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Effect of magnesium infusion on thoracic epidural analgesia

INTRODUCTION: Patients of lung volume reduction surgery (LVRS) having an ASA status III or more are likely to be further downgraded by surgery to critical levels of pulmonary function. AIM: To compare the efficacy of thoracic epidural block with (0.125%) bupivacaine, fentanyl combination and (0.125%...

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Autores principales: Gupta, Sampa Dutta, Mitra, Koel, Mukherjee, Maitreyee, Roy, Suddhadeb, Sarkar, Aniruddha, Kundu, Sudeshna, Goswami, Anupam, Sarkar, Uday Narayan, Sanki, Prakash, Mitra, Ritabrata
Formato: Texto
Lenguaje:English
Publicado: Medknow Publications 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3101755/
https://www.ncbi.nlm.nih.gov/pubmed/21655018
http://dx.doi.org/10.4103/1658-354X.76512
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author Gupta, Sampa Dutta
Mitra, Koel
Mukherjee, Maitreyee
Roy, Suddhadeb
Sarkar, Aniruddha
Kundu, Sudeshna
Goswami, Anupam
Sarkar, Uday Narayan
Sanki, Prakash
Mitra, Ritabrata
author_facet Gupta, Sampa Dutta
Mitra, Koel
Mukherjee, Maitreyee
Roy, Suddhadeb
Sarkar, Aniruddha
Kundu, Sudeshna
Goswami, Anupam
Sarkar, Uday Narayan
Sanki, Prakash
Mitra, Ritabrata
author_sort Gupta, Sampa Dutta
collection PubMed
description INTRODUCTION: Patients of lung volume reduction surgery (LVRS) having an ASA status III or more are likely to be further downgraded by surgery to critical levels of pulmonary function. AIM: To compare the efficacy of thoracic epidural block with (0.125%) bupivacaine, fentanyl combination and (0.125%) bupivacaine, fentanyl combination with adjunctive intravenous magnesium infusion for the relief of postoperative pain in patients undergoing LVRS. METHODS: Patients were operated under general anesthesia. Thirty minutes before the anticipated completion of skin closure in both groups, (Group A and Group B) 7 ml of (0.125%) bupivacaine calculated as 1.5 ml/thoracic segment space for achieving analgesia in dermatomes of T4, T5, T6, T7, and T8 segments, along with fentanyl 50 μg (0.5 ml), was administered through the catheter, activating the epidural block, and the time was noted. Thereafter, in patients of Group A, magnesium sulfate injection 30 mg/kg i.v. bolus was followed by infusion of magnesium sulfate at 10 mg/kg/hr and continued up to 24 hours. Group B was treated as control. RESULTS AND ANALYSIS: A significant increase in the mean and maximum duration of analgesia in Group A in comparison with Group B (P<0.05) was observed. Total epidural dose of fentanyl and bupivacaine required in Group A was significantly lower in comparison with Group B in 24 hours. DISCUSSION: Requirement of total doses of local anesthetics along with opioids could be minimized by magnesium infusion; therefore, the further downgradation of patients of LVRS may be prevented. CONCLUSION: Intravenous magnesium can prolong opioid-induced analgesia while minimizing nausea, pruritus, and somnolence.
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spelling pubmed-31017552011-06-08 Effect of magnesium infusion on thoracic epidural analgesia Gupta, Sampa Dutta Mitra, Koel Mukherjee, Maitreyee Roy, Suddhadeb Sarkar, Aniruddha Kundu, Sudeshna Goswami, Anupam Sarkar, Uday Narayan Sanki, Prakash Mitra, Ritabrata Saudi J Anaesth Original Article INTRODUCTION: Patients of lung volume reduction surgery (LVRS) having an ASA status III or more are likely to be further downgraded by surgery to critical levels of pulmonary function. AIM: To compare the efficacy of thoracic epidural block with (0.125%) bupivacaine, fentanyl combination and (0.125%) bupivacaine, fentanyl combination with adjunctive intravenous magnesium infusion for the relief of postoperative pain in patients undergoing LVRS. METHODS: Patients were operated under general anesthesia. Thirty minutes before the anticipated completion of skin closure in both groups, (Group A and Group B) 7 ml of (0.125%) bupivacaine calculated as 1.5 ml/thoracic segment space for achieving analgesia in dermatomes of T4, T5, T6, T7, and T8 segments, along with fentanyl 50 μg (0.5 ml), was administered through the catheter, activating the epidural block, and the time was noted. Thereafter, in patients of Group A, magnesium sulfate injection 30 mg/kg i.v. bolus was followed by infusion of magnesium sulfate at 10 mg/kg/hr and continued up to 24 hours. Group B was treated as control. RESULTS AND ANALYSIS: A significant increase in the mean and maximum duration of analgesia in Group A in comparison with Group B (P<0.05) was observed. Total epidural dose of fentanyl and bupivacaine required in Group A was significantly lower in comparison with Group B in 24 hours. DISCUSSION: Requirement of total doses of local anesthetics along with opioids could be minimized by magnesium infusion; therefore, the further downgradation of patients of LVRS may be prevented. CONCLUSION: Intravenous magnesium can prolong opioid-induced analgesia while minimizing nausea, pruritus, and somnolence. Medknow Publications 2011 /pmc/articles/PMC3101755/ /pubmed/21655018 http://dx.doi.org/10.4103/1658-354X.76512 Text en © Saudi Journal of Anaesthesia http://creativecommons.org/licenses/by/2.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Gupta, Sampa Dutta
Mitra, Koel
Mukherjee, Maitreyee
Roy, Suddhadeb
Sarkar, Aniruddha
Kundu, Sudeshna
Goswami, Anupam
Sarkar, Uday Narayan
Sanki, Prakash
Mitra, Ritabrata
Effect of magnesium infusion on thoracic epidural analgesia
title Effect of magnesium infusion on thoracic epidural analgesia
title_full Effect of magnesium infusion on thoracic epidural analgesia
title_fullStr Effect of magnesium infusion on thoracic epidural analgesia
title_full_unstemmed Effect of magnesium infusion on thoracic epidural analgesia
title_short Effect of magnesium infusion on thoracic epidural analgesia
title_sort effect of magnesium infusion on thoracic epidural analgesia
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3101755/
https://www.ncbi.nlm.nih.gov/pubmed/21655018
http://dx.doi.org/10.4103/1658-354X.76512
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