Does race-ethnicity affect upper airway stimulation adherence and treatment outcome of obstructive sleep apnea? Journal of clinical sleep medicine : JCSM : official publication of the American Academy of Sleep Medicine Khan, M., Stone, A., Soose, R. J., Cohen, S. M., Howard, J., Capasso, R., Itayem, D., Gillespie, M. B., Mehra, R., Chio, E., Strollo, P. J., Menzl, A., Kaplan, A., Ni, Q. 2022

Abstract

STUDY OBJECTIVES: Untreated obstructive sleep apnea (OSA) is associated with excessive daytime sleepiness, decreased quality of life, and cardiovascular disease. Positive airway pressure (PAP) is the first-line therapy for OSA, however, adherence is difficult. Upper airway stimulation (UAS) is an FDA approved treatment of OSA. The objective of this study was to evaluate for a difference in treatment efficacy and adherence of upper airway stimulation therapy for OSA between individuals who are White and non-White using data from the ADHERE registry.METHODS: ADHERE registry is a multicenter prospective study of real-world experience of UAS for treatment of OSA in the US and Europe. Propensity score matching was used to create a balanced data set between the White and non-White groups. T-tests at a significance level of 5% were used to compare numeric values between groups.RESULTS: There were 2,755 participants of the ADHERE registry. 27 were excluded due to not having a race identified. 125 participants identified as non-White, 2,603 identify as White, and 27 did not provide race information. Propensity score matching was used to select 110 participants with 55 White and 55 non-White for the non-inferiority analysis. We did not find a difference in adherence, treatment AHI, changes in Epworth Sleepiness Scale Score, or clinical global impression after intervention score between White and non-White individuals.CONCLUSIONS: Our study found that there was no statistically significant difference in adherence or efficacy with UAS therapy between White and non-White individuals. However, the percent of non-White people implanted is low which suggests a need to expand access to this therapy for non-White populations with OSA who cannot tolerate PAP therapy.

View details for DOI 10.5664/jcsm.10068

View details for PubMedID 35681251