Improving Outcomes in Pediatric Obstructive Sleep Apnea With Computational Fluid Dynamics (OSA-MRI)
Obstructive Sleep Apnea
About this trial
This is an interventional diagnostic trial for Obstructive Sleep Apnea focused on measuring OSA, 129Xe, MRI, CFD simulations
Eligibility Criteria
Inclusion Criteria:
- Male or Female
- Subjects between the ages of 5 to 18 only for Aim 1 and xenon use
- Subjects 3-18 years of age for Aims 2 and 3
- Subjects with persistent moderate or severe OSA after adenotonsillectomy. - -- Persistent moderate or severe OSA will be defined as an oAHI > 5 per hour of sleep.
- Clinical indication or suspicion of upper-airway obstruction. Examples include but not limited to hypertrophy of the lingual tonsils, disproportionately large tongue, or micrognathia.
- Subjects who have failed a trial of CPAP.
- Subjects whose parents elect to pursue surgery without a trial of CPAP.
- Subjects who require a surgical procedure for OSA based on the clinical assessment of the surgeon (otolaryngologist or plastic surgeon).
Exclusion Criteria:
- Children adequately treated with CPAP.
- Children with braces/metal rods.
- Children who have a contraindication to sedative.
- Standard MRI exclusion criteria as set forth by the CCHMC Department of Radiology.
Sites / Locations
- Cincinnati Children's Hospital Medical CenterRecruiting
Arms of the Study
Arm 1
Arm 2
Experimental
Experimental
Phase 1 - Contrast 129Xe MRI ages 5-18
Phase 2 - Contrast 129Xe MRI ages 3-18
The research team will collect data characterizing upper airway anatomy, motion, and airflow. In patients, these data may be recorded before and after surgery. The data may include some or all of the following: (1) Static and dynamic proton MRI of the airway. (2) Respiratory airflow measurements. (3) Phase contrast MRI of inhaled gas. (4) Data from clinical PSGs. (5) Measurements may be repeated at different levels of CPAP.
The research team plans to collect data characterizing upper airway anatomy, motion, and airflow. In patients, these data may be recorded before and after surgery. The data may include some or all of the following: (1) Static and dynamic proton MRI of the airway. (2) Respiratory airflow measurements. (3) Data from clinical PSGs. (5) Measurements may be repeated at different levels of CPAP.