2013
DOI: 10.1583/13-4428c.1
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Commentary: From Bespoke to Off-the-Shelf: The t-Branch Stent-Graft for Total Endovascular TAAA Repair

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Cited by 3 publications
(4 citation statements)
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“…Usually, we do not reinforce stent grafts with self-expanding bare stents unless kinking has been evident or in case of a short landing zone of the target vessel (<20 mm). A similar strategy has been presented by other authors [26,30,31]. We used Lifestent as a relining support for Viabahn stent grafts in one case because of the long distance between the branch and the orifice of the left renal artery.…”
Section: Discussionmentioning
confidence: 97%
See 1 more Smart Citation
“…Usually, we do not reinforce stent grafts with self-expanding bare stents unless kinking has been evident or in case of a short landing zone of the target vessel (<20 mm). A similar strategy has been presented by other authors [26,30,31]. We used Lifestent as a relining support for Viabahn stent grafts in one case because of the long distance between the branch and the orifice of the left renal artery.…”
Section: Discussionmentioning
confidence: 97%
“…The current 34 mm diameter of the t-Branch system limits its use as a standalone device, because it requires off-the-shelf proximal extensions [ 31 ]. The ideal proximal landing zone for the t-Branch device is 24–30 mm (outer to outer wall), which may result in 12–29% oversizing [ 39 ].…”
Section: Discussionmentioning
confidence: 99%
“…Several studies have demonstrated promising early results, though longerterm data are pending. [36][37][38] Gore has also developed an off-the-shelf device intended for thoracoabdominal aortic aneurysms, the Gore Excluder Thoracoabdominal Branch Endoprosthesis. The Gore Thoracoabdominal Aortic Aneurysm Clinical Study is evaluating a device in Brazil with hopes to begin a subsequent feasibility study in the United States (W. L. Gore & Associates, Flagstaff, AZ).…”
Section: Aortic Branched Devicesmentioning
confidence: 99%
“…Currently, fenestrated-branched endovascular aneurysm repair (F/B-EVAR) is used in the United States, in the context of Food and Drug Administration (FDA)-sponsored investigational device exemption (IDE) trials, to treat TAAA in patients who are at high risk for open repair 11, 12, 13, 14, 15. Whereas off-the-shelf and physician-modified designs confer certain advantages, company-manufactured, custom-made devices are well suited to endovascular repair of Carrel patch aneurysms 11, 12, 13, 16. In cases of prior open repair, in which reimplantation and patch degeneration often lead to significant distortions of the normal anatomic configuration, custom-made F/B-EVAR can be designed to be patient specific and to accommodate a variety of branch vessel anatomy.…”
mentioning
confidence: 99%