role of blood components in clinical practice
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Dr. Sanjay Upreti
Assistant Professor
Department of Pathology
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What is Blood component
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Whole Blood vs ComponentsWhole blood- red cells suspended in a proteinsolution
Wastage More side effects
Not available in western countries
Components
Specific Therapy
More patients can be benefitted
Increased shelf life
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Whole blood
Red cells Plasma Platelets
(Fresh frozenplasma (FFP)
Cryoprecipitate Cryosupernatant
plasma (CSP)F lX*
ImmuneGlobulin
Albumin
Fractionatedproducts
F Vlla*
F Vlll*
Granulocytes
* Now available as recombinant products
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BloodProducts
Whole blood
Red cellcomponent
Plateletcomponent
Plasma products
Component derivatives
Red blood cell
conc./suspension
(PRBC)
Single donation
unit (PC)
Fresh frozen
plasma (FFP)
Albumin
Washed Red
Cells Conc.
Pooled unit Liquid plasma Coagulation
factors
Leucocyte
depleted red cells
Single donor
apheresisplatelets (SDAP)
Cryoprecipitate immunoglobulins
Frozen red cells - irradiated PC Cryo poor
plasma
- irradiatedPRBC
Viral inactivatedlasma
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Composition Whole blood Red cell concentrate
(PRBC)
Red cell suspension
Preparation Separate plasma at 2-
60C under
gravity/centrifugation
Separate plasma and
add additive soln. e.g.
ADSOL
1 unit increase Hb by 1gm% 1-1.5gm% 1-1.5%
Volume (ml) 350-450 150-200 150-200
Maximum storage
time at 2-60C
35 days : CPDA 35 days: CPDA 42 days-ADSOL
Advantages Easier to prepare Low viscosity, more
shelf life
Disadvantages Higher viscosity Expensive
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PRBC Indications-
Component of choice for virtually all patients with a
deficit of oxygen carrying capacity, e.g., blood loss oranemia.
Transfusion Trigger-
>10 gm/dl- Probably no transfusion required
7-10 gm/dl- Transfusion may be requierd
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Storage lesions Viability
2-3 DPG Levels
Potassium plasma Hb
REVERSIBLE No or very little clinical significance
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Washed RBCWashed with NS
Removes 99% of plasma proteins, electrolytes and
antibodies No significant leukoreduction.
20% cells lost
Use within 24 hours.
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Washed RBCsIndications-
IgA Deficient individuals
Repeated allergic reactions Intrauterine transfusion
Pts with T activated cells
Very occassionaly- severe autoimmune hemolytic
anaemia
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Leukodepleted RBC < 5 x 10 6Leukocyte/unit
Reduce the risk of
1. Febrile non hemolytic reactions2. CMV Transmission
3. HLA Allo-immunization leading to plateletrefractoriness.
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Leukodepleted RBC1. Filteration
Prestorage leukodepletion
Leukodepletion at time of issue Bedside leukodepletion
2. Buffy Coat Removal
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Irradiated Blood Components
Indication- To prevent TA- GVHD
Usually due to use of fresh whole bloodfrom related donors/ immuno-compromised pts
Pathophysiology- escape of donor Tlymphocytes present in cellular blood
components in the recipient & subsequentclonal expansion of these cells with immunedestruction of host tissues.
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s/s- fever,dermatitis, erythroderma, hepatitis,enterocolitis, pancytopenia, hypocellular marrow,
Instrument- Blood irradiator
Dose- 25Gy Irradiation indicated for-
1. all relative donors
2. immunocompromised patients
3. neonates undergoing exchange transfusion
4. Pts with Hodgkins disease
5. Pt of CLL receiving fludarbine phosphate
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Platelets TransfusionIndications
Bleeding d/t thrombocytopenia/abnormal platelet
functions Prophylactically- 10,000/cumm instable pts.
Platelet transfusion trigger -50,000/cumm for mostsurgeries.
Neurosurgery/ophthalmic surgery- 100,000/cumm
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Effectiveness of platelet
transfusion 1 unit of platelet concentrate will increase the platelet
count by 5-10K in the average adult;
Dose:1 unit platelet concentrate per 10 kg body weight
or 1 unit apheresis platelets Patients repeatedly transfused - alloimmunized and
refractory to platelet transfusion-HLA matched orcross-matched platelets may be required
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Platelets TransfusionContraindications
ITP
Platelet refractoriness TTP
Heparin induced thrombocytopenia