Transfusion medicine Flashcards
Blood donations tested for?
- ABO group and RhD type
Infection
Which infections are blood donations tested for?
- HIV 1+2 abs
- Hepatitis BsAg
- Hepatitis C ab
- Syphilis ab
- HTLV ab
Processing of blood donations?
- Leucocyte depletion
- centrifuged:
- red cells
- platelets
- Plasma - Platelets sampled for
bacterial testing - Special processes (eg irradiation, washing, hyperconcentration)
Plasma centrifuged to which components?
Fresh frozen plasma
Cryoprecipitate
Red cells in blood donations
- shelf life?
- storage temp?
- how much time once out of fridge
- 35 day shelf life
- at 4 degrees
- transfuse < 4 h after removing from fridge
2 methods of getting them platelet concentrates in blood donations?
I. Pool 4-6 donors blood
II. Apheresis
- single donor
Platelet concentrates in blood donations
- shelf time?
- storage temp
- max for 7 days
2. Storage: 22oC
Fresh frozen component in blood donations
- storage
- shelf-time
- special processing
- Plasma frozen to -30oC
- 2 yr storage
- I.Viral inactivation
-Methylene Blue
II. Solvent detergent
treatment (Octaplas)
Fresh frozen component in blood donations use?
For clotting factor replacement if bleeding
Cryoprecipitate
- how is it formed?
- use
- Precipitate that forms
when thawing FFP - Fibrinogen
When to give blood transfusion in anaemia?
If below Hb < 7g/dL
acute haemolytic transfusion reaction timing?
are defined as fever and other symptoms/ signs of haemolysis within 24 hours of transfusion
acute haemolytic transfusion reaction types?
I. transfusion-related acute lung injury (TRALI),
II. transfusion-associated circulatory overload (TACO),
III. transfusion-associated dyspnoea (TAD)
acute haemolytic transfusion reaction sx?
Fever, renal failure
Donor PLASMA compatibility: (also same with Platelets, FFP, cryoprecipitate)
Different from RBC compatibility A receives from A or AB B receives from B or AB O receives from any AB receives from AB
Blood clotting pathway (haemostasis)
- Collagen and tissue factor exposed
- Von Willebrand Factor binds collagen
- Platelets adhere to vWF-collagen
- Platelets activate and aggregate
- Tissue factor initiates rapid thrombin generation on activated platelets
- Thrombin converts fibrinogen to fibrin and
completes platelet activation - Stable fibrin-platelet clot is formed
How TF (tissue factor) initiates rapid thrombin generation on activated platelets
by causing release of Proteases FVII, FX, FIX, FXI and Co-factors FVIII and FV
3 regulations of haemostasis
- vWF activity is regulated by ADAMTS 13
- Thrombin is regulated by Antithrombin and Activated protein C
- Fibrin cleaved by Plasmin into fibrin degradation products (D-dimer)
2 types of clinical disorders of haemostasis?
- Primary haemostasis disorders
- Coagulation pathway disorders
Primary haemostasis disorders cause?
- defects in
Platelets,
VWF,
vessel wall
Primary haemostasis disorders sx?
- mucocutaneous bleeding eg epistaxis, purpura
- immediate bleeding
Coagulation pathway disorders causes?
- defects in:
- Coagulation factors
- fibrinogen
Coagulation pathway disorders presentation
- deep tissue bleeding (joints)
- delayed bleeding (weak clot forms and breaks, followed by secondary bleeding)
Both can cause GI/CNS bleeds
Laboratory investigations of bleeding?
1. Platelet count + blood film Indicates platelet number (not function) 2. Coagulation screen I. PT time II. aPTT time