2. Whole
Blood
Red Blood Plasma
Cells
Platelets Fresh Frozen Cryoprecipitate
Leuko-reduced Plasma
RBC
Washed RBC
Derivatives
Irradiated RBC
Albumin
Immunoglobulin
Factors VIII & IX
3. Compose of RBC, plasma, WBC, platelets
Restores blood volume and oxygen carrying capacity
Maximise use of WB: Preparation of specific blood
components and plasma derivatives
Platelets not functional and clotting Factors V and VIII are
greatly reduced
Indication
Extensive bleeding to replace the loss of both red cell mass
and plasma volume
Massive transfusion: such as major trauma case, certain
surgical procedures
4. Cellular Components – Red Blood Cell Products
Platelets
Plasma Components – Fresh Frozen Plasma
Cryoprecipitate
Plasma Derivatives – Albumin
Immunoglobulin
Factors VIII, IX
5. Cellular Components – Red Blood Cell Products
Platelets
Plasma Components – Fresh Frozen Plasma
Cryoprecipitate
Plasma Derivatives – Albumin
Immunoglobulin
Factors VIII, IX
6. Most plasma removed from whole blood
Provide oxygen-carrying capacity without unnecessary volume
Platelets removed
Lack of clotting factors in RBC: 1 FFP given every 4 units
transfused. High volume transfusions result in decreased clotting
factors
Indication
Anaemia
Blood loss during surgery
Thalassaemia
7. Washed with sterile normal saline to remove most of the
plasma proteins, antibodies and platelets
Not leukoreduced –some leukocytes removed but not enough
to prevent alloimmunization
Shelf-life of 24hrs – preparation in an open system and most
of the anticoagulant-preservative solution removed.
Indication
Patients with recurrent febrile reactions
Urticarial reactions
Anaphylactic reactions
8. Prepared by filtration method: Reduce
leukocyte count to less than 5 x 106
Indication
Prevent febrile nonhaemolytic transfusion
reactions due to donor leukocytes
Decrease post-transfusion reactions due to HLA
alloimmunization
Reduce transmission of CMV infections, since
CMV lives in WBCs
9. Gamma irradiation inactivates donor lymphocytes
Graft vs host disease (GVHD) is reduced in
immunocompromised or immunodeficient patients
Indications
Prevention of post-transfusion GVHD eg bone
marrow transplant recipients
11. Anticoagulants - Prevent blood clotting
Preservatives - Provide cells with nutrients during
storage; maintain red cell viability and function
12. CPDA-1
Citrate – Anticoagulant (binds to calcium)
- Calcium essential component of clotting cascade
- Binding to calcium decreases clotting ability
Phosphate – Maintain 2,3-diphosphoglycerate (2,3-DPG)
levels in red cell
- 2,3-DPG essential for movement of oxygen from
RBCs to body tissues
Dextrose – Sugar substrate needed to generate ATP
Adenine – Synthesis of ATP allowing longer shelf life of 35
days
13. SAGM – Sodium chloride, Adenine, Glucose and Mannitol
Nutrition source for red cells
Supports integrity of red cell membrane to reduce haemolysis
Maintain high ATP levels in RBCs
Extending shelf life from 35 to 42 days
Lowers viscosity = faster transfusion
14. Compose of platelets, WBC and plasma
Aid in clotting
Viable for 5 days
Maintained at 20-24°C with constant agitation
Cold temperatures and lack of agitation decrease the viability of
the platelets
Indications
Massive bleeding or undergoing invasive
surgery
Platelet dysfunction
Thrombocytopenia - ↓ platelet count
15. Cellular Components – Red Blood Cell Products
Platelets
Plasma Components – Fresh Frozen Plasma
Cryoprecipitate
Plasma Derivatives – Albumin
Immunoglobulin
Factors VIII, IX
16. Plasma
Contains all coagulation factors including
labile Factors V and VIII
No platelets and RBCs
Stored at -30°C for up to 12 months
Indications
Treat bleeding due to coagulation factor
deficiencies eg. massive transfusion
Plasma exchange – Treatment of TTP
(Thrombotic thrombocytopenic purpura )
patient’s plasma is replaced by donor plasma
17. Fibrinogen
Factors VIII and XIII
von Willebrand’s factor
Prepared by freezing plasma at -70°C followed by thawing at
4°C. Once thawed, the precipitate that forms is centrifuged to
sediment the cryoprecipitate
Indications
Fibrinogen deficiency
Treatment of hemophilia A (Factor VIII deficiency)
von Willebrand’s disease
Massive haemorrhage
18. Cellular Components – Red Blood Cell Products
Platelets
Plasma Components – Fresh Frozen Plasma
Cryoprecipitate
Plasma Derivatives – Albumin
Immunoglobulin
Factors VIII, IX
19. Prepared by fractionation of plasma
No coagulation factors or blood group antibodies
5% and 20% albumin solutions
Indications
Hypovolaemia – decrease in blood plasma due to burns, bleeding.
Eg. Severe burns, act as volume expansion by replacing protein
loss from burn site
Hypoalbuminaemia - Liver failure
20. Compose of IgG antibodies – used in
replacement IgG therapy
Maintain adequate antibody levels to
prevent infections and confers passive
immunity
Indications
Treatment of hypoglobulinaemia (reduced
gamma globulins) or agammaglobulinaemia
(absent)
Autoimune diseases such as immune
thrombocytopenia
21. Prepared from fractionation of plasma that contains Factor
VIII
Product treated to reduce risk of viral transmission
Indication
Control bleeding in haemophilia A patients with:
congenital Factor VIII deficiency
acquired Factor VIII deficiency
Factor VIII inhibitors
22. Compose of: Factors II, VII, IX and X.
Factor IX makes up 5% of this product
Indication
Hemophilia B( Factor IX deficiency)
Congenital Factor VII or X deficiency
Factor IX inhibitors
23. Granulocyte concentrate
Composed of: granulocytes, RBCs,
WBCs, plasma, platelets
Shelf-life 24hrs at 20-24°C
Indication
Severe neutropenia with severe bacterial
or fungal infections
Fever unresponsive to antibiotic therapy
24. Rh Immune Globulin (RhIg)
Protect Rh-negative mother who is
pregnant with Rh-positive infant
Usually given in pregnancy and
immediately after birth
Indication
Prevention of Rh(D) HDN
25. AND MORE!!!
Antithrombin III
Alpha-1-proteinase inhibitor
Fibrinogen
Thrombin
Protein C
(Too many to list)
26. Types of blood donation:
Whole blood donation
Apheresis donation: Plasma or platelet donation
Advantage of apheresis donation
Donations can be made every month (whole blood
donations - 3mths)
Allows larger amount of platelets to be collected from a
single donor compared to whole blood donations
Minimise patient’s exposure from multiple donors’ blood