Abstract

Introduction

In-laboratory titration polysomnography (PSG) is standard to determine optimal therapeutic continuous positive airway pressure (CPAP) in children with obstructive sleep apnea syndrome (OSAS) treated with CPAP. Use of auto titrating CPAP devices (autoCPAP) as an alternative is not well studied in children. We hypothesized that autoCPAP-derived pressures (PAUTO) correlate with the gold standard of titration PSG pressure (PPSG).

Methods

Retrospective study of children cared for in a pediatric sleep center initiated on autoCPAP between 2007 and 2017 who had a titration PSG. Children who used autoCPAP ≥ 120 minutes on the nights used within 90 days of titration PSG and whose residual obstructive apnea hypopnea index (OAHI) decreased by ≥ 75% were included in the analysis. PAUTO were obtained from usage downloads and compared to PPSG. PPSG predictive factors were analyzed by median regression. Non-parametric methods were used for analysis.

Results

110 children were initiated on autoCPAP and 44 satisfied inclusion criteria. Age (mean±SD) was 12.9±4.0 years, 63.6% were obese (BMI ≥ 95%). PPSG median[IQR] was 8[7-11] cmH2O, PAUTO mean pressure (PMEAN) 6.2[5.6-7.6] cmH2O, peak mean pressure (PPEAKMEAN) 9.4[7.7-11.1] cmH2O, and average device pressure < 90% of the time (P90) 8.1[7.2-9.7] cmH2O. All three PAUTO correlated with PPSG (rho 0.34, 0.36, 0.33, respectively; p <0.05). PMEAN was significantly lower than the other three pressures (p<0.0002). Median regression analysis demonstrated that after adjusting for patient characteristics such as age, BMI, obesity status, baseline OAHI, race and gender, PAUTO remained significant predictors of PPSG (p<0.05). There were no significant interactions between these patient characteristics and PAUTO.

Conclusion

AutoCPAP can be effectively used in children. PPEAKMEAN and P90 are in better agreement with PPSG. PMEAN was lower than PPSG underscoring that autoCPAP decreases pressure when less pressure is needed. Long-term studies of autoCPAP for the treatment of OSAS in children are needed to determine its impact on adherence and health outcomes in children.

Support (If Any)

T32HL07713, K01HL130719

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