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Updated: Nov 20, 2025

A Precision Medicine Tool for Measurement and Monitoring of Hemoglobin S in Sickle Cell Disease Patients Receiving Transfusion Therapy
Delayed Hemolytic Transfusion Reaction in a Sickle Cell Disease Patient: A Case Report.
Mohammed Saleh1,2, Vishnu Priya Mallipeddi2, Ahmed Ali3
1Internal Medicine, University of Missouri, Columbia, USA.
Delayed hemolytic transfusion reactions (DHTR) complicate sickle cell disease (SCD) management. Misinterpreting DHTR symptoms as vaso-occlusive crisis can worsen anemia and lead to hyper-hemolytic crisis in SCD patients.
Area of Science:
- Hematology
- Transfusion Medicine
- Sickle Cell Disease Research
Background:
- Alloimmunization is a known complication in patients with sickle cell disease (SCD).
- Delayed hemolytic transfusion reactions (DHTR) are a significant consequence of alloimmunization in SCD.
- DHTR presents diagnostic and management challenges for healthcare providers treating SCD patients.
Observation:
- A case report details a 33-year-old African female with hemoglobin SS (Hb SS) SCD and a history of transfusions.
- The patient presented with vaso-occlusive crisis (VOC) symptoms triggered by sepsis from E. coli pyelonephritis.
- She received packed red blood cells (PRBC) for worsening anemia and VOC, subsequently developing a DHTR.
Findings:
- The patient experienced a delayed hemolytic transfusion reaction (DHTR) following PRBC transfusion.
- DHTR exacerbated her anemia and vaso-occlusive crisis (VOC).
- Symptoms of DHTR were initially mistaken for a worsening pain crisis.
Implications:
- DHTR requires careful consideration in SCD patients presenting with worsening anemia or VOC symptoms.
- Early recognition and management of DHTR are crucial to prevent severe complications like hyper-hemolytic crisis.
- This case highlights the importance of vigilance for transfusion reactions in transfused SCD populations.
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