The efficacy and side effects of hydroxyurea in young children with sickle cell disease are unknown. The authors followed-up eight young children (mean age 3.7 years) during therapy with hydroxyurea for an average of 137 weeks. Total and fetal hemoglobin levels rose with hydroxyurea therapy. Hospital admission rates and total hospital days decreased during hydroxyurea therapy. No unexpected toxicity occurred, and growth and development were unaffected. This pilot study suggests that hydroxyurea is safe and effective in young children with sickle cell disease.
机构:
Childrens Hosp, Div Hematol Oncol, Dept Med, Boston, MA 02115 USA
Harvard Univ, Sch Med, Boston, MA USAChildrens Hosp, Div Hematol Oncol, Dept Med, Boston, MA 02115 USA
Heeney, Matthew M.
Ware, Russell E.
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机构:
St Jude Childrens Res Hosp, Dept Hematol, Memphis, TN 38105 USAChildrens Hosp, Div Hematol Oncol, Dept Med, Boston, MA 02115 USA
机构:
Childrens Hosp, Dept Med, Div Hematol Oncol, Boston, MA 02115 USA
Harvard Univ, Sch Med, Dept Pediat, Boston, MA 02115 USAChildrens Hosp, Dept Med, Div Hematol Oncol, Boston, MA 02115 USA
Heeney, Matthew M.
Ware, Russell E.
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h-index: 0
机构:
St Jude Childrens Res Hosp, Dept Hematol, Memphis, TN 38105 USAChildrens Hosp, Dept Med, Div Hematol Oncol, Boston, MA 02115 USA