Blood Products

ByRavindra Sarode, MD, The University of Texas Southwestern Medical Center
Reviewed/Revised Mar 2024
View Patient Education

    Whole blood can provide improved oxygen-carrying capacity, volume expansion, and replacement of clotting factors and was previously recommended for rapid massive blood loss. However, because component therapy is equally effective in most circumstances and is a more efficient use of donated blood, whole blood transfusions were not available in the United States for several decades. The low titer (for anti-A) whole blood type O is now being increasingly used for trauma resuscitation as a universal blood type based on data suggesting improved survival when compared with component therapy (1).

    Red blood cells (RBCs)

    Packed RBCs are stored between 1 and 6° C temperature for up to 42 days. Packed RBCs are the component of choice to increase hemoglobin (Hb) in a patient with anemia. Indications depend on the patient. Oxygen-carrying capacity may be adequate with Hb levels as low as 7 g/dL (70 g/L) in healthy patients, but transfusion may be indicated with higher Hb levels in patients with decreased cardiopulmonary reserve or ongoing bleeding. One unit of RBCs increases an average adult’s Hb by approximately 1 g/dL (10 g/L), and the hematocrit (Hct) by approximately 3%, above the pretransfusion value. When only volume expansion is required, other fluids can be used concurrently or separately. In patients with multiple blood group antibodies or with antibodies to high-frequency RBC antigens, RBCs with rare phenotypes of antigens are used; these are usually frozen for storage.

    Washed RBCs are free of almost all traces of plasma, most white blood cells, and platelets. They are generally given to patients who have severe reactions to plasma (eg, severe allergies, paroxysmal nocturnal hemoglobinuria, IgA immunization). In IgA-immunized patients, blood collected from IgA-deficient donors may be preferable for transfusion.

    WBC-depleted RBCs (leukoreduced RBCs) are prepared with special filters that remove 99.99% of white blood cells. They are indicated for patients who have experienced nonhemolytic febrile transfusion reactions, for exchange transfusions, for patients who require cytomegalovirus-negative blood that is unavailable, and possibly for the prevention of human leukocyte antigen (HLA) alloimmunization to help prevent refractoriness to platelet transfusion (failure to achieve the target level of blood platelets after platelet transfusion).

    Fresh frozen plasma

    Fresh frozen plasma (FFP) is an unconcentrated source of all clotting factors without platelets. The FFP is stored at -18° C for up to 1 year. Indications include correction of coagulopathic bleeding secondary to clotting factor deficiencies for which specific factor replacements are unavailable or to multifactor deficiency states (eg, massive transfusion, disseminated intravascular coagulation [DIC], liver failure). FFP is used for urgent warfarinfactor Xa inhibitors or direct thrombin inhibitors. FFP can supplement RBCs when whole blood is unavailable for neonatal exchange transfusion. FFP should not be used simply for volume expansion or correction of mild to moderate coagulopathy before surgical procedures especially in patients with cirrhosis who are not bleeding, because the coagulation defects may not be corrected and there is a risk that the additional plasma given will increase portal pressure and promote bleeding.

    Pathogen-inactivated plasma obtained by treatment using the solvent detergent method is available to avoid transmission of almost all pathogens. Convalescent plasma has been used in the past during Ebola and influenza H1N1 epidemics.

    Cryoprecipitate

    Cryoprecipitate is a concentrate prepared from FFP and also stored at -18° C. Each concentrate usually contains approximately 80 units each of factor VIII and von Willebrand factor and approximately 250 mg of fibrinogen. It also contains ADAMTS13 (an enzyme that is deficient in congenital thrombotic thrombocytopenic purpura), and factor XIII. Although originally used for hemophilia and von Willebrand disease, cryoprecipitate is currently used as a source of fibrinogen in acute DIC with bleeding, treatment of uremic bleeding, cardiothoracic surgery (fibrin glue), obstetric emergencies such as placental abruption and HELLP syndrome (hemolysis, elevated liver enzymes, and low platelet count), and rare factor XIII deficiency when human coagulation factor XIII concentrate is unavailable. In general, it should not be used for other indications. A pathogen-inactivated pooled cryoprecipitate is available that can be used as a source of fibrinogen. It has the advantage that it can be thawed and stored at room temperature for up to 5 days unlike standard cryoprecipitate that needs to be thawed from -18° C and used within 4 hours.

    White blood cells (WBCs)

    Granulocytes may be transfused when sepsis occurs in a patient with profound persistent neutropenia (neutrophils < 500/mcL [0.5 × 109/L]) who is unresponsive to antibiotics. Granulocytes are stored at room temperature and must be given within 24 hours of harvest; however, testing for HIV, hepatitis, human T-cell lymphotropic virus, and syphilis may not be completed before infusion. Because of improved antibiotic therapy and medications that stimulate granulocyte production during chemotherapy, granulocytes are seldom used.

