What to Transfuse: Specifications for Red Cell Products

What to know

This thalassemia resource for healthcare providers contains information about transfusion management of beta (β) thalassemia. It covers information about β thalassemia and describes key considerations for selecting red blood cell products for people with β thalassemia who receive regular blood transfusions.

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Key facts about β thalassemia

  • β thalassemia is caused by β-globin gene variants that reduce the production of adult hemoglobin (HbA), which may cause anemia.
  • Chronic anemia can have serious consequences for people with β thalassemia. Children may experience: reduced activity, growth problems and delayed puberty, hepatosplenomegaly, osteopenia, and cognitive impairment. Adults may experience: fatigue, decline in capacity to work or perform usual activities, cognitive impairment, osteopenia, fractures, hypersplenism, and reduced quality of life.
  • The primary management of severe anemia in β thalassemia is regular red blood cell (RBC) transfusions.

Healthcare providers can work with their blood bank partners to develop thalassemia-specific red blood cell transfusion protocols. In selecting RBC products for patients receiving regular transfusions, it's important for the clinical team to carefully consider which products emphasize efficacy (hemoglobin response) while also minimizing risk of hemolytic and non-hemolytic transfusion complications.

What type of RBC product is needed by people with β thalassemia?

The optimization of RBC products is vital when transfusing people with β thalassemia. The Thalassemia Western Consortium recommends

  • Leukoreduction of RBC units via filtration during the pre-storage period to prevent febrile non-hemolytic transfusion reactions
  • Storage of RBC units in additive solutions (lower hematocrit and higher volume) or citrate phosphate dextrose-adenine (higher hematocrit and lower volume)
  • Using non-apheresis-derived RBC units for transfusions in adults due to smaller hemoglobin increments with apheresis-derived units
  • Washed RBC units for individuals who experience severe, recurrent allergic reactions
  • RBC units that are less than 2 weeks old, when possible, to reduce the impact of the storage lesion on red cell survival
  • Using non-irradiated RBC units, as routine use of irradiated RBC units may be detrimental

What type of RBC antigen matching is needed by people with β thalassemia?

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Doctor going over medical chart with patient

Prevention of red cell alloimmunization is an important goal of transfusion management in thalassemia. Ideally, an individual's RBC genotyping is performed once the decision to initiate regular transfusions is made. The results of this typing determine their risk for developing alloantibodies and/or autoantibodies and determine the extent to which antigen-matched blood is needed. The Thalassemia Western Consortium recommends:

  • Individuals without a history of alloimmunization are given RBC units matched to Cc, Ee, and K blood group antigens
  • Individuals with one or more alloantibodies are given RBC units matched to Cc, Ee, K, Jka/b, Fya/b, and Ss blood group antigens

It is important for providers to maintain an accurate antibody history, as an antibody screen can become negative over time, and individuals with a history of developing antibodies need antigen-negative blood to prevent hemolytic transfusion reactions.


Lal A, Wong T, Keel S, Pagano M, Chung J, Kamdar A, et al. The transfusion management of beta thalassemia in the United States. Transfusion. 2021;1-13.


The Thalassemia Transfusion Resources were supported by cooperative agreement number CDC-RFA-DD19-1903, funded by the Centers for Disease Control and Prevention (CDC). They were developed by Georgia State University Research Foundation, Inc., Joan & Sanford I. Weill Medical College of Cornell University, and The Regents of the University of California San Francisco in collaboration with CDC. The materials have been developed as a supplemental (user-friendly) resource for healthcare providers, blood banks, and persons with thalassemia and their families to provide key information from a recent evidence-based report that details recommendations for the transfusion management of beta thalassemia in the United States.

These materials are not part of the CDC guidelines and recommendations. The original evidence-based report and recommendations were developed in 2021 by a multi-disciplinary committee, the Thalassemia Western Consortium, consisting of members from 10 hematology centers that was partially funded under a prior cooperative agreement CDC-RFA-DD14-1406. While the Consortium was supported with federal funding, their work on clinical recommendations for transfusion practices was independent of CDC, and the contents of the resulting published report are solely the responsibility of the authors and do not necessarily represent the official views of, nor an endorsement by, CDC or the Department of Health and Human Services.

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