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FELLOWS’ CORNER endpoints of recurrent angina at one year and a combined endpoint of target-lesion failure between 1 and 5 years (in which analysis the subjects from ABSORB III will be included); the early and medium-term safety of the scaffold will continue to be an question of interest as more experience increases with the delivery system and a more varied patient population. Importantly, BVS have promising uses in specific sub-populations, including cardiac transplant recipients, patients with radiation-induced coronary disease, peripheral interventions, spontaneous coronary artery dissections, and congenital heart disease patients. Both cardiac allograft vasculopathy and radiation appear to cause constrictive remodeling of the coronaries, and both populations are generally young, tend to have simple lesions and face the need for re-interventioncharacteristics which make them particularly wellsuited for BVS; a randomized trial of the Absorb BVS is under way in patients post-cardiac transplant.16 The increased stent flexibility seen in BVS is of interest in peripheral interventions, in particular in segments with vessel deformation such as the superficial femoral artery a nd the popliteal artery behind the knee.17 A novel application for BVS is in the treatment of large vessel stenosis in infants and small children, particu- larly useful in view of the growth of the child and need for re-intervention. Successful use of BVS has been reported in branch pulmonary artery stenosis,18, 19 Blalock-Taussig shunt thrombosis, coronary stenosis, and in coarctation of the aorta.20, 21 This innovation in the field of interventional cardiology holds promises in both prevalent coronary disease and niche populations in which it serves an unmet need, and further data is needed on its safety and risk-benefit profile. ■ Ada C. Stefanescu Schmidt is a Fellow-in-Training at the Massachusetts General Hospital in Boston, MA. She is doing outcomes research in interventional cardiology at the Brigham and Women’s Hospital, and is interested in adult congenital heart disease. REFERENCES 1. Serruys PW, de Jaegere P, Kiemeneij F, et al. N Engl J Med. 1994;331:489-95. 2. Block PC. Circulation. 1990;81:IV2-4. 3. Levine GN, Bates ER, Bittl JA, et al. J Am Coll Cardiol. 2016. 4. Administration USFaD. Absorb GT1™ Bioresorbable Vascular Scaffold (BVS) System - P150023. 2016. 5. Serruys PW, Ormiston JA, Onuma Y et al. Lancet. 2009;373:897-910. 6. Kereiakes DJ, Meredith IT, Windecker S et al. Circulation Cardiovascular Interventions. 2015;8. 7. Danzi GB, Sesana M, Arieti M, et al. Catheter Cardiovasc Interv. 2015;86:984-91. 8. Ellis SG, Kereiakes DJ, Metzger DC, et al. N Engl J Med. 2015. 9. Sabate M, Windecker S, Iniguez A, et al. Eur Heart J. 2016;37:229-40. 10. Capodanno D, Gori T, Nef H, et al. EuroIntervention. 2015;10:1144-53. 11. Gori T, Wiebe J, Capodanno D, et al. EuroIntervention. 2015;11. 12. Tamburino C, Capranzano P, Gori T, et al. JACC Cardiovasc Interv. 2016;9:440-9. 13. Stone GW, Gao R, Kimura T et al. Lancet. 2016;387:127789. 14. Kimura T, Kozuma K, Tanabe K, et al. Eur Heart J. 2015;36:3332-42. 15. Gao R, Yang Y, Han Y, et al. J Am Coll Cardiol. 2015;66:2298-309. 16. Pighi M, Tomai F, Petrolini A, et al. J Cardiovasc Transl Res. 2016;9:40-48. 17. Linni K, Ugurluoglu A, Hitzl W, et al. A. J Endovasc Ther. 2014;21:493-502. 18. Zartner P, Cesnjevar R, Singer H, et al. Catheter Cardiovasc Interv. 2005;66:590-4. 19. McCrossan BA, McMahon CJ, Walsh KP. Catheter Cardiovasc Interv. 2016;87:324-8. 20. Hascoet S, Baruteau A, Jalal Z, et al. Arch Cardiovasc Dis. 2014;107:462-75. 21. Schranz D, Zartner P, Michel-Behnke I, et al. Catheter Cardiovasc Interv. 2006;67:671-3.