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Updated: Jul 18, 2026

A Murine Model of Stent Implantation in the Carotid Artery for the Study of Restenosis
Published on: May 14, 2013
XIENCE V everolimus-eluting coronary stent system: a novel second generation drug-eluting stent
1Academic Medical Center, University of Amsterdam, Department of Cardiology, Meibergdreef 9, PO Box 22660, 1105 AZ Amsterdam, The Netherlands. m.a.beijk@amc.uva.nl
Insights
Drug-eluting stents (DES) effectively treat coronary artery disease by reducing restenosis. The XIENCE V everolimus-eluting stent shows promise with improved deliverability and sustained drug elution for better vascular compatibility.
Area of Science:
- Cardiovascular Medicine
- Biomaterials Science
Background:
- Drug-eluting stents (DES) are crucial in percutaneous coronary intervention, reducing restenosis and clinical events.
- Current approved DES include sirolimus-eluting stents (SES), paclitaxel-eluting stents (PES), and zotarolimus-eluting stents (ZES).
Purpose of the Study:
- To evaluate the safety and efficacy of the XIENCE V everolimus-eluting coronary stent system.
- To compare the performance of the everolimus-eluting stent with earlier-generation DES.
Main Methods:
- The study references findings from SPIRIT I, FUTURE I, and II trials involving the everolimus-eluting stent.
- Assessment of clinical and angiographic outcomes, deliverability, radiopacity, and vascular compatibility.
Main Results:
- The everolimus-eluting stent demonstrated safety and tolerability.
- Favorable clinical and angiographic results were observed.
- The XIENCE V system offers enhanced deliverability, radiopacity, and sustained drug elution via a durable polymer.
Conclusions:
- The XIENCE V everolimus-eluting coronary stent system is a safe and effective option for coronary artery disease treatment.
- It presents potential advantages over previous DES generations, including improved vascular compatibility.
Abstract:
Drug-eluting stents (DES) have been shown to be safe and significantly reduce clinical events and angiographic restenosis in the percutaneous treatment of coronary artery disease. Currently, three DES have been approved in Europe and Northern America: the sirolimus-eluting stent (SES), the paclitaxel-eluting stent (PES) and the zotarolimus-eluting stent (ZES). Everolimus, an analog of sirolimus, is an immunosuppressive and antiproliferative agent. In three studies, the SPIRIT I, FUTURE I and II, the everolimus-eluting stent has proven to be safe, well-tolerated and has shown very favorable clinical and angiographic results. Compared with earlier-generation DES, the XIENCE V everolimus-eluting coronary stent system (Advanced Cardiovascular Systems Inc., an Abbott Vascular Company, CA, USA) may provide enhanced deliverability, radiopacity with thinner strut filaments and, owing to a durable polymer, sustained drug elution and vascular compatibility.
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