If you have obstructive sleep apnea, your airway tends to collapse when you sleep. After snoring, gasping and choking your way through the night, you’re getting by on little rest the next day.
Cleveland Clinic is a non-profit academic medical center. Advertising on our site helps support our mission. We do not endorse non-Cleveland Clinic products or services. Policy
The most common solution is CPAP (continuous positive airway pressure). While your partner may appreciate quieter nights, chances are you’re not a big fan.
“It’s the standard treatment for obstructive sleep apnea, but about half the people don’t like it very much,” explains surgical sleep medicine specialist Alan Kominsky, MD.
A Cleveland Clinic study found that just 44% of the patients prescribed CPAP for obstructive sleep apnea were still using it three years later.
A new implantable device
Another option is an implantable, programmable device approved by the U.S. Food and Drug Administration in 2014. The Inspire® upper airway stimulation device looks like a heart pacemaker.
It has two leads. One senses your breathing. The other stimulates the nerve that controls the tongue, to move it forward and open your throat.
“A pivotal trial demonstrated the device’s safety and effectiveness in a small group of patients with moderate to severe obstructive sleep apnea,” says Dr. Kominsky. Five years later, those improvements have been measured and are persistent.
The airway stimulation device is available at select U.S. medical centers, including Cleveland Clinic. To be eligible for it:
- You must be age 22 or older.
- Your AHI (apnea-hypopnea index) must be between 15 and 65.
- Your body mass index must be lower than 32.
- You must have failed the use of CPAP.
Eligible patients must have a recent sleep study. The next step is to perform sleep endoscopy. This outpatient procedure begins with sedation so that doctors can insert an endoscope into the airway. This lets them view the pattern of airway collapse to confirm the device will help.
The stimulator system is then implanted under general anesthesia in an outpatient procedure.
“One month after the procedure, we turn the device on,” says Dr. Kominsky. “One month after that, we perform a repeat sleep study. This helps us make adjustments to ensure the device will deliver the maximum benefit.”