Abdominal wall healing in incisional hernia using different biomaterials in rabbits
Autor(a) principal: | |
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Data de Publicação: | 2013 |
Outros Autores: | , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNIFESP |
Texto Completo: | http://dx.doi.org/10.1590/S0102-86502013000400011 http://repositorio.unifesp.br/handle/11600/7681 |
Resumo: | PURPOSE: To investigate abdominal wound healing using specific biomaterials in incisional hernias. METHODS: Incisional hernias were produced in 40 rabbits, after that they were reoperated with or without the use of meshes: PREMILENE® (PPL), ULTRAPRO® (UP), PROCEED® (PCD) or repairing without mesh (TRANSPALB). After 30 days a macroscopic and microscopic study of the part withdrawn from the abdominal wall was performed. RESULTS: Macroscopic: adhesion Area: PPL> UP and PCD (p = 0.031). Vascularization: PPL> UP and PCD (p = 0.001). PPL groups (p = 0.032) and PCD (p <0.001) showed greater meshes shrinkages when compared to UP. Microscopic: neutrophils: PCD> PPL, UP and TRANSPALB (p = 0.010); eosinophils: PPL> UP, and TRANSPALB PCD (p = 0.010); granulation tissue: PPL and PCD> UP and TRANSPALB (p <0.001); macrophages : PPL, UP and PCD> TRANSPALB (p <0.001); lymphocytes: PPL and PCD> UP (p = 0.009) and TRANSPALB (p <0.001); giant cells: PPL, UP and PCD> TRANSPALB (p <0.001); viscera adhered: PPL and UP> PCD and TRANSPALB (p <0.001). CONCLUSION: All types of meshes caused the formation of adhesions. The UP and PCD groups showed lower area and vascularization of the adhesions. The PPL and PCD groups showed higher meshes shrinkage and there was a predominance of acute inflammatory process in the PCD group. |
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Abdominal wall healing in incisional hernia using different biomaterials in rabbitsWound HealingAbdominal Wall. Hernia, VentralSurgical MeshAdhesionsBiomaterialsMaterials TestingAnimal ExperimentationRabbitsPURPOSE: To investigate abdominal wound healing using specific biomaterials in incisional hernias. METHODS: Incisional hernias were produced in 40 rabbits, after that they were reoperated with or without the use of meshes: PREMILENE® (PPL), ULTRAPRO® (UP), PROCEED® (PCD) or repairing without mesh (TRANSPALB). After 30 days a macroscopic and microscopic study of the part withdrawn from the abdominal wall was performed. RESULTS: Macroscopic: adhesion Area: PPL> UP and PCD (p = 0.031). Vascularization: PPL> UP and PCD (p = 0.001). PPL groups (p = 0.032) and PCD (p <0.001) showed greater meshes shrinkages when compared to UP. Microscopic: neutrophils: PCD> PPL, UP and TRANSPALB (p = 0.010); eosinophils: PPL> UP, and TRANSPALB PCD (p = 0.010); granulation tissue: PPL and PCD> UP and TRANSPALB (p <0.001); macrophages : PPL, UP and PCD> TRANSPALB (p <0.001); lymphocytes: PPL and PCD> UP (p = 0.009) and TRANSPALB (p <0.001); giant cells: PPL, UP and PCD> TRANSPALB (p <0.001); viscera adhered: PPL and UP> PCD and TRANSPALB (p <0.001). CONCLUSION: All types of meshes caused the formation of adhesions. The UP and PCD groups showed lower area and vascularization of the adhesions. The PPL and PCD groups showed higher meshes shrinkage and there was a predominance of acute inflammatory process in the PCD group.UNIFESP Paulista Medical School Postgraduate Program in Interdisciplinary Surgical SciencesUNIFESP Paulista Medical School Gastrointestinal DivisionUniversity of Medical Sciences of Minas Gerais FCMMG Surgery DepartmentFederal University of Minas Gerais Department of General PathologyFCMMGUNIFESP, Paulista Medical School Postgraduate Program in Interdisciplinary Surgical SciencesUNIFESP, Paulista Medical School Gastrointestinal DivisionSciELOSociedade Brasileira para o Desenvolvimento da Pesquisa em CirurgiaUniversidade Federal de São Paulo (UNIFESP)University of Medical Sciences of Minas Gerais FCMMG Surgery DepartmentFederal University of Minas Gerais Department of General PathologyFCMMGAramayo, Ana Letícia Gomes [UNIFESP]Lopes Filho, Gaspar de Jesus [UNIFESP]Barbosa, Cirênio de AlmeidaAmaral, Vânia da FonsecaCosta, Luciano Assis2015-06-14T13:45:21Z2015-06-14T13:45:21Z2013-04-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersion307-316application/pdfhttp://dx.doi.org/10.1590/S0102-86502013000400011Acta Cirurgica Brasileira. Sociedade Brasileira para o Desenvolvimento da Pesquisa em Cirurgia, v. 28, n. 4, p. 307-316, 2013.10.1590/S0102-86502013000400011S0102-86502013000400011.pdf0102-8650S0102-86502013000400011http://repositorio.unifesp.br/handle/11600/7681WOS:000317522300011engActa Cirurgica Brasileirainfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP2024-07-28T19:23:33Zoai:repositorio.unifesp.br/:11600/7681Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestbiblioteca.csp@unifesp.bropendoar:34652024-07-28T19:23:33Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false |
dc.title.none.fl_str_mv |
Abdominal wall healing in incisional hernia using different biomaterials in rabbits |
title |
