Please use this identifier to cite or link to this item: https://dora.health.qld.gov.au/qldresearchjspui/handle/1/4619
Title: Sleep, function, behaviour and cognition in a cohort of children with down syndrome
Authors: Chawla, Jasneek 
Burgess, S.
Heussler, Helen 
Bernard, A.
Issue Date: 2021
Source: 11, (10), 2021
Journal: Brain Sciences
Abstract: Objective: To describe the sleep problems experienced by children with Down syndrome attending a tertiary sleep clinic and relationship with behaviour, function and cognition. Methods: Data were collected from children with Down syndrome aged 3–18 years old. Carers completed the Abbreviated Child Sleep Habits Questionnaire, Child Behaviour Checklist and Life-Habits Questionnaire at enrolment. Cognitive assessment (Stanford-Binet 5) was undertaken by a trained psychologist. Children received management for their sleep problem as clinically indicated. Results: Forty-two subjects with a median age of 6.8 years (Interquartile Range-IQR 4.5, 9.8) were enrolled. A total of 92% were referred with snoring or symptoms of Obstructive Sleep Apnoea (OSA), with 79% of those referred having had previous ENT surgery. Thus, 85% of all participants underwent a sleep study and 61% were diagnosed with OSA (OAHI ≥ 1/h). Based on questionnaires, 86% of respondents indicated that their child had a significant sleep disorder and non-respiratory sleep problems were common. Non-respiratory problems included: trouble going to sleep independently (45%), restless sleep (76%), night-time waking (24%) and bedtime resistance (22%). No significant correlations were found between sleep measures (behavioural and medical sleep problems) and the behavioural, functional or cognitive parameters. Conclusion: Sleep disorders were very common, especially non-respiratory sleep problems. OSA was common despite previous surgery. No association was found between sleep-related problems (snoring, sleep-study-confirmed OSA or non-respiratory sleep problem) and parent-reported behavioural problems, functional impairments or intellectual performance. This may reflect limitations of the measures used in this study, that in this population ongoing problems with daytime function are not sleep related or that a cross-sectional assessment does not adequately take into account the impacts of past disease/treatments. Further research is required to further evaluate the tools used to evaluate sleep disorders, the impact of those disorder on children with Down syndrome and interventions which improve both sleep and daytime function.L20140967552021-10-21
2021-10-26
DOI: 10.3390/brainsci11101317
Resources: https://www.embase.com/search/results?subaction=viewrecord&id=L2014096755&from=exporthttp://dx.doi.org/10.3390/brainsci11101317 |
Keywords: Down syndrome;Duchenne muscular dystrophy;ear nose throat surgery;electrocardiography;electroencephalography;electromyography;electronic medical record;electrooculography;emotional disorder;electroencephalograph electrodepressure transducer;thermistor;carbon dioxide;melatonin;adenoidectomy;adenotonsillectomy;female;functional disease;heart disease;heart rhythm;home oxygen therapy;human;information processing;language delay;language development;male;nose airflow;parasomnia;plethysmography;polysomnography;preschool child;problem behavior;pulse oximetry;questionnaire;retrospective study;school child;sleep;sleep disorder;sleep disordered breathing;sleep quality;snoring;thorax;tonsillectomy;transcutaneous carbon dioxide monitoring;wakefulness;thyroid disease;anxiety;article;attention deficit hyperactivity disorder;autism;behavior;body mass;bruxism;child;clinical article;cognition;comorbidity;cross-sectional study;data analysis;daytime somnolence;developmental delay;disease severity
Type: Article
Appears in Sites:Children's Health Queensland Publications

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