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The relationship between pain and sleep in pediatric sickle cell disease
Dakshin Padmanabhan1, Tiffany Tucker2, Donna Murdaugh1,3
1Division of Pediatric Hematology and Oncology, Department of Pediatrics, University of Alabama at Birmingham, Birmingham, Alabama, USA.
Insights
Pain significantly disrupts sleep in children with sickle cell disease (SCD). Patient-reported outcomes reveal strong links between pain interference and sleep disturbances, underscoring the need for integrated care.
Area of Science:
- Pediatric Hematology
- Sleep Medicine
- Pain Management
Background:
- Sickle cell disease (SCD) frequently causes pain and sleep disturbances in children.
- Understanding the relationship between pain and sleep is crucial for improving quality of life in pediatric SCD patients.
Purpose of the Study:
- To investigate the associations between pain and sleep disturbances in pediatric SCD patients.
- To characterize sleep chronotype and social jetlag in this population.
Main Methods:
- A cross-sectional survey of 105 pediatric patients (aged 8-17) with SCD.
- Utilized PROMIS (Patient Reported Outcomes Measurement System) for pain interference, sleep disturbance, and sleep-related impairment.
- Assessed chronotype and social jetlag using the μMCTQ (Ultra-short Munich Chronotype Questionnaire).
Main Results:
- Pain interference strongly correlated with sleep disturbance (r=0.49) and sleep-related impairment (r=0.46).
- Female participants reported higher sleep-related impairment than males.
- Patients with recent emergency department visits for pain experienced greater sleep disturbance and impairment.
Conclusions:
- Pain interference is significantly associated with both sleep disturbance and sleep-related impairment in pediatric SCD.
- PROMIS measures effectively identify patients with pain and sleep issues.
- Further longitudinal studies are needed to establish causality between pain and sleep in SCD.
Background:
Pain and sleep disturbances are prevalent complications experienced by pediatric patients with sickle cell disease (SCD). This study aims to identify associations between pain and sleep, and to characterize sleep chronotype and social jetlag in children and adolescent patients with SCD.
Methods:
We performed a cross-sectional survey of 105 pediatric patients with SCD aged 8-17 years using PROMIS (Patient Reported Outcomes Measurement System) pain interference, sleep disturbance, and sleep-related impairment item banks. The μMCTQ (Ultra-short Munich Chronotype Questionnaire) assessed chronotype and social jetlag. Analyses were performed to assess associations between PROMIS measures, sleep patterns, and clinical variables.
Results:
Female participants reported higher T-scores for sleep-related impairment than males (females: 56.7 ± 10 vs. males 50.2 ± 9.4, p = .0009). Patients with one or more emergency department (ED) visits for pain in the last 12 months reported greater sleep disturbance (55.0 ± 8.5 vs. 50.7 ± 10, p = .046) and sleep-related impairment (57.1 ± 9.3 vs. 52.1 ± 10.2, p = .03) than patients without any ED visits for pain in the last 12 months. Pain interference was significantly associated with both sleep disturbance (r = .49, p < .0001) and sleep-related impairment (r = .46, p < .0001). The average mid-sleep time was 4:14 ± 1:44 a.m. and the average social jetlag (hh:mm) was 2:32 ± 1:35.
Conclusion:
Our study demonstrates that pain interference is associated with both sleep disturbance and sleep-related impairment. PROMIS measures can identify patients that suffer from pain and sleep disturbances and highlights the need to conduct longitudinal prospective studies to define the directionality of pain and sleep in SCD.
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