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Carprofen for perioperative analgesia causes early anastomotic leakage in the rat ileum
BACKGROUND: There is increasing evidence that perioperative use of NSAIDs may compromise the integrity of intestinal anastomoses. This study aims to characterize the negative effects of carprofen on early anastomotic healing in the rat ileum. RESULTS: In 159 male Wistar rats an anastomosis was const...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3582476/ https://www.ncbi.nlm.nih.gov/pubmed/23270317 http://dx.doi.org/10.1186/1746-6148-8-247 |
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author | van der Vijver, Rozemarijn J van Laarhoven, Cees JHM Lomme, Roger MLM Hendriks, Thijs |
author_facet | van der Vijver, Rozemarijn J van Laarhoven, Cees JHM Lomme, Roger MLM Hendriks, Thijs |
author_sort | van der Vijver, Rozemarijn J |
collection | PubMed |
description | BACKGROUND: There is increasing evidence that perioperative use of NSAIDs may compromise the integrity of intestinal anastomoses. This study aims to characterize the negative effects of carprofen on early anastomotic healing in the rat ileum. RESULTS: In 159 male Wistar rats an anastomosis was constructed in the ileum. In experiment 1 eighty-four rats were divided over control and experimental groups, which received daily buprenorphine or carprofen, respectively, as an analgesic and were killed on day 1, 2 or 3 after surgery. In experiment 2 three groups of 15 rats received carprofen either immediately after surgery or with a delay of 1 or 2 days. Animals were killed after 3 days of carprofen administration. In experiment 3 three groups of 10 rats received different doses (full, half or quarter) of carprofen from surgery. In significant contrast to buprenorphine, which never did so, carprofen induced frequent signs of anastomotic leakage, which were already present at day 1. If first administration was delayed for 48 hours, the leakage rate was significantly reduced (from 80 to 20%; p = 0.0028). Throughout the study, the anastomotic bursting pressure was lowest in animals who displayed signs of anastomotic leakage. Loss of anastomotic integrity did not coincide with reduced levels of hydroxyproline or increased activity of matrix metalloproteinases. CONCLUSIONS: Carprofen interferes with wound healing in the rat ileum at a very early stage. Although the mechanisms responsible remain to be fully elucidated, one should be aware of the potential of NSAIDs to interfere with the early phase of wound repair. |
format | Online Article Text |
id | pubmed-3582476 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-35824762013-02-27 Carprofen for perioperative analgesia causes early anastomotic leakage in the rat ileum van der Vijver, Rozemarijn J van Laarhoven, Cees JHM Lomme, Roger MLM Hendriks, Thijs BMC Vet Res Research Article BACKGROUND: There is increasing evidence that perioperative use of NSAIDs may compromise the integrity of intestinal anastomoses. This study aims to characterize the negative effects of carprofen on early anastomotic healing in the rat ileum. RESULTS: In 159 male Wistar rats an anastomosis was constructed in the ileum. In experiment 1 eighty-four rats were divided over control and experimental groups, which received daily buprenorphine or carprofen, respectively, as an analgesic and were killed on day 1, 2 or 3 after surgery. In experiment 2 three groups of 15 rats received carprofen either immediately after surgery or with a delay of 1 or 2 days. Animals were killed after 3 days of carprofen administration. In experiment 3 three groups of 10 rats received different doses (full, half or quarter) of carprofen from surgery. In significant contrast to buprenorphine, which never did so, carprofen induced frequent signs of anastomotic leakage, which were already present at day 1. If first administration was delayed for 48 hours, the leakage rate was significantly reduced (from 80 to 20%; p = 0.0028). Throughout the study, the anastomotic bursting pressure was lowest in animals who displayed signs of anastomotic leakage. Loss of anastomotic integrity did not coincide with reduced levels of hydroxyproline or increased activity of matrix metalloproteinases. CONCLUSIONS: Carprofen interferes with wound healing in the rat ileum at a very early stage. Although the mechanisms responsible remain to be fully elucidated, one should be aware of the potential of NSAIDs to interfere with the early phase of wound repair. BioMed Central 2012-12-27 /pmc/articles/PMC3582476/ /pubmed/23270317 http://dx.doi.org/10.1186/1746-6148-8-247 Text en Copyright ©2012 van der Vijver et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article van der Vijver, Rozemarijn J van Laarhoven, Cees JHM Lomme, Roger MLM Hendriks, Thijs Carprofen for perioperative analgesia causes early anastomotic leakage in the rat ileum |
title | Carprofen for perioperative analgesia causes early anastomotic leakage in the rat ileum |
title_full | Carprofen for perioperative analgesia causes early anastomotic leakage in the rat ileum |
title_fullStr | Carprofen for perioperative analgesia causes early anastomotic leakage in the rat ileum |
title_full_unstemmed | Carprofen for perioperative analgesia causes early anastomotic leakage in the rat ileum |
title_short | Carprofen for perioperative analgesia causes early anastomotic leakage in the rat ileum |
title_sort | carprofen for perioperative analgesia causes early anastomotic leakage in the rat ileum |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3582476/ https://www.ncbi.nlm.nih.gov/pubmed/23270317 http://dx.doi.org/10.1186/1746-6148-8-247 |
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