| Literature DB >> 28035747 |
Djamila Labib Ghafuri1, Shruti Chaturvedi2, Mark Rodeghier3, Sarah-Jo Stimpson4, Brandi McClain4, Jeannie Byrd4, Michael R DeBaun4.
Abstract
In a retrospective cohort study, we tested the hypothesis that when prescribing hydroxyurea (HU) to children with sickle cell anemia (SCA) to prevent vaso-occlusive events, there will be a secondary benefit of maintaining low transcranial Doppler (TCD) velocity, measured by imaging technique (TCDi). HU was prescribed for 90.9% (110 of 120) of children with SCA ≥5 years of age and followed for a median of 4.4 years, with 70% (n = 77) receiving at least one TCDi evaluation after starting HU. No child prescribed HU had a conditional or abnormal TCDi measurement. HU initiation for disease severity prevention decreases the prevalence of abnormal TCDi velocities.Entities:
Keywords: hydroxyurea therapy; red cells; sickle cell disease; transcranial Doppler velocity
Mesh:
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Year: 2016 PMID: 28035747 DOI: 10.1002/pbc.26401
Source DB: PubMed Journal: Pediatr Blood Cancer ISSN: 1545-5009 Impact factor: 3.167