Abdominal wall healing in incisional hernia using different biomaterials in rabbits |
spellingShingle |
Abdominal wall healing in incisional hernia using different biomaterials in rabbits Aramayo, Ana Letícia Gomes [UNIFESP] Wound Healing Abdominal Wall. Hernia, Ventral Surgical Mesh Adhesions Biomaterials Materials Testing Animal Experimentation Rabbits |
title_short |
Abdominal wall healing in incisional hernia using different biomaterials in rabbits |
title_full |
Abdominal wall healing in incisional hernia using different biomaterials in rabbits |
title_fullStr |
Abdominal wall healing in incisional hernia using different biomaterials in rabbits |
title_full_unstemmed |
Abdominal wall healing in incisional hernia using different biomaterials in rabbits |
title_sort |
Abdominal wall healing in incisional hernia using different biomaterials in rabbits |
author |
Aramayo, Ana Letícia Gomes [UNIFESP] |
author_facet |
Aramayo, Ana Letícia Gomes [UNIFESP] Lopes Filho, Gaspar de Jesus [UNIFESP] Barbosa, Cirênio de Almeida Amaral, Vânia da Fonseca Costa, Luciano Assis |
author_role |
author |
author2 |
Lopes Filho, Gaspar de Jesus [UNIFESP] Barbosa, Cirênio de Almeida Amaral, Vânia da Fonseca Costa, Luciano Assis |
author2_role |
author author author author |
dc.contributor.none.fl_str_mv |
Universidade Federal de São Paulo (UNIFESP) University of Medical Sciences of Minas Gerais FCMMG Surgery Department Federal University of Minas Gerais Department of General Pathology FCMMG |
dc.contributor.author.fl_str_mv |
Aramayo, Ana Letícia Gomes [UNIFESP] Lopes Filho, Gaspar de Jesus [UNIFESP] Barbosa, Cirênio de Almeida Amaral, Vânia da Fonseca Costa, Luciano Assis |
dc.subject.por.fl_str_mv |
Wound Healing Abdominal Wall. Hernia, Ventral Surgical Mesh Adhesions Biomaterials Materials Testing Animal Experimentation Rabbits |
topic |
Wound Healing Abdominal Wall. Hernia, Ventral Surgical Mesh Adhesions Biomaterials Materials Testing Animal Experimentation Rabbits |
description |
PURPOSE: To investigate abdominal wound healing using specific biomaterials in incisional hernias. METHODS: Incisional hernias were produced in 40 rabbits, after that they were reoperated with or without the use of meshes: PREMILENE® (PPL), ULTRAPRO® (UP), PROCEED® (PCD) or repairing without mesh (TRANSPALB). After 30 days a macroscopic and microscopic study of the part withdrawn from the abdominal wall was performed. RESULTS: Macroscopic: adhesion Area: PPL> UP and PCD (p = 0.031). Vascularization: PPL> UP and PCD (p = 0.001). PPL groups (p = 0.032) and PCD (p <0.001) showed greater meshes shrinkages when compared to UP. Microscopic: neutrophils: PCD> PPL, UP and TRANSPALB (p = 0.010); eosinophils: PPL> UP, and TRANSPALB PCD (p = 0.010); granulation tissue: PPL and PCD> UP and TRANSPALB (p <0.001); macrophages : PPL, UP and PCD> TRANSPALB (p <0.001); lymphocytes: PPL and PCD> UP (p = 0.009) and TRANSPALB (p <0.001); giant cells: PPL, UP and PCD> TRANSPALB (p <0.001); viscera adhered: PPL and UP> PCD and TRANSPALB (p <0.001). CONCLUSION: All types of meshes caused the formation of adhesions. The UP and PCD groups showed lower area and vascularization of the adhesions. The PPL and PCD groups showed higher meshes shrinkage and there was a predominance of acute inflammatory process in the PCD group. |
publishDate |
2013 |
dc.date.none.fl_str_mv |
2013-04-01 2015-06-14T13:45:21Z 2015-06-14T13:45:21Z |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://dx.doi.org/10.1590/S0102-86502013000400011 Acta Cirurgica Brasileira. Sociedade Brasileira para o Desenvolvimento da Pesquisa em Cirurgia, v. 28, n. 4, p. 307-316, 2013. 10.1590/S0102-86502013000400011 S0102-86502013000400011.pdf 0102-8650 S0102-86502013000400011 http://repositorio.unifesp.br/handle/11600/7681 WOS:000317522300011 |
url |
http://dx.doi.org/10.1590/S0102-86502013000400011 http://repositorio.unifesp.br/handle/11600/7681 |
identifier_str_mv |
Acta Cirurgica Brasileira. Sociedade Brasileira para o Desenvolvimento da Pesquisa em Cirurgia, v. 28, n. 4, p. 307-316, 2013. 10.1590/S0102-86502013000400011 S0102-86502013000400011.pdf 0102-8650 S0102-86502013000400011 WOS:000317522300011 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Acta Cirurgica Brasileira |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
307-316 application/pdf |
dc.publisher.none.fl_str_mv |
Sociedade Brasileira para o Desenvolvimento da Pesquisa em Cirurgia |
publisher.none.fl_str_mv |
Sociedade Brasileira para o Desenvolvimento da Pesquisa em Cirurgia |
dc.source.none.fl_str_mv |
reponame:Repositório Institucional da UNIFESP instname:Universidade Federal de São Paulo (UNIFESP) instacron:UNIFESP |
instname_str |
Universidade Federal de São Paulo (UNIFESP) |
instacron_str |
UNIFESP |
institution |
UNIFESP |
reponame_str |
Repositório Institucional da UNIFESP |
collection |
Repositório Institucional da UNIFESP |
repository.name.fl_str_mv |
Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP) |
repository.mail.fl_str_mv |
biblioteca.csp@unifesp.br |
_version_ |
1814268311080271872 |