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Coping strategies and laboratory pain in children with sickle cell disease

K M Gil1, J L Edens, J J Wilson

  • 1Department of Psychology, University of North Carolina, Chapel Hill 27599-3270, USA.

Insights

Children with sickle cell disease (SCD) using active coping strategies reported less pain. Future interventions should focus on these coping mechanisms for managing SCD pain.

Area of Science:

  • Pediatric Pain Management
  • Hematology
  • Psychology

Background:

  • Coping strategies influence pain, healthcare use, and adjustment in children with sickle cell disease (SCD).
  • The precise mechanisms linking coping strategies to pain perception in pediatric SCD remain unclear.

Purpose of the Study:

  • To investigate the relationship between coping strategies and pain perception in children with SCD using a laboratory pain task.
  • To explore the utility of laboratory pain models for assessing pain in pediatric SCD.

Main Methods:

  • 41 children with SCD underwent a standardized laboratory pain task.
  • Sensory decision theory and hierarchical regression analyses were employed.
  • Coping strategies and adjustment were assessed via parent and child self-report measures.

Main Results:

  • Active cognitive and behavioral coping strategies were associated with a reduced tendency to report pain.
  • Age was controlled for in the hierarchical regression analyses.
  • The findings highlight the role of active coping in modulating pain perception.

Conclusions:

  • Active coping strategies can mitigate pain reporting in children with SCD.
  • Laboratory pain models are valuable tools for studying pediatric SCD pain.
  • Intervention studies should target the enhancement of coping strategies for SCD pain management.

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