Stents Drug Eluting

This channel includes news and new technology innovations for drug eluting stents (DES). These drug coated stents were developed to solve a frequent problem with bare metal stents, which can cause neointimal hyperplasia (scar tissue growth) in some patients. The antiproliferative drugs used on DES prevent the growth of tissue. One downside of DES is the requirement for patients to take long-term antiplatelet therapy to prevent the possible formation of clots on these stents. Newer generation DES use technologies help the vessels heal faster, which may allow reduce the duration of dual antiplatelet therapy (DAPT), or use a single drug, usually eliminating aspirin. This section includes news for both metallic and bioresorbable drug-eluting stents and related clinical trial data.

Technology

The FDA recently cleared Boston Scientific Corp.’s PROMUS Everolimus-Eluting Coronary Stent System.


Boston Scientific ...

Home September 09, 2008
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News

September 5, 2008 - The results of the SYNTAX study, a head-to-head comparison between drug-eluting stents (DES) using ...

Home September 04, 2008
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Technology

The FDA recently cleared Boston Scientific Corp.’s PROMUS Everolimus-Eluting Coronary Stent System and Abbott Vascular’s ...

Home September 03, 2008
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Feature | Venkat Rajan, medical research analyst, Frost & Sullivan

This comparison chart features three categories of stents: coronary, carotid and peripheral. We gratefully acknowledge ...

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September 2, 2008 - The safety debate about drug-eluting stents (DES) is still ongoing and in these times of uncertainty ...

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September 2, 2008 – Boston Scientific Corp. today announced positive one-year results from the European and ...

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September 2, 2008 - Data from the landmark SYNTAX trial indicates patients with very complex coronary artery disease can ...

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September 2, 2008 - Patients with both diabetes and advanced blockages in at least three heart vessels will find good ...

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August 28, 2008 – In patients with diabetes, the CYPHER Sirolimus-eluting coronary stent outperformed the Taxus stent ...

Home August 27, 2008
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August 27, 2008 - Cordis Corp. today said it received CE mark approval to market the CYPHER SELECT Plus Sirolimus ...

Home August 26, 2008
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Technology

Medtronic Inc. recently announced the initiation of the first investigational sites in the U.S. to participate in ...

Home August 25, 2008
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August 25, 2008 - A study conducted by the Cardiovascular Research Institute, Washington Hospital Center, Washington, D ...

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Technology

OrbusNeich will showcase its Genous Stent at TCT 2008, a stent that was CE Marked in 2005. The company’s data ...

Home August 06, 2008
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Technology


XTENT Inc.'s Custom NX stent system reportedly allows physicians to customize the length and diameter of the ...

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News

July 31, 2008 - Medtronic Inc. said today it initiated the first investigational sites in the U.S. to participate in ...

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