Abstract
Purpose
Sleep disordered breathing (SDB) is common in children, resulting in extensive waiting lists for specialist clinics. There is an urgent need for a valid method of triaging patients and the OSA-18, a disease-specific tool, is an attractive candidate for this role. We aimed to examine the OSA-18 as a measurement tool in detail and to determine whether the score or aspects of it could be used as a screening tool for SDB in children.
Methods
Retrospective analysis of 582 children (6 months to 16.4 years)—216 underwent overnight PSG and 366 overnight oximetry. Confirmatory factor analysis (CFA) and exploratory factor analysis (EFA) were conducted. Receiver operating characteristic curve analysis assessed the diagnostic accuracy of the factors for the presence of OSA. Rasch analysis was used to assess the structure of the items (1–18) and categories of response (Likert scale).
Results
The CFA with a forced five-factor structure, revealed three factors with Eigenvalues >1, and explained 73.7 % of the variance. EFA resulted in a two-factor structure, explaining 60.3 % of the variance. Assessment of sensitivity and specificity showed a high false-positive rate, irrespective of the factor structure tested. Rasch analysis showed poor discrimination between adjacent categories on the Likert scale.
Conclusion
This study confirmed that the predictive value of the OSA-18 for SDB severity is weak. Some questions perform better than others statistically, and the seven categories of response introduce significant statistical noise, raising the possibility that modification of the OSA-18 may improve its performance in the prediction of OSA severity.
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Acknowledgments
The authors would like to thank the children and families who participated in this study and the staff of the Melbourne Children’s Sleep Centre for their support. The authors thank Andrew Stephanou (Australian Council for Educational Research) for performing the Rasch analysis.
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Ethical approval for this study was granted by the Monash Health and Monash University Human Research Ethics Committees. Written informed consent was obtained from parents at the time of the clinical testing for use of data pertaining to the diagnostic PSG or home oximetry for research purposes. There was no monetary incentive for participation.
Funding
This study was supported by a National Health and Medical Research Council of Australia project grant (491001 and 1010810) and the Victorian Government’s Operational Infrastructure Support Program.
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All authors certify that they have no affiliations with or involvement in any organization or entity with any financial interest (such as honoraria; educational grants; participation in speakers’ bureaus; membership, employment, consultancies, stock ownership, or other equity interest; and expert testimony or patent-licensing arrangements), or non-financial interest (such as personal or professional relationships, affiliations, knowledge or beliefs) in the subject matter or materials discussed in this manuscript.
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Lisa M. Walter and Sarah N. Biggs are co-first authors.
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Walter, L.M., Biggs, S.N., Cikor, N. et al. The efficacy of the OSA-18 as a waiting list triage tool for OSA in children. Sleep Breath 20, 837–844 (2016). https://doi.org/10.1007/s11325-015-1289-5
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DOI: https://doi.org/10.1007/s11325-015-1289-5