Transient scaffolding using bioresorbable drug-eluting polymeric platforms aims to improve late clinical outcomes through restoration of vasomotion, adaptive shear stress, late plaque regression and expansive remodelling. However, long-term data are scarce. Several studies have reported the midterm comparison of the Absorb™ bioresorbable scaffold (Abbott Vascular, Santa Clara, CA, USA) with its metallic stent counterpart, XIENCE® (Abbott Vascular). Preclinical evaluation has shown that scaffold degradation is complete by 36 months3. The aim of this report is to present the first four-year comparative evaluation after the expected full resorption of the scaffold device.,
Department of Cardiology

Chevalier, B., Cequier, A., Dudek, D., Haude, M., Carrié, D., Sabaté, M., … Serruys, P. (2018). Four-year follow-up of the randomised comparison between an everolimus-eluting bioresorbable scaffold and an everolimus-eluting metallic stent for the treatment of coronary artery stenosis (ABSORB II Trial). EuroIntervention, 13(13), 1561–1564. doi:10.4244/EIJ-D-17-00873