Challenges in the treatment and prevention of delayed hemolytic transfusion reactions with hyperhemolysis in sickle cell disease patients-Reference-Cited by-同舟云学术

Challenges in the treatment and prevention of delayed hemolytic transfusion reactions with hyperhemolysis in sickle cell disease patients

Published:2019-03-08 Issue:5 Volume:59 Page:1698-1705
ISSN:0041-1132
Container-title:Transfusion
language:en
Short-container-title:Transfusion

Author:

Dean Christina L.¹^ORCID,Maier Cheryl L.¹,Chonat Satheesh²³,Chang Andres⁴,Carden Marcus A.⁵,El Rassi Fuad⁴,McLemore Morgan L.⁴,Stowell Sean R.¹,Fasano Ross M.¹⁴

Affiliation:

1. Center for Transfusion and Cellular Therapy, Department of Pathology and Laboratory MedicineEmory University School of Medicine Atlanta Georgia

2. Department of PediatricsEmory University School of Medicine Atlanta Georgia

3. Aflac Cancer and Blood Disorders CenterChildren's Healthcare of Atlanta Atlanta Georgia

4. Department of Hematology and Medical OncologyWinship Cancer Institute of Emory University Atlanta Georgia

5. Department of Pediatrics and MedicineUniversity of North Carolina School of Medicine Chapel Hill North Carolina

Publisher

Wiley

Subject

Hematology,Immunology,Immunology and Allergy

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/trf.15227

Reference47 articles.

1. High prevalence of red blood cell alloimmunization in sickle cell disease despite transfusion from Rh-matched minority donors

2. Hemoglobin A clearance in children with sickle cell anemia on chronic transfusion therapy

3. Impact of red blood cell alloimmunization on sickle cell disease mortality: a case series

4. Delayed haemolytic transfusion reaction in adults with sickle cell disease: a 5-year experience

5. Alloimmunization in Sickle Cell Anemia and Transfusion of Racially Unmatched Blood

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