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Severe inflammatory reaction induced by peritoneal trauma is the key driving mechanism of postoperative adhesion formation
BACKGROUND: Many factors have been put forward as a driving mechanism of surgery-triggered adhesion formation (AF). In this study, we underline the key role of specific surgical trauma related with open surgery (OS) and laparoscopic (LS) conditions in postoperative AF and we aimed to study peritonea...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3266192/ https://www.ncbi.nlm.nih.gov/pubmed/22082071 http://dx.doi.org/10.1186/1471-2482-11-30 |
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author | Pismensky, Sergei V Kalzhanov, Zhomart R Eliseeva, Marina Yu Kosmas, Ioannis P Mynbaev, Ospan A |
author_facet | Pismensky, Sergei V Kalzhanov, Zhomart R Eliseeva, Marina Yu Kosmas, Ioannis P Mynbaev, Ospan A |
author_sort | Pismensky, Sergei V |
collection | PubMed |
description | BACKGROUND: Many factors have been put forward as a driving mechanism of surgery-triggered adhesion formation (AF). In this study, we underline the key role of specific surgical trauma related with open surgery (OS) and laparoscopic (LS) conditions in postoperative AF and we aimed to study peritoneal tissue inflammatory reaction (TIR), remodelling specific complications of open surgery (OS) versus LS and subsequently evaluating AF induced by these conditions. METHODS: A prospective randomized study was done in 80 anaesthetised female Wistar rats divided equally into 2 groups. Specific traumatic OS conditions were induced by midline incision line (MIL) extension and tissue drying and specific LS conditions were remodelled by intraperitoneal CO(2 )insufflation at the 10 cm of water. TIR was evaluated at the 24(th), 72(nd), 120(th )and 168(th )hour by scoring scale. Statistical analysis was performed by the non-parametric t test and two-way ANOVA using Bonferroni post-tests. RESULTS: More pronounced residual TIR was registered after OS than after LS. There were no significant TIR interactions though highly significant differences were observed between the OS and LS groups (p < 0.0001) with regard to surgical and time factors. The TIR change differences between the OS and LS groups were pronounced with postoperative time p < 0.05 at the 24(th )and 72(nd); p < 0.01 - 120(th )and p < 0.001 - 168(th )hrs. Adhesion free wounds were observed in 20.0 and 31.0% of cases after creation of OS and LS conditions respectively; with no significant differences between these values (p > 0.05). However larger adhesion size (41.67 ± 33.63) was observed after OS in comparison with LS (20.31 ± 16.38). The upper-lower 95% confidential limits ranged from 60.29 to 23.04 and from 29.04 to 11.59 respectively after OS and LS groups with significant differences (p = 0.03). Analogous changes were observed in adhesion severity values. Subsequently, severe TIR parameters were followed by larger sizes of severe postoperative adhesions in the OS group than those observed in the LS group. CONCLUSIONS: MIL extension and tissue drying seem to be the key factors in the pathogenesis of adhesion formation, triggering severe inflammatory reactions of the peritoneal tissue surrounding the MIL resulting in local and systemic consequences. CO(2 )insufflation however, led to moderate inflammation and less adhesion formation. |
format | Online Article Text |
id | pubmed-3266192 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-32661922012-01-26 Severe inflammatory reaction induced by peritoneal trauma is the key driving mechanism of postoperative adhesion formation Pismensky, Sergei V Kalzhanov, Zhomart R Eliseeva, Marina Yu Kosmas, Ioannis P Mynbaev, Ospan A BMC Surg Research Article BACKGROUND: Many factors have been put forward as a driving mechanism of surgery-triggered adhesion formation (AF). In this study, we underline the key role of specific surgical trauma related with open surgery (OS) and laparoscopic (LS) conditions in postoperative AF and we aimed to study peritoneal tissue inflammatory reaction (TIR), remodelling specific complications of open surgery (OS) versus LS and subsequently evaluating AF induced by these conditions. METHODS: A prospective randomized study was done in 80 anaesthetised female Wistar rats divided equally into 2 groups. Specific traumatic OS conditions were induced by midline incision line (MIL) extension and tissue drying and specific LS conditions were remodelled by intraperitoneal CO(2 )insufflation at the 10 cm of water. TIR was evaluated at the 24(th), 72(nd), 120(th )and 168(th )hour by scoring scale. Statistical analysis was performed by the non-parametric t test and two-way ANOVA using Bonferroni post-tests. RESULTS: More pronounced residual TIR was registered after OS than after LS. There were no significant TIR interactions though highly significant differences were observed between the OS and LS groups (p < 0.0001) with regard to surgical and time factors. The TIR change differences between the OS and LS groups were pronounced with postoperative time p < 0.05 at the 24(th )and 72(nd); p < 0.01 - 120(th )and p < 0.001 - 168(th )hrs. Adhesion free wounds were observed in 20.0 and 31.0% of cases after creation of OS and LS conditions respectively; with no significant differences between these values (p > 0.05). However larger adhesion size (41.67 ± 33.63) was observed after OS in comparison with LS (20.31 ± 16.38). The upper-lower 95% confidential limits ranged from 60.29 to 23.04 and from 29.04 to 11.59 respectively after OS and LS groups with significant differences (p = 0.03). Analogous changes were observed in adhesion severity values. Subsequently, severe TIR parameters were followed by larger sizes of severe postoperative adhesions in the OS group than those observed in the LS group. CONCLUSIONS: MIL extension and tissue drying seem to be the key factors in the pathogenesis of adhesion formation, triggering severe inflammatory reactions of the peritoneal tissue surrounding the MIL resulting in local and systemic consequences. CO(2 )insufflation however, led to moderate inflammation and less adhesion formation. BioMed Central 2011-11-14 /pmc/articles/PMC3266192/ /pubmed/22082071 http://dx.doi.org/10.1186/1471-2482-11-30 Text en Copyright ©2011 Pismensky 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 Pismensky, Sergei V Kalzhanov, Zhomart R Eliseeva, Marina Yu Kosmas, Ioannis P Mynbaev, Ospan A Severe inflammatory reaction induced by peritoneal trauma is the key driving mechanism of postoperative adhesion formation |
title | Severe inflammatory reaction induced by peritoneal trauma is the key driving mechanism of postoperative adhesion formation |
title_full | Severe inflammatory reaction induced by peritoneal trauma is the key driving mechanism of postoperative adhesion formation |
title_fullStr | Severe inflammatory reaction induced by peritoneal trauma is the key driving mechanism of postoperative adhesion formation |
title_full_unstemmed | Severe inflammatory reaction induced by peritoneal trauma is the key driving mechanism of postoperative adhesion formation |
title_short | Severe inflammatory reaction induced by peritoneal trauma is the key driving mechanism of postoperative adhesion formation |
title_sort | severe inflammatory reaction induced by peritoneal trauma is the key driving mechanism of postoperative adhesion formation |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3266192/ https://www.ncbi.nlm.nih.gov/pubmed/22082071 http://dx.doi.org/10.1186/1471-2482-11-30 |
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