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Published on: December 6, 2016
Mandibular advancement splint titration in obstructive sleep apnoea.
A J Campbell1, G Reynolds, H Trengrove
1Department of Medicine, University of Otago, Wellington South, New Zealand.
Titratable mandibular advancement splints (MAS) effectively treated obstructive sleep apnea (OSA) in most patients. While polysomnography (PSG) feedback improved device use, it did not yield greater symptom or apnea-hypopnoea index (AHI) improvements compared to self-adjustment.
Area of Science:
- Sleep Medicine
- Dental Sleep Medicine
- Respiratory Medicine
Background:
- Mandibular advancement splints (MAS) are used to treat obstructive sleep apnea (OSA).
- Titratable MAS may offer better patient tolerance, but optimal adjustment protocols require investigation.
- This study investigates two adjustment methods for titratable MAS in OSA patients.
Purpose of the Study:
- To evaluate the effectiveness of a titratable MAS in patients with moderate OSA (AHI 10-40/h) and BMI < 35 kg/m².
- To compare subjective self-adjustment versus objective adjustment based on polysomnography (PSG) feedback.
- To assess changes in apnea-hypopnoea index (AHI) and OSA symptoms.
Main Methods:
- Twenty-eight patients with symptomatic OSA were randomized to self-adjustment or PSG-guided adjustment.
- The MAS was initially set at 70% maximal protrusion.
- Outcomes (AHI, OSA symptoms) were compared at baseline and after 6 weeks.
Main Results:
- Overall, 71% of patients showed improved or resolved OSA (AHI < 5/h or >50% reduction).
- Objective adjustment (with PSG feedback) led to higher reported nightly device use (91% vs. 63%).
- Both adjustment methods yielded similar significant improvements in AHI and symptoms; PSG feedback did not further reduce AHI after 3 weeks.
Conclusions:
- Titratable MAS effectively improved or resolved OSA in a majority of selected patients.
- While PSG-based feedback increased device use, it did not offer superior clinical outcomes compared to self-adjustment.
- A follow-up sleep study is recommended to confirm MAS efficacy.
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