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.

Feature | Dave Fornell

Over the past year several new drug-eluting stents (DES) stents have been released and SYNTAX trial data proved ...

Home September 17, 2009
Home
Feature | Stents Bioresorbable | Dave Fornell

 



Metal stents are foreign objects that can irritate vessels and cause stent thrombosis, prevent vessel ...

Home September 17, 2009
Home
Feature | Dave Fornell

The polymer coating on drug-eluting stents (DES) used to carry the antiproliferative drugs cause an increased risk ...

Home September 16, 2009
Home
News

Sept. 14, 2009 – Abbott said today the Chinese State Food and Drug Administration (SFDA) has approved the XIENCE ...

Home September 14, 2009
Home
Feature | Dave Fornell

Gregg W. Stone, M.D., offered a preview Sept. 10 of some of the key, late-breaking clinical trials and trends in ...

Home September 10, 2009
Home
News

September 3, 2009 – Abbott said last week it received approval from Health Canada for the XIENCE V Everolimus ...

Home September 03, 2009
Home
News

September 2, 2009 – Abbott announced Monday at the European Society of Cardiology Congress the widespread ...

Home September 02, 2009
Home
News

September 1, 2009 – Cordis Corp. said first patient has been enrolled in the CYPRESS study, which will assess ...

Home September 01, 2009
Home
News

August 13, 2009 – Abbott today announced the expansion of the company's XIENCE V USA post-approval study designed ...

Home August 13, 2009
Home
News

August 11, 2009 – Physicians in the United Kingdom yesterday completed patient implants using the first CE mark ...

Home August 11, 2009
Home
Technology

July 16, 2009 – Boston Scientific Corp. today said its received approval from the FDA to market its TAXUS Liberte ...

Home July 16, 2009
Home
News

July 14, 2009 – Despite the fact that drug-eluting stent (DES) implantation reduces restenosis and the need for ...

Home July 14, 2009
Home
News

June 23, 2009 – Abbott said today it received CE mark (Conformite Europeenne) for its next-generation Xience PRIME ...

Home June 23, 2009
Home
News

June 18, 2009 – Abbott this week initiated SPIRIT PRIME, a clinical trial to study the performance of the company ...

Home June 18, 2009
Home
News

June 8, 2009 - The Bypass Angioplasty Revascularization Investigation With Diabetes Trial (BARI-2D) is a useful ...

Home June 08, 2009
Home
Subscribe Now