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Thoracic epidural analgesia: a new approach for the treatment of acute pancreatitis?

This review article analyzes, through a nonsystematic approach, the pathophysiology of acute pancreatitis (AP) with a focus on the effects of thoracic epidural analgesia (TEA) on the disease. The benefit–risk balance is also discussed. AP has an overall mortality of 1 %, increasing to 30 % in its se...

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Autores principales: Windisch, Olivier, Heidegger, Claudia-Paula, Giraud, Raphaël, Morel, Philippe, Bühler, Léo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4855315/
https://www.ncbi.nlm.nih.gov/pubmed/27141977
http://dx.doi.org/10.1186/s13054-016-1292-7
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author Windisch, Olivier
Heidegger, Claudia-Paula
Giraud, Raphaël
Morel, Philippe
Bühler, Léo
author_facet Windisch, Olivier
Heidegger, Claudia-Paula
Giraud, Raphaël
Morel, Philippe
Bühler, Léo
author_sort Windisch, Olivier
collection PubMed
description This review article analyzes, through a nonsystematic approach, the pathophysiology of acute pancreatitis (AP) with a focus on the effects of thoracic epidural analgesia (TEA) on the disease. The benefit–risk balance is also discussed. AP has an overall mortality of 1 %, increasing to 30 % in its severe form. The systemic inflammation induces a strong activation of the sympathetic system, with a decrease in the blood flow supply to the gastrointestinal system that can lead to the development of pancreatic necrosis. The current treatment for severe AP is symptomatic and tries to correct the systemic inflammatory response syndrome or the multiorgan dysfunction. Besides the removal of gallstones in biliary pancreatitis, no satisfactory causal treatment exists. TEA is widely used, mainly for its analgesic effect. TEA also induces a targeted sympathectomy in the anesthetized region, which results in splanchnic vasodilatation and an improvement in local microcirculation. Increasing evidence shows benefits of TEA in animal AP: improved splanchnic and pancreatic perfusion, improved pancreatic microcirculation, reduced liver damage, and significantly reduced mortality. Until now, only few clinical studies have been performed on the use of TEA during AP with few available data regarding the effect of TEA on the splanchnic perfusion. Increasing evidence suggests that TEA is a safe procedure and could appear as a new treatment approach for human AP, based on the significant benefits observed in animal studies and safety of use for human. Further clinical studies are required to confirm the clinical benefits observed in animal studies.
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spelling pubmed-48553152016-05-05 Thoracic epidural analgesia: a new approach for the treatment of acute pancreatitis? Windisch, Olivier Heidegger, Claudia-Paula Giraud, Raphaël Morel, Philippe Bühler, Léo Crit Care Review This review article analyzes, through a nonsystematic approach, the pathophysiology of acute pancreatitis (AP) with a focus on the effects of thoracic epidural analgesia (TEA) on the disease. The benefit–risk balance is also discussed. AP has an overall mortality of 1 %, increasing to 30 % in its severe form. The systemic inflammation induces a strong activation of the sympathetic system, with a decrease in the blood flow supply to the gastrointestinal system that can lead to the development of pancreatic necrosis. The current treatment for severe AP is symptomatic and tries to correct the systemic inflammatory response syndrome or the multiorgan dysfunction. Besides the removal of gallstones in biliary pancreatitis, no satisfactory causal treatment exists. TEA is widely used, mainly for its analgesic effect. TEA also induces a targeted sympathectomy in the anesthetized region, which results in splanchnic vasodilatation and an improvement in local microcirculation. Increasing evidence shows benefits of TEA in animal AP: improved splanchnic and pancreatic perfusion, improved pancreatic microcirculation, reduced liver damage, and significantly reduced mortality. Until now, only few clinical studies have been performed on the use of TEA during AP with few available data regarding the effect of TEA on the splanchnic perfusion. Increasing evidence suggests that TEA is a safe procedure and could appear as a new treatment approach for human AP, based on the significant benefits observed in animal studies and safety of use for human. Further clinical studies are required to confirm the clinical benefits observed in animal studies. BioMed Central 2016-05-04 2016 /pmc/articles/PMC4855315/ /pubmed/27141977 http://dx.doi.org/10.1186/s13054-016-1292-7 Text en © Windisch et al. 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Review
Windisch, Olivier
Heidegger, Claudia-Paula
Giraud, Raphaël
Morel, Philippe
Bühler, Léo
Thoracic epidural analgesia: a new approach for the treatment of acute pancreatitis?
title Thoracic epidural analgesia: a new approach for the treatment of acute pancreatitis?
title_full Thoracic epidural analgesia: a new approach for the treatment of acute pancreatitis?
title_fullStr Thoracic epidural analgesia: a new approach for the treatment of acute pancreatitis?
title_full_unstemmed Thoracic epidural analgesia: a new approach for the treatment of acute pancreatitis?
title_short Thoracic epidural analgesia: a new approach for the treatment of acute pancreatitis?
title_sort thoracic epidural analgesia: a new approach for the treatment of acute pancreatitis?
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4855315/
https://www.ncbi.nlm.nih.gov/pubmed/27141977
http://dx.doi.org/10.1186/s13054-016-1292-7
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