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Infliximab’s influence on anastomotic strength and degree of inflammation in intestinal surgery in a rabbit model

BACKGROUND: Infliximab, a TNF-α inhibitor, is a potent anti-inflammatory drug in the treatment of inflammatory bowel diseases. Recent studies have investigated the effect of infliximab treatment on postoperative complications such as anastomotic leakage, however, with conflicting results and conclus...

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Autores principales: Frostberg, Erik, Ström, Petter, Gerke, Oke, Qvist, Niels
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4017771/
https://www.ncbi.nlm.nih.gov/pubmed/24762063
http://dx.doi.org/10.1186/1471-2482-14-23
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author Frostberg, Erik
Ström, Petter
Gerke, Oke
Qvist, Niels
author_facet Frostberg, Erik
Ström, Petter
Gerke, Oke
Qvist, Niels
author_sort Frostberg, Erik
collection PubMed
description BACKGROUND: Infliximab, a TNF-α inhibitor, is a potent anti-inflammatory drug in the treatment of inflammatory bowel diseases. Recent studies have investigated the effect of infliximab treatment on postoperative complications such as anastomotic leakage, however, with conflicting results and conclusions. The purpose of this study was to investigate whether a single dose infliximab has an adverse effect on the anastomotic healing process, observed as reduced anastomotic breaking strength and histopathologically verified lower grade of inflammatory response, in the small intestine of a rabbit. METHODS: Thirty New Zealand rabbits (median weight 2.5 kg) were allocated to treatment with an intravenous bolus of either 10 mg/kg infliximab (n = 15) or placebo (n = 15). One week later all rabbits underwent two separate end-to-end anastomoses in the jejunum under general anesthesia. At postoperative day three, the anastomotic breaking strength was determined and histopathological changes were examined. RESULTS: The mean value of anastomotic breaking strength in the placebo group was 1.89 ± 0.36 N and the corresponding value was 1.81 ± 0.33 N in the infliximab treated rabbits. There was no statistically significant difference between the groups (p = 0.51). The infliximab-treated rabbits had a significant lower degree of inflammatory infiltration response compared to the placebo group (p = 0.047). CONCLUSIONS: Our conclusion, limited by the small sample sizes in both groups, is that a single dose of infliximab, given one week prior to surgery, does not have an impact on the anastomotic breaking strength on the third postoperative day in the small intestine of rabbits.
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spelling pubmed-40177712014-05-13 Infliximab’s influence on anastomotic strength and degree of inflammation in intestinal surgery in a rabbit model Frostberg, Erik Ström, Petter Gerke, Oke Qvist, Niels BMC Surg Research Article BACKGROUND: Infliximab, a TNF-α inhibitor, is a potent anti-inflammatory drug in the treatment of inflammatory bowel diseases. Recent studies have investigated the effect of infliximab treatment on postoperative complications such as anastomotic leakage, however, with conflicting results and conclusions. The purpose of this study was to investigate whether a single dose infliximab has an adverse effect on the anastomotic healing process, observed as reduced anastomotic breaking strength and histopathologically verified lower grade of inflammatory response, in the small intestine of a rabbit. METHODS: Thirty New Zealand rabbits (median weight 2.5 kg) were allocated to treatment with an intravenous bolus of either 10 mg/kg infliximab (n = 15) or placebo (n = 15). One week later all rabbits underwent two separate end-to-end anastomoses in the jejunum under general anesthesia. At postoperative day three, the anastomotic breaking strength was determined and histopathological changes were examined. RESULTS: The mean value of anastomotic breaking strength in the placebo group was 1.89 ± 0.36 N and the corresponding value was 1.81 ± 0.33 N in the infliximab treated rabbits. There was no statistically significant difference between the groups (p = 0.51). The infliximab-treated rabbits had a significant lower degree of inflammatory infiltration response compared to the placebo group (p = 0.047). CONCLUSIONS: Our conclusion, limited by the small sample sizes in both groups, is that a single dose of infliximab, given one week prior to surgery, does not have an impact on the anastomotic breaking strength on the third postoperative day in the small intestine of rabbits. BioMed Central 2014-04-24 /pmc/articles/PMC4017771/ /pubmed/24762063 http://dx.doi.org/10.1186/1471-2482-14-23 Text en Copyright © 2014 Frostberg 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 credited.
spellingShingle Research Article
Frostberg, Erik
Ström, Petter
Gerke, Oke
Qvist, Niels
Infliximab’s influence on anastomotic strength and degree of inflammation in intestinal surgery in a rabbit model
title Infliximab’s influence on anastomotic strength and degree of inflammation in intestinal surgery in a rabbit model
title_full Infliximab’s influence on anastomotic strength and degree of inflammation in intestinal surgery in a rabbit model
title_fullStr Infliximab’s influence on anastomotic strength and degree of inflammation in intestinal surgery in a rabbit model
title_full_unstemmed Infliximab’s influence on anastomotic strength and degree of inflammation in intestinal surgery in a rabbit model
title_short Infliximab’s influence on anastomotic strength and degree of inflammation in intestinal surgery in a rabbit model
title_sort infliximab’s influence on anastomotic strength and degree of inflammation in intestinal surgery in a rabbit model
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4017771/
https://www.ncbi.nlm.nih.gov/pubmed/24762063
http://dx.doi.org/10.1186/1471-2482-14-23
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