First Patient in Biosense Webster’s Multi-Electrode RF Balloon Catheter Study

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26/03/2018

Heart arrhythmia specialist company, Biosense Webster, Inc., has enrolled and treated the first patient in Europe to its SHINE  clinical study.

Johnson and Johnson company Biosense Webster says its multicenter study will evaluate the its next generation multi-electrode radiofrequency (RF) balloon catheter for its ability to isolate pulmonary veins when treating paroxysmal or intermittent atrial fibrillation (AF).

The first patient was treated at Barts Hospital in London, United Kingdom, by Richard Schilling, MD, Professor of Cardiology. The clinical study will enroll up to 230 patients across multiple sites in Europe.

Cardiac ablation is a minimally-invasive procedure that neutralizes parts of the abnormal electrical pathways causing arrhythmia. In the procedure, doctors thread a flexible balloon catheter through blood vessels to the left atrium of the heart. Once there, the balloon is inflated near the pulmonary veins and RF energy is applied to create lines of scar tissue to prevent the pulmonary veins from emitting faulty electrical impulses that can trigger AF.

The new RF balloon catheter used in the study is designed to deliver directionally-tailored energy using multiple electrodes. The device will be used in combination with the company’s integrated multi-electrode circular diagnostic catheter to potentially improve procedural efficiency.

“AF is fast becoming one of the world’s most significant public health issues affecting millions of lives and placing a critical burden on healthcare systems,” said Shlomi Nachman, Company Group Chair of Johnson & Johnson Medical Devices Cardiovascular & Specialty Solutions. “Biosense Webster is committed to delivering solutions that help clinicians reach more patients and we look forward to completing this important study and bringing new technologies to the market.”


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