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Transition to adult care in sickle cell disease: A longitudinal study of clinical characteristics and disease severity.

Mariam KayleSharron L DochertyRichard SloanePaula TanabeGary MaslowWei PanNirmish Shah
Published in: Pediatric blood & cancer (2018)
Whereas most AYAs had stable severity, nearly a quarter had increasing severity, over time. AYAs with increasing severity had more complications, were more likely to transfer to adult care, and demonstrated higher and longer adult SCD care utilization compared with AYAs with stable severity.
Keyphrases
  • healthcare
  • sickle cell disease
  • palliative care
  • quality improvement
  • risk factors
  • young adults