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It’s important to recognise, respond to and report suspected adverse events.
Once you suspect an adverse reaction, follow the steps for managing suspected transfusion reactions.
Classification of transfusion-related adverse reactions and estimated incidence
- Immunological acute (<24 hours)
-
Adverse event Incidence* Acute haemolytic transfusion reaction (AHTR) 1:76,000 Fatal acute haemolytic reaction 1:1.8 million Febrile non-haemolytic transfusion reaction (FNHTR) 0.1%–1%
(with universal leucocyte depletion)
Mild allergic reactions (urticarial) 1%–3% Severe allergic reactions (anaphylaxis) 1:20,000–1:50,000 Transfusion-related acute lung injury (TRALI) 1:1,200–1:190,000 - Non-immunological acute (<24 hours)
-
Adverse event Incidence* Complications of massive transfusion Variable Non-immune mediated haemolysis (physical or chemical destruction of blood) Rare Transfusion transmitted bacterial infection (for clinically apparent reactions) due to platelets Approximately 1:250,000
(in Australia)
Transfusion transmitted bacterial infection (for clinically apparent reactions) due to red cells Approximately 1:2.5 million
(in Australia)
Transfusion-associated circulatory overload (TACO) 1% - Immunological delayed (>24hours)
-
Adverse event Incidence* Delayed haemolytic transfusion reaction (DHTR) 1:2,500–1:11,000 Post-transfusion purpura (PTP) Rare Transfusion-associated graft versus host disease (TA-GVHD) Rare Alloimmunisation - RBC antigens 1% Alloimmunisation - HLA antigens 10% Transfusion-related immune modulation (TRIM) Not known - Non-immunological delayed (>24hours)
-
Adverse event Incidence* Iron overload requiring chelation therapy May occur after >20 RBC units Iron overload with organ dysfunction May occur after 50-100 RBC units Transfusion-transmissible infections For incidence rates refer to risk estimates for transfusion-transmissible infections
* May be based on overseas data.
Further information
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