated. The aim of this study was to evaluate and compare the efficacy, haemodynamic and adverse effects of dexmedetomidine with those of tramadol, when used for control of post-spinal anaesthesia shivering. METHODS: A prospective, randomised, and double-blind study was conducted in 50 American Society of Anaesthesiologists Grade I and II patients of either gender, aged between 18 and 65 years, scheduled for various surgical procedures under spinal anaesthesia. The patients were randomised in two groups of 25 patients each to receive either dexmedetomidine 0.5 μg/kg or tramadol 0.5 mg/kg as a slow intravenous bolus. Grade of shivering, onset of shivering, time for cessation of shivering, recurrence, response rate, and adverse effects were observed at scheduled intervals. Unpaired t-test was used for analysing the data. RESULTS: Time taken for cessation of shivering was significantly less with dexmedetomidine when compared to tramadol. Nausea and vomiting was observed only in tramadol group (28% and; 20% respectively). There was not much difference in the sedation profile of both the drugs. CONCLUSION: We conclude that although both drugs are effective, the time taken for cessation of shivering is less with dexmedetomidine when compared to tramadol. Moreover, dexmedetomidine has negligible adverse effects, whereas tramadol is associated with significant nausea and vomiting. Medknow Publications & Media Pvt Ltd 2014 /pmc/articles/PMC4090989/ /pubmed/25024466 http://dx.doi.org/10.4103/0019-5049.135031 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 Mittal, Geeta Gupta, Kanchan Katyal, Sunil Kaushal, Sandeep Randomised double-blind comparative study of dexmedetomidine and tramadol for post-spinal anaesthesia shivering |
title | Randomised double-blind comparative study of dexmedetomidine and tramadol for post-spinal anaesthesia shivering |
title_full | Randomised double-blind comparative study of dexmedetomidine and tramadol for post-spinal anaesthesia shivering |
title_fullStr | Randomised double-blind comparative study of dexmedetomidine and tramadol for post-spinal anaesthesia shivering |
title_full_unstemmed | Randomised double-blind comparative study of dexmedetomidine and tramadol for post-spinal anaesthesia shivering |
title_short | Randomised double-blind comparative study of dexmedetomidine and tramadol for post-spinal anaesthesia shivering |
title_sort | randomised double-blind comparative study of dexmedetomidine and tramadol for post-spinal anaesthesia shivering |
topic | Clinical Investigation |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4090989/ https://www.ncbi.nlm.nih.gov/pubmed/25024466 http://dx.doi.org/10.4103/0019-5049.135031 |
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