· Introduction
· Storage lesion
· Overload
· Dilution
· Metabolic
· Immune
· Infective
Red cell unit contents |
· Red cells · Small volume plasma · Preservative: sodium, adenine, glucose, mannitol |
Massive transfusion |
· 50% blood volume in 4 hours, or 100% of BV in 24 hours · 10 units = 2.5L = 50% blood volume |
Ideal ratio of RBC:FFP:plt |
· 1:1:1 units = 4:2*:1 bags · May be situation-dependent (*4 in Victoria) |
Lethal triad |
· Acidosis · Hypothermia · Coagulopathy |
Cells |
· Red cells: spheroidal, rigid, fragile; 25% loss at 4/52 · White cells: inactivate but still antigenic · Platelets: inactivated at 48 hours? |
Coag factors |
· Minimal since plasma removed · FV 50% at 3/52 · FVIII 30% at 3/52 |
Metabolic |
· Temp 4°C · pH 7.4->6.7 (due to additives) · K+ 4->30mM · Ca2+ 2mmol/L -> ? (due to 3mg citrate) · ATP 75% · [2,3-DPG]: 50% at 2/52, 5% at 4/52 (due to low temp) · ↑Free haemoglobin |
Fluid |
· ↑Blood volume -> ↑preload · May cause heart failure · High risk if LV impairment |
Iron |
· Haemolysis -> Hb breakdown -> ↑free haemoglobin · Risk of haemochromatosis -> damage to liver, pancreas, heart, pituitary |
Microaggregates |
· Microvascular occlusion -> multi-organ dysfunction (especially lung) |
Coag factors |
· Dilutional coagulopathy o Coag factors esp fibrinogen o Platelets |
Plasma |
· Hyperviscosity o ↑risk thromboembolism o ↑resistance to flow, ↑myocardial work |
↓Temperature |
· Arrest if rapid via CVC · Coagulopathy |
↓pH |
· Arrest if rapid via CVC · Negative inotropy · Generalized metabolic dysfunction |
↑K+ |
· Arrhythmia, arrest if rapid via CVC · Most K+ taken up by RBC upon transfusion |
↓Ca2+ |
· Arrhythmia, muscle weakness · (Note hypocalcaemia severe enough to cause coagulopathy would already have caused cardiac arrest) |
↓2,3-DPG |
· Left shift oxyhaemoglobin dissociation curve -> ↓tissue oxygenation |
Acute |
· Febrile non-haemolytic (cytokines) · Febrile haemolytic (incompatibility) o ABO: intravascular (DIC, renal failure, death) o RhD: extravascular (haemolysis) · Anaphylaxis (Type 1 hypersensitivity against plasma protein) · TRALI (? donor antibody ? host priming by illness) |
Delayed |
· Alloimmunisation o Delayed haemolysis (anamnestic response to Kell, Kidd, Duffy) o Haemolytic disease of the newborn (anti-RhD IgG crosses placenta) o Post-transfusion purpura (anti-platelet antibody -> consumption) · Cancer recurrence (immune suppression) · Graft vs host (donor WBC multiplies in immunocompromised host) |
Bacteria |
· Platelets (room temp) > RBC · Certain bacteria can multiply in the cold |
Viruses |
· HBV, HCV, HIV; CMV |
Other |
· Parasites (e.g. P.falciparum malaria) · Prion |
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