OSA – A wake up call for Dentists

A truly next-generation device, ARES™ (FDA approved) is worn on the forehead and stores up to three nights of nocturnal data. Comfortable and designed to be worn in all sleep positions, ARES™ was created to be worn at home, where it’s easier to gather an accurate profile of the patient’s breathing and sleep. Engineered to integrate physiological data acquired in-home with clinical history and anthropomorphic data to determine the presence and severity of obstructive sleep apnea (OSA).
Form Completion:
Complete and fax the
Home Sleep Study
Order Form
Mail Delivery:
SleepMed will verify
benefits coverage and
contact the patient to
schedule delivery of the
home sleep test device
Home Sleep Study:
Patient receives the device
and completes a 1-2 night
home sleep study. SleepMed
will contact the patient on
the night of the study to
provide education on use.
Device Return:
Patient returns the
device via prepaid /
pre-addressed mailer.
Data Interpretation:
SleepMed will perform a
technical edit of the raw
study data and have a
professional interpretation
completed by a boarded
sleep physician, then fax
the final study report to
you for review.
Oral Appliances in the Market
refuse CPAP and could be eligible for Oral Appliance
AHI potentially suitable for Oral Appliance
Clinical research shows that it is linked strongly to a range of serious, even life-threatening, chronic diseases such as stroke, heart failure, hypertension, diabetes, obesity and coronary heart disease. However, awareness is low and we believe that about 90% of people who have OSA remain undiagnosed and untreated. Dentists are waking up to the opportunity and SleepMed is here to help.