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Component
Preparation & Therapy
Renee Wilkins, PhD, MLS(ASCP)cm
CLS 325/435
School of Health Related Professions
University of Mississippi Medical Center
Basic Blood Components
 Red Blood Cells
 Platelets
 Fresh Frozen Plasma (FFP)
 Cryoprecipitated Anti-hemophilic
Factor
 Granulocytes
Terms to know:
 Whole blood: blood collected before
separation into components
 Components: parts of whole blood
that are separated
 Closed system: a sterile system of
blood collection
 Open system: when the collection is
exposed to air, decreasing expiration
date
Collection basics
 Blood is collected in a primary bag
that contains anticoagulant-
preservatives
 Satellite bags may also be attached,
depending on what components are
needed
 Anticoagulant-preservatives minimize
biochemical changes and increase
shelf life
Plasma
hemoglobin
Plasma K+
Viable cells
pH
ATP
2,3-DPG
Plasma Na+
Helps release oxygen
from hemoglobin (once
transfused, ATP & 2,3-
DPG return to normal)
K+Na+
Blood Component
Preparation
 Components of whole blood are
centrifuged:
 “light spin” – short time, low RPM
 “heavy spin” – longer spin, high RPM
 Procedures are in the AABB Technical
Manual
Centrifuged blood
Buffy Coat
(WBCs & Platelets)
Red Blood Cells
Plasma/serum
Whole Blood
 Component Requirements
 Stored: 1-6° C
 Shipping: 1-10° C
 21 or 35 days depending on
preservative (CPD, CP2D, or CPDA-1)
Whole Blood
 Consists of RBCs, WBCs, platelets and
plasma (with anticoagulant)
 1 unit increases Hgb 1 g/dL and Hct 3%
 When is it used?
 Patients who are actively bleeding and
lost >25% of blood volume
 Exchange transfusion
Red Blood Cells
 RBCs
 1-6° C (stored); 1-10° C (shipped)
 21, 35, or 42 days depending on
preservative or additive
 Hematocrit should be ≤80%
 One unit increases hematocrit 3%
 Once the unit is “opened” it has a
24 hour expiration date!
24
hours
Red Blood Cells
 RBCs (frozen)
 ≤ -65°C for 10 years
 RBCs (deglycerolized or washed)
 Good at 1-6°C for 24 hours
 RBCs (irradiated)
 1-6°C for 28 days
Red Blood Cells
 RBCs are usually given because of
their hemoglobin content
 They increase the mass of circulating
red blood cells in situations where
blood loss occurs
RBCs
 Conditions include:
 Oncology patients (chemo/radiation)
 Trauma victims
 Cardiac, orthopedic, and other surgery
 End-stage renal disease
 Premature infants
 Sickle cell disease ( Hgb A)
RBC Types
 Leukocyte-Reduced RBCs are for:
 patients who receive a lot of
transfusions to prevent antibody
production toward WBC antigens
 Patients transfused outside of a
hospital
 Patients who have reacted to
leukocytes in the past
http://www.pall.com/39378_39479.asp
Leukocyte
Reduction Filters
(maintains closed system)
Final unit must have less
than 5 x 106 WBCs
RBC Types
 Frozen RBCs
 Glycerol is added to
cryoprotect the unit
 Glycerol prevents cell
lysis
 Why?
• Freezing RBCs
preserves rare units or
extends to life of
autologous units
RBC Types
 Deglycerolized RBCs
 RBCs that have had the
glycerin removed
 Thawed at 37°C
 A blood cell processor
washes the cells with varying
concentrations of saline
 Considered “open”, expires in
24 hrs.
