Barrett's esophagus management
The power to eradicate Barrett's esophagus† is in your hands.1
Treatment with radiofrequency ablation (RFA) can lead to significantly improved outcomes for patients with Barrett's esophagus (BE), including:
Medtronic is committed to saving patients’ lives by helping you work towards better patient outcomes and prevent disease progression, with our reliable treatments.
The Barrx™ radiofrequency ablation system includes a bipolar radiofrequency energy generator designed to precisely control depth and uniformity of tissue ablation in the GI tract.
The Barrx™ flex RFA energy generator provides the flexibility to choose either a Barrx™ 360 RFA balloon catheter or a Barrx™ 360 express RFA balloon catheter for larger circumferential treatment areas or a Barrx™ RFA focal catheter for treatment of smaller focal areas.
Barrx™ RFA is a proven, effective and durable therapy.4
This quick guide explains which catheters to use for each condition (Barrett's esophagus, GAVE, Radiation proctitis) and the respective ablation/cleaning protocols and energy settings.
The Barrx™ 360 express RFA balloon catheter and the Barrx™ channel RFA endoscopic catheter simulator application is now available on the Apple App Store®.
This educational application offers an interactive experience that provides useful information about procedural steps, handling, and usage of these devices — in a 3D simulated environment.‡
This app is suitable for iPad®, and is free to download and install.
Many publications demonstrate the efficacy of Barrx™ RFA for the treatment of Barrett's esophagus.
Conclusion:
The rate of neoplastic progression to high-grade dysplasia and adenocarcinoma is significantly reduced by RFA. RFA therapy should be considered in patients with a confirmed diagnosis of low-grade dysplasia.
Authors: Phoa K, van Vilsteren FI, Weusten BM, et al.
Published in: American Medical Association (JAMA) 2014;311:1209-1217.
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† Complete eradication occurred in 92.6% of cases.
‡ This app is for simulation purposes only and does not reflect actual use of the device in a clinical setting with actual equipment. It is also not to be used for training purposes but for demonstration only. While every reasonable precaution has been taken in the preparation of this guide, Medtronic assumes no responsibility for errors or omissions, nor for the uses made of the materials contained herein and the decisions based on such use. This document does not contain all of the information necessary for the proper care and treatment of patients. As such, no individual may rely on the information presented herein in forming a comprehensive treatment program or in treating any patient. No warranties are made, expressed or implied, with regard to the contents of this work or to its applicability to specific patients or circumstances. Medtronic shall not be liable for direct, indirect, special, incidental or consequential damages arising out of the use or inability to use the contents of this guide.
* Does not apply to the Barrx™ 360 express RFA balloon catheter
§ 94% is the calculated relative risk reduction [ (26-1.5)/26] = 25/26 *100. From [25.0% (1.5%for ablation vs 26.5%for control; 95%CI, 14.1%-35.9%; P < .001]
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