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A comparative study of pre-operative oral clonidine and pregabalin on post-operative analgesia after spinal anesthesia
OBJECTIVES: Pregabalin and clonidine have anti-nociceptive properties. This study assesses their efficacy in prolonging the analgesic effect of spinal anesthesia and post-operative analgesic requirement in patients undergoing vaginal hysterectomy. MATERIALS AND METHODS: A total of 90 females in the...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Medknow Publications & Media Pvt Ltd
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4173598/ https://www.ncbi.nlm.nih.gov/pubmed/25886102 http://dx.doi.org/10.4103/0259-1162.128907 |
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author | Prasad, Anu Bhattacharyya, Susmita Biswas, Atanu Saha, Mrityunjaya Mondal, Sudeshna Saha, Dona |
author_facet | Prasad, Anu Bhattacharyya, Susmita Biswas, Atanu Saha, Mrityunjaya Mondal, Sudeshna Saha, Dona |
author_sort | Prasad, Anu |
collection | PubMed |
description | OBJECTIVES: Pregabalin and clonidine have anti-nociceptive properties. This study assesses their efficacy in prolonging the analgesic effect of spinal anesthesia and post-operative analgesic requirement in patients undergoing vaginal hysterectomy. MATERIALS AND METHODS: A total of 90 females in the age group of 30-60 years were randomly allocated in to three groups of 30 each, to receive either oral clonidine (150 μg) or oral pregabalin (150 mg) or oral multivitamin as placebo 1.5 h before spinal anesthesia with 3ml (15 mg) of 0.5% hyperbaric bupivacaine. Intensity of pain was measured on a visual analog scale (VAS) at the end of operation (0 h) then at 1,2,4,6,12 and 24 h thereafter. Diclofenac sodium intramuscularly 1 mg/kg was provided when the VASscore was >4 in the study period. Sedation was defined by Ramsay sedation scale at 0,6,12 and 24 h. Side-effects such as nausea and vomiting, respiratory depression and dryness of mouth were noted. RESULTS: The VAS scores were significantly less in the pregabalin group compared with the clonidine group at 6,12 and 24 h post-operatively with a P < 0.0001. More sedation was seen in the clonidine group than in the pregabalin group (P < 0.05). Analgesic consumption and VAS scores were lower in clonidine and pregabalin group compared with the placebo group (P < 0.05). CONCLUSION: Oral pregabalin (150 mg) prolongs the post-operative pain relief after spinal anesthesia but produces less sedation compared with oral clonidine (150 μg). |
format | Online Article Text |
id | pubmed-4173598 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-41735982014-10-22 A comparative study of pre-operative oral clonidine and pregabalin on post-operative analgesia after spinal anesthesia Prasad, Anu Bhattacharyya, Susmita Biswas, Atanu Saha, Mrityunjaya Mondal, Sudeshna Saha, Dona Anesth Essays Res Original Article OBJECTIVES: Pregabalin and clonidine have anti-nociceptive properties. This study assesses their efficacy in prolonging the analgesic effect of spinal anesthesia and post-operative analgesic requirement in patients undergoing vaginal hysterectomy. MATERIALS AND METHODS: A total of 90 females in the age group of 30-60 years were randomly allocated in to three groups of 30 each, to receive either oral clonidine (150 μg) or oral pregabalin (150 mg) or oral multivitamin as placebo 1.5 h before spinal anesthesia with 3ml (15 mg) of 0.5% hyperbaric bupivacaine. Intensity of pain was measured on a visual analog scale (VAS) at the end of operation (0 h) then at 1,2,4,6,12 and 24 h thereafter. Diclofenac sodium intramuscularly 1 mg/kg was provided when the VASscore was >4 in the study period. Sedation was defined by Ramsay sedation scale at 0,6,12 and 24 h. Side-effects such as nausea and vomiting, respiratory depression and dryness of mouth were noted. RESULTS: The VAS scores were significantly less in the pregabalin group compared with the clonidine group at 6,12 and 24 h post-operatively with a P < 0.0001. More sedation was seen in the clonidine group than in the pregabalin group (P < 0.05). Analgesic consumption and VAS scores were lower in clonidine and pregabalin group compared with the placebo group (P < 0.05). CONCLUSION: Oral pregabalin (150 mg) prolongs the post-operative pain relief after spinal anesthesia but produces less sedation compared with oral clonidine (150 μg). Medknow Publications & Media Pvt Ltd 2014 /pmc/articles/PMC4173598/ /pubmed/25886102 http://dx.doi.org/10.4103/0259-1162.128907 Text en Copyright: © Anesthesia: Essays and Researches 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 | Original Article Prasad, Anu Bhattacharyya, Susmita Biswas, Atanu Saha, Mrityunjaya Mondal, Sudeshna Saha, Dona A comparative study of pre-operative oral clonidine and pregabalin on post-operative analgesia after spinal anesthesia |
title | A comparative study of pre-operative oral clonidine and pregabalin on post-operative analgesia after spinal anesthesia |
title_full | A comparative study of pre-operative oral clonidine and pregabalin on post-operative analgesia after spinal anesthesia |
title_fullStr | A comparative study of pre-operative oral clonidine and pregabalin on post-operative analgesia after spinal anesthesia |
title_full_unstemmed | A comparative study of pre-operative oral clonidine and pregabalin on post-operative analgesia after spinal anesthesia |
title_short | A comparative study of pre-operative oral clonidine and pregabalin on post-operative analgesia after spinal anesthesia |
title_sort | comparative study of pre-operative oral clonidine and pregabalin on post-operative analgesia after spinal anesthesia |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4173598/ https://www.ncbi.nlm.nih.gov/pubmed/25886102 http://dx.doi.org/10.4103/0259-1162.128907 |
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