2. • Blood product: Therapeutic substance prepared from
human blood.
• Whole blood :One unit of non-separated donor blood.
• Blood component: constituent separated from whole blood
by differential centrifugation or that is obtained directly from
donor by apheresis
3.
4. WHY ??
• To avoid wastage of collected whole blood.
• Administration of specific replacement therapy.
• To avoids transfusion of unnecessary blood elements that are not
required by the patient.
5.
6. Blood : Anticoagulant Ratio
• 14 ml of CPD/CPDA is used in preserving 100 ml blood
• 63 ml for a 450 ml collection
• 49 ml for 350 ml collection
• At the end of the collection , venous blood (pH 7.35) mixed
with anticoagulant-preservative solution (pH 5.0 to 5.6) with
resulting pH of 7.05 in the mixture.
7.
8.
9. Methods of blood components separation
• Differential centrifugation of whole blood
• Apheresis
10.
11.
12.
13.
14.
15. • Whole blood is stored in a refrigerator at 4°-6°C.
• Shelf life (If CPDA is anticoagulant) - 35 days.
• Must be ABO identical.
• Transfusion:
-should commence within 30 minutes.
- should complete within 4 hours of starting.
• Transfusion of one unit raises hemoglobin by 1 gm/dl or
hematocrit by 3%.
16. Indications:
• Acute blood loss with hypovolemia
• Exchange transfusion in neonates
• Non-availability of red cell concentrate.
Contraindications:
• Chronic anemia with compromised cardiovascular functions
17. Blood components
• Cellular components:
Red cells:
Packed red cells
Red cells in additive solution,
Leukocyte-poor red cells,
Washed red cells,
Frozen red cells,
Irradiated red cells
Platelets:
Platelet concentrate,
Apheresis platelets
19. • Packed red cells:
-Prepared by removing most of the plasma from one unit of
whole blood.
1. By allowing to sediment overnight in a refrigerator at 2-
6°C
2. Spun in a refrigerated centrifuge.
Red cells(65-80%)+ small amount of plasma(20-35%)
- Hematocrit 70-75%
It has high viscosity and therefore the rate of infusion should
be slow
20. • Transfusion of one unit increases hemoglobin by 1 gm%.
• Indications:
• Chronic severe anemia
• Severe anemia to reduce chance of circulatory overload.
• Anemia in elderly
• Acute blood loss (transfused along with a crystalloid or a
colloid solution)
21. • Red cells in additive solution (Red cell suspension):
• Red cells + minimal residual plasma + additive solution.
(SAGM-- saline, adenine, glucose, and mannitol).
-shelf life - 42 days.
22.
23. • Leukocyte-poor red cells:
Red cells contain < 5 × 106 white cells per bag.
Methods for leukocyte depletion:
1.Leukocyte-reduction filters.
2.Removal of buffy coat.
It should contain at least 85% of original red cells.
24. Indications for leucocyte-poor red cells are:
1.Prevention of HLA immunization in patients who are
likely to receive allogeneic bone marrow
transplantation.
2. Prevention of febrile nonhemolytic transfusion
reactions.
3. Prevention of transmission of cytomegalovirus.
25.
26. • Washed red cells:
washed with normal saline to remove plasma proteins, Ab’s,
white cells, and platelets.
Used for IgA-deficient individuals (has they developed anti-
IgA antibodies, as exposure will lead to anaphylaxis)
Shelf life- 24hrs( if stored at 4-6degrees)
Around 20% red cells are lost
27. • Frozen red cells:
Red cells + glycerol = freeze at -65degrees
Shelf life =10 years.
After glycerolization (washing with saline)-used with in 24hrs(4-
6degrees)
Uses:
Storage for donor red cells with rare blood groups.
For future autologous transfusion.
28. • Irradiated red cells:
-Gamma-irradiation of red cells inactivates lymphocytes and
prevents graft vs. host disease.
Storage: 4-6degrees for 28 days
Indications:
Intrauterine or premature neonate transfusions.
Individuals with immunodeficiency.
33. • Suitable if HLA-matched platelets are required
• If patient has developed refractoriness to platelet transfusion due to
the formation of alloantibodies against HLA antigens.
Platelet refractoriness means poor increment following platelet
transfusion.
35. • Indications
• Bleeding due to decreased platelet production.
• Bleeding in hereditary disorders of platelet function.
• Massive blood transfusion.
• Viral diseases associated with thrombocytopenia.
• Contraindications
• Thrombotic thrombocytopenic purpura.
• Hemolytic uremic syndrome
36. Guidelines for platelet transfusion
Non bleeding patients with failure of platelet production:
Pt count<10,000/ul
Invasive procedure with platelet count<50,000/ul.
Bleeding patients
DIC with<50,000/ul
Active bleeding & Pt count<50,000/ul
39. • Solvent/detergent plasma:
-It is increasingly used in clinical practice.
-It lowers the risk of viral transmission –HBV,HCV & HIV.
-Treating the plasma with TNPB and detergent triton X-100, which
inactivates the viruses.
