Obstructive sleep apnea syndrome (OSAS) is a sleep breathing disorder characterized by periods of cessation (apnea) and/or reduction (hypopnea) of oronasal airflow during sleep accompanied by drops in the blood oxygen level caused by repetitive upper airway obstructions.
1 Identifying the site of obstruction and the pattern of airway collapse during sleep are essential key points to guide nonventilatory treatment decision making processes for OSAS in adults. Several studies have shown that upper airway endoscopic findings from tests performed while the patient is awake do not correspond exactly to obstructive sleep events.
2,3 First introduced by Croft and Pringle
4 in 1991, drug-induced sleep endoscopy (DISE) is a diagnostic technique providing a dynamic anatomical analysis of the upper airways during the pharmacologic induction of artificial sleep. Direct observation of anatomical modifications, such as collapse, vibrations, apnea or hypopnea, and their localization, is provided by a flexible fiber optic nasopharyngoscope. The lack of standardization in the DISE technique, including sedation, operation procedure, and classification, has produced several variations in the performance of DISE.
5 In particular, the detection of obstructive events depends on the direct visual observation of changes in upper airway caliber, causing a subjective interpretation of the test results and, consequently, poor intraobserver and interobserver reliability when otolaryngology surgeons not experienced in the technique are involved.
6