2011
DOI: 10.1016/j.ejvs.2011.06.008
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Final Results of the Prospective European Trial of the Endurant Stent Graft for Endovascular Abdominal Aortic Aneurysm Repair

Abstract: The Endurant Stent Graft was successfully delivered and deployed in all cases and performed safely and effectively in all patients, including those with unfavourable proximal neck anatomy.

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Cited by 54 publications
(46 citation statements)
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“…Technical specifications of the Endurant Stent Graft System have been published previously. 11,12 Preoperatively, each patient had a customised plan made with respect to stent diameters and length, dependent on their aortic and iliac dimensions. For optimal sealing, it was advised to oversize the stent diameter by approximately 20% based on inner vessel diameter.…”
Section: Study Proceduresmentioning
confidence: 99%
See 1 more Smart Citation
“…Technical specifications of the Endurant Stent Graft System have been published previously. 11,12 Preoperatively, each patient had a customised plan made with respect to stent diameters and length, dependent on their aortic and iliac dimensions. For optimal sealing, it was advised to oversize the stent diameter by approximately 20% based on inner vessel diameter.…”
Section: Study Proceduresmentioning
confidence: 99%
“…The Endurant Stent Graft System received CE mark approval in July 2008 and Food and Drug Administration (FDA) approval in December 2010. After a safety assessment trial conducted in Europe, 11 the Endurant Stent Graft Natural Selection Global Postmarket Registry (ENGAGE) was undertaken to quantify the performance of this recently released endograft within the context of contemporary, real-world use. Herein, we report the perioperative and 1-year results of this global, multicentre, prospective 1262-patient study of the Endurant Stent Graft System.…”
mentioning
confidence: 99%
“…[7] Experience and new stent graft systems reduce this requirement to below 1%. [8][9][10] Yavuz et al [11] also reported this problem in their study.…”
mentioning
confidence: 59%
“…21 Serious adverse events were comparable between the high (.60u) and moderate (,60u) angulation groups. There were no device migrations, stent fractures, aortic ruptures, or conversions, but 3 secondary endovascular procedures were performed for outflow vessel stenosis, graft limb occlusion, and iliac extension (none in the high angulation group).…”
Section: ¤ ¤mentioning
confidence: 85%