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BATMAN to the rescue: TMVR technique helps cardiologists reduce risk of LVOT obstruction

How BATMAN technique can reduce risk of LVOT obstruction during TMVR

The BATMAN technique. Illustration courtesy of JACC: Cardiovascular Interventions and Giustino et al.

LVOT obstruction is a serious complication of TMVR. BATMAN may help protect patients from LVOT obstruction without leading to any additional risks.

  • Read more about BATMAN to the rescue: TMVR technique helps cardiologists reduce risk of LVOT obstruction

Inflammation may help explain how GLP-1 drugs prevent AFib

Kenneth Bilchick, MD, MS, Director of Electrophysiology Research, and a professor of cardiovascular medicine at the University of Virginia, explains GLP-1 receptor agonists (GLP-RAs) may do more than drive weight loss—showing a significantly lower risk of atrial fibrillation.

Kenneth Bilchick, MD, spoke to Cardiovascular Business about new data he presented at Heart Rhythm 2026. 

  • Read more about Inflammation may help explain how GLP-1 drugs prevent AFib

How TAVR valve implant depth impacts clinical outcomes

cardiologists heart doctors

TAVR procedures with a higher implant depth are associated with certain clinical benefits after one year, according to a new study of data from more than 600 patients.

  • Read more about How TAVR valve implant depth impacts clinical outcomes

FDA warns public about Johnson & Johnson heart pump controllers after patient death

The FDA has identified another safety concern with Johnson & Johnson MedTech's Automated Impella Controllers. This comes after the devices were linked to five separate recalls in 2025.

Image courtesy of Johnson & Johnson MedTech.

The FDA has identified another safety concern with Johnson & Johnson MedTech's Automated Impella Controllers. This comes after the devices were linked to five separate recalls in 2025. 

  • Read more about FDA warns public about Johnson & Johnson heart pump controllers after patient death

Advocacy group wants TAVR changes, urging Trump admin to ‘stop getting in between patients and their doctors’

2024 has been a banner year for structural heart treatments, especially those focused on the tricuspid valve. In February, for example, Edwards Lifesciences made history when its Evoque transcatheter tricuspid valve replacement (TTVR) system became the first device of its kind to gain U.S. Food and Drug Administration (FDA) approval for treating tricuspid regurgitation (TR). Two months later, Abbott’s TriClip transcatheter edge-to-edge repair (TEER) system also gained FDA approval for the treatment of TR.

The Alliance for Aging Research wants CMS to go through with policy changes that could make many more patients eligible for TAVR. The agency is currently considering the changes, and a final decision is expected in June. 

  • Read more about Advocacy group wants TAVR changes, urging Trump admin to ‘stop getting in between patients and their doctors’

Medtronic recalls thousands of surgical devices due to contamination risk

warning safety alert recall healthcare issue

This Class II recall includes more than 18,000 cannulae used during cardiac surgery.

  • Read more about Medtronic recalls thousands of surgical devices due to contamination risk

'Compelling' study shows promise of new pulmonary embolectomy system

Jupiter Endovascular's Vertex Pulmonary Embolectomy System showed positive results in its SPIRARE II pivotal trial.

"Pulmonary embolism is fundamentally a cardiovascular disease, where restoration of hemodynamic stability, beyond simple clot removal, is the key determinant of patient recovery,” one researcher explained. 

  • Read more about 'Compelling' study shows promise of new pulmonary embolectomy system

Artivion acquires medtech company behind FDA-approved endovascular device for $135M

Nexus Aortic Arch System Artivion Endospan

The Nexus Aortic Arch System from Artivion.

The purchase price could end up being closer to $200 million if certain commercial milestones are met.

  • Read more about Artivion acquires medtech company behind FDA-approved endovascular device for $135M

Shockwave Medical's new IVL catheter overcomes previous limitations

Ziad Ali, MD, DPhil, director of the DeMatteis Cardiovascular Institute, St. Francis Hospital and Heart Center, spoke with Cardiovascular Business about his center's experience using the recently released Johnson & Johnson MedTech next-generation Shockwave C2 Aero Coronary IVL Catheter to treat calcified coronary artery disease. Ali said his center was the first in the world to use the catheter in August 2025 and has since gained experience in roughly 80 cases.

Ziad Ali, MD, said the new device has completely changed the way he and his colleagues treat patients with calcified coronary artery disease. 

  • Read more about Shockwave Medical's new IVL catheter overcomes previous limitations

SMART update: Self-expanding TAVR valves still linked to superior durability after 3 years

Medtronic Evolut FX TAVR valve. Medtronic has received an additional CE mark approval for its Evolut Pro+ and FX transcatheter aortic valve replacement (TAVR) valves; they can now be used for redo TAVR in addition to traditional TAVR procedures.

These three-year data represent a major update to one of the more noteworthy TAVR trials in recent memory.

  • Read more about SMART update: Self-expanding TAVR valves still linked to superior durability after 3 years

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