Individual-level behavioral interventions to support optimal development of children with sickle cell disease: A systematic review

Pediatr Blood Cancer. 2023 Mar;70(3):e30178. doi: 10.1002/pbc.30178. Epub 2022 Dec 30.

Abstract

This review aimed to identify and describe individual-level behavioral interventions for children 0-18 years of age with sickle cell disease (SCD). PRISMA guidelines were followed at each stage of this review. Twenty-seven studies were included, representing six intervention types: disease knowledge (n = 7), self-management (n = 7), pain management (n = 4), school functioning (n = 4), cognitive health (n = 4), and mental health (n = 2). Most interventions targeted older children (5+ years), while only two examined interventions for children 0-3 years. This review suggests that offering education about disease knowledge, self-management, and pain management interventions can be beneficial for this population. Future research is needed to understand interventions to support young children and the impact of SCD on development.

Keywords: child development; developmental delay; intervention; rehabilitation; sickle cell disease.

Publication types

  • Systematic Review
  • Review

MeSH terms

  • Adolescent
  • Anemia, Sickle Cell* / therapy
  • Behavior Therapy* / methods
  • Child
  • Child, Preschool
  • Humans
  • Infant
  • Infant, Newborn
  • Pain Management
  • Patient Education as Topic
  • Self-Management