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Continuous Manual Exchange Transfusion for Patients with Sickle Cell Disease: An Efficient Method to Avoid Iron Overload
Published on: March 14, 2017
Delayed hemolytic transfusion reaction in sickle cell disease
Leslie P Scheunemann1, Kenneth I Ataga
1Department of Medicine, University of North Carolina, Chapel Hill, North Carolina 27599-7305, USA.
Delayed hemolytic transfusion reactions are serious complications in sickle cell disease patients. Prompt diagnosis and management are crucial for acute pain episodes after red blood cell transfusions.
Area of Science:
- Hematology
- Transfusion Medicine
Background:
- Delayed hemolytic transfusion reactions (DHTRs) are a significant risk for patients with sickle cell disease (SCD).
- These reactions can be life-threatening and complicate SCD management.
Purpose of the Study:
- To review the clinical features, pathophysiology, laboratory evaluation, and management of DHTRs in SCD patients.
- To emphasize the importance of considering DHTRs in the differential diagnosis of acute pain.
Main Methods:
- Literature review of clinical features, pathophysiology, laboratory evaluation, and management strategies for DHTRs in SCD.
- Analysis of diagnostic criteria and treatment protocols.
Main Results:
- DHTRs present with diverse clinical manifestations and complex pathophysiology.
- Early laboratory identification and appropriate management are key to patient outcomes.
Conclusions:
- DHTRs require inclusion in the differential diagnosis for acute pain episodes post-transfusion in SCD.
- Awareness and timely intervention can mitigate the severity of these reactions.
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