Abbott has received Health Canada authorisation for its Esprit BTK Everolimus Eluting Resorbable Scaffold System, a dissolvable stent developed for patients with chronic limb-threatening ischemia (CLTI) affecting below-the-knee arteries.
Traditionally, balloon angioplasty has been the standard treatment, where a balloon presses arterial blockages against the vessel wall to restore blood flow. However, the approach often leads to recurrent narrowing and repeat interventions. Abbott’s new scaffold, made from a material similar to dissolving sutures, offers a minimally invasive alternative. Inserted via a catheter-based leg incision, it props the artery open while releasing the drug everolimus to aid healing.
The device provides support for up to three years before dissolving, allowing the vessel to function on its own. Results from the LIFE-BTK trial, presented at the 2024 VIVA Conference, showed a 48% reduction in repeat procedures compared to balloon angioplasty, demonstrating improved long-term outcomes.
30-09-2025