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Updated: Dec 10, 2025

Drug-Induced Sleep Endoscopy DISE with Target Controlled Infusion TCI and Bispectral Analysis in Obstructive Sleep Apnea
Published on: December 6, 2016
Propofol versus dexmedetomidine during drug-induced sleep endoscopy (DISE) for pediatric obstructive sleep apnea
Erin M Kirkham1, Karen Hoi2, Jonathan B Melendez2
1Department of Otolaryngology: Head & Neck Surgery, Mott Children's Hospital, University of Michigan Medical Center, 1540 E. Hospital Dr. CW 5-702, SPC 4241, Ann Arbor, MI, 48109, USA. ekirkham@umich.edu.
Insights
This study found no significant difference in airway obstruction during DISE between children sedated with propofol or dexmedetomidine. Further randomized trials are needed to confirm these findings on pediatric sleep apnea assessment.
Area of Science:
- Pediatric Anesthesiology
- Sleep Medicine
- Otolaryngology
Background:
- Obstructive sleep apnea (OSA) is common in children.
- Drug-induced sleep endoscopy (DISE) is crucial for OSA diagnosis.
- Sedation choice may influence DISE findings.
Purpose of the Study:
- To compare DISE findings in children sedated with propofol versus dexmedetomidine.
- To investigate if anesthetic agents affect the degree of upper airway obstruction during DISE.
- Hypothesized higher obstruction with propofol at dynamic airway levels.
Main Methods:
- Retrospective review of 117 children (age 1-18) undergoing DISE.
- Comparison of obstruction severity (Chan-Parikh scale ≥ 2) between propofol and dexmedetomidine sedation groups.
- Logistic regression analysis adjusted for confounders.
Main Results:
- No statistically significant difference in ≥ 50% airway obstruction between propofol and dexmedetomidine groups.
- This finding held true across all airway levels (velum, lateral walls, tongue base, supraglottis, adenoid).
- Confounder adjustment did not alter the non-significant difference.
Conclusions:
- Propofol and dexmedetomidine sedation yield similar DISE obstruction patterns in children.
- The choice of these sedatives does not appear to significantly impact the assessment of upper airway collapse.
- Prospective, randomized studies are recommended for definitive confirmation.
Purpose:
To test for differences in DISE findings in children sedated with propofol versus dexmedetomidine. We hypothesized that the frequency of ≥ 50% obstruction would be higher for the propofol than dexmedetomidine group at the dynamic levels of the airway (velum, lateral walls, tongue base, and supraglottis) but not at the more static adenoid level.
Methods:
A single-center retrospective review was performed on children age 1-18 years with a diagnosis of sleep disordered breathing or obstructive sleep apnea (OSA) who underwent DISE from July 2014 to Feb 2019 scored by the Chan-Parikh scale sedated with either propofol or dexmedetomidine (with or without ketamine). Logistic regression was used to test for a difference in the odds of ≥ 50% obstruction (Chan-Parikh score ≥ 2) at each airway level with the use of dexmedetomidine vs. propofol, adjusted for age, sex, previous tonsillectomy, surgeon, positional OSA, and ketamine co-administration.
Results:
Of 117 subjects, 57% were sedated with propofol and 43% with dexmedetomidine. Subjects were 60% male, 66% Caucasian, 31% obese, 38% syndromic, and on average 6.5 years old. Thirty-three percent had severe OSA and 41% had previous tonsillectomy. There was no statistically significant difference in the odds of ≥ 50% obstruction between the two anesthetic groups at any level of the airway with or without adjustment for potential confounders.
Conclusion:
We did not find a significant difference in the degree of upper airway obstruction on DISE in children sedated with propofol versus dexmedetomidine. Prospective, randomized studies would be an important next step to confirm these findings.
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