This will serve as a guide for the specific indications, storage requirements and stability of the different blood components.
Whole Blood, Packed Red Blood Cells: 1-6 degrees Celsius.
Plasma, Cyroprecipitated AHF: -18 degrees Celsius.
Platelets: 20-24 degrees Celsius with continuous gentle agitation.
Granulocytes: 20-24 degrees Celsius without agitation.
Whole Blood: When refrigerated a unit of whole blood has a shelf life between 21-35 days depending on the additive that is used. Must be transfused within 4 hours when at room temperature.
Packed Red Cells: Packed red cells are stable for up to 42 days refrigerated, but they can also be frozen with glycerol as a cyroprotectant for up to 10 years. They must be deglycerolized by washing and thawed prior to transfusion and must be transfused within 24 hours once thawed.
Platelets: Platelets have a shelf live of only 5 days. Some hospitals and clinics are extending the shelf life out to 7 days with continuous bacterial testing to ensure there is no contamination.
Plasma: Plasma products must be processed and frozen within 8 hours of collection and are stable for 12 months. Once thawed they must be transfused within 24 hours.
Thawed Plasma: Has an expiration of 5 days.
Cryo: Cyro AHF once pooled and frozen has a stability of up to 12 months.
Granulocytes: Granulocytes must be transfused within 24 hours after donation.
Whole Blood: Used to replace the loss of both RBC mass and plasma volume. The product is 550-600 mL of whole blood, with a hematocrit of about 40%.
Packed Red cells: Usually the red cell product of choice. 330 mL of red cells, hematocrit of about 55-65% with an additive solution.
Platelets: Platelets derived from whole blood must contain at least 5.5×10^10 platelets in 40-70 mL of plasma in at least 90% of the units tested. Platelets donated through apheresis must contain at least 3×10^11/L platelets in 100-500 mL of plasma. One apheresis platelet collection is equivalent to six pooled random donor platelet concentrates.
Plasma: Can be derived from whole blood or apheresis collection. Plasma contains albumin, coagulation factors, fibrinolytic proteins, and immunoglobulins. Fresh frozen plasma (FFP) derived from whole blood is usually 220-300 mL and units derived from apheresis usually contain 400-600 mL. The plasma must be frozen within 8 hours of collection.
Cryoprecipitated Antihemophilic Factor (AHF): AHF is prepared from FFP. It is slowly thawed, then refrozen within one hour of thawing. AHF typically contains 5-20 mL of plasma with 80-120 U/concentrate of Factor VIII, 150-250 mg/concentrate of fibrinogen, 40-70% of vWF, and 20-30% of Factor XIII that would normally be present in FFP. Making it the treatment of choice for Von Willebrands Disease and Hemophiliacs.
Red cell transfusions are used to treat hemorrhage and to improve oxygen delivery to tissues. The decision to transfuse red cells should be based on the patients clinical condition. Indications for red cell transfusion include acute sickle cell crisis, acute blood loss of greater than 30% of blood volume, or patients with symptomatic anemia that can’t function without red cell repleting. The threshold for transfusion of red cells should be a hemoglobin of 7 g/dL in adults and children. Maintenance can be at a level of >7-9 g/dL. One unit of red cells should increase the hemoglobin by 1 g/dL and hematocrit by 3%.
Washed Red Cells
Washed red cells are washed with saline to remove any residual plasma proteins. These are used for patients with a history of allergic transfusion reactions. These patients have an IgA deficiency and have developed anti-IgA.
Leukocyte reduced red cells decrease the incidence of febrile transfusion reactions. They are indicated for those at high risk of transfusion-associated GVHD or transfusion-related immune suppression. For a unit to be considered leukocyte reduced, there must be less than 5×10^6 leukocytes.
Irradiated Red Cells
Used for patients with a history of febrile transfusion reactions or patients that are immunocompromised immediately after an allogeneic bone marrow or stem cell transplant. Patients at risk for HLA-GVHD will receive irradiated red cells.
Plasma transfusion are recommended for patients with active bleeding and an international normalized ratio (INR) greater than 1.6. Its indicated for patients on anticoagulant therapy that are undergoing an invasive procedure. Plasma should not be administered for a high INR without active bleeding. Plasma is indicated for patients with inherited clotting factor deficiencies for which there is no safe recombinant factor available. Those factors are II, V, X, and XI. Plasma is used as an emergent reversal of warfarin (coumadin) toxicity to prevent intracranial hemorrhage. It is also used in acute disseminated intravascular coagulation (DIC) or other thrombotic microangiopathies such as thrombotic thrombocytopenic purpura (TTP) or hemolytic uremic syndrome (HUS). Plasma is often times transfused with red cells during massive transfusions; with the definition of massive transfusion being greater than 5,000 mL in an adult of average weight (70 kg).
Platelet transfusions are indicated to prevent hemorrhage in patients with thrombocytopenia or those with functional platelet defects. Contradictions for platelet therapy are patients with TTP and heparin-induced thrombocytopenia (HIT) as transfusion in these clinical situations can result in exacerbation of thrombosis. Platelet transfusions can be used prophylactically in invasive surgeries with no active bleeding and commonly used in active bleeding situations along with transfusion of FFP and red cells. One unit of apheresis platelets should increase the platelet count in adults by 30-60×10^9/L.
Transfusion of neonates is complicated and should be based on upon clinical reasons with consideration to the platelet count. If the count is <20×10^3/mL, you should always transfuse if possible. When you reach 20-30×10^3/mL you should consider transfusion, but weigh all possibilities. In a case of active bleeding, transfusion is absolutely appropriate, but all factors should be considered. Transfusion is also indicated in there is signs of a coagulation disorder, intraventricular or intraparenchymal cerebral hemorrhage, an invasive procedure, or if there is alloimmune neonatal thrombocytopenia.
Cryo contains high concentrations of factor VIII and fibrinogen and is used especially in cases of hypofibrinogenemia. Hypofibrinogenemia is typically seen in the setting of massive hemorrhage or in a consumptive coagulopathy such as DIC. Indications for cyroprecipitate AHF are factor VIII and factor XIII deficiency, congenital fibrinogen deficiency, and von Willebrand disease.
Indicated for patients with fever, neutropenia, septicemia or an antibiotic resistant bacterial infection.