The same principle as centrifuged anticoagulated blood, wherein distinct layers develop
Citrate
The primary anticoagulant in apheresis procedures (ACD)
Additional donor guidelines
At least 48 hours elapsed time after apheresis donation
A donor must not exceed more than 2x a week or 24x in a year unless otherwise allowed by the blood bank physician
A donor must be tested to detect cytopenia
If a donor donates whole blood, at least 3 months/ 2 months/ 56 days/ 8 weeks must be elapsed before he can donate for pheresis
Extracorporeal blood must not exceed 15% of the donor's total blood volume
If plateletpheresis is to be performed, a donor must have above 150 x 10^9 L
Possible adverse reactions to plasma expanders must be determined
Intermittent flow centrifugation (IFC)
Blood is processed in batches or cycles, hence the term intermittent
Continuous flow centrifugation (CFC)
The processes of blood withdrawal, processing, and reinfusion are performed simultaneously in an ongoing manner
Plateletpheresis
Equivalent to 6–10 random platelet concentrates, containing 3 x 10^11 platelets
Plateletpheresis
Used to treat patients who have abnormally elevated platelet counts (>1,000,000 uL), e.g. Polycythemia Vera
Leukapheresis
Removal of WBCs
HES (HydroxyethylStarch)
Sedimenting agent used for granulocyte collection which causes rouleaux formation of RBCs, allowing WBCs to be harvested more efficiently
Corticosteroids
Administered to donors 12–24 hours before pheresis to increase the number of circulating granulocytes by pulling them from the marginal pool to the circulating pool
Leukapheresis
Used to treat patients with leukemia (> 100,000/uL WBC), Hairy Cell Leukemia, AML (Acute Myeloid Leukemia), Cutaneous T Cell Lymphoma
Lymphocytapheresis
Removal of lymphocytes, involves immunosuppression
Lymphocytapheresis
Used to treat Rheumatoid Arthritis, SLE, Kidney Transplant Rejection, Autoimmune Disease, Alloimmune Disease
Neocytapheresis
Transfusion of young RBCs called "neocytes"
Neocytapheresis
Used for pediatric patients with Thalassemia Syndrome
Erythrocytapheresis
Considered an exchange procedure, where a predetermined quantity of red cells is removed from the patient and replaced with homologous blood
Erythrocytapheresis
Used for Sickle Disease (Priapism), Impending stroke, Malaria, Babesia, patients with abnormal RBC appearance
Therapeutic plasmapheresis (plasma exchange)
Replacement fluids used: NSS, NSA, PPF, FFP
Therapeutic plasmapheresis
Used for patients with TTP and HUS, to remove the offending agent in the plasma causing clinical symptoms in cases of Paraproteinemia (Multiple Myeloma, Waldenstrom Macroglobulinemia), Familial Hypercholesterolemia, to collect rare RBC and WBC antibodies, and beneficial in diseases that involve malfunction of the immune system (e.g. SLE, RA)
Many of the adverse events seen with transfusion are related to the fact that transfusion is the introduction of foreign cells into the recipient, and non-cellular plasma and plasma-derived products involve the introduction of foreign proteins into the recipient that may cause a transfusion reaction
AABB requirements for laboratory investigation of a transfusion reaction
Clerical check of the component bag, label, paperwork, and pre-transfusion patient specimen
Repeat ABO testing on the post-transfusion sample
Visual check of the pre- and post-transfusion specimens for hemolysis
Direct antiglobulin test (DAT) on the post-transfusion specimen
Quarantine additional components prepared from the same donor selection
Report findings to the transfusion service supervisor or medical doctor
Pre-transfusion blood
Used for crossmatching, kept for up to 3 weeks, signs and symptoms may manifest during transfusion or within 21–28 days
Post-transfusion blood
Collected during the onset of the transfusion reaction, used to double-check with the unit, test for DAT
Classification of a transfusion reaction
Immediate or delayed type
Hemolytic or non-hemolytic
Immune or non-immune
Acute/immediate type transfusion reaction
Onset of signs and symptoms is within 24 hours, during or after transfusion
Delayed type transfusion reaction
Onset of signs and symptoms will occur after 14–21 days or 28 days
Hemolytic transfusion reaction
Positive DAT, there's an excessive lysis of RBC
Non-hemolytic transfusion reaction
Negative DAT
Laboratory tests confirming hemolysis
Decreased fibrinogen
Decreased or absent haptoglobin
Increased unconjugated bilirubin
Increased LDH
Hemoglobinuria and hemoglobinemia
Decreased Hgb/Hct
Serologic evidence of immune-mediated hemolytic transfusion reaction
Positive DAT
Positive elution with identification of 1 or more alloantibodies
Most severe type of transfusion reaction, associated with intravascular hemolysis, triggered by IgM antibodies against ABO
Acute/immediate hemolytic transfusion reaction
Manifested within 24 hours with signs and symptoms like fevers, chills, dyspnea, hypotension, bleeding, and can lead to severe complications like DIC and renal failure
Most common type of transfusion reaction, characterized by an increase in temperature of greater than 1°C after transfusion, caused by the interaction of the recipient's antibodies against the donor's HLA in WBCs or platelets