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Updated: May 6, 2026

A Precision Medicine Tool for Measurement and Monitoring of Hemoglobin S in Sickle Cell Disease Patients Receiving Transfusion Therapy
Optimizing adolescent transition to adult care for sickle cell disease
Stephenie Cerns1, Colleen McCracken, Claire Rich
1Inpatient Medicine/Hematology-Oncology/Palliative Care Unit, Froedtert Hospital, Milwaukee, WI, USA.
Abstract:
Transitioning health care from a pediatric to an adult environment in a patient with sickle cell disease presents challenges. A program developed to assist with transition is described.
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