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Airway Balloon Dilation
Airway stenosis is a congenital or acquired narrowing that obstructs the passage of air to the lungs. Symptoms include stridor, wheezing, hoarseness, shortness of breath and respiratory distress. Patients who have severe airway stenosis are often dependent on a tracheotomy tube to breathe.
The most common cause of acquired airway stenosis is endotracheal intubation, resulting in 90% of cases. Other causes include external trauma, thermal or caustic injuries, chronic inflammatory diseases, infection, and cancer.
The following diagram outlines the balloon dilation process:
The INSPIRA AIR® Balloon Dilation System is introduced into the airway under direct visualization. The airway stylet facilitates atraumatic access across narrow stenosis.
The balloon is gently inflated, applying controlled radial pressure to the stricture. After dilation, the balloon is deflated and withdrawn from the airway.
INSPIRA AIR® Balloon Dilation System
ACCLARENT® Balloon Inflation Device
1. Kim, S.S., Khalpey, Z., Hsu, C. and Little, A.G. (2017). Changes in Tracheostomy and Intubation-Related Tracheal Stenosis: Implications for Surgery. Ann Thorac Surg.;104:964–70.
Acclarent Devices are intended for use by or under the direction of a physician who is trained in the use of Acclarent Technology. INSPIRA AIR® Balloon Dilation System use has described risks, including serious complications such as airway obstruction, airway rupture (partial or complete) resulting in pneumomediastinum, pneumothorax and mediastinitis, chest pain, bronchospasm, atelectasis, pulmonary edema and bleeding. 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: US law restricts this device to sale by or on the order of a physician.
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 11/18/2019