Over 100 California Auctions End Today - Bid Now
Over 350 Total Lots Up For Auction at Two Locations - CO 05/12, PA 05/15

Abbott's dissolving stent gets support from FDA advisory panel

by Gail Kalinoski, Contributing Reporter | March 16, 2016
Business Affairs Cardiology Population Health Risk Management

However, in a San Diego Union-Tribune/Associated Press report, health writer Matthew Perrone noted that there were some company studies that showed slightly higher rates of cardiovascular complications with the Absorb device compared to the Xience metal stents, particularly when inserted into smaller arteries. The AP report stated the difference of 1.7 percent was “not deemed statistically significant.”

The AP story also points to two prominent cardiologists – Dr. David Holmes and Dr. Michael Mack – who wrote an editorial in the February Journal of the American College of Cardiology that said the Absorb stent had not shown superior results.

stats Advertisement
DOTmed text ad

Training and education based on your needs

Stay up to date with the latest training to fix, troubleshoot, and maintain your critical care devices. GE HealthCare offers multiple training formats to empower teams and expand knowledge, saving you time and money

stats

The Tech Times reported federal regulators with the FDA had found heart attack and stent-related blood clots were more likely to occur with use of the Absorb dissolving stent compared to Xience.

Drug coatings were first added to stents in 2003 to help prevent scar tissue buildup from reclogging arteries. But later studies found arteries with stents could still get blood clots, so Abbott and other manufacturers turned to developing dissolving stents.

Absorb is already being sold in at least 100 countries, including in Europe.

Back to HCB News

You Must Be Logged In To Post A Comment