Coronary Artery Disease Clinical Trial
Official title:
SWiss Evaluation of Bioabsorbable Polymer-coated Everolimus-eluting Coronary sTent The SWEET Registry
Bioresorbable polymer drug eluting stents (DES) are an indisputable improvement over
first-generation DES with promising results on long-term adverse events. But the thicker
polymer and/or strut may hinder its deliverability. Complex procedures challenge stent
deliverability and stent delivery failure impacts clinical prognosis.
This registry aimed to assess the immediate performance of the third-generation Synergy
everolimus-eluting stent (sEES) and its 12-month clinical follow-up in an all-comer
population.
All consecutive patients treated with the SYNERGY stent at our institutions were prospectively included in the SWEET registry. Baseline and procedural characteristics were collected at index procedure. Clinical follow-up was performed at 1 month and 1 year by clinic visit or follow-up call. The study end point was a composite of cardiac death (CD), myocardial infarction (MI) and target lesion revascularization (TLR) at 1 year. ;
Observational Model: Case Control, Time Perspective: Retrospective
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