Inspire Sleep Apnea Device Mri Safety

Inspire sleep apnea therapy review final verdict this device is suitable for people who are above the age of 18 years and suffer from moderate to severe obstructive sleep apnea.

Inspire sleep apnea device mri safety.

Food and drug administration fda approval for its next generation device the inspire 3028 implantable pulse generator which includes magnetic resonance mr conditional labeling allowing patients to undergo magnetic resonance imaging mri safely. It is the only fda approved obstructive sleep apnea treatment that works inside the body with just the click of a button. As a result osa patients may experience a high degree of daytime sleepiness. Depending on the model of your inspire system you may be able to undergo mri on the head and extremities provided certain conditions and precautions are followed.

A wire is placed in the chest wall. Minneapolis june 5 2017 inspire medical systems inc manufacturer of the only fda approved implantable device for obstructive sleep apnea osa has received u s. Inspire upper airway stimulation uas is used to treat a subset of patients with moderate to severe obstructive sleep apnea osa apnea hypopnea index ahi of greater than or equal to 15 and less than or equal to 65. There is a yellow mr triangle on the back of the patient id card if your patient has the inspire generator model 3028.

However they are eligible to have ct scans x rays and ultrasound images taken anywhere in the body. This device called an upper airway stimulator consists of a small pulse generator placed under the skin in the upper chest. Inspire uas is used in adult patients 22 years of age and older who have been confirmed to fail or cannot tolerate positive airway pressure pap treatments such as continuous positive. Inspire was fda approved in 2014 and has been proven both safe and effective in multiple clinical studies.

Untreated obstructive sleep apnea osa has a negative impact on sleep and the body s ability to recover during sleep. Inspire therapy has not been tested in people with a bmi greater than 32. It should be used after you have tried positive airway pressure treatments and they have not worked or you could not tolerate them. An implanted device called inspire.

If your patient has the inspire generator model 3024 they are not eligible for mri scans. If so they are eligible for mri head and extremity scans provided specific guidelines in the manual are followed. Please check your inspire patient id card to determine if you are able to get an mri under specific conditions. By proving compliance there should be no issues renewing your commercial driver s license.