Single donor plasma or AHG poor plasma:
It is the plasma separated from outdated blood or plasma from which
anti haemophilic factors has been separated.
-It contains all stable factors.
40. Indications for fresh frozen plasma:
• Multiple coagulation factor deficiencies
• Disseminated intravascular coagulation.
• Inherited deficiency of a coagulation factor for which
no specific replacement therapy is available.
• Thrombotic thrombocytopenic purpura
41. • Cryoprecipitate contains volume-10-15ml .
- F VIII 80-100units/concentrate
- Von Willebrand factor 40-70% of FFP
- Fibrinogen 150-250mg/concentrate
- F XIII 20-30% of FFP
- Fibronectin 55mg.
42. - Indications for cryoprecipitate :
- Deficiency of fibrinogen
- Deficiency of F XIII
- F VIII deficiency (if F VIII concentrate is not available)
- Von Willebrand disease.
43. PLASMA DERIVATIVES
• Manufactured by fractionation of large volumes of pooled human
plasma.
• Plasma derivatives are:
1. Human albumin solutions.
2. F VIII concentrate.
3.Prothrombin complex concentrate.
4. Immunoglobulins
44. • Human albumin solutions:
• uses are:
1. Replacement fluid in therapeutic plasma exchange.
2. For treatment of diuretic-resistant edema of hypoproteinemia.
F VIII concentrate:
1.It is the treatment of choice for treatment of hemophilia A .
2.Severe von Willebrand disease.
45. • Prothrombin complex concentrate (PCC):
Contains factors II, VII, IX, and X, and also protein C and S.
Uses of PCC are:
1. Deficiency of F IX
2. Inherited deficiency of factors II, VII, and X.
A serious risk of PCC is thrombotic complications due to the presence
of small amounts of activated coagulation factors.
46. • Immunoglobulins:
• They are of two types: specific and nonspecific.
• Specific immunoglobulins:
• They are obtained from donors who have specific high titer IgG
antibodies.
• Anti-RhD immunoglobulin is prepared so it is used for prevention of
sensitization to RhD antigen in Rh negative women giving birth to a
Rh-positive baby.
• Hepatitis B immune globulin
• Varicella-zoster immune globulin.
• Tetanus immune globulin.
47. • Non-specific immunoglobulins:
• These are derived from the pooled plasma of non-selected donors.
Indications:
1. Passive prophylaxis of viral infections like hepatitis, rubella, and
measles.
2.Treatment of hypogammaglobulinaemia.
3.Autoimmune thrombocytopaenic purpura to induce a rise in platelet
count.
4. Neonatal sepsis.
To Inactivate T-lymphocytes, sometimes these t-cells go and attack the host causing graft vs host reaction
From day of irrradiatin.or expiery date which ever is earlier.
Whose immune system is not developed.
Buffy coat removal method
First- hard spin,for 3 layers speration in single step
Second-light spin, in which platelet concentrate are sperated.
Tell random donor platelet
Immune causes
Non immune causes—splenomegaly,infections,drugs
Buffy coat removal method (if top and bottom blood bags are used &automated blood component sperator used)
First- hard spin,for 3 layers speration in single step
Second-light spin, in which platelet concentrate are sperated
One unit platelet concentrate- from single buffy coat.
Pooled platelet concentrate-from pooling of 4-5 buffy coats.—it aguments the quality of platelets.
Advantage:1-high yield of plasma(if we use PAS)
2.Lower leukocyte contamination
Amegakaryocytic thrombocytopenia-leukemia,hypoplastic anaemia,chemotherapy,bone marrow transplantation.,marrow infiltration by carcinoma or leukemia
FFP-usually measures 175-250ml, containing 70-80units/dl of F-8,F-9,Vwf and cfs.
CP- contains avg volume of 15ml,with 80-120 units of F-8,250MG OF FIBRINOGEN. Appox 40-70% of vWF
TNPB- tri n-butyl phosphate detergent-triton X100
AHG poor plasma-advantages- used for replacement of prothrombin factors and for volume replacement.
AGH-anti hemophilic globulin
: liver disease, warfarin overdose, massive blood transfusion.
FFP for infusion is 12-15ml/kg
ABO compatible FFP should be used.
CP- contains avg volume of 15ml,with 80-120 units of F-8,250MG OF FIBRINOGEN. Appox 40-70% of vWF
Heat and chemical inactivation.
1.Albumin is prepared by cold ethanol fractionation of pooled plasma and is sterilized during manufacture to destroy viruses and bacteria.
2. Freeze-dried F VIII concentrate is prepared by fractionation from large pools of fresh frozen plasma. To reduce the risk of transmission of viral infections, it is treated with heat or chemicals during manufacturing process
-Immunoglobulins are obtained by cold ethanol fractionation of large pools of human plasma
-Anti-RhD immunoglobulin is prepared from plasma of Rh-negative donors who have produced anti-D following immunization; it is used for prevention of sensitization to RhD antigen in Rhnegative women giving birth to a Rh-positive baby.
-Tetanus immune globulin that are used for passive prophylaxis of infections
RABIES