1996
DOI: 10.1016/s1078-5884(96)80141-9
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A new animal model for abdominal aortic aneurysms: Initial results using a multiple-wire stent

Abstract: A pulsatile, non-thrombogenic aortic aneurysm model approaching human dimensions has been successfully developed for the study of endoprostheses prior to their clinical use. Endovascular placement of a plain, multiple-wire Wallstent was associated with reductions in aneurysm pulsatility, pulse pressure within the sac and maximum aneurysm diameter over the study period. Stenting was associated with thrombosis of the excluded aneurysm sac in 50% of cases.

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Cited by 27 publications
(13 citation statements)
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“…Infusion of elastase in an isolated segment of the aorta to create an aneurysm model has been reported in rats [5,6], but again, similar results could hardly be effectively reproduced in large animals [7][8][9]. The most effective methods to develop an aneurysm model for larger animals have been use of an anterior patch and use of a pouch made of autogenous fascia, vein, jejunum, or synthetic polyethylene terephthalate [10][11][12][13].…”
Section: Original Researchmentioning
confidence: 82%
“…Infusion of elastase in an isolated segment of the aorta to create an aneurysm model has been reported in rats [5,6], but again, similar results could hardly be effectively reproduced in large animals [7][8][9]. The most effective methods to develop an aneurysm model for larger animals have been use of an anterior patch and use of a pouch made of autogenous fascia, vein, jejunum, or synthetic polyethylene terephthalate [10][11][12][13].…”
Section: Original Researchmentioning
confidence: 82%
“…An independent group reported good renal artery patency, renal perfusion pressure and kidney function after placement of an uncovered self-expanding Wallstent (Schneider AG, Bulach, Switzerland) in the abdominal aorta across renal artery origins [100,189]. It was supported that despite covering renal artery origins with a Wallstent during EVAR, these arteries remained widely patent with no evidence of renal infarction of microemboli formation [100,189].…”
Section: Experimental Models For Endovascular Aaa Repair (Evar)mentioning
confidence: 99%
“…The interposition graft model has been reproduced in dogs, pigs and sheep, with grafts made from crimped woven Dacron [93][94][95][96][97], biomedical grade elastomeric polyurethane [95], autologous jugular vein [98] or gastric serosa patches [99] and segments of glutaraldehyde-treated bovine internal jugular vein [100] to mimic an aneurysm. Another disadvantage is that these aneurysms do not show progressive enlargement thus differing from human AAAs [93][94][95][96][97][98][99][100]. A disadvantage of this model noted in all animals is the presence of moderate to severe fibrous reaction around the artificial aneurysm and in the sac wall.…”
Section: Interposition Graft Modelmentioning
confidence: 99%
“…created a model by interpositioning a fusiform segment of glutaraldehyde-tanned bovine internal jugular vein into the infrarenal aortas of large white pigs [91]. The resulting aneurysm had an aorta to aneurysm diameter ratio of 1:2.…”
Section: Animal Modelsmentioning
confidence: 99%