Key interventional cardiology takeaways from the SCAI 2022 conference

Early clinical evaluation of the Alleviant System to create no-implant interatrial shunts to treat heart failure patients with preserved and reduced ejection fraction (HFpEF and HFrEF) demonstrated procedural safety and feasibility with a promising efficacy signal through six months.
One of the newest technologies to be discussed at SCAI 2022 was a no-implant interatrial shunt device to treat heart failure patients with preserved and reduced ejection fraction (HFpEF and HFrEF), which showed safety and feasibility with a promising efficacy signal through six months.

The key interventional cardiology takeaways from sessions presented at the Society for Cardiovascular Angiography and Interventions (SCAI) 2022 annual meeting.

More than 68,000 stents recalled after multiple injuries

The Advanta V12 and iCast (bottom image) balloon expandable covered stents were recalled by Atrium/Getinge because the balloons may not deflate quickly when using thicker contrast for endovascular use.

The Advanta V12 (top) and iCast (bottom) balloon expandable covered stents were recalled by Atrium Medical, a subsidiary of Getinge, because the balloons may not deflate quickly when using thicker contrast for endovascular use. The iCast device is available in the United States, and the Advanta device is not. 

Dozens of customers have reported issues with the device’s balloon or catheter hub separating from the delivery system, mostly during off-label use in a patient's blood vessels.