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* From the Departments of Pediatrics (Dr. Kirk and Ms. Bohn) and Medicine (Drs. Flemons and Remmers), University of Calgary, Calgary, AB, Canada.
Correspondence to: Valerie Kirk, MD, FCCP, 1820 Richmond Rd, SW Calgary, AB Canada T2T 5C7; e-mail: val.kirk{at}calgaryhealthregion.ca
Study objectives: To measure the accuracy and reliability of a portable home oximetry monitor with an automated analysis for the diagnosis of obstructive sleep apnea (OSA) in children.
Design: Prospective cohort study.
Setting: Alberta Lung Association Sleep Center, Alberta Childrens Hospital Sleep Clinic.
Study subjects: Consecutive, otherwise healthy children, aged 4 to 18 years, presenting to the Pediatric Sleep Service at the Alberta Childrens Hospital for assessment of possible OSA.
Interventions: All subjects underwent 2 nights of monitoring in the home with an oximetry-based portable monitor with an automatic internal scoring algorithm. A third night of monitoring was done simultaneously with computerized laboratory polysomnography according to American Thoracic Society guidelines.
Measurements and results: Both test-retest reliability of the portable monitor-based desaturation index (DI) between 2 nights at home and between laboratory and home were high using the Bland and Altman analysis (mean agreement, 0.32 and 0.64; limits of agreement, - 8.00 to 8.64 and - 0.75 to 6.50, respectively). The polysomnographic apnea-hypopnea index (AHI) agreed poorly with the portable monitor DI (mean difference, 1.27; limits of agreement, - 12.02 to 15.02). The sensitivity and specificity of the monitor for the identification of moderate sleep apnea (polysomnography AHI > 5/h) were 67% and 60%, respectively.
Conclusion: Portable monitoring based only on oximetry alone is not adequate for the identification of OSA in otherwise healthy children.
Key Words: abbreviated monitoring ambulatory monitoring children diagnosis obstructive sleep apnea oximetry sleep apnea syndromes
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