Efficacy of Oral Appliances on Obstructive Sleep Apnea During Pregnancy

Study design : Intervention Pilot Study uncontrolled experimental cohort

Population: 32 pregnant women with sleep apnea with an apnea - hypopnea index ( AHI ) ≥ 10 events / hr .

Methodology: The mandibular advancement appliance will be used with the chip DentiTracs to measure adhesion. Participation in this project requires five visits to the research team, including 3 visits at home. Participants will be recruited and granted in obstetrics MUHC. The questionnaires will be filled (Epworth Sleepiness Scale, Pittsburgh sleep quality and functional (FOSQ)). A sleep recording (PSG type II) will be done at home to confirm the diagnosis. The recording equipment will be returned to the research team by mail. During the second visit (clinical orthodontics), dental impressions in alginate will be made. At the 3rd visit (clinical orthodontics), the mandibular advancement appliance will be adjusted and instructions will be given. A weekly phone call follow-up will be ensured during this period of adjustment of the appliance. The fourth visit (at home) will consist of a sleep recording to evaluate the effect of treatment. A questionnaire comfort / secondary effects will be administered. For patients who have started their participation during their second trimester, a sleep recording at home (4a visit) will be realized in Q3 to assess whether it is necessary to change the titration of the appliance. The 5th visit (orthodontic clinic) will be 3-6 months after delivery. Participants will fulfill all the mentioned questionnaires and make a sleep recording at home without the appliance. Replace the appliance in place if AHI> 10. During the 4th and 5th visits, anthropometric data (ie, weight), and objective adhesion will be taken

Inclusion criteria

• Adult women (≥ 18 years old)
• Pregnant women (between14 and 34 weeks)
• Sleep apnea with respiratory disturbance index (RDI) ≥ 5 events/hour
• Snoring or sleep apnea testimony by chamber partner

Exclusion criteria

• Severe sleep apnea
• Evidence of a respiratory sleep disorder other than sleep apnea
• Body mass index greater than 40
• Use of medication that could affect breathing or sleep
• Abnormalities of the upper airway (oversized amygdala)
• Severe temporomandibular disorder
• Periodontal problems and untreated caries
• Poor dental hygiene
• Possible retention of OAM (Not enough teeth to retain the OAM in the mouth )