RBC Types
 Washed RBCs
 Not effective in reducing WBCs
 For patients (with anti-IgA) that may
react with plasma proteins containing
IgA
 Reactions may be allergic, febrile, or
anaphylactic
RBC Types
 Irradiated RBCs
 Prevents T-cell proliferation that may cause
transfusion-associated graft versus host
disease (GVHD)
 GVHD is fatal in 90% of those affected
 Used for:
• Donor units from a blood relative
• HLA-matched donor unit
• Intrauterine transfusion
• Immunodeficiency
• Premature newborns
• Chemotherapy and irradiation
• Patients who received marrow or stem cells
Platelets
 Important in maintaining hemostasis
 Help stop bleeding and form a platelet
plug (primary hemostasis)
 People who need platelets:
 Cancer patients
 Bone marrow recipients
 Postoperative bleeding
How platelets are processed
 Requires 2 spins:
 Soft – separates RBCs and WBCs from
plasma and platelets
 Heavy
• platelets in platelet rich plasma (PRP) will
be forced to the bottom of a satellite bag
• 40-60 mL of plasma is expelled into
another satellite bag, while the remaining
bag contains platelet concentrate
Preparation of platelet
concentrate
RBCs PRP
Plasma
Platelet
concentrate
Platelets
 Storage Temperature
 20-24°C for 5 days (constant
agitation)
 Each unit should contain at least 5.5 x
1010 platelets (platelet concentrate)
 Each unit should elevate the platelet
count by 5-10,000 µL in a 165 lb
person
Types of platelets
 Pooled platelets
 Used to reach therapeutic dose
 An “open system” occurs when pooling
platelets, resulting in an expiration of 4 hours
 Platelet, pheresis – therapeutic dose (from
one donor) without having to pool platelets
 3x1011 minumum
 HLA matched – for those with HLA
antibodies
 Leukocyte reduced - used to prevent febrile
non-hemolytic reactions and HLA
alloimmunization
Fresh Frozen Plasma (FFP)
 Plasma that is frozen within 8 hours of
donation
 -18°C or colder for 1 year
 Provides coagulation factors for
 Bleeding
 Abnormal clotting due to massive transfusion
 Patients on warfarin who are bleeding
 Treatment of TTP and HUS
 Factor deficiencies
 ATIII deficiency
 DIC when fibrinogen is <100 mg/dL
Fresh Frozen Plasma
 FFP is thawed before transfusion
 30-37°C waterbath for 30-45 minutes
 Stored 1-6°C and transfused within 24
hours
 Needs to be ABO compatible
Cryoprecipitate
 Cryoprecipitated antihemophilic factor
(AHF) or “Cryo” is the precipitated protein
portion that results after thawing FFP
 Contains:
 von Willebrand’s factor (plt. adhesion)
 Fibrinogen
• 150 mg in each unit
 Factor VIII
• About 80 IU in each unit
 Fibrinonectin
Cryoprecipitate
 Same storage as FFP (cannot be re-frozen as FFP
once it is separated); -18 for 1 year
 If thawed, store at room temp 4 hrs
 The leftover plasma is called cryoprecipitate
reduced or plasma cryo
 Good for thrombocytopenic purpura (TTP)
 CRYO is used for
 2° treatment for Factor VIII deficiency (Hemophilia A)
 2 ° treatment for von Willebrand’s Disease
 Congenital or acquired fibrinogen deficiency
 FXIII deficiency
 “Fibrin Glue” applied to surgical sites
FFP
Frozen
within 8
hours
Thawed
FFP
Cryoprecipitate
(VIII, vW)
Plasma cryoprecipitate, reduced
(TTP, FII, V, Vii, IX, X, XI)
Thaw at 30-37°C
Store at RT 4 hrs
Refrozen with 24 hrs of
separation
Store at ≤18°C 1 yr
5 day expiration at 1-6°C
Granulocytes
Lymphocyte Monocyte
Neutrophils Eosinophils Basophils
Granulocytes
 Neutrophils are the most numerous,
involved in phagocytosis of
bacteria/fungi
 Although rare, it is useful for infants
with bacteremia
 Prepared by hemapheresis
 ≥ 1.0 x 1010
 Maintained at room temp for 24 hours
Labeling of components
 ISBT labeling
 International Society of Blood
Transfusion recommendations
regarding the uniform labeling of lood
products for international bar code
recognition by computers
References
 Rudmann, S. V. (2005). Textbook of Blood Banking and Transfusion
Medicine (2nd Ed.). Philadelphia, PA: Elsevier Saunders.
 Blaney, K. D. and Howard, P. R. (2000). Basic & Applied Concepts of
Immunohematology. St. Louis, MO: Mosby, Inc.
