New research at the 20th Anniversary Meeting of the American Academy of Dental Sleep Medicine (AADSM) in Minneapolis quantified the efficacy of mandibular advancement splints (MAS) using a self-administered, at-home device to monitor snoring and sleep-related breathing disorders. Clinical assessment of MAS efficacy in the treatment of snoring and obstructive sleep apnea (OSA) is based predominantly on subjective reports by the patient and partner, and less commonly, on the apnea hypopnea index (AHI), which is the average number of pauses in breathing that occur per hour of sleep. The current study used the Sonomat, a portable, unobtrusive device that has sensors contained within a mattress overlay. These sensors measure AHI by detecting and recording snoring, breathing, and body movements. Results show that MAS treatment reduced the average AHI from 10.3 events per hour to 3.8 events per hour. The respiratory event movement index, which records more types of events than AHI, was reduced from 15.9 events per hour to 7.6 events per hour. There was also a decrease in the percentage of patients who snored from 38% without the MAS to 15% with the MAS. Snoring decreased overall, but 12 of the 42 subjects still snored for greater than 25% of the night, with several having substantial increases in snoring. “The primary findings in our study were that MAS devices were effective in the treatment of OSA by reducing AHI in moderate and severe OSA patients,” said principal investigator and lead author Joachim Ngiam, BDS. “Overall, significant reductions in snoring were found to occur with MAS therapy with greater changes seen in OSA patients.” Despite favorable reductions in AHI with MAS treatment, snoring may persist and patients may question treatment success, indicating a need for quantification of therapy efficacy.
(Source: AADSM, June 11, 2011)
