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CARDIOVASCULAR
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The XIENCE™ DES is proven to offer unparalleled patient outcomes during and long after percutaneous coronary interventions (PCI).1 Implanted in over 15 million patients and studied in 120+ clinical trials,* XIENCE™ Stent provides consistent long-term safety data beyond 10 years.2 XIENCE™ Stent allows interventional cardiologists (ICs) to achieve the positive outcomes they want for their patients.

Reach for Xience

XIENCE Sierra™ Drug Eluting Stent System

The newest DES in the XIENCE™ family, XIENCE Sierra™ Stent has an enhanced design that offers exceptional deliverability, pushability, post dilatation expansion as well as an ultra-low profile and smoother crossing.

XIENCE Alpine™ Everolimus Eluting Coronary Stent System

XIENCE Alpine™ Stent, like all XIENCE™ Stents, features a unique combination of design, drug, and fluoropolymer—with the fluoropolymer coating shown to be significantly more anti-thrombotic than other DES.3

* Data on file at Abbott. The 15 million implants is based on DES data through Q1 2020.

† Tests performed by and data on file at Abbott.

References

  1. Zanchin C, et al. JACC Cardiovasc Interv. 2019;12(17):1665-1675. • Serruys P, et al. N Engl J Med. 2010;363(2):136-146. • Shiomi H, et al.  JACC Cardiovasc Interv. 2019;12:637-647. • Kufner S, et al. Circulation. 2019:139(3):325-333. • Palmerini T, et al. Lancet. 2012;379(9824);1393-1402. • Bangalore S, et al. Circ Cardiovasc Interv. 2013;6:378-390. • Pilgrim T, et al. Lancet. 2014;384:2111-2122. • Pilgrim T, et al. Lancet 2018;392:737-746.
  2. Kufner S, et al. Circulation. 2019:139(3):325-333. Shiomi H, et al. J Am Coll Cardiol Interv. 2019;12:637-647.
  3. Jinnouchi H, et al. J Am Coll Cardiol. 2019;74:Suppl B – TCT-291.

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