This study randomized 3514 patients to a thin-strut biodegradable polymer everolimus-eluting stent (SYNERGY) vs. a sirolimus-eluting stent (ORSIRO) vs. a durable polymer zotarolimus-eluting stent (RESOLUTE INTEGRITY).
The combined endpoint, the rate of target vessel failure, was similar for all three devices (8.3% for the zotarolimos-eluting stent, 6.8% for the everolimus-eluting stent, and 6.6% for the sirolimus-eluting stent).
Landmark analyses at one year had revealed an advantage in favor of new devices as regards the rates of revascularization and other secondary endpoints. However, at the two-year follow-up, these differences were leveled out.
Original title: Two-Year Clinical Outcome of All-Comers Treated with Three Highly Dissimilar Contemporary Coronary Drug-Eluting Stents in the Randomized BIO-RESORT Trial.
Presenter: Marlies M. Kok.
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