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Drug-Induced Sleep Endoscopy DISE with Target Controlled Infusion TCI and Bispectral Analysis in Obstructive Sleep Apnea
Published on: December 6, 2016
A case-control study of Drug-Induced Sleep Endoscopy (DISE) in pediatric population: A proposal for indications
Maria Antonietta Collu1, Eduard Esteller2, Fiorella Lipari3
1Otorhinolaryngology Department, Cliniche Universitarie, Sassari, Italy.
Insights
Drug-Induced Sleep Endoscopy (DISE) significantly alters treatment plans for pediatric Obstructive Sleep Apnoea Syndrome (OSAS), especially in non-conventional and persistent cases. This diagnostic tool is crucial for tailoring interventions beyond standard procedures.
Area of Science:
- Pediatric Otolaryngology
- Sleep Medicine
- Diagnostic Endoscopy
Background:
- Obstructive Sleep Apnoea Syndrome (OSAS) is a common condition in children.
- Standard diagnostic methods for pediatric OSAS include history, questionnaires, physical exams, and polysomnography.
- The role of Drug-Induced Sleep Endoscopy (DISE) in refining diagnosis and treatment for pediatric OSAS requires further elucidation.
Purpose of the Study:
- To determine if and when Drug-Induced Sleep Endoscopy (DISE) changes the diagnosis and treatment plan for pediatric Obstructive Sleep Apnoea Syndrome (OSAS).
- To identify specific pediatric OSAS patient subgroups who would benefit most from undergoing DISE.
- To evaluate the impact of DISE on surgical planning beyond standard tonsillectomy and adenoidectomy (T&A).
Main Methods:
- A case-control study involving 150 children diagnosed with OSAS undergoing DISE.
- Patients were categorized into conventional, disproportional, and persistent OSAS subgroups based on clinical and polysomnography criteria.
- Surgical plans were modified if DISE findings led to interventions other than T&A, with outcomes compared between cases and controls.
Main Results:
- DISE altered surgical plans in 4.5% of conventional OSAS, 17.5% of disproportional OSAS, and 72.7% of persistent OSAS cases (p < 0.005).
- A change in treatment plan due to DISE was significantly associated with a non-conventional OSAS status (OR = 6).
- The persistent OSAS subgroup showed the highest rate of DISE-guided treatment modification.
Conclusions:
- Drug-Induced Sleep Endoscopy (DISE) is a safe and valuable procedure for pediatric OSAS patients.
- DISE is particularly recommended for non-syndromic pediatric OSAS patients with non-conventional or persistent disease patterns.
- The findings support considering DISE in a broader range of pediatric OSAS cases beyond those previously identified.
Objective:
To evaluate whether and when Drug-Induced Sleep Endoscopy (DISE) changes diagnosis and treatment plan in pediatric Obstructive Sleep Apnoea Syndrome (OSAS) with the aim to identify specific subgroups of patients for whom DISE should be especially considered.
Methods:
A case-control study of DISE in 150 children with OSAS. Pre-operative OSA were assessed through detailed history, Chervin questionnaire, physical examination and overnight polysomnography. The group of study was divided into three subgroups according to clinical and polysomnographyc criteria: conventional OSAS, disproportional OSAS and persistent OSAS. Endoscopic evaluation of the upper airway during DISE was scored using Chan classification. Surgical treatment was tailored individually upon the basis of sleep endoscopy findings: performance of any surgery other than tonsillectomy and adenoidectomy (T&A) was considered as a change of the treatment plan. Cases and controls were compared considering presence and absence of DISE-directed extra surgery, respectively.
Results:
150 patients with mean age (SD) 56.09 (23.94) months and mean apnoea-hypopnea index (AHI) of 5.79 (6.52) underwent DISE. The conventional subgroup represented the 58.67% of the sample (n = 88), while the disproportional one counted for the 26.67% (n = 40), and the persistent one for 14.66% (n = 22) of the population. Sleep endoscopy changed the surgical plan in 4.5% of conventional OSAS, 17.5% of disproportional OSAS and 72.7% of persistent OSAS (p < 0.005). Overall, a change of the treatment plan operated by DISE was associated with a non-conventional OSAS status (OR = 6; 95% CI = 1.6-26.4).
Conclusions:
DISE is a safe procedure in children suffering from OSAS, and, despite being unnecessary in conventional cases of OSA, DISE should be considered not only in syndromic children, as previously demonstrated, but also in the general non-syndromic pediatric population, in the case of non-conventional OSA patients, and in children with persistent OSAS.
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