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Night-to-night variation of pulse oximetry in children with sleep-disordered breathing
Rachael M Burke1,2, Barbara Maxwell2, Carolyn Hunter2
1Centre for Infection and Immunity, Queen's University Belfast, Belfast, UK.
Insights
Overnight oximetry shows significant night-to-night variation in children, especially those with Down syndrome. Recording three nights provides more reliable sleep-disordered breathing screening results.
Area of Science:
- Pediatric Pulmonology
- Sleep Medicine
- Clinical Diagnostics
Background:
- Sleep-disordered breathing is a serious concern in pediatric patients, particularly those with Down syndrome.
- Overnight pulse oximetry is a standard screening tool, but interpretation and optimal recording duration remain unclear.
Purpose of the Study:
- To evaluate night-to-night variability in overnight oximetry readings.
- To determine the impact of Down syndrome on oximetry result consistency.
- To assess the clinical utility of multiple nights of oximetry recording.
Main Methods:
- Retrospective observational study of 214 children undergoing overnight oximetry.
- Inclusion of 30 children with Down syndrome.
- Analysis of trace adequacy, basal SpO2, adjusted index of desaturations, and time with SpO2 <90%.
Main Results:
- Substantial night-to-night variation observed across all pediatric groups.
- Greater variability noted in children with Down syndrome compared to other diagnoses.
- Intraclass correlation for adjusted index was lower in Down syndrome (0.54) vs. others (0.88).
Conclusions:
- Significant day-to-day fluctuations in overnight oximetry readings are common.
- Children with Down syndrome exhibit more pronounced variability, complicating interpretation.
- Increasing recordings from one to three nights enhances clinical information for diagnosing sleep-disordered breathing.
Background:
Sleep-disordered breathing is a common and serious feature of many paediatric conditions and is particularly a problem in children with Down syndrome. Overnight pulse oximetry is recommended as an initial screening test, but it is unclear how overnight oximetry results should be interpreted and how many nights should be recorded.
Methods:
This retrospective observational study evaluated night-to-night variation using statistical measures of repeatability for 214 children referred to a paediatric respiratory clinic, who required overnight oximetry measurements. This included 30 children with Down syndrome. We measured length of adequate trace, basal SpO2, number of desaturations (>4% SpO2 drop for >10 s) per hour ('adjusted index') and time with SpO2<90%. We classified oximetry traces into normal or abnormal based on physiology.
Results:
132 out of 214 (62%) children had three technically adequate nights' oximetry, including 13 out of 30 (43%) children with Down syndrome. Intraclass correlation coefficient for adjusted index was 0.54 (95% CI 0.20 to 0.81) among children with Down syndrome and 0.88 (95% CI 0.84 to 0.91) for children with other diagnoses. Negative predictor value of a negative first night predicting two subsequent negative nights was 0.2 in children with Down syndrome and 0.55 in children with other diagnoses.
Conclusions:
There is substantial night-to-night variation in overnight oximetry readings among children in all clinical groups undergoing overnight oximetry. This is a more pronounced problem in children with Down syndrome. Increasing the number of attempted nights' recording from one to three provides useful additional clinical information.
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