Evaluation of Sleep Stages During Drug-Induced Sleep Endoscopy in Pediatric Patients with Obstructive Sleep Apnea: A

Audrey Abend1, Chase Hintelmann1, Katherine H Dinh1

  • 1Rutgers Robert Wood Johnson Medical School, New Brunswick, New Jersey, USA.

Insights

This pilot study explored sleep stages in children with obstructive sleep apnea (OSA) during drug-induced sleep endoscopy (DISE). Most children experienced N2 sleep, with no REM sleep observed, providing initial insights into DISE neurophysiology.

Area of Science:

  • Pediatric Sleep Medicine
  • Neurophysiology
  • Sleep Endoscopy

Background:

  • Drug-induced sleep endoscopy (DISE) is crucial for evaluating upper airway obstruction in pediatric obstructive sleep apnea (OSA).
  • Understanding the neurophysiological changes during DISE-induced sleep is limited.
  • This study investigates sleep stages in children undergoing DISE.

Purpose of the Study:

  • To demonstrate the safety and feasibility of collecting sleep stage data during DISE in pediatric OSA patients.
  • To characterize the sleep architecture of pediatric OSA patients during DISE.

Main Methods:

  • Prospective cohort pilot study conducted at an academic medical center.
  • Recruited 13 pediatric patients (3-13 years) with OSA, excluding those with craniofacial abnormalities or non-English/Spanish speaking.
  • Collected electroencephalogram (EEG), electrooculogram (EOG), and electromyogram (EMG) data during DISE, primarily using dexmedetomidine sedation.

Main Results:

  • EEG, EOG, and EMG data were successfully collected and scored.
  • Sleep stages observed included N1 (6 subjects), N2 (12 subjects), and N3 (5 subjects).
  • The majority of sleep time was spent in N2 sleep; no REM sleep was recorded.

Conclusions:

  • This pilot study offers the first insights into sleep stages during DISE in pediatric OSA patients.
  • Further research is needed to explore the neurophysiology and anesthetic effects during DISE.
  • Findings highlight the potential for detailed sleep analysis during DISE procedures.
Abstract