Endovascular model of abdominal aortic aneurysm induction in swine

Detalhes bibliográficos
Autor(a) principal: Lederman, Alex
Data de Publicação: 2014
Outros Autores: Saliture Neto, Fernando Tavares, Ferreira, Rimarcs [UNIFESP], Figueiredo, Luis Francisco Poli de, Otoch, Jose Pinhata, Aun, Ricardo, Silva, Erasmo Simao da
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNIFESP
Texto Completo: http://repositorio.unifesp.br/handle/11600/37803
http://dx.doi.org/10.1177/1358863X14534006
Resumo: Abdominal aortic aneurysms are among the main causes of death. the high morbidity and mortality associated with aneurysm rupture and repair represents a challenge for surgeons and high risk for patients. Although experimental models are useful to understand, train, and develop new treatment and diagnostic methods for this pathology, animal models developed to date are far from ideal. Animals are either too small and do not represent the pathology of humans, or the procedures employ laparotomy, or the aortic behavior does not resemble that of a true aneurysm. We developed a novel, less invasive and effective method to induce true aortic aneurysms in Large White pigs. Animals were submitted to an endovascular chemical induction using either calcium chloride (25%) or swine pancreatic elastase. Controls were exposed to saline solution. All animals were operated on using the same surgical technique under general anesthesia. They were followed weekly with ultrasound examinations and at 4 weeks the aorta was harvested. Although elastase induced only arterial dilation, imaging, histological, and biomechanical studies of the aorta revealed the formation of true aneurysms in animals exposed to calcium chloride. Aneurysms in the latter group had biomechanical failure properties similar to those of human aneurysms. These findings indicate that the endovascular approach is viable and does not cause retroperitoneal fibrosis.
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spelling Lederman, AlexSaliture Neto, Fernando TavaresFerreira, Rimarcs [UNIFESP]Figueiredo, Luis Francisco Poli deOtoch, Jose PinhataAun, RicardoSilva, Erasmo Simao daUniversidade de São Paulo (USP)Hosp Israelita Albert EinsteinUniversidade Federal de São Paulo (UNIFESP)2016-01-24T14:37:20Z2016-01-24T14:37:20Z2014-06-01Vascular Medicine. London: Sage Publications Ltd, v. 19, n. 3, p. 167-174, 2014.1358-863Xhttp://repositorio.unifesp.br/handle/11600/37803http://dx.doi.org/10.1177/1358863X1453400610.1177/1358863X14534006WOS:000337579800002Abdominal aortic aneurysms are among the main causes of death. the high morbidity and mortality associated with aneurysm rupture and repair represents a challenge for surgeons and high risk for patients. Although experimental models are useful to understand, train, and develop new treatment and diagnostic methods for this pathology, animal models developed to date are far from ideal. Animals are either too small and do not represent the pathology of humans, or the procedures employ laparotomy, or the aortic behavior does not resemble that of a true aneurysm. We developed a novel, less invasive and effective method to induce true aortic aneurysms in Large White pigs. Animals were submitted to an endovascular chemical induction using either calcium chloride (25%) or swine pancreatic elastase. Controls were exposed to saline solution. All animals were operated on using the same surgical technique under general anesthesia. They were followed weekly with ultrasound examinations and at 4 weeks the aorta was harvested. Although elastase induced only arterial dilation, imaging, histological, and biomechanical studies of the aorta revealed the formation of true aneurysms in animals exposed to calcium chloride. Aneurysms in the latter group had biomechanical failure properties similar to those of human aneurysms. These findings indicate that the endovascular approach is viable and does not cause retroperitoneal fibrosis.Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Univ São Paulo, Univ Hosp, São Paulo, BrazilHosp Israelita Albert Einstein, São Paulo, BrazilUniversidade Federal de São Paulo, Escola Paulista Med, São Paulo, BrazilUniv São Paulo, Fac Med, São Paulo, BrazilUniversidade Federal de São Paulo, Escola Paulista Med, São Paulo, BrazilFAPESP: 2010/07307-6Web of Science167-174engSage Publications LtdVascular Medicinehttp://www.uk.sagepub.com/aboutus/openaccess.htminfo:eu-repo/semantics/openAccessaortic aneurysmbiomechanicscalcium chlorideelastasepig modelEndovascular model of abdominal aortic aneurysm induction in swineinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlereponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP11600/378032022-06-02 09:02:17.392metadata only accessoai:repositorio.unifesp.br:11600/37803Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestopendoar:34652022-06-02T12:02:17Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false
