We conducted a pilot study to evaluate the accuracy of a custom built non-contact pressure-sensitive device in diagnosing obstructive sleep apnea (OSA) severity as an alternative to in-laboratory polysomnography (PSG) and a Type 3 in-home sleep apnea test (HSAT). Fourteen patients completed PSG sleep studies for one night with simultaneous recording from our load-cell-based sensing device in the bed. Subjects subsequently installed pressure sensors in their bed at home and recorded signals for up to four nights. Machine learning models were optimized to classify sleep apnea severity using a standardized American Academy of Sleep Medicine (AASM) scoring of the gold standard studies as reference. On a per-night basis, our model reached a correct OSA detection rate of 82.9% (sensitivity = 88.9%, specificity = 76.5%), and OSA severity classification accuracy of 74.3% (61.5% and 81.8% correctly classified in-clinic and in-home tests, respectively). There was no difference in Apnea Hypopnea Index (AHI) estimation when subjects wore HSAT sensors versus load cells (LCs) only (p-value = 0.62). Our in-home diagnostic system provides an unobtrusive method for detecting OSA with high sensitivity and may potentially be used for long-term monitoring of breathing during sleep. Further research is needed to address the lower specificity resulting from using the highest AHI from repeated samples.
- Apnea-Hypopnea index
- Automated obstructive sleep apnea diagnosis
- Contact-less load cell sensor
- Long-term breathing monitoring
- Unobtrusive obstructive sleep apnea diagnosis
ASJC Scopus subject areas
- Clinical Biochemistry