Abbott receives CE mark for Aveir dual chamber leadless pacemaker system

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Abbott has received CE mark in Europe for the Aveir dual chamber (DR) leadless pacemaker system.

The Aveir DR leadless pacemaker system utilises a new method of delivering dual chamber therapy as it is comprised of two unique devices—one that paces the right ventricle (Aveir VR) and one that paces the right atrium (Aveir AR). Each device is roughly one-tenth the size of a traditional pacemaker and smaller than a AAA battery.

Unlike traditional pacemakers, leadless devices are implanted directly into the heart through a minimally invasive procedure, eliminating cardiac leads. As a result, leadless pacemakers reduce people’s exposure to potential lead and infection-related complications and offer a less restrictive and shorter recovery period post-implantation.

“Receiving CE mark for AVEIR DR is a historic moment in European cardiac care. This technology redefines how we approach the treatment of heart rhythm abnormalities,” said Reinoud Knops (Amsterdam University Medical Center, Amsterdam, The Netherlands). “As the world’s first dual chamber leadless pacemaker, Aveir DR is a game changer, expanding our capacity to address complex heart conditions, and significantly reducing complication risk and enhance patient comfort.”

Through Abbott’s proprietary i2i (implant-to-implant) communication technology, Aveir DR provides synchronised pacing between two leadless pacemakers on every heartbeat based on a person’s clinical needs. The i2i technology utilises high-frequency pulses to relay messages via the naturally conductive characteristics of the body’s blood between the paired, co-implanted devices. Conductive communication uses far less battery current than inductive, radio-frequency, or Bluetooth® communication, which are alternatives often used in implantable medical devices or traditional pacemakers.

“Since its inception, pacemaker technology has remained fundamentally unchanged as seamless synchronisation of two leadless pacemakers has been a significant challenge,” said Leonard Ganz, divisional vice president of medical affairs and chief medical officer at Abbott’s cardiac rhythm management business. “Aveir DR addresses a critical need for people living with slow heart rhythms and enhances people’s quality of life with its revolutionary leadless design.”

The AVEIR DR i2i global clinical investigation study showed that Aveir DR met its three prespecified primary endpoints for safety and efficacy. Results through three-months post-implant showed a 98.3% system implant success rate and more than 97% of people had a successful atrio-ventricular synchrony, so that the upper and lower chambers were beating normally, despite different postures and gaits.


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