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10 Component Preparation

The document outlines the goals and processes involved in blood component preparation, emphasizing the importance of providing optimal therapy through safer blood components compared to whole blood. It details the procedures for collection, testing, separation, labeling, storage, and distribution of various blood components, including packed red blood cells, platelets, and plasma. Additionally, it discusses the significance of anticoagulants, storage conditions, and specific indications for different blood products.

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0% found this document useful (0 votes)
27 views3 pages

10 Component Preparation

The document outlines the goals and processes involved in blood component preparation, emphasizing the importance of providing optimal therapy through safer blood components compared to whole blood. It details the procedures for collection, testing, separation, labeling, storage, and distribution of various blood components, including packed red blood cells, platelets, and plasma. Additionally, it discusses the significance of anticoagulants, storage conditions, and specific indications for different blood products.

Uploaded by

michellouise17
Copyright
© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
Available Formats
Download as PDF, TXT or read online on Scribd

Enclonar, Kimberly / MLS 3A

Component Preparation
April 28, 2021
Meshane Bato-on, RMT

Goals of Blood Component Preparation


• To provide the optimal therapy to patients needing
blood transfusion
• Blood components are a lot safer than whole blood
• Blood component therapy = optimal therapy
• FDA Storage Lesion
o Collection • Biochemical changes that affect RBC viability and
o Testing survival
o Separation • At least 75% of original red cells in the recipients
o Labeling circulation within 24 hours and <1% hemolysis
o Storage • Neonates require "fresh" RBC products
o Distribution
• ↑ plasma Hgb, K+
• ↓ Viable cells, plasma pH and Na+, RBC ATP & 2,3-
Collection DPG
• Blood is collected in a primary bag which contains the
anticoagulant-preservative mixture Materials Needed
• Satellite bag = closed system • Swing Bucket centrifuge
• "Red Blood Cells Low Volume" • Refrigerator
o When the whole blood collection does not meet • Expressor
the volume requirements of the collection bag • Electric sealer
and anticoagulant has not been adjusted • Type of blood bag:
o 450mL = 63mL (300-404mL) o Single, double, triple, quadruple bags
o 500mL = 70mL (330-419mL)
o Can't make Blood Components
▪ Platelets • Packed RBC
▪ FFP o Leukoreduced RBC
▪ CRYO 1317 o Frozen RBC
o Washed RBC
Anticoagulant/Preservative Storage o Irradiated RBC
Limit • Plasma (light spin)
o Platelet Rich Plasma (heavy spin)
CPD/citrate-phosphate-dextrose 21
▪ Plt concentrate (pH 6.2)
CP2D/Citrate-phosphate-2-dextrose 21 □ Irradiated plt concentrate
CPDA-1/citrate-phosphate-dextrose-adenine 35 □ Leukoreduced plt concentrate
o Plt poor plasma
AS-1 (Adsol); AS-5 (Nutricel)/dextrose, 42
▪ Fresh Frozen Plasma/PF24
adenine, mannitol, saline
□ Cryoprecipitate
AS-3 (Optisol)/dextrose, adenine, saline, 42
citrate Blood Component Preparation
• Red cells move to the bottom because they are the
Dextrose Supports ATP generation by glycolytic heaviest component, whereas the platelets and
pathway plasma components remain on top.
o Light spin = short time, low RPM
Adenine Acts as a substrate for red cell ATP ▪ Platelet concentration
synthesis o Heavy spin = longer spin, high RPM
Citrate Prevents coagulation by chelating • Refrigerator = 1-6C
calcium, also protects RBC membrane • Plts = room temp with agitation or 20-24C
Sodium Prevents excessive decrease pH Heavy Spin Light Spin
biphosphate 5000g for 5min 2000g for 3min
Mannitol Osmotic diuretic acts as a membrane (PRBC, plt. Conc)
stabilizer 5000g for 7 min 3200rpm for 2-3min
(cryo, cell free plasma)
Anticoagulant adjustment in underweight donors 3200 rpm for 5min
• Allowable amount of blood to drawn in mL
Platelets: 20-25C Others: 1-6C
o
Checklist for Receiving Blood
• Amount of anticoagulant needed: • Transport temp: 1-10C
o • Temperature acceptable for component
• Appearance: Clots, discoloration, hemolysis
• Amount of anticoagulant to remove • Container closure
o • Attached segments intact: RBCs
Enclonar, Kimberly / MLS 3A
• Expiration date and time Washed RBCs
• Shipping list correct • Indicated for patients who react to the small amount
• Intact labels of plasma proteins that remain in a unit of RBCs.
• Reactions can be
Whole Blood o Allergic
• RBCs, WBCs, platelets, and plasma proteins with the o Febrile
anticoagulant-preservative solution o Anaphylactic
• 1-6C • IgA deficiency and clinically significant anti-IgA
• Storage time: will depend on additive • Intrauterine transfusion - fetus
• Related to circulatory overload • Saline Washing
• Whole blood is indicated for patients who are actively o 0.9% saline, 1000mL
