Hyperhaemolysis in sickle cell disease — an unusual and potentially life‐threatening complication
Author:
Affiliation:
1. Royal Children's Hospital, Melbourne, VIC.
2. Australian Red Cross Blood Service, Melbourne, VIC.
3. Thalassaemia Service, Monash Medical Centre, Melbourne, VIC.
Publisher
AMPCo
Subject
General Medicine
Link
https://onlinelibrary.wiley.com/doi/pdf/10.5694/j.1326-5377.2010.tb03509.x
Reference11 articles.
1. The sickle cell hemolytic transfusion reaction syndrome
2. Delayed Hemolytic Transfusion Reaction/Hyperhemolysis Syndrome in Children With Sickle Cell Disease
3. Hyperhemolysis during the evolution of uncomplicated acute painful episodes in patients with sickle cell anemia
4. Clinical significance of RBC alloantibodies and autoantibodies in sickle cell patients who received transfusions
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3. American Society of Hematology 2020 guidelines for sickle cell disease: transfusion support;Blood Advances;2020-01-27
4. Successful management of the potentially fatal hyperhaemolysis syndrome of sickle cell anaemia with a regimen including bortezomib and Hemopure;Journal of Clinical Pharmacy and Therapeutics;2019-06-25
5. Hyperhemolysis in Patients With Hemoglobinopathies: A Single-Center Experience and Review of the Literature;Transfusion Medicine Reviews;2015-10
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