This is a multicentric voluntary observational study with a retrospective evaluation of prospectively collected data concerning the treatment of visceral aneurysms with flow diversion stent Derivo Peripher and Derivo 2 (DED, Acandis GmbH) Follow-up will include clinical and radiological (CT) evaluation at least 12 months after the intervention. The enrollment period will be of 65 months (01/jan/2020-30/jun/2025). Sample size will be of 100 patients.
Study Type
OBSERVATIONAL
Enrollment
100
Flow diverter stenting
AOU Città della Salute e della Scienza di Torino
Torino, TO, Italy
RECRUITINGEfficacy of the stenting in terms of patency and side branches
stent patency and side branches (the absence of stenosis greater than 50% of the stent's internal lumen and the side branches' lumen)
Time frame: 12 months
Efficacy of the stenting in terms of aneurysm thrombosis rate
aneurysm (partial or complete, \>50% or 100%) thrombosis
Time frame: 12 months
Efficacy of the stenting in terms of aneurysm volume assessment
aneurysm volume assessment (percentage of volume reduction respect to the initial volume)
Time frame: 12 months
Safety in terms of morbidity
morbidity (any adverse events occured during follow up for any causes and by causes associated with treatment)
Time frame: 12 months
Safety in terms of mortality
mortality (any cause of death related to pathology or not)
Time frame: 12 months
Safety in terms of technical issues
technical issues (any adverse event during stent placement)
Time frame: 12 months
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