Eustachian Tube Balloon Dilation

Persistent Eustachian tube dysfunction (ETD) is the inability of the Eustachian tube to adequately perform its functions and failure of the Eustachian tube to open and/or close properly.1 

 

With Eustachian Tube Balloon Dilation, a small balloon catheter is used to insert a small balloon through the patient’s nose and into the Eustachian tube. Once inflated, the balloon opens up a pathway for mucus and air to flow through the Eustachian tube, which may help restore proper function. After the Eustachian tube is dilated, the balloon is deflated and the catheter is removed.2 

Eustachian Tube Balloon Dilation

The following diagrams outline the balloon dilation process. 

Step 1: The ACCLARENT AERA® Eustachian Tube Balloon Dilation System is introduced into the Eustachian tube under direct visualization.

Step 1: The ACCLARENT AERA® Eustachian Tube Balloon Dilation System is introduced into the Eustachian tube under direct visualization.

Step 2: The ACCLARENT AERA® balloon is then inflated for 2 minutes, applying controlled radial pressure to the epithelial layer. The shearing or crushing of portions of the epithelium, sparing the basal layer, allows for rapid healing.

Step 2: The ACCLARENT AERA® balloon is then inflated for 2 minutes, applying controlled radial pressure to the epithelial layer. The shearing or crushing of portions of the epithelium, sparing the basal layer, allows for rapid healing.

Step 3: After dilation, the balloon is deflated and withdrawn from the Eustachian tube

Step 3: After dilation, the balloon is deflated and withdrawn from the Eustachian tube

References

1. Grimmer, J.F., & Poe, D.S. (2005) Update on Eustachian Tube Dysfunction and the Patulous Eustachian Tube. Curr Opin Otolaryngol Head and Heck Surg, 13: 277‐ 282.
2. ACCLARENT AERA® Eustachian Tube Balloon Dilation System Instructions for Use. Irvine, CA: Acclarent, Inc; 2018. IFU005146 Rev E

Disclosures

ACCLARENT AERA® Eustachian Tube Balloon Dilation System is intended for use by physicians who are trained on Acclarent Technology.

Eustachian tube balloon dilation has associated risks, including tissue and mucosal trauma, infection, or possible carotid artery injury. Prior to use, it is important to read the Instructions for Use and to understand the contraindications, warnings, and precautions associated with these devices.

Caution: Federal (US) law restricts the sale, distribution or use of these devices to, by or on the order of a physician. Third party trademarks used herein are trademarks of their respective owners. This content is intended for audience within the US only.

This site is published by Acclarent, Inc. which is solely responsible for its contents. It is intended for visitors from the United States.

© Acclarent, Inc. 2019. Last Updated on 2/12/20

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