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Updated: Jul 25, 2025

Drug-Induced Sleep Endoscopy DISE with Target Controlled Infusion TCI and Bispectral Analysis in Obstructive Sleep Apnea
Published on: December 6, 2016
Multilevel Airway Obstruction Phenotypes in Adult OSA
Bartholomew Bacak1, Lee Porterfield1, Sveta Karelsky1
1University of Rochester Medical Center Rochester New York USA.
Three distinct airway obstruction phenotypes were identified using drug-induced sleep endoscopy (DISE) in adults. These multilevel phenotypes suggest different collapse patterns and may guide future treatment strategies for sleep apnea.
Area of Science:
- Sleep Medicine
- Otolaryngology
- Respiratory Physiology
Background:
- Airway obstruction during sleep is a key factor in obstructive sleep apnea.
- Drug-induced sleep endoscopy (DISE) is a valuable tool for visualizing airway collapse.
- Understanding multilevel airway obstruction phenotypes is crucial for effective treatment.
Purpose of the Study:
- To describe multilevel phenotypes of airway obstruction identified via DISE in adults.
- To correlate these phenotypes with demographic and polysomnographic data.
Main Methods:
- Retrospective chart review of DISE video recordings from adult patients.
- Cross-correlation matrix analysis to identify significant correlations between anatomical subsites.
- Calculation of mean differences and confidence intervals for phenotype comparisons.
Main Results:
- Three distinct phenotypes were identified: T2-E2 (tongue base/epiglottis collapse), V2C-O2LPW (velum/oropharynx collapse), and V0/1-O2T (velum/tonsillar hypertrophy).
- Phenotype 1 (T2-E2) associated with older age, lower BMI, and smaller neck circumference.
- Phenotype 2 (V2C-O2LPW) associated with higher BMI, larger neck circumference, and higher apnea-hypopnea index.
- Phenotype 3 (V0/1-O2T) associated with younger age.
Conclusions:
- Three distinct multilevel airway obstruction phenotypes were identified using DISE.
- These phenotypes represent different patterns of anatomical collapse.
- The identification of these phenotypes may impact understanding of pathophysiology and treatment selection.
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