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Published on: March 14, 2017
Pain, coping, and sleep in children and adolescents with sickle cell disease
Joyce Kelly Graves1, Eufemia Jacob
1School of Nursing, University of California Los Angeles, Los Angeles, CA, USA.
Insights
Children with sickle cell disease (SCD) experience pain that impacts sleep and coping strategies. Nurses should assess pain, coping, and sleep concurrently to improve patient outcomes.
Area of Science:
- Pediatric Hematology
- Pain Management
- Sleep Medicine
Background:
- Sickle cell disease (SCD) is a chronic condition often associated with significant pain.
- Pain in SCD can profoundly impact a child's quality of life, including sleep and coping mechanisms.
Purpose of the Study:
- To investigate the interrelationships between pain, pain coping strategies, and sleep quality in children with SCD.
- To identify demographic and clinical factors influencing pain, coping, and sleep in this population.
Main Methods:
- A cross-sectional study involving 66 participants (39 children, 27 adolescents) with SCD.
- Data collected using electronic visual analog scale (eVAS), Pain Coping Questionnaire, and Pittsburg Sleep Quality Index.
Main Results:
- Two-thirds of participants reported pain; no significant associations found with age, gender, pain intensity, or frequency.
- Common coping strategies included information seeking, problem-solving, and social support.
- Significant negative correlations noted in males between pain severity and behavioral distraction/catastrophizing.
- Over 91% experienced sleep disturbances, with 18.2% using sleep medication frequently.
- No significant differences in sleep quality were associated with age, gender, pain intensity, or frequency.
Conclusions:
- Pain in children with SCD significantly affects sleep patterns and coping behaviors.
- Concurrent assessment of pain, coping, and sleep is crucial for effective nursing care.
- Promoting sleep hygiene and positive coping strategies is recommended during painful episodes.
Purpose:
The study examined the relationships among pain, pain coping, and sleep, and assessed factors (age, gender, frequency, and intensity of pain) that affect pain, coping, and sleep in children with sickle cell disease (SCD).
Methods:
Participants (66) were 39 children (M = 11.5 years) and 27 adolescents (M = 15.5 years) with SCD who completed an electronic visual analog scale (eVAS), Pain Coping Questionnaire, and Pittsburg Sleep Quality Index.
Results:
About two-thirds of the children reported pain the previous month. No significant differences were found between pain and age, gender, pain intensity, or frequency. Most children coped with pain by seeking information, problem solving, seeking social support, and positive self-statements. There were significant negative correlations in males between worse pain severity and behavioral distraction and internalizing or catastrophizing. The majority (91.2%) had mild to severe sleep disturbances, with 18.2% requiring sleeping medication three or more times a week. There were no significant differences between sleep and age, gender, pain intensity, or frequency.
Conclusion:
Children with SCD experience pain that affects sleep patterns and the way they cope with pain. Nurses need to concurrently assess pain, coping, and sleep and promote sleep hygiene and positive coping strategies during pain episodes.
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