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How Will New Bioabsorbable Polymer Drug Eluting Stents Impact Dapt Duration?

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How will new bioabsorbable polymer drug-eluting stents impact DAPT duration? Ian J Sarembock, MB, ChB, MD, FACC; Dean J Kereiakes, MD, FACC
The Heart & Vascular Service Line and The Lindner Center for Research and Education, The Christ Hospital Health Network, Cincinnati, Ohio The evolution of percutaneous coronary intervention (PCI) from plain old balloon angioplasty (POBA) in 1977, to bare metal stents (BMS) in 1986, through the revolutionary introduction of drug-eluting stents (DES) in 2003 which successfully treated the “Achilles heal” of BMS (neointimal proliferation and restenosis) has provided significant iterative improvement in platform design and performance. Adverse clinical events to 1-year following stent …show more content…

Stents that deliver anti-proliferative drugs from durable polymer, have reduced both clinical and angiographic restenosis compared with bare metal stents without increasing adverse events (AEs) including death or myocardial infarction (MI) (1-2). However, permanent polymers may be associated with hypersensitivity reactions, delayed and/or incomplete vascular healing which may contribute to an increased risk of both late (30 days to 1 year) and very late (beyond 1 year) stent thrombosis (ST) which was particularly evident following first generation DES (5,6). Even newer durable polymers with enhanced biocompatibility and improved clinical outcomes have still been incriminated in chronic inflammation, thrombosis and neoatherosclerosis (which occurs earlier and with increased prevalence following both 1st and 2nd generation DES (7,8,9). To reduce the risk of stent thrombosis and MI, the 2016 ACC/AHA Guideline Focused Update on Duration of Dual Antiplatelet Therapy in Patients With Coronary Artery Disease provides guidance regarding the duration of dual antiplatelet therapy following DES deployment for both stable coronary artery disease (CAD) as well as acute coronary syndromes (ACS) (10). Patients should receive clopidogrel (or an alternative P2Y12 inhibitor) in addition to aspirin for a minimum of 6 months (stable CAD) or 12 months (ACS) unless there is high bleeding risk (10). Longer treatment duration may be prescribed on an individualized basis for

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