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January 21, 2020
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Leadless pacemaker for patients with atrioventricular block nets FDA approval

Larry Chinitz

The FDA has approved the first leadless pacemaker with atrioventricular synchrony, according to a press release from Medtronic.

Perspective from Bruce L. Wilkoff, MD

The new leadless pacemaker (Micra AV, Medtronic) is indicated for the treatment of patients with atrioventricular block.

According to the release, this new device is similar in size and shape to the company’s original leadless pacemaker (Micra Transcatheter Pacing System, Medtronic), but features atrial sensing algorithms to detect cardiac movement, which enables the device to adjust ventricular pacing to coordinate with the atrium.

As Healio previously reported, the first version of the leadless pacemaker was approved in 2016.

“With the approval of Micra AV, more pacemaker patients qualify for a new treatment option that offers the advantages of leadless pacing — including a minimally invasive implant procedure and a cosmetically invisible device,” Larry Chinitz, MD, cardiac electrophysiologist and director of NYU Langone’s Heart Rhythm Center, said in the release. “Although complications with traditional pacemakers are infrequent, when they occur, they’re expensive to treat and can be invasive for the patient. Real-world use of Micra has shown a 63% reduction in major complications compared to traditional pacemakers.”

The approval is based on the results of the MARVEL 2 study that was presented at the 2019 American Heart Association Scientific Sessions, as Healio previously reported. Researchers found that patients with atrioventricular block implanted with device experienced improvements in atrioventricular synchrony and stroke volume when under algorithm-based atrioventricular synchronous pacing compared with when under VVI pacing. - by Scott Buzby

Disclosure: Chinitz reports he is on the speaker’s bureau for Abbott, Biotronik and Medtronic and is a consultant/advisory board member for Medtronic.