Hospital-based study reveals intermediate health-related quality of life and high pain burden in pediatric sickle cell disease, highlighting the need for systematic pain protocols.
SCD), encompassing domains such as pain, pain impact, emotions, treatment, and communication. The total score indicated intermediate HRQoL, with the pain impact domain showing the lowest scores, highlighting the importance of systematic pain management. Associations were observed between age, disease complications, household composition, and specific HRQoL domains, suggesting that both clinical burden and family context influence patient-reported outcomes. These findings underscore the multifactorial nature of HRQoL in pediatric SCD and support the development of standardized outpatient and emergency pain management protocols, alongside family-centered care, to improve quality of life in this population.
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Andrade et al. (2026) studied this question.
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