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.

News

March 29, 2012 — In the second year of an ongoing trial, the Resolute zotarolimus-eluting stent (Medtronic) achieved a ...

Home March 29, 2012
Home
Feature

March 27, 2012 — Biodegradable polymer drug-eluting stents (DES) provide better long-term safety and efficacy than ...

Home March 27, 2012
Home
Feature | Mark Paquin

April 15, 2012, will mark the 10th anniversary of the approval of the first drug-eluting stent (DES). Ten years ago, the ...

Home March 16, 2012
Home
News

March 9, 2012 — Boston Scientific Corp. announced the launch of the Promus Element everolimus-eluting coronary stent sys ...

Home March 09, 2012
Home
News

March 6, 2012 — In a development that brings advanced combination therapy treatment of peripheral artery disease (PAD) t ...

Home March 06, 2012
Home
News

February 24, 2012 ­– The U.S. Food and Drug Administration (FDA) this week granted the first coronary stent indication ...

Home February 24, 2012
Home
Technology

February 20, 2012 — Medtronic announced U.S. Food and Drug Administration (FDA) approval of the Resolute Integrity drug ...

Home February 20, 2012
Home
News

February 1, 2012 — Boston Scientific announced the first patient use and European market launch of the Promus Element ...

Home February 01, 2012
Home
News

January 23, 2012 – Boston Scientific Corp. said the U.S. District Court for the District of New Jersey has found all the ...

Home January 24, 2012
Home
News

January 9, 2012 – A registry that includes every patient in Sweden having percutaneous coronary intervention (PCI) found ...

Home January 09, 2012
Home
News

December 22, 2011 ­– Abbott today announced the initiation of ESPRIT I, a first-of-its-kind clinical trial in Europe ...

Home December 22, 2011
Home
Technology

December 12, 2011 - Boston Scientific recently announced U.S. Food and Drug Administration (FDA) approval for the Promus ...

Home December 12, 2011
Home
News

December 9, 2011 — Abbott announced Thursday the initiation of ABSORB II, the first randomized, controlled, multi-center ...

Home December 09, 2011
Home
News

November 21, 2011 — Micell Technologies Inc. announced the release of preliminary data from the first-in-human clinical ...

Home November 21, 2011
Home
News

November 15, 2011The risk of late stent thrombosis (ST) in the first generation of drug-eluting stents continues for ...

Home November 15, 2011
Home
Subscribe Now