    Immune globulins

    Rh immune globulin (RhIg), given IM or IV, prevents development of maternal Rh antibodies that can result from fetomaternal hemorrhage. The standard dose of intramuscular RhIg (300 mcg) must be given to an Rh-negative mother immediately after abortion or delivery (live or stillborn) unless the infant is Rho(D) and Du negative or the mother’s serum already contains anti-Rho(D). If fetomaternal hemorrhage is > 30 mL, a larger dose is needed. If hemorrhage of this amount is suspected, testing of the volume of fetomaternal hemorrhage begins with the screening rosette test, which, if positive, is followed by a quantitative test (eg, Kleihauer-Betke test).

    RhIg is also used to treat immune thrombocytopenia (ITP), in which case it is given IV.

    Other immune globulins are available for postexposure prophylaxis for patients exposed to a number of infectious diseases, including cytomegalovirus, hepatitis A, hepatitis B, measles, rabies, respiratory syncytial virus, rubella, tetanus, smallpox, and chickenpox (for usage, see under specific disease).

    Platelets

    Platelet concentrates are used

    • To prevent bleeding in asymptomatic severe thrombocytopenia (platelet count < 5,000 to 10,000/mcL [<5 × 109/L to 10 × 109/L])

    • For bleeding patients with less severe thrombocytopenia (platelet count < 50,000/mcL [< 50 × 109/L])

    • For bleeding patients with platelet dysfunction due to antiplatelet medications (other than aspirin) but with a normal platelet count

    • For patients receiving massive transfusion that causes dilutional thrombocytopenia

    Platelet concentrates are also sometimes used before invasive surgery, particularly with extracorporeal circulation for > 2 hours (which often makes platelets dysfunctional). One platelet concentrate unit increases the platelet count by approximately 10,000/mcL (10 × 109/L), and adequate hemostasis is achieved with a platelet count of approximately 10,000/mcL (10 × 109/L) in a patient without complicating conditions, and approximately 50,000/mcL (50 × 109/L) for those undergoing surgery. Therefore, platelet concentrates derived from a pool of 4 to 5 units of whole blood are commonly used in adults.

    Platelet concentrates are usually prepared by automated devices that harvest the platelets and return unneeded components (eg, RBCs, plasma) to the donor. This procedure, called plateletpheresis, provides enough platelets from a single donation (equivalent to 4 to 5 whole blood platelet units) for transfusion to an adult, which, because it minimizes infectious and immunogenic risks, is preferred to multiple donor transfusions in certain conditions.

    Certain patients may not respond to platelet transfusions (called refractoriness), possibly because of splenic sequestration, platelet consumption due to disseminated intravascular coagulation, or destruction due to HLA or platelet-specific antigen alloimmunization (and immune-mediated destruction). If patients are refractory to transfusion, they are tested for alloimmunization if possible. Patients with immune-mediated destruction may respond to pooled whole blood platelets (because of greater likelihood that some units are HLA compatible), platelets from family members, or ABO- or HLA-matched platelets. HLA alloimmunization may be mitigated by transfusing WBC-depleted RBCs and WBC-depleted platelet concentrates.

    Pathogen-inactivated platelets, inactivated by using a chemical (amotosalen), are also available for clinical use. Most platelets are stored at 20 to 22° C for up to 5 to 7 days. Platelets can also be stored at 1 to 6° C for up to 14 days. During cold storage, platelets are partially activated and thus, hemostatically more functional than room temperature storage platelets; therefore, cold storage platelets are used during surgery or in a patient who is bleeding.

    Other products

    Irradiated blood products are used to prevent graft-versus-host disease in patients who are at risk.

    Many attempts have been made to develop blood substitutes using inert chemicals (eg, perfluorocarbons) or hemoglobin solutions to carry and deliver oxygen to tissues. Although these hemoglobin substitutes had promising ability to deliver oxygen to tissues during an emergency, several clinical trials have failed due to increased mortality and severe adverse cardiovascular toxicities (eg, hypotension). Attempts to regenerate platelets and RBCs from various stem cell sources are underway.

    Hematopoietic stem cells from autologous or allogenic donors can be transfused as a way of reconstituting hematopoietic function (particularly immune function) in patients undergoing myeloablative or myelotoxic therapy.

    Reference

    1. 1. McCoy CC, Brenner M, Duchesne J, et al. Back to the Future: Whole Blood Resuscitation of the Severely Injured Trauma Patient. Shock 2021;56(1S):9-15. doi:10.1097/SHK.0000000000001685

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