This study aims to assess the effectiveness of an investigational algorithm in the treatment of obstructive sleep apnea.
Participants willing to give written informed consent.
Participants who can read and comprehend English.
Participants who ≥ 18 years of age
Participants who have been using a ResMed AirSense 10 or 11 device.
Participants using Bilevel flow generators.
Participants using CPAP, AutoSet for Her
Participants who are or may be pregnant.
Participants with a preexisting lung disease/ condition that would predispose them to pneumothorax (for example: COPD, lung cancer; fibrosis of the lungs; recent (< 2years) case of pneumonia or lung infection; lung injury.