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How Well Do Children with Cystic Fibrosis Sleep? An Actigraphic and Questionnaire-Based Study
Moya Vandeleur1, Lisa M Walter2, David S Armstrong3
1The Ritchie Centre, Department of Pediatrics, Monash University and Hudson Institute of Medical Research, Melbourne, Victoria, Australia; Department of Respiratory Medicine, Royal Children's Hospital, Melbourne, Victoria, Australia.
Insights
Children with cystic fibrosis (CF) experience poorer sleep quality and efficiency than healthy peers, even when clinically stable. Sleep disturbances in CF are linked to disease severity, impacting daytime alertness.
Area of Science:
- Pediatric Pulmonology
- Sleep Medicine
- Clinical Research
Background:
- Cystic Fibrosis (CF) affects multiple organ systems, including potentially impacting sleep.
- Objective and subjective sleep assessment is crucial for understanding the overall health of children with CF.
Purpose of the Study:
- To objectively and subjectively measure sleep patterns and quality in clinically stable children with CF compared to healthy controls.
- To investigate the relationship between sleep quality and CF disease severity.
Main Methods:
- Actigraphy for 14 days to assess sleep patterns and quality.
- Pulse oximetry for overnight peripheral capillary oxygen saturation.
- Pediatric Daytime Sleepiness Scale (PDSS), Sleep Disturbance Scale for Children, and Obstructive Sleep Apnea-18 for subjective assessments.
Main Results:
- Children with CF exhibited significantly lower total sleep time and sleep efficiency than controls, with more frequent awakenings.
- CF disease severity markers (e.g., FEV1, oxygen saturation) correlated with sleep parameters.
- Children with CF reported significantly higher sleep disturbance and daytime sleepiness scores.
Conclusions:
- Children with CF have impaired sleep quality and efficiency, even during clinical stability, characterized by increased nighttime wakefulness.
- Objective sleep disturbances and subjective daytime sleepiness in CF are associated with disease severity.
- Parental reports of sleep disturbance may not always align with objective measures or disease severity.
Objective:
To measure sleep patterns and quality, objectively and subjectively, in clinically stable children with cystic fibrosis (CF) and healthy control children, and to examine the relationship between sleep quality and disease severity.
Study Design:
Clinically stable children with CF and healthy control children (7-18 years of age) were recruited. Sleep patterns and quality were measured at home with actigraphy (14 days). Overnight peripheral capillary oxygen saturation was measured via the use of pulse oximetry. Daytime sleepiness was evaluated by the Pediatric Daytime Sleepiness Scale (PDSS) and subjective sleep quality by the Sleep Disturbance Scale for Children and Obstructive Sleep Apnea-18.
Results:
A total of 87 children with CF and 55 control children were recruited with no differences in age or sex. Children with CF had significantly lower total sleep time and sleep efficiency than control children due to frequent awakenings and more wake after sleep onset. In children with CF, forced expiratory volume in 1 second and overnight peripheral capillary oxygen saturation nadir correlated positively with total sleep time and sleep efficiency and negatively with frequency of awakenings and wake after sleep onset. Patients with CF had significantly greater Sleep Disturbance Scale for Children (45 vs 35; P < .001), Obstructive Sleep Apnea-18 (35 vs 24; P < .001), and PDSS scores (14 vs 11; P < .001). There was a negative correlation between PDSS and forced expiratory volume in 1 second (r = -0.23; P < .05).
Conclusions:
Even in periods of clinical stability, children with CF get less sleep than their peers due to more time in wakefulness during the night rather than less time spent in bed. Objective measures of sleep disturbance and subjective daytime sleepiness were related to disease severity. In contrast, parents of children with CF report high levels of sleep disturbance unrelated to disease severity.
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