When I was a cardiology fellow in Philadelphia in 2003 I was fortunate to be one of the first physicians in the country to implant a first of its kind CYPHER drug coated stent. Prior to the advent of drug coated stents, patients received bare metal stents that were mired with the achilles heel of interventional cardiology: restenosis. This is when scar tissue formed inside of the stent infra-structure and resulted in fairly frequent repeat procedures to open the same treatment area as before. The drug coated stents appeared to resolve much of this issue but restenosis and even stents clotting off remained an important issue.

These polymers are now used in a wide range of bioresorbable implants, including: orthopedic devices such as plates, pins and screws; drug delivery systems such as solid implants and gel based systems; suture anchors; peripheral bioresorbable stents (organic stents); and surgical mesh and clips. As a sub-investigator in the Absorb III clinical trial and having enrolled patients into the study it was exciting to recently implant these approved stents in patients in the real world setting. It truly is a revolution in the stenting arena.
