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Sickle cell disease in the United States: looking back and forward at 100 years of progress in management and survival

Am J Hematol. 2010 May;85(5):346-53. doi: 10.1002/ajh.21676.

Abstract

The past 100 years since James Herrick's first description of sickle cell disease in the United States have been characterized by the gradual development of management strategies. We review the progress in sickle cell disease management in the United States over the past 100 years, with emphasis on the diverse forces surrounding advances in disease management. Mortality and survival data are presented chronologically, with an attempt to highlight improvements in survival associated with specific advancements for pediatric and adult care. Finally, the future course for sickle cell disease management is explored, given the continued work in advancing the field.

Publication types

  • Review

MeSH terms

  • Adolescent
  • Adult
  • Anemia, Sickle Cell / diagnosis
  • Anemia, Sickle Cell / drug therapy*
  • Anemia, Sickle Cell / mortality
  • Antisickling Agents / therapeutic use*
  • Child
  • Child, Preschool
  • Health Policy / legislation & jurisprudence*
  • Health Policy / trends
  • Humans
  • Infant
  • Mass Screening / legislation & jurisprudence*
  • Mass Screening / trends
  • Middle Aged
  • Patient Rights
  • Survival Analysis
  • United States / epidemiology
  • Young Adult

Substances

  • Antisickling Agents