News | Ablation Systems | May 22, 2018

LuxCath Showcases OmniView Light-Guided Ablation Catheter at HRS 2018

Device sees into tissue to assess catheter-tissue contact and lesion progression during cardiac ablation in real time

LuxCath Showcases OmniView Light-Guided Ablation Catheter at HRS 2018

May 22, 2018 — LuxCath LLC showcased the next generation of its proprietary OmniView light-guided catheter ablation system at the 2018 Heart Rhythm Society (HRS) conference, May 9-12 in Boston. The OmniView light-guided ablation catheter is the only technology, according to the company, that can see into tissue during cardiac ablation and assess catheter-tissue contact and lesion progression in real time. This offers electrophysiologists a simple and more definitive end point for lesion quality, increasing the potential for complete and more effective cardiac ablation.

Cardiac ablation is a well-accepted treatment option for cardiac arrhythmias, performed more than 800,000 times every year globally. Currently, electrophysiologists rely on a range of indirect surrogate endpoints, such as temperature, power, duration and contact force, to assess lesion quality during the cardiac ablation procedure. However, these surrogate endpoints have been shown to be variable and potentially unreliable, and they do not directly assess tissue response in real time. Literature has shown single-procedure recurrence rates of 20-40 percent when ablating atrial fibrillation (AF), the most common form of arrhythmia.

The LuxCath OmniView light-guided catheter delivers and couples light into the tissue via an optical fiber embedded in the ablation catheter to assess tissue metabolic activity. The optical signal can be used to assess stability of catheter-tissue contact, tissue composition and lesion formation. The quality of these lesions is critical, as arrhythmia will recur if the lesions are not complete and uniform across the affected tissue. As lesions are formed, natural tissue fluorescence diminishes, indicating tissue destruction. This feedback mechanism allows the electrophysiologist to better assess the quality of the lesion formed. The next generation of the OmniView is orientation-independent, emitting light and seeing in all directions, allowing for optical signals at all angles of tissue contact.

“LuxCath has developed a promising and much needed technology with the OmniView light-guided ablation catheter, which has the potential to improve lesion quality and reduce procedure time while also making the procedure less operator dependent,” said Vivek Reddy, M.D., director of cardiac arrhythmia service for The Mount Sinai Hospital and the Mount Sinai Health System, and a LuxCath scientific advisory board member. “The light-guided technology is designed to signal to the operator when there is stable and consistent tissue contact, which is critical in achieving complete lesions. If the OmniView can deliver on the promise of its approach, light guidance has the potential to be the primary sensory modality in the catheter ablation treatment of AF.”

Separately, the company has announced the establishment of a scientific advisory board, with members including Reddy as well as:

  • David Haines, M.D., section head, Heart Rhythm, Beaumont Hospital, Royal Oak, Mich.;
  • Pierre Jais, M.D., co-director, L’institut de rythmologie et modélisation cardiaque, Bordeaux, France;
  • Andrea Natale, M.D., executive medical director, Texas Cardiac Arrhythmia Institute at St. David’s Medical Center; and
  • Jeremy Ruskin, M.D., founder, director, Cardiac Arrhythmia Service, Massachusetts General Hospital.

For more information: www.luxcath.com

 

Related Content

Biosense Webster Announces Initial Results From First-in-Human QDOT-FAST Study
News | Ablation Systems | May 16, 2019
Johnson & Johnson Medical Devices Companies announced that Biosense Webster, Inc.’s QDot Micro catheter...
CardioFocus Announces Results From HeartLight X3 Ablation System Pivotal Study
News | Ablation Systems | May 16, 2019
CardioFocus Inc. announced the presentation of results from its pivotal confirmatory study evaluating the HeartLight X3...
New Global Consensus Statement Addresses Catheter Ablation of Ventricular Arrhythmias
News | Ablation Systems | May 14, 2019
The Heart Rhythm Society (HRS) in partnership with three other professional societies issued an international consensus...
Netherlands Hospital to Install State-of-the-Art MRI Ablation Center
News | Ablation Systems | May 13, 2019
Imricor announced the signing of a commercial agreement with the Haga Hospital in The Hague, Netherlands to outfit a...
A CyberHeart cardiac ablation radiotherapy treatment plan showing where the radiation beam will ablate for a noninvasive pulmonary vein isolation procedure. Varian acquires, buys, purchases Cyberheart.

A CyberHeart cardiac ablation radiotherapy treatment plan showing where the radiation beams will ablate for a noninvasive pulmonary vein isolation procedure to treat an arrhythmia.

Feature | Ablation Systems | May 10, 2019 | Dave Fornell, Editor
May 10, 2019 — Radiation oncology vendor Varian announced it acquired the start-up company CyberHeart, which has deve
Ablation Reduces Risk of Dementia in Patients With AFib and Carotid Artery Disease
News | Ablation Systems | May 08, 2019
Even though many medical practitioners may opt not to perform procedures on higher-risk patients, new research finds it...
CardioFocus Announces European CE Mark Approval Of HeartLight X3 System
News | Ablation Systems | April 16, 2019
CardioFocus Inc. announced the European CE Mark approval of the HeartLight X3 Endoscopic Ablation System.
First Patient Treated With QDot Micro Ablation Catheter
News | Ablation Systems | February 04, 2019
Biosense Webster has enrolled and treated the first patient in its U.S. Investigational Device Exemption (IDE) study...
FDA Approves TactiCath Contact Force Ablation Catheter, Sensor Enabled
Technology | Ablation Systems | January 21, 2019
Abbott announced U.S. Food and Drug Administration (FDA) approval of the TactiCath Contact Force Ablation Catheter,...
First Patient Treated in STELLAR Atrial Fibrillation IDE Study
News | Ablation Systems | November 30, 2018
Johnson & Johnson Medical Devices Companies announced that Biosense Webster Inc. has enrolled and treated the first...
Overlay Init