Home > Riviste > The Journal of Cardiovascular Surgery > Fascicoli precedenti > The Journal of Cardiovascular Surgery 2014 October;55(5) > The Journal of Cardiovascular Surgery 2014 October;55(5):699-704

ULTIMO FASCICOLO
 

JOURNAL TOOLS

eTOC
Per abbonarsi
Sottometti un articolo
Segnala alla tua biblioteca
 

ARTICLE TOOLS

Estratti
Permessi

 

ORIGINAL ARTICLES  VASCULAR SECTION 

The Journal of Cardiovascular Surgery 2014 October;55(5):699-704

Copyright © 2014 EDIZIONI MINERVA MEDICA

lingua: Inglese

Rationale and design of the EAGLE Registry: EVAR with Endurant® in challenging anatomy

Stokmans R. A. 1, 2, Broos P. P. 1, Cuypers Ph. W. M. 1, Forbes T. L. 3, Vahl A. C. 4, Swartbol P. 5, Van Sambeek M. R. 1, Teijink J. A. 1, 2

1 Department of Vascular Surgery, Catharina Hospital, Eindhoven, the Netherlands; 2 Department of Epidemiology, CAPHRI Research School, Maastricht University, the Netherlands; 3 Division of Vascular Surgery, London Health Sciences Centre, University of Western Ontario, London, Canada; 4 Department of Vascular Surgery, Onze Lieve Vrouwe Gasthuis, Amsterdam, the Netherlands; 5 Department of Vascular Surgery, Ziekenhuisgroep Twente, Almelo, the Netherlands


PDF


AIM: The aim of this study was to collect clinical information on the performance of the Endurant® (II) Stent Graft System for endovascular repair in anatomically challenging infrarenal aneurysms, and to critically assess whether the current instructions for anatomic eligibility for endovascular treatment with this system are still applicable.
METHODS: Initiated by doctors, EAGLE is a prospective, non-interventional study, aiming to enrol 250 patients in 20 experienced centres across several countries worldwide. EAGLE focuses on patients with challenging angulation or neck length. To minimize the risk of selection bias and enhance data quality, EAGLE eligibility will be determined by an independent core-lab and efforts will be made to secure consecutive enrolment of challenging cases. The EAGLE database is designed to merge with the on-going ENGAGE database, which enables comparative analysis of cases and results.
RESULTS: The primary endpoint is treatment success at 30 days, 12 months and yearly up to 5 years postimplant.
CONCLUSION: Separate studies on the performance of EVAR in challenging anatomy are necessary to demonstrate safety and effectiveness of the latest generation stent-grafts, which is essential in making a balanced judgment about the optimal management of AAAs.

inizio pagina