Resultados de los tipos de endoprótesis en la reparación endovascular del aneurisma aórtico abdominal: experiencia a largo plazo de un centro colombiano de alta complejidad, el primer ejemplo latinoamericano

Abstract

Introduction: Endovascular abdominal aortic aneurysm repair (EVAR) devices are associated with a higher rate of complications at 5-year follow-up. At least 30% of patients with EVAR devices require some type of reintervention (whether endovascular or open) at 10-year follow-up. These complications include endoleak, abdominal aortic aneurysms rupture, graft migration, occlusion or infection. The objective of this paper was to determine the rates of failure for each type of EVAR stent-graft used in our local population. Also, this paper is the first step to create a Colombian and Latin American transnational EVAR device registry. Material and method: Single-center retrospective observational cohort study. Thirty-four patients with abdominal aortic aneurysms (AAA) treated with EVAR were included from 2011 through 2017. Data were collected from the patients’ electronic medical records.Results: The stent-graft Endologicx Ba (Endologix, Irvine, CA, United States), Excluder (W.L. Gore, Newark, DE, United States), Zenith (Cook Medical, Bloomington, IN, United States), and Nellix endovascular aneurysm sealing system (EVAS) (Endologix, Santa Rosa, CA, United States) were not associated with any endoleaks or any type of complications after the EVAR procedure. The Aorfix (Lombard, Didcot, United Kingdom), and Endurant (Medtronic, Minneapolis, MN, United States) stent-grafts had rates of type II endoleak (in 1 and 2 patients) of 2.9% and 5.8%, respectively that closed spontaneously. No stent-graft developed type I, III or IV endoleaks or any endovascular or open reinterventions were needed. Conclusions: This study shows that the different types of stent-graft used for to treat AAA with EVAR can be used in a safe and feasible way with good postoperative clinical outcomes in the Latin American population.