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Sleep patterns in pediatric sickle cell disease
Lauren C Daniel1, Mitzie Grant, Sanjeev V Kothare
1Department of Psychology, Drexel University, Philadelphia, Pennsylvania 19104, USA. lcd34@drexel.edu
Insights
Children with sickle cell disease (SCD) experience more night waking and sleep-disordered breathing behaviors than healthy children. These sleep issues are linked to disease severity, complications, and socioeconomic status.
Area of Science:
- Pediatric Sleep Medicine
- Hematology
- Child Health
Background:
- Limited research exists on general sleep behaviors in children with sickle cell disease (SCD).
- Previous studies focused on specific sleep disorders like sleep-disordered breathing and hypoxemia in this population.
- Understanding general sleep patterns is crucial for comprehensive care.
Purpose of the Study:
- To compare sleep patterns and behaviors in children with SCD versus healthy controls.
- To investigate associations between demographic/disease factors and sleep in children with SCD.
Main Methods:
- Parents of children aged 4-10 with SCD (n=54) and healthy controls (n=52) completed the Children's Sleep Habits Questionnaire.
- Demographic and disease factors (genotype, healthcare use, complications, SES) were reviewed from medical charts for the SCD group.
Main Results:
- Children with SCD showed significantly more night waking and sleep-disordered breathing behaviors than controls.
- In the SCD group, parasomnias correlated with socioeconomic status (SES), enuresis, severe genotypes, SCD complications, and healthcare use.
- Sleep-disordered breathing was associated with SES, enuresis, and SCD complications.
Conclusions:
- Children with SCD exhibit more disrupted sleep than peers with similar backgrounds, highlighting the need for routine sleep assessment.
- Higher rates of reported sleep-disordered breathing and night waking necessitate interventions to improve sleep quality and daytime function.
- Addressing sleep disruptions can enhance the overall quality of life for children with SCD.
Background:
Research examining sleep in children with sickle cell disease (SCD) has focused on the increased occurrence of specific sleep disorders (i.e., sleep-disordered breathing, hypoxemia, nocturnal enuresis), but no research exists describing general sleep behaviors of children with SCD. The purpose of the current study was to compare sleep patterns and sleep behaviors in children with SCD and healthy controls and examine the associations of demographic and disease factors with sleep in the SCD group.
Procedure:
The Children's Sleep Habits Questionnaire was completed by parents of 4- to 10-year-old children with SCD (n = 54) and children attending well-care clinics in the same urban hospital (n = 52). Within the SCD group, demographic and disease factors [i.e., genotype, healthcare utilization, SCD complications, and socioeconomic status (SES)] were determined by medical chart review.
Results:
Parents of children with SCD reported significantly more behaviors associated with night waking and sleep-disordered breathing than the control group. Within the SCD group, parasomnias were related to SES, enuresis, more severe genotypes, SCD complications, and healthcare utilization. Sleep-disordered breathing was also related to SES, enuresis, and SCD complications.
Conclusions:
Results indicate the importance of routinely assessing sleep in children with SCD as they are more likely to exhibit disrupted sleep than children with similar demographic backgrounds. Given significantly higher rates of parent reported sleep-disordered breathing and night waking in this population, it is important to consider interventions to minimize disruptions to overnight sleep and improve daytime functioning for quality of life in children with SCD.
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