The etiology of ETD may be linked to3:

  • Viral upper respiratory tract infection
  • Chronic sinusitis
  • Allergic rhinitis
  • Adenoid hypertrophy
  • Tobacco smoke
  • Reflux
  • Cleft palate
  • Radiation therapy
  • Reduced mastoid air cell system
  • Exposure to nitrous oxide

There is limited evidence to support current approaches to ETD treatments3

Different approaches to the treatment of ETD are available, but only one randomized controlled trial has been conducted. And in that study, nasal steroids showed no effect on ETD symptoms.

Other current ETD treatments:

  • Auto pressure equalization technique
  • Treatment with decongestants
  • Treatment with antihistamines
  • Surgical procedures including ventilation tubes, laser tuboplasty, and microdebrader tuboplasty

Why use the ACCLARENT AERA® Eustachian Tube Balloon Dilation System?

It was the first available device in the United States specifically designed to dilate the Eustachian tubes for patients with persistent ETD supported by a prospective, multicenter, randomized clinical trial.

Become
ACCLARENT AERA®
trained

Contact your local
representative or call
877-775-2789 if you are
a physician interested in
learning more about
ACCLARENT AERA® Eustachian
Tube Balloon Dilation System training.

Call
877-775-2789
to learn more
about training.

References

  1. Browning GG, Catehouse S. The prevalence of middle ear disease in the adult British population. Clin Otolaryngol Allied Sci. 1992; 17(4):317-321.

  2. Ockermann T, Reineke U, Upile T, Ebmeyer J, Sudhoff HH. Balloon dilatation eustachian tuboplasty: a clinical study. Laryngoscope.2010;120(7):1411-1416.

  3. Randrup TS, Ovesen T. Balloon Eustachian tuboplasty: a systematic review. Otolaryngol Head Neck Surg. 2015;152(3):383-392.

Indications For Use

The ACCLARENT AERA® Eustachian Tube Balloon Dilation System is intended to dilate the Eustachian tube for treatment of persistent Eustachian tube dysfunction in adults ages 18 and older.

Important Safety Information

ACCLARENT AERA® 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.

View ACCLARENT AERA® Instructions for Use