2015
DOI: 10.1177/1526602815618492
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Global Experience With the Nellix Endosystem for Ruptured and Symptomatic Abdominal Aortic Aneurysms

Abstract: EVAS in the acute setting appears safe and feasible and concordant with the literature for endovascular aneurysm repair. More robust prospective and comparative data are required to establish the position of the technique in the treatment algorithm of acute AAA.

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Cited by 31 publications
(24 citation statements)
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“…7e9 Subsequent publications have reported successful use outside the original IFU, in combination with parallel stents (chimney EVAS or ChE-VAS), 10 for the salvage for failed conventional EVAR 11 and for ruptured AAA. 8 All papers have relatively short follow up (<2 years). Despite seemingly favourable results, there has been progressive and substantial refinement with regard to the device IFU such that the morphological suitability for on-label EVAS has been considerably narrowed.…”
Section: Introductionmentioning
confidence: 99%
“…7e9 Subsequent publications have reported successful use outside the original IFU, in combination with parallel stents (chimney EVAS or ChE-VAS), 10 for the salvage for failed conventional EVAR 11 and for ruptured AAA. 8 All papers have relatively short follow up (<2 years). Despite seemingly favourable results, there has been progressive and substantial refinement with regard to the device IFU such that the morphological suitability for on-label EVAS has been considerably narrowed.…”
Section: Introductionmentioning
confidence: 99%
“…In spite of these difficulties and although there is few experience by treatment the ruptured abdominal aortic aneurysma with the Nellix endosystem and in especially in conjunction with the chimney procedure [14,15], we decided to use the Nellix ® endosystem for both reasons: (i) to allow for secure sealing of the aortic rupture side as well as the insufficiency of the proximal anastomosies side and (ii) to safely seal potential gutters around the renal stentgrafts.…”
Section: Discussionmentioning
confidence: 99%
“…Therefore, when Nellix was launched few years ago, there was a high expectation on limiting the rate of type II endoleaks. Nevertheless, the device did not perform at the standards that it was initially expected, probably because in most of the cases it was used outside the instructions for use (IFU) [4043]. Specifically, the IFU instructed aortic proximal neck diameter range of 18 to 28 mm, minimum aortic proximal neck length ≥ 10 mm, proximal aortic neck angulation of ≤ 60°, aortic aneurysm with a blood lumen diameter ≤ 70 mm, ratio of maximum aortic aneurysm diameter to maximum aortic blood lumen diameter < 1.4, and distal iliac artery seal zone with length of ≥10 mm and diameter range of 9 to 25 mm.…”
Section: Type II Endoleaksmentioning
confidence: 99%