Laser, video technology combine in new atrial fibrillation treatment
University of Illinois at Chicago Health News Jun 03, 2017
The University of Illinois Hospital & Health Sciences System is the first hospital in the Midwest to offer an improved minimally invasive treatment for atrial fibrillation, also called AF or AFib.
Pulmonary vein isolation, or PVI, is a first–line treatment for patients whose atrial fibrillation does not respond, or no longer responds, to medication. In PVI, a specialist uses catheters to access the heart and deliver small doses of energy to destroy the tissue that causes the heart to beat irregularly.
The new treatment, performed by an electrophysiologist using the HeartLight Endoscopic Ablation System, uses a laser to destroy the problem tissue, in place of the radio waves used in standard PVI. The laserÂs visual guidance provides physicians with a direct view into the heart that was previously unavailable.
The Food and Drug Administration approved the new system a year ago. In early trials, patients experienced similar rates of success as with standard PVI – one study showed 61 percent experiencing freedom from AF at 12 months. But electrophysiologists think that the technology may help improve long–term success rates by creating a more pinpointed and long–lasting therapeutic lesion.
Dr. Erik Wissner, director of cardiac electrophysiology at UI Health, has experience using the HeartLight system in Germany, where it has been approved since 2009. He performed the first commercial procedure in the U.S. on May 4. He says that greater precision in the interventional treatment of AF is good for patients.
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Pulmonary vein isolation, or PVI, is a first–line treatment for patients whose atrial fibrillation does not respond, or no longer responds, to medication. In PVI, a specialist uses catheters to access the heart and deliver small doses of energy to destroy the tissue that causes the heart to beat irregularly.
The new treatment, performed by an electrophysiologist using the HeartLight Endoscopic Ablation System, uses a laser to destroy the problem tissue, in place of the radio waves used in standard PVI. The laserÂs visual guidance provides physicians with a direct view into the heart that was previously unavailable.
The Food and Drug Administration approved the new system a year ago. In early trials, patients experienced similar rates of success as with standard PVI – one study showed 61 percent experiencing freedom from AF at 12 months. But electrophysiologists think that the technology may help improve long–term success rates by creating a more pinpointed and long–lasting therapeutic lesion.
Dr. Erik Wissner, director of cardiac electrophysiology at UI Health, has experience using the HeartLight system in Germany, where it has been approved since 2009. He performed the first commercial procedure in the U.S. on May 4. He says that greater precision in the interventional treatment of AF is good for patients.
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