 Flynn, J. C. (1998). Essentials of Immunohematology.

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Component prep and therapy

  • 1. Component Preparation & Therapy Renee Wilkins, PhD, MLS(ASCP)cm CLS 325/435 School of Health Related Professions University of Mississippi Medical Center
  • 2. Basic Blood Components  Red Blood Cells  Platelets  Fresh Frozen Plasma (FFP)  Cryoprecipitated Anti-hemophilic Factor  Granulocytes
  • 3. Terms to know:  Whole blood: blood collected before separation into components  Components: parts of whole blood that are separated  Closed system: a sterile system of blood collection  Open system: when the collection is exposed to air, decreasing expiration date
  • 4. Collection basics  Blood is collected in a primary bag that contains anticoagulant- preservatives  Satellite bags may also be attached, depending on what components are needed  Anticoagulant-preservatives minimize biochemical changes and increase shelf life
  • 5. Plasma hemoglobin Plasma K+ Viable cells pH ATP 2,3-DPG Plasma Na+ Helps release oxygen from hemoglobin (once transfused, ATP & 2,3- DPG return to normal) K+Na+
  • 6. Blood Component Preparation  Components of whole blood are centrifuged:  “light spin” – short time, low RPM  “heavy spin” – longer spin, high RPM  Procedures are in the AABB Technical Manual
  • 7. Centrifuged blood Buffy Coat (WBCs & Platelets) Red Blood Cells Plasma/serum
  • 8.
  • 9. Whole Blood  Component Requirements  Stored: 1-6° C  Shipping: 1-10° C  21 or 35 days depending on preservative (CPD, CP2D, or CPDA-1)
  • 10. Whole Blood  Consists of RBCs, WBCs, platelets and plasma (with anticoagulant)  1 unit increases Hgb 1 g/dL and Hct 3%  When is it used?  Patients who are actively bleeding and lost >25% of blood volume  Exchange transfusion
  • 11. Red Blood Cells  RBCs  1-6° C (stored); 1-10° C (shipped)  21, 35, or 42 days depending on preservative or additive  Hematocrit should be ≤80%  One unit increases hematocrit 3%  Once the unit is “opened” it has a 24 hour expiration date! 24 hours
  • 12. Red Blood Cells  RBCs (frozen)  ≤ -65°C for 10 years  RBCs (deglycerolized or washed)  Good at 1-6°C for 24 hours  RBCs (irradiated)  1-6°C for 28 days
  • 13. Red Blood Cells  RBCs are usually given because of their hemoglobin content  They increase the mass of circulating red blood cells in situations where blood loss occurs
  • 14. RBCs  Conditions include:  Oncology patients (chemo/radiation)  Trauma victims  Cardiac, orthopedic, and other surgery  End-stage renal disease  Premature infants  Sickle cell disease ( Hgb A)
  • 15. RBC Types  Leukocyte-Reduced RBCs are for:  patients who receive a lot of transfusions to prevent antibody production toward WBC antigens  Patients transfused outside of a hospital  Patients who have reacted to leukocytes in the past
  • 16. http://www.pall.com/39378_39479.asp Leukocyte Reduction Filters (maintains closed system) Final unit must have less than 5 x 106 WBCs
  • 17. RBC Types  Frozen RBCs  Glycerol is added to cryoprotect the unit  Glycerol prevents cell lysis  Why? • Freezing RBCs preserves rare units or extends to life of autologous units
  • 18. RBC Types  Deglycerolized RBCs  RBCs that have had the glycerin removed  Thawed at 37°C  A blood cell processor washes the cells with varying concentrations of saline  Considered “open”, expires in 24 hrs.