dc.title.en.fl_str_mv Endovascular model of abdominal aortic aneurysm induction in swine
title Endovascular model of abdominal aortic aneurysm induction in swine
spellingShingle Endovascular model of abdominal aortic aneurysm induction in swine
Lederman, Alex
aortic aneurysm
biomechanics
calcium chloride
elastase
pig model
title_short Endovascular model of abdominal aortic aneurysm induction in swine
title_full Endovascular model of abdominal aortic aneurysm induction in swine
title_fullStr Endovascular model of abdominal aortic aneurysm induction in swine
title_full_unstemmed Endovascular model of abdominal aortic aneurysm induction in swine
title_sort Endovascular model of abdominal aortic aneurysm induction in swine
author Lederman, Alex
author_facet Lederman, Alex
Saliture Neto, Fernando Tavares
Ferreira, Rimarcs [UNIFESP]
Figueiredo, Luis Francisco Poli de
Otoch, Jose Pinhata
Aun, Ricardo
Silva, Erasmo Simao da
author_role author
author2 Saliture Neto, Fernando Tavares
Ferreira, Rimarcs [UNIFESP]
Figueiredo, Luis Francisco Poli de
Otoch, Jose Pinhata
Aun, Ricardo
Silva, Erasmo Simao da
author2_role author
author
author
author
author
author
dc.contributor.institution.none.fl_str_mv Universidade de São Paulo (USP)
Hosp Israelita Albert Einstein
Universidade Federal de São Paulo (UNIFESP)
dc.contributor.author.fl_str_mv Lederman, Alex
Saliture Neto, Fernando Tavares
Ferreira, Rimarcs [UNIFESP]
Figueiredo, Luis Francisco Poli de
Otoch, Jose Pinhata
Aun, Ricardo
Silva, Erasmo Simao da
dc.subject.eng.fl_str_mv aortic aneurysm
biomechanics
calcium chloride
elastase
pig model
topic aortic aneurysm
biomechanics
calcium chloride
elastase
pig model
description Abdominal aortic aneurysms are among the main causes of death. the high morbidity and mortality associated with aneurysm rupture and repair represents a challenge for surgeons and high risk for patients. Although experimental models are useful to understand, train, and develop new treatment and diagnostic methods for this pathology, animal models developed to date are far from ideal. Animals are either too small and do not represent the pathology of humans, or the procedures employ laparotomy, or the aortic behavior does not resemble that of a true aneurysm. We developed a novel, less invasive and effective method to induce true aortic aneurysms in Large White pigs. Animals were submitted to an endovascular chemical induction using either calcium chloride (25%) or swine pancreatic elastase. Controls were exposed to saline solution. All animals were operated on using the same surgical technique under general anesthesia. They were followed weekly with ultrasound examinations and at 4 weeks the aorta was harvested. Although elastase induced only arterial dilation, imaging, histological, and biomechanical studies of the aorta revealed the formation of true aneurysms in animals exposed to calcium chloride. Aneurysms in the latter group had biomechanical failure properties similar to those of human aneurysms. These findings indicate that the endovascular approach is viable and does not cause retroperitoneal fibrosis.
publishDate 2014
dc.date.issued.fl_str_mv 2014-06-01
dc.date.accessioned.fl_str_mv 2016-01-24T14:37:20Z
dc.date.available.fl_str_mv 2016-01-24T14:37:20Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.citation.fl_str_mv Vascular Medicine. London: Sage Publications Ltd, v. 19, n. 3, p. 167-174, 2014.
dc.identifier.uri.fl_str_mv http://repositorio.unifesp.br/handle/11600/37803
http://dx.doi.org/10.1177/1358863X14534006
dc.identifier.issn.none.fl_str_mv 1358-863X
dc.identifier.doi.none.fl_str_mv 10.1177/1358863X14534006
dc.identifier.wos.none.fl_str_mv WOS:000337579800002
identifier_str_mv Vascular Medicine. London: Sage Publications Ltd, v. 19, n. 3, p. 167-174, 2014.
1358-863X
10.1177/1358863X14534006
WOS:000337579800002
url http://repositorio.unifesp.br/handle/11600/37803
http://dx.doi.org/10.1177/1358863X14534006
dc.language.iso.fl_str_mv eng
language eng
dc.relation.ispartof.none.fl_str_mv Vascular Medicine
dc.rights.driver.fl_str_mv http://www.uk.sagepub.com/aboutus/openaccess.htm
info:eu-repo/semantics/openAccess
rights_invalid_str_mv http://www.uk.sagepub.com/aboutus/openaccess.htm
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 167-174
dc.publisher.none.fl_str_mv Sage Publications Ltd
publisher.none.fl_str_mv Sage Publications Ltd
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
_version_ 1802764128367935488