The society says it is discussing virtual options to deliver the educational content to attendees at a later date.

Of note, the update is endorsed by EACTS, resolving some lingering left main debate, amid lots of other revised advice.

The majority of FDA-recalled devices made it to market via the 510(k) pathway, which doesn’t require new clinical or safety data.

There is no need for alarm, say researchers, but the publicly reported data deserve further study.

There is no need for alarm, say researchers, but the publicly reported data deserve further study.

In the RIBS trials, Abbott’s old BVS had the highest risks of TLR, specifically beyond 1 year, and safety worries when used for ISR.

In the RIBS trials, Abbott’s old BVS had the highest risks of TLR, specifically beyond 1 year, and safety worries when used for ISR.

In interviews with TCTMD, US cardiologists in that special role say care has shifted from paternalism to shared decision-making.