Affiliation:
1. Department of Otorhinolaryngology, Division of Sleep Surgery University of Pennsylvania Perelman School of Medicine Philadelphia Pennsylvania USA
2. Department of Medicine, Division of Sleep Medicine University of Pennsylvania Perelman School of Medicine Philadelphia Pennsylvania USA
3. Department of Medicine, Division of Sleep Medicine Universidad Peruana Cayetano Heredia School of Medicine Lima Peru
Abstract
AbstractObjectivePositive airway pressure (PAP) titration during drug‐induced sleep endoscopy (DISE) provides objective measures of upper airway collapsibility. While skeletal measurements relate to collapsibility measures on DISE, the influence of soft tissue dimensions on upper airway collapsibility is not known. We analyzed the relationship of measures of upper airway soft tissue volumes, specifically soft palate, pharyngeal lateral walls, and tongue, with metrics of collapsibility.Study DesignCross‐sectional analysis from a prospective cohort.SettingAcademic medical center.MethodsPatients seeking PAP alternative therapies for obstructive sleep apnea (OSA) underwent standardized supine computed tomography (CT) acquisition and DISE protocols. The CT analysis primarily focused on soft tissue volumes and, secondarily, on airway and skeletal volumetric measures. DISE with PAP administration (DISE‐PAP) enabled the determination of the pressure at which inspiratory airflow first commenced (pharyngeal critical pressure, PcritA) and the pressure at which inspiratory flow limitation was abolished (pharyngeal opening pressure, PhOP). Both unadjusted and adjusted correlation analyses were performed to understand the relationship between upper airway anatomy and either PcritA or PhOP.ResultsOne hundred thirty‐nine subjects completed both CT and DISE‐PAP. On average, patients were male (70.5%), white (84.2%), middle‐aged (56.6 ± 13.5 years), and overweight (29.6 ± 4.7 kg/m2), with moderate‐severe apnea‐hypopnea index (29.7 ± 21.3 events/h). Adjusted for age, sex, body mass index, and skeletal volumes, soft palate, and lateral pharyngeal wall volumes were not associated with PhOP or PcritA, but a larger tongue was associated with more positive PhOP (⍴ = 0.20, P = .02), and more positive PcritA (⍴ = 0.16, P = .07). Exploratory analyses revealed smaller minimum cross‐sectional retropalatal area and intramandibular volume were also associated with increased collapsibility measures.ConclusionAfter controlling for clinical factors and skeletal volume, greater tongue volume was associated with more severe collapsibility during DISE. These results, in concert with previous work, suggest that greater tongue volume in a smaller skeletal dimensions contribute to the severity of airway collapsibility, a key driver of OSA pathogenesis.