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Piedmont Heart Institute leads the East Coast in Transcatheter Mitral Valve Replacement

Published: January 5, 2026
Piedmont Heart

Atlanta, Ga. (January 5, 2026) – Piedmont Heart Institute physicians Pradeep K. Yadav, MD, Director of Structural Interventions, and Vinod H. Thourani, MD, Marcus Chairman of Cardiovascular Surgery, successfully performed the first Transcatheter Mitral Valve Replacement (TMVR) on the East Coast (and second in the country) using the commercial Sapien M3 valve system – a state of the art, fully-percutaneous, trans-septal valve replacement for the treatment of mitral regurgitation.

This achievement further places Piedmont Heart Institute at the forefront of advanced heart valve therapies offered in the region, expanding life-changing options for patients with limited alternatives.

Both Dr. Yadav and Dr. Thourani were investigators and on the steering committee of the pivotal trial that studied Sapien M3 valve and co-authored results recently published in The Lancet, one of the most prestigious peer-reviewed scientific journals. The U.S. Food and Drug Administration (FDA) approved the Sapien M3 valve on Dec. 22, 2025, for the treatment of severe mitral regurgitation for patients who are not good candidates for surgery or Transcatheter Edge to Edge Repair (TEER).

“This is a historic moment as it fills the huge unmet clinical need for mitral valve patients,” said Dr. Yadav. “Our experience with Sapien M3 has been exceptional with very predictable results and incredible safety, even with elderly patients with comorbidities. The procedure is very teachable as it builds on existing skills, and we look forward to disseminating to our broader physician community.”

Said Dr. Thourani: “This is a major step forward in the management for the treatment of mitral regurgitation in those patients considered high risk for traditional valve surgery. As one of the leaders in the country for transcatheter valve therapies, I am glad that we are able to provide this life-saving technology to our patients in the Southeastern U.S. This significantly adds to our armamentarium to treat these complex patients!”

Sapien M3 is the first TMVR system to receive FDA approval for the treatment of mitral regurgitation – a condition that causes blood flow backward in the heart and can lead to heart failure if left untreated. Traditional solutions often required open-heart surgery or were limited to repair techniques like Transcatheter Edge to Edge Repair (TEER). The M3 system now offers:

  • Expanded treatment for patients who were unsuitable for surgery or TEER.
  • Valve replacement that can treat complex anatomies including calcification of the mitral valve with predictable results.
  • Minimally invasive deployment through a small access in the femoral vein, allowing faster recovery.
  • Demonstrated safety and effectiveness in clinical trials with significant reduction in mitral regurgitation and improved patient outcomes.

Piedmont Heart Institute, which treats patients from all 50 states, is a national destination for clinical care. Piedmont Heart clinicians are leading clinical trials, publishing frequently in the world’s leading medical journals and presenting at scientific sessions worldwide. Piedmont is one of the nation’s top-enrolling centers in studies that include valvular heart disease, complex coronary intervention, renal denervation and beyond. For more information on the Piedmont Heart Institute Marcus Valve Center, please call 404.605.5151.

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