Research AppraisalRandomised Controlled Trial

Clinical impact of customised positive airway pressure (PAP) therapy interfaces (3DPiPPIn): a single site randomised controlled trial

ThoraxMansell, Stephanie K, Mandal, Swapna, Gowing, Francesca et al.14 May 2026DOI

Clinical Snapshot

60CEBM
Evidence: StrongRandomised Controlled Trial

PICO Framework

P — Population160 adults naïve to PAP therapy with sleep disordered breathing (AHI ≥15 events/hour)
I — InterventionCustomised 3D-printed oronasal interface cushions created from structured light facial scans
C — ComparatorConventional oronasal PAP therapy interfaces
O — OutcomesPrimary: residual AHI at 6 months. Secondary: interface leak, therapy compliance, patient-reported symptoms

Bottom Line

This well-designed RCT of 160 PAP-naïve adults with OSA found that customised 3D-printed interfaces performed worse than conventional interfaces across all measured outcomes. At 6 months, customised interfaces were associated with a non-significant 1.5 events/hour increase in residual AHI, significantly higher interface leak (30 L/min difference), and reduced compliance. The study challenges assumptions about personalised interface design and suggests current 3D printing technology may not be ready for clinical implementation. Australian clinicians should continue using conventional interfaces, which remain effective and cost-efficient. The negative results highlight the importance of rigorous testing before adopting new technologies, even when they appear theoretically superior. Future research should address manufacturing limitations before re-evaluating customised interfaces.

Evidence: Strong

Key Findings

  • P Value: p=0.059 for primary outcome

  • Effect Size: Median AHI difference of 1.5 events/hour favouring conventional interfaces

  • Primary Outcome: 1.5 events/hour increase in AHI with customised interfaces (p=0.059)

  • Nnt Or Sensitivity: Number needed to harm: approximately 1 in 1.3 patients may experience worse AHI control

  • Confidence Interval: Not provided for primary outcome

Clinical Application

Limited by requirement for 3D scanning equipment and printing facilities Results support continued use of conventional interfaces available through PBS. 3D printing technology not yet ready for routine clinical implementation in Australian sleep centres Adults with moderate-severe OSA (AHI ≥15) initiating PAP therapy

Abstract

INTRODUCTION: Positive airway pressure (PAP) therapy is the recognised treatment for sleep disordered breathing (SDB), delivered via a tight-fitting face mask (interface). Conventional interfaces do not consider facial geometries, often resulting in poor fit and ineffective therapy. Three-dimensional (3D) printing of customised interfaces may improve comfort and outcomes. OBJECTIVES: To evaluate the clinical impact of customised versus conventional oronasal interfaces in adults with obstrcutive sleep apnoea (OSA). The primary outcome was residual Apnoea Hypopnea Index (AHI) at 6 months; secondary outcomes included interface leak, therapy concordance and patient reported symptoms. METHODS: A randomised controlled trial with 160 adults naïve to PAP therapy and diagnosed with SDB (AHI ≥15 events/hour). Randomisation was minimised by age and ethnicity. Structured light facial scans (POP2, Revopoint, China) were used to produce 3D printed moulds (Fuse 30+, Formlabs, Massachusetts, USA) for silicone injected oronasal customised interface cushions.AHI was compared using quantile regression to account for the skewed distribution of the AHI data. Secondary outcomes were compared using logistic, quantile and linear regressions. RESULTS: 160 participants were recruited (intervention: 82, control: 78). Customised interfaces were associated with a 1.5 (events/hour) increase in AHI (p=0.059), higher interface leak (difference in medians 30.0 L/min, 95% CI 7.36 to 40.14, p<0.0001) and lower compliance (difference in compliance 0.78, 95% CI 0.05 to 1.54, p=0.04) at 6 months. CONCLUSIONS: This trial did not demonstrate customised oronasal interfaces were superior to conventional interfaces. Future research should focus on addressing design and manufacturing limitations before any potential advantages can be evaluated. TRIAL REGISTRATION NUMBER: ISRCTN74082423.

References

  1. 1.Mansell, S. K., Mandal, S., Gowing, F., Ridout, D., Kilbride, C., Olsen, O., Hilton, S., Main, E., & Schievano, S. (2026). Clinical impact of customised positive airway pressure (PAP) therapy interfaces (3DPiPPIn): a single site randomised controlled trial. Thorax. https://doi.org/10.1136/thorax-2025-224135
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