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Transfusion

Leukocyte Reduced Red Cells and Platelets

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Units of whole blood, red blood cells, and platelets contain significant numbers of leukocytes while fresh frozen plasma and cryoprecipitate do not. Transfusion of leukocytes has been associated with several adverse sequelae, including:
  • Febrile transfusion reactions
  • Transfusion related acute lung injury (TRALI)
  • HLA alloimmunization of chronically transfused patients
  • Refractoriness to platelet transfusions
  • Leukotropic (CMV and HTLV) virus transmission
  • Immune suppression
  • Graft vs. Host Disease


Leukocytes can be removed immediately after collection or at the bedside using third generation adsorption filters that remove 99.9% of leukocytes. Pre-storage leukoreduction has the additional advantages of preventing cytokine release from white blood cells during storage and elimination of the need for bedside filters that have slower flow rates than standard blood filters. Prestorage leukocyte reduction has also been proven to more consistently remove enough white blood cells to meet the definition of a leukocyte reduced unit. If bedside leukoreduction is necessary, one unit of red blood cells can be transfused through a single filter. A pool of 8-10 random donor platelet concentrates can be transfused through a single platelet filter.

On September 18, 1998, the Blood Products Advisory Committee of the FDA recommended universal leukoreduction of all cellular blood components, except granulocytes. Many other countries already required universal leukoreduction of blood components. On September 28, 1998, the Transfusion Committee at Saint Luke's Hospital in Kansas City decided that all patients at Saint Luke's Hospital should receive leukoreduced red blood cells and platelets. The hospital transfusion service implemented the new policy on November 1. Leukocyte reduced components are more expensive. However, the Biological Practices Committee stated that the clinical benefits far exceed the increase in blood component cost. The advantages of leukocyte removal include decreased risk of:
  • Febrile reactions
  • HLA alloimmunization & platelet refractoriness
  • Viral transmission
  • Graft vs. Host Disease
  • Postoperative infection
  • Immune suppression
  • Post transfusion purpura
If a hospital has not implemented universal leukoreduction, leukocyte reduced blood components should be used in the following situations:

Established Indications:
Prevention of febrile reactions following two documented febrile reactions
Febrile reaction and demonstrable WBC antibodies
Prevention of transfusion related acute lung injury
Prevention of HLA alloimmunization in multi-transfused patients including:
  • Chronic hemolytic anemia
  • Aplastic anemia
  • Myelodysplastic syndromes
  • Myeloproliferative syndromes
Bone marrow transplant candidates
Heart transplant recipients
Substitute for CMV negative components, when none are available
HIV infected patients
Antepartum transfusions for CMV negative women

The most common indication for using leukocyte reduced blood components is the prevention of febrile transfusion reactions.

TRALI is most often caused by the passive transfusion of a blood component containing high-titer anti-HLA antibodies, which react with the recipient's leukocytes (80-90%). However, it may also be caused by anti-HLA antibodies in the recipient's plasma reacting with leukocytes in transfused units of whole blood, red blood cells, or platelets (10-20%). Transfusing leukocyte reduced blood components to such recipients requiring subsequent transfusions can prevent TRALI caused by this second mechanism. Leukocyte reduction will not prevent acute lung injury resulting from high titers of HLA antibodies in the donor unit.

Leukocyte reduced components may also delay or prevent alloimmunization to HLA and leukocyte-specific antigens in chronically transfused patients and, thereby, delay the onset of refractoriness to random donor platelet transfusions. Patients expected to receive only a few blood components, such as during elective surgery, do not derive much benefit from the additional expense.

Some viruses such as CMV reside in granulocytes. Pre-storage leukocyte reduction eliminates the risk of CMV transmission. Leukocyte reduction has convincingly been shown to reduce the incidence of CMV seroconversion in CMV negative leukemia patients treated with chemotherapy and bone marrow transplantation. Leukocyte removal filtration can be used in the following clinical situations when CMV negative components are not available:

Indications for Substituting Leukocyte Reduced for CMV Negative Blood
  • Seronegative pregnant women requiring transfusions.
  • Intravascular fetal transfusions if the mother is seronegative.
  • Premature neonates 1200 g or less born of CMV seronegative mothers.
  • Seronegative organ, bone marrow, or stem cell transplant recipients who receive seronegative tissue.
  • Seronegative patients who are candidates for autologous bone marrow or stem cell transplant.
  • As a substitute for CMV negative units when CMV negative are not available.
  • Immunodeficient patients; either acquired or hereditary.
  • Seronegative patients with lymphoma.
  • HIV infected patients.
Leukocyte reduced units will not prevent graft versus host disease. Plasma components such as FFP and cryoprecipitate do not need to be leukoreduced because they contain so few leukocytes.

Administration of pre-storage leukoreduced RBCs and platelets is the same as regular units. The use of bedside leukoreduction filters may significantly slow flow rates, which precludes their use in emergent situations where multiple rapid transfusions are required. External pressure devices should not be used, because they reduce the efficiency of leukocyte removal.