MedStar Washington Hospital Center is first in Baltimore-Washington region to implant novel, dual-chamber leadless pacemaker

MedStar Washington Hospital Center is First in Baltimore-Washington Region to Implant Novel, Dual-chamber Leadless Pacemaker

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Dr Eldadah performs a procedure to place a leadless pacemaker in a patient at MedStar Washington Hospital Center.

Patients with slow heart rhythm can benefit from new option

Washington, DC, July 22, 2022 — The cardiac electrophysiology team at MedStar Washington Hospital Center successfully implanted the first dual-chamber leadless pacemaker system in the Baltimore-Washington region this week. Known as the Aveir™ DR Leadless Pacemaker System, this breakthrough technology is being clinically evaluated as part of a worldwide clinical trial sponsored by Abbott, and MedStar Washington Hospital Center was the only hospital in the region selected to participate. The device is not yet commercially available, and its design specifications are subject to change. Patients with slow heart rates who need pacing therapy are candidates for this trial. In May 2022, the MedStar cardiac electrophysiology team was also the first in the region to implant the Aveir™ VR single-chamber leadless pacemaker.

Patients of any age, but most commonly older people, can experience abnormal slowing of the pulse, which may cause fatigue, dizziness, passing out, and diminished quality of life. Traditional pacing therapy has required threading wires through a vein to the heart and connecting them to a metal, disc-shaped pacemaker implanted under the skin of the chest.

Thanks to the design of this investigational device, treatment can now be delivered by two mini pacemakers—each smaller than a AAA battery—that are inserted via a catheter in the large vein in the thigh. Under X-ray guidance and without any incisions, the two devices are secured within the upper and lower chambers of the heart, respectively, to normalize rhythm. The investigational device has also been designed to be readily retrieved and removed if needed.

                  A close up photo of a gloved hand holding a leadless pacemaker device in a clinical setting.

This major leap forward offers patients an excellent option to treat abnormally slow heart rates,” said Zayd Eldadah, MD, PhD, director of Cardiac Electrophysiology at MedStar Health and principal investigator of the Aveir DR i2i clinical trial. “No wires implanted in veins, no metal device under the skin, and not even a surgical incision means the design offers the potential for less risk, greater comfort, and fewer post-procedure restrictions.”

Compared to traditional pacing, leadless technology can eliminate inflammation, scars, and long-term problems such as wire insulation breaks, vein blockage, and device infection. The procedure typically takes less than an hour, and patients can go home the same day.

“The pacemaker’s impressive battery life is a key benefit,” said Cyrus Hadadi, MD, associate director of Cardiac Arrhythmia Research at MedStar Washington Hospital Center. “It also offers a real-time mapping design capability that allows physicians to measure heart electric signals, offering options to allow for improved positioning of the devices.”

                   A close up of a computer screen showing the placement of a leadless pacemaker device in the cardiac electrophysiology lab.

Most patients needing pacemaker therapy require dual-chamber systems to best regulate their rhythm. “In place of wires, the Aveir uses the patient’s own blood to transmit electrical information between the heart’s upper and lower chambers—a very clever and energy-efficient innovation,” added Dr. Eldadah, who performed the region’s first implant on July 19. “This device has the potential to be a transformational advance for patients—perhaps the medical equivalent of graduating from a rotary-dial landline to a smartphone.”

The Aveir DR i2i study is designed to assess the safety and effectiveness of the Abbott Aveir™ DR Leadless Pacemaker System in patients with abnormal heart rhythms. Patients enrolled in the study will receive Abbott’s Aveir DR leadless pacemaker device through a minimally invasive, catheter-based procedure. It will enroll up to 550 patients at up to 80 sites worldwide and data collected will be submitted to support global regulatory approvals.

For more information about the study, please contact study coordinator, Dr. Nebu Alexander, at