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Therapeutic phlebotomy is safe in children with sickle cell anaemia and can be effective treatment for transfusional iron overload
Authors:Banu Aygun  Nicole A. Mortier  Karen Kesler  Alexandre Lockhart  William H. Schultz  Alan R. Cohen  Ofelia Alvarez  Zora R. Rogers  Janet L. Kwiatkowski  Scott T. Miller  Pamela Sylvestre  Rathi Iyer  Peter A. Lane  Russell E. Ware  the Stroke With Transfusions Changing to Hydroxyurea Trial Investigators
Affiliation:1. Steven and Alexandra Cohen Children's Medical Center, New Hyde Park, NY, USA;2. Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA;3. Rho Inc., Chapel Hill, NC, USA;4. Children's Hospital of Philadelphia and the Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA, USA;5. University of Miami, Miami, FL, USA;6. University of Texas Southwestern Medical Center at Dallas, Dallas, TX, USA;7. SUNY Downstate, Brooklyn, NY, USA;8. Duckworth Pathology Group, Memphis, TN, USA;9. University of Mississippi Medical Center, Jackson, MS, USA;10. Emory University/Children's Healthcare of Atlanta, Atlanta, GA, USA
Abstract:Serial phlebotomy was performed on sixty children with sickle cell anaemia, stroke and transfusional iron overload randomized to hydroxycarbamide in the Stroke With Transfusions Changing to Hydroxyurea trial. There were 927 phlebotomy procedures with only 33 adverse events, all of which were grade 2. Among 23 children completing 30 months of study treatment, the net iron balance was favourable (?8·7 mg Fe/kg) with significant decrease in ferritin, although liver iron concentration remained unchanged. Therapeutic phlebotomy was safe and well‐tolerated, with net iron removal in most children who completed 30 months of protocol‐directed treatment.
Keywords:sickle cell  iron overload  phlebotomy  liver iron
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