  • 19. RBC Types  Washed RBCs  Not effective in reducing WBCs  For patients (with anti-IgA) that may react with plasma proteins containing IgA  Reactions may be allergic, febrile, or anaphylactic
  • 20. RBC Types  Irradiated RBCs  Prevents T-cell proliferation that may cause transfusion-associated graft versus host disease (GVHD)  GVHD is fatal in 90% of those affected  Used for: • Donor units from a blood relative • HLA-matched donor unit • Intrauterine transfusion • Immunodeficiency • Premature newborns • Chemotherapy and irradiation • Patients who received marrow or stem cells
  • 21. Platelets  Important in maintaining hemostasis  Help stop bleeding and form a platelet plug (primary hemostasis)  People who need platelets:  Cancer patients  Bone marrow recipients  Postoperative bleeding
  • 22. How platelets are processed  Requires 2 spins:  Soft – separates RBCs and WBCs from plasma and platelets  Heavy • platelets in platelet rich plasma (PRP) will be forced to the bottom of a satellite bag • 40-60 mL of plasma is expelled into another satellite bag, while the remaining bag contains platelet concentrate
  • 23. Preparation of platelet concentrate RBCs PRP Plasma Platelet concentrate
  • 24. Platelets  Storage Temperature  20-24°C for 5 days (constant agitation)  Each unit should contain at least 5.5 x 1010 platelets (platelet concentrate)  Each unit should elevate the platelet count by 5-10,000 µL in a 165 lb person
  • 25. Types of platelets  Pooled platelets  Used to reach therapeutic dose  An “open system” occurs when pooling platelets, resulting in an expiration of 4 hours  Platelet, pheresis – therapeutic dose (from one donor) without having to pool platelets  3x1011 minumum  HLA matched – for those with HLA antibodies  Leukocyte reduced - used to prevent febrile non-hemolytic reactions and HLA alloimmunization
  • 26. Fresh Frozen Plasma (FFP)  Plasma that is frozen within 8 hours of donation  -18°C or colder for 1 year  Provides coagulation factors for  Bleeding  Abnormal clotting due to massive transfusion  Patients on warfarin who are bleeding  Treatment of TTP and HUS  Factor deficiencies  ATIII deficiency  DIC when fibrinogen is <100 mg/dL
  • 27. Fresh Frozen Plasma  FFP is thawed before transfusion  30-37°C waterbath for 30-45 minutes  Stored 1-6°C and transfused within 24 hours  Needs to be ABO compatible
  • 28. Cryoprecipitate  Cryoprecipitated antihemophilic factor (AHF) or “Cryo” is the precipitated protein portion that results after thawing FFP  Contains:  von Willebrand’s factor (plt. adhesion)  Fibrinogen • 150 mg in each unit  Factor VIII • About 80 IU in each unit  Fibrinonectin
  • 29. Cryoprecipitate  Same storage as FFP (cannot be re-frozen as FFP once it is separated); -18 for 1 year  If thawed, store at room temp 4 hrs  The leftover plasma is called cryoprecipitate reduced or plasma cryo  Good for thrombocytopenic purpura (TTP)  CRYO is used for  2° treatment for Factor VIII deficiency (Hemophilia A)  2 ° treatment for von Willebrand’s Disease  Congenital or acquired fibrinogen deficiency  FXIII deficiency  “Fibrin Glue” applied to surgical sites
  • 30. FFP Frozen within 8 hours Thawed FFP Cryoprecipitate (VIII, vW) Plasma cryoprecipitate, reduced (TTP, FII, V, Vii, IX, X, XI) Thaw at 30-37°C Store at RT 4 hrs Refrozen with 24 hrs of separation Store at ≤18°C 1 yr 5 day expiration at 1-6°C
  • 32. Granulocytes  Neutrophils are the most numerous, involved in phagocytosis of bacteria/fungi  Although rare, it is useful for infants with bacteremia  Prepared by hemapheresis  ≥ 1.0 x 1010  Maintained at room temp for 24 hours
  • 33. Labeling of components  ISBT labeling  International Society of Blood Transfusion recommendations regarding the uniform labeling of lood products for international bar code recognition by computers
  • 34. References  Rudmann, S. V. (2005). Textbook of Blood Banking and Transfusion Medicine (2nd Ed.). Philadelphia, PA: Elsevier Saunders.  Blaney, K. D. and Howard, P. R. (2000). Basic & Applied Concepts of Immunohematology. St. Louis, MO: Mosby, Inc.  Flynn, J. C. (1998). Essentials of Immunohematology.