Identificador persistente para citar o vincular este elemento: http://hdl.handle.net/10553/75924
Campo DC Valoridioma
dc.contributor.authorUson-Gargallo, Jen_US
dc.contributor.authorCrisostomo, Ven_US
dc.contributor.authorLoscertales, Ben_US
dc.contributor.authorSun, Fen_US
dc.contributor.authorSanchez-Margallo, FMen_US
dc.contributor.authorMartin-Cancho, MFen_US
dc.contributor.authorMaynar Moliner, Manuelen_US
dc.date.accessioned2020-11-24T15:42:27Z-
dc.date.available2020-11-24T15:42:27Z-
dc.date.issued2006en_US
dc.identifier.issn0894-1939en_US
dc.identifier.otherWoS-
dc.identifier.urihttp://hdl.handle.net/10553/75924-
dc.description.abstractThe purpose of this work was to develop an abdominal aortic aneurysm (AAA) model that resembles human aneurysms with potential for further growth, patent collateral vessels, and a predictable tendency to rupture, and that can be used in the development of new endoprostheses and implant training. An infrarenal AAA model was created in five domestic swine using an autologous gastric serosal patch. Pre- and postsurgical digital substraction aortograms (DSA) were obtained to document the appearance and dimensions of the aneurysm. Animals were followed up with DSA and ultrasonography on days 7, 14, 30, 45, 60, and 90 after model creation. Aneurysmal diameters were measured with both techniques in all examinations. On day 90, animals were euthanized, target arteries were harvested, and pathological evaluation was performed. The nonparametric Wilcoxon test was used to assess any differences in measured diameters. All the animals survived the surgical procedure. The aneurysmal diameters increased from 8.14 +/- 2.15 to 13.28 +/- 1.18 mm immediately after surgery (p<.05), but no subsequent significant growth of the aneurysmal sac was seen during follow-up. In this experimental setting, measurements obtained with DSA were slightly larger than those obtained with ultrasound. Two animals died of AAA rupture on days 6 and 10 (40% rupture rate). Pathological examination showed lack of elastic laminae and increased collagen content in the aortic patch. Thus, model showed a tendency to rupture, but no significant potential for further aneurysmal growth. It might be useful for training in endovascular therapies, but its usefulness for preclinical endovascular device testing is limited by its lack of growth potential.en_US
dc.languageengen_US
dc.relation.ispartofJournal of Investigative Surgeryen_US
dc.sourceJournal Of Investigative Surgery [ISSN 0894-1939], v. 19 (2), p. 97-104, (Marzo-Abril 2006)en_US
dc.subject32 Ciencias médicasen_US
dc.subject321301 Cirugía abdominalen_US
dc.subject.otherAnimal-Modelen_US
dc.subject.otherThrombusen_US
dc.subject.otherRuptureen_US
dc.subject.otherGraftsen_US
dc.subject.otherRepairen_US
dc.subject.otherAbdominal Aortic Aneurysmen_US
dc.subject.otherAnimal Modelen_US
dc.subject.otherGastric Serosaen_US
dc.subject.otherSwineen_US
dc.titleA new model of abdominal aortic aneurysm with gastric serosa patch: Surgical technique and short-term evaluationen_US
dc.typeinfo:eu-repo/semantics/Articleen_US
dc.typeArticleen_US
dc.identifier.doi10.1080/08941930600569415en_US
dc.identifier.scopus33645007137-
dc.identifier.isi000235906800005-
dc.contributor.authorscopusid6603379138-
dc.contributor.authorscopusid8537585200-
dc.contributor.authorscopusid12784378500-
dc.contributor.authorscopusid57085682500-
dc.contributor.authorscopusid6507750669-
dc.contributor.authorscopusid6506491475-
dc.contributor.authorscopusid7005962555-
dc.identifier.eissn1521-0553-
dc.description.lastpage104en_US
dc.identifier.issue2-
dc.description.firstpage97en_US
dc.relation.volume19en_US
dc.investigacionCiencias de la Saluden_US
dc.type2Artículoen_US
dc.contributor.daisngid1371671-
dc.contributor.daisngid492319-
dc.contributor.daisngid5288477-
dc.contributor.daisngid1483572-
dc.contributor.daisngid1353916-
dc.contributor.daisngid2814894-
dc.contributor.daisngid30319800-
dc.description.numberofpages8en_US
dc.utils.revisionen_US
dc.contributor.wosstandardWOS:Uson-Gargallo, J-
dc.contributor.wosstandardWOS:Crisostomo, V-
dc.contributor.wosstandardWOS:Loscertales, B-
dc.contributor.wosstandardWOS:Sun, F-
dc.contributor.wosstandardWOS:Sanchez-Margallo, FM-
dc.contributor.wosstandardWOS:Martin-Cancho, MF-
dc.contributor.wosstandardWOS:Maynar, M-
dc.date.coverdateMarzo 2006en_US
dc.identifier.ulpgcen_US
dc.contributor.buulpgcBU-MEDen_US
dc.description.jcr1,107
dc.description.jcrqQ3
dc.description.scieSCIE
item.grantfulltextnone-
item.fulltextSin texto completo-
crisitem.author.deptGIR IUIBS: Tecnología Médica y Audiovisual-
crisitem.author.deptIU de Investigaciones Biomédicas y Sanitarias-
crisitem.author.orcid0000-0001-9154-0712-
crisitem.author.parentorgIU de Investigaciones Biomédicas y Sanitarias-
crisitem.author.fullNameMaynar Moliner,Manuel-
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