bleeding and who have lost more than 25% of their • Storage temp: 1-6C
blood volume • Shelf life: 24hours after washing
• Increases • Anemia, IgA deficiency, PNH
o Hgb to 1g/dL
o Hct 3% Irradiated RBCs
• Hemostat - stopper • Viable T cells in cellular blood components may cause
• AS-1 = RBCs transfusion-associated GVHD, which is fatal in more
than 90% of affected patients
Packed Red Blood Cells • Graft-versus-host disease (GVHD)
• Erythrocytes o Immune condition that occurs in a patient after
• ↑ RBC mass = ↑Hgb deliver transplantation when immune cells present in
• ↑ Hgb to 1g/dL; Hct to 3% donor tissue (the graft) attach the host's own
• Open system = transfuse within 24hrs tissues
• Storage: 1-6C • 2500cGy, or 25Gy (center) - gamma radiation
• For: • 15Gy (delivered to any part of the blood unit)
o Sickle cell anemia • Storage temp: 1-6C
o Cancer • Shelf life: 28 days from irradiation
o Bleeding/Trauma • Intrauterine transfusion, immunocompromised
• Celsium 137 or Cobalt 60 isotopes
Leukoreduced RBCs o Ultraviolet irradiation
• Leukocyte-reduced RBCs are prepared with a method o X-rays
known to retain at least 85% of the original RBCs and o Radiochromic Film Label - Quality Control
reduce the leukocyte number in the final component • ↓ Atp, 2,3-DPG
to <5x106 in each unit • ↑ Potassium
• Prevent:
o TRALI Fresh Frozen Plasma
o Febrile-non hemolytic transfusion reactions • Contains all coagulation factors including labile
▪ Biological Response Modifiers (BRMs) - factors V and VIII
fever o Cold labile = 7, 11
o Transmission of EBV, CMV, Human T-cell Virus • Storage temp: ≤18C after thawing 1-6C
• Does not prevent graft vs host diseae • Shelf life: 12 months, after thawing within 6 hours
• Filtration - Leukocyte filters • Indication:
o Polyester or Cellulose acetate nonwoven fibers o For patients who are actively bleeding & have
• Done before storing Packed RBCs multiple clotting factor deficiencies
• FFP: Plasma frozen within 8 hours of collection and
Frozen RBCs stored at or below -18C for up to 1 year or stored at
• RBCs can be frozen for long-term preservation to or below -65C for 7 years
maintain an inventory of rare units or extend the • Plasma frozen within 8-24hours of phlebotomy (PF24)
availability of autologous units stored -18C or colder
• Freezing extends storage up to 10years from • Thawing - water bath
collection when stored at or below -65C
• Frozen in glycerol within 6 days of collection Cryoprecipitate
o 40% glycerol: ≤ -65C • Cryo Antihemophilic Factor contains: 8, vWF, 13,
o 20% glycerol: ≤ -120C Fibrinogen
o Storage: 10years after phlebotomy, 24 hours • Cryo-poor contains: 2, 5, 7, 9, 10, 11, ADAMTS 13 (use
after deglycerolization roman numerals)
o Anemia • Storage temp: ≤18C, after thawing room temp
• Deglycerolization o Frozen: 1 year
o Decreasing osmolar solutions of saline o Thawed: 6hr
▪ 12% saline o Pooled: 4hr
▪ 1.6% saline • Hemophilia A, vWD, Dysfibrinogenemia, Factor XIII
▪ 0.2% saline with dextrose deficiency
o Must be transfused after 24 hours • Thawed: 1-6C
o Check supernatant for remnants of glycerol and • Formation of white precipitate
hemolysis • Heavy spin
• Plasma Cryoprecipitate Reduced
o Refrozen at -18C or colder, 12-month expiration
date
Enclonar, Kimberly / MLS 3A
o Replacement solution for therapeutic Platelets
plasmapheresis for the treatment of thrombotic Random- • Contain a minimum of 5.5x1010
thrombocytopenic purpura donor plts • 20-24C with gentle agitation until
transfusion
• Shelf-life: 5 days
Apheresis Plts • Should contain a minimum of 3x1011
plts in 90% of the sampled units 20-
24C with gentle agitation until
transfusion
• Shelf life: 5 days
Pooled Plts • Accomplished by transferring the plt
concentrates into a transfer set
• 20-24C with gentle agitation until
transfusion
• Shelf life: 4 hours (due to open
system)
Irradiated • Made from either random donor or
Platelet Concentrate plts single donor
• Contraindicated: ITP, DIC, TTP
• Irradiation requirements the same
• Storage temp: 20-24C with RBC
• Shelf life: 5 days with agitation
• Prevent bleeding, quanti and quali plt disorders Plt • Febrile nonhemolytic reactions and
• Contain at least 5.5x1010 platelets and maintained at Leukocytes HLA alloimmunization leukocytes
pH ≥6.2 Reduced • Random Donor platelets: 8.3x105
• 1 unit should raise the plt count by 5000-10000/uL in leukocytes
a 75kg px
• For Apheresis
o Actively bleeding patients who are • General term for taking away targeted cell type
thrombocytopenic (<50,000/uL) • Cytapheresis - blood cells
o Cancer patients during chemotherapy • Plasmapheresis - plasma
o Thrombocytopenic preoperative patients • Storage temp: 20-24C
• Evaluation of the effectiveness of plt transfusions is • Shelf-life: 24 hours
important in determining whether the patient is • Neutropenia with infection
o Refractory or Unresponsive to the plt
transfusions
• Corrected Count Increment (CCI) of 5000/uL at
10mins to 1hour posttransfusion may indicate a
refractory state to plt therapy

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