The Inspire® Procedure is an FDA-approved obstructive sleep apnea device that can help treat and prevent sleep apnea for children with Down syndrome who cannot use Continuous Positive Airway Pressure (CPAP) therapy and are not effectively treated by adenotonsillectomy (surgical removal of the tonsils and adenoids).

This small device is implanted under the skin near a patient's collarbone during a minimally invasive procedure. It is controlled by a small hand-held remote to turn on therapy when sleeping and a mobile application to track and share sleep data with your child's care team. While sleeping, Inspire opens the airway, preventing sleep apnea and allowing your child to sleep peacefully.

Because Inspire is a simple, low-maintenance therapy that works without the use of a mask or hose, children can rest and get an adequate amount of sleep. Caregivers report their children with Down syndrome have less daily tiredness and show increased alertness and energy after consistently using Inspire.

Criteria for Patients
  • Thirteen years of age or older.
  • Moderate to severe obstructive sleep apnea.
  • An apnea-hypopnea index between 10 and 50.
  • Either an inability to tolerate or does not benefit from traditional CPAP therapy.
Safety

Inspire's safety and efficacy were evaluated during the STAR clinical trial. Five-year STAR trial outcomes show patients using Inspire experience significant reductions in sleep apnea events and substantially improve quality-of-life measures. Over 150 peer-reviewed publications on Inspire have shown results consistent with those seen in the STAR trial.

Learn More

To learn more about Inspire and how it can benefit your child, please call (562) 728-5230 to consult with an Ear, Nose & Throat (ENT) specialist. 

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