0572 Conclusive AHI from RIP-Only Type III HSAT: Comparison of RIP-Based and Cannula-Based AI Analyses in a Large Multicenter Cohort

Abstract Introduction Type III home sleep apnea tests (HSAT) rely on respiratory flow measurement to score apneas and hypopneas. Although respiratory inductance plethysmography (RIP) has traditionally been viewed as an effort signal, contemporary implementations can capture respiratory morphology with sufficient fidelity to support RIP as a primary measurement of breathing. We evaluated whether a RIP-only Type III HSAT configuration (without nasal cannula) can deliver conclusive AHI-based severity classification comparable to full-montage attended polysomnography (PSG). Methods We performed a retrospective multicenter study using 5,771 Type I/II PSGs manually scored by registered technologists and board-certified sleep physicians. Two HSAT signal configurations were simulated from the same recordings: (1) a nasal-cannula HSAT configuration (nasal pressure, thoracoabdominal RIP, oximetry) and (2) a RIP-only HSAT configuration (thoracoabdominal RIP, oximetry). Both were processed by DeepRESP v2.0 (K252330), an FDA-cleared medical device, to score sleep/wake, respiratory events, and derive the AHI. PSG-scored AHI served as the reference. Positive-, negative-, and overall percentage agreement (PPA, NPA, OPA) with AHI thresholds (≥5, ≥15, ≥30 events/hour) were computed with 95% confidence intervals. Subgroup summaries characterized heterogeneity across age, sex, body mass index, race/ethnicity, and AHI. Results The cohort was clinically diverse: adults 18–88 years old, 35% female, 58% with body mass index ≥30 kg/m2, with AHI values spanning normal to severe. For AHI ≥5, RIP-only HSAT achieved PPA 93.7%, NPA 63.5%, OPA 92.8%, compared with nasal-cannula HSAT PPA 91.0%, NPA 78.0%, OPA 90.6%. For AHI ≥15, RIP-only HSAT achieved PPA 81.0%, NPA 91.1%, OPA 83.4%, versus nasal-cannula PPA 78.1%, NPA 93.9%, OPA 81.7%. Agreement at AHI ≥30 remained similarly high for both configurations. Across thresholds, RIP-only performance was within a few percentage points of the nasal-cannula configuration. Conclusion RIP-only Type III HSAT analyzed by AI can yield conclusive AHI-based severity classification that closely tracks attended PSG and performs comparably to a nasal-cannula-based HSAT configuration. These findings demonstrate that high-quality RIP signals—without a nasal cannula—can provide robust breathing information for AHI estimation, reducing inconclusive HSAT studies and decreasing the likelihood of repeat testing. Support (if any) None

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Journal
SLEEP
Published
2026-05-01
DOI
https://doi.org/10.1093/sleep/zsag091.0571
Primary Topic
Obstructive Sleep Apnea Research
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article
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article

0572 Conclusive AHI from RIP-Only Type III HSAT: Comparison of RIP-Based and Cannula-Based AI Analyses in a Large Multicenter Cohort

Sigurdur Aegir Jonsson, Ernir Erlingsson, Kristófer Montazeri, Eydís Arnardóttir et al.
SLEEP
Obstructive Sleep Apnea Research
article

0572 Conclusive AHI from RIP-Only Type III HSAT: Comparison of RIP-Based and Cannula-Based AI Analyses in a Large Multicenter Cohort

Sigurdur Aegir Jonsson, Ernir Erlingsson, Kristófer Montazeri, Eydís Arnardóttir, Jon Agustsson, Eysteinn Finnsson, Heidi Riney, Daniel Wilcox, Scott Sands, Rósa Hugosdóttir, Megan McPhee, Þóra Sigmarsdottir, Guðný Árnadóttir
article en

Abstract

Abstract Introduction Type III home sleep apnea tests (HSAT) rely on respiratory flow measurement to score apneas and hypopneas. Although respiratory inductance plethysmography (RIP) has traditionally been viewed as an effort signal, contemporary implementations can capture respiratory morphology with sufficient fidelity to support RIP as a primary measurement of breathing. We evaluated whether a RIP-only Type III HSAT configuration (without nasal cannula) can deliver conclusive AHI-based severity classification comparable to full-montage attended polysomnography (PSG). Methods We performed a retrospective multicenter study using 5,771 Type I/II PSGs manually scored by registered technologists and board-certified sleep physicians. Two HSAT signal configurations were simulated from the same recordings: (1) a nasal-cannula HSAT configuration (nasal pressure, thoracoabdominal RIP, oximetry) and (2) a RIP-only HSAT configuration (thoracoabdominal RIP, oximetry). Both were processed by DeepRESP v2.0 (K252330), an FDA-cleared medical device, to score sleep/wake, respiratory events, and derive the AHI. PSG-scored AHI served as the reference. Positive-, negative-, and overall percentage agreement (PPA, NPA, OPA) with AHI thresholds (≥5, ≥15, ≥30 events/hour) were computed with 95% confidence intervals. Subgroup summaries characterized heterogeneity across age, sex, body mass index, race/ethnicity, and AHI. Results The cohort was clinically diverse: adults 18–88 years old, 35% female, 58% with body mass index ≥30 kg/m2, with AHI values spanning normal to severe. For AHI ≥5, RIP-only HSAT achieved PPA 93.7%, NPA 63.5%, OPA 92.8%, compared with nasal-cannula HSAT PPA 91.0%, NPA 78.0%, OPA 90.6%. For AHI ≥15, RIP-only HSAT achieved PPA 81.0%, NPA 91.1%, OPA 83.4%, versus nasal-cannula PPA 78.1%, NPA 93.9%, OPA 81.7%. Agreement at AHI ≥30 remained similarly high for both configurations. Across thresholds, RIP-only performance was within a few percentage points of the nasal-cannula configuration. Conclusion RIP-only Type III HSAT analyzed by AI can yield conclusive AHI-based severity classification that closely tracks attended PSG and performs comparably to a nasal-cannula-based HSAT configuration. These findings demonstrate that high-quality RIP signals—without a nasal cannula—can provide robust breathing information for AHI estimation, reducing inconclusive HSAT studies and decreasing the likelihood of repeat testing. Support (if any) None

SLEEPVol. 49(Supplement_1)
Harvard University Press (US), Rex Medical (United States) (US)
Openalex Percentile: Top 7%
Obstructive Sleep Apnea Research
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