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Background <p>The apnea–hypopnea index (AHI) is the standard metric for grading obstructive sleep apnea (OSA) severity but does not capture cumulative oxygen desaturation; hypoxic burden (HB), integrating desaturation area per hour, may better reflect physiological load, but its diagnostic performance remains uncertain.</p> Methods <p>We conducted a retrospective diagnostic study of adults undergoing Peripheral Arterial Tonometry—Home Sleep Apnea Testing (PAT-HSAT) (WatchPAT®) between 2016 and 2025. After prespecified exclusions, 1,171 patients with AHI3% ≥ 5 events/h were included. HB (%·min/h) was derived from Oxygen Desaturation Index (ODI4%) linked desaturation events and normalized by total sleep time (TST). Diagnostic accuracy for moderate-to-severe (AHI3% ≥ 15 events/h) and severe OSA (AHI3% ≥ 30 events/h) was assessed using receiver operating characteristic (ROC) analyses and standard performance metrics. HB distributions were examined across American Academy of Sleep Medicine (AASM) categories.</p> Results <p>Substantial heterogeneity in HB was observed within AASM severity categories. HB values discordant with AASM-defined severity were present in 30.0% of mild, 49.2% of moderate, and 26.6% of severe OSA patients, affecting 35.4% of the overall cohort. HB showed good discrimination for moderate-to-severe OSA (AUC 0.867, 95% CI 0.846–0.888) and strong discrimination for severe OSA (AUC 0.897, 95% CI 0.879–0.916). An HB threshold ≥ 16.6%·min/h showed high sensitivity (90.1%) for moderate-to-severe OSA, while ≥ 29.5%·min/h showed high specificity (88.3%) for severe OSA.</p> Conclusion <p>HB derived from PAT-HSAT identifies clinically relevant heterogeneity within AASM severity categories and provides good diagnostic discrimination. By capturing cumulative hypoxemic load beyond event frequency, HB complements AHI-based classification and may refine severity stratification.</p> Clinical trial registration <p>Not applicable.</p>

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Hypoxic burden calculation in patients with obstructive sleep apnea diagnosed by peripheral arterial tonometry: diagnostic accuracy and clinical implications

  • 期刊论文

  • 出版模式：

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  • 发表日期：

    2026年4月2日

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  • Diego Ignacio Vanegas,
  • Andrés Felipe Blanco,
  • Fernando Adolfo Vanegas,
  • Francisco José Hurtado

摘要

Background

The apnea–hypopnea index (AHI) is the standard metric for grading obstructive sleep apnea (OSA) severity but does not capture cumulative oxygen desaturation; hypoxic burden (HB), integrating desaturation area per hour, may better reflect physiological load, but its diagnostic performance remains uncertain.

Methods

We conducted a retrospective diagnostic study of adults undergoing Peripheral Arterial Tonometry—Home Sleep Apnea Testing (PAT-HSAT) (WatchPAT®) between 2016 and 2025. After prespecified exclusions, 1,171 patients with AHI3% ≥ 5 events/h were included. HB (%·min/h) was derived from Oxygen Desaturation Index (ODI4%) linked desaturation events and normalized by total sleep time (TST). Diagnostic accuracy for moderate-to-severe (AHI3% ≥ 15 events/h) and severe OSA (AHI3% ≥ 30 events/h) was assessed using receiver operating characteristic (ROC) analyses and standard performance metrics. HB distributions were examined across American Academy of Sleep Medicine (AASM) categories.

Results

Substantial heterogeneity in HB was observed within AASM severity categories. HB values discordant with AASM-defined severity were present in 30.0% of mild, 49.2% of moderate, and 26.6% of severe OSA patients, affecting 35.4% of the overall cohort. HB showed good discrimination for moderate-to-severe OSA (AUC 0.867, 95% CI 0.846–0.888) and strong discrimination for severe OSA (AUC 0.897, 95% CI 0.879–0.916). An HB threshold ≥ 16.6%·min/h showed high sensitivity (90.1%) for moderate-to-severe OSA, while ≥ 29.5%·min/h showed high specificity (88.3%) for severe OSA.

Conclusion

HB derived from PAT-HSAT identifies clinically relevant heterogeneity within AASM severity categories and provides good diagnostic discrimination. By capturing cumulative hypoxemic load beyond event frequency, HB complements AHI-based classification and may refine severity stratification.

Clinical trial registration

Not applicable.