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Updated: Jun 4, 2025

A Precision Medicine Tool for Measurement and Monitoring of Hemoglobin S in Sickle Cell Disease Patients Receiving Transfusion Therapy
Initial outcomes in a sickle cell disease transition clinic
Katheryne Madrazo-Aguirre1, Jean-Antoine Ribeil1,2, Amy E Sobota1,3
1Boston University Chobanian & Avedisian School of Medicine, Boston, MA.
A multidisciplinary transition clinic effectively prepares young adults with sickle cell disease (SCD) for adult care. Meeting adult providers eased patient concerns about managing SCD and transitioning care.
Area of Science:
- Hematology
- Pediatrics
- Adult Medicine
Background:
- Transitioning from pediatric to adult care for sickle cell disease (SCD) patients presents challenges, including increased healthcare utilization, costs, and mortality risk.
- Effective preparation is vital to mitigate these risks and ensure continuity of care.
- A multidisciplinary transition clinic was established to facilitate this process.
Purpose of the Study:
- To evaluate the effectiveness of a multidisciplinary transition clinic in preparing young adults with SCD for adult care.
- To assess patient engagement and identify key concerns during the transition period.
Main Methods:
- Chart review of patients (aged 20-27) attending the transition clinic between September 2021 and May 2023.
- Data collection included visit frequency, topics discussed, and patient attitudes towards transition.
- Analysis of patient concerns and feelings regarding the transition process.
Main Results:
- Eighty-two percent of patients (22 total) utilized the transition clinic.
- Most patients attended their first adult care visit within 2.4 months of their last transition visit.
- Key patient concerns included medication adherence (hydroxyurea), reproductive health, and educational support; discussions alleviated anxiety.
Conclusions:
- A collaborative transition clinic model successfully prepares young adults with SCD for adult care.
- Early introduction to adult SCD providers significantly alleviates patient concerns.
- Future research will focus on long-term patient integration into adult care settings.
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08:23Characterization of Sickling During Controlled Automated Deoxygenation with Oxygen Gradient Ektacytometry
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05:23Continuous Manual Exchange Transfusion for Patients with Sickle Cell Disease: An Efficient Method to Avoid Iron Overload
Published on: March 14, 2017
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