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A Precision Medicine Tool for Measurement and Monitoring of Hemoglobin S in Sickle Cell Disease Patients Receiving Transfusion Therapy
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A Precision Medicine Tool for Measurement and Monitoring of Hemoglobin S in Sickle Cell Disease Patients Receiving Transfusion Therapy

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Shared decision making for hydroxyurea treatment initiation in children with sickle cell anemia

Lori E Crosby1,2, Lisa M Shook2,3, Russell E Ware2,3,4

  • 1Division of Behavioral Medicine and Clinical Psychology, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio.

Pediatric Blood & Cancer
|October 14, 2014
PubMed

Keywords:
decision‐makingguidelinespediatricssickle cell anemiatherapeutics

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