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BB Week 1

Donation and units

QuestionAnswer
Clinical significance of ABO Antibodies IgM and activate complement
Anti-A,B reagent Used to confirm Type O donations
Anti-A,B antibody Produced in some Type O patients and is a separate antibody from Anti-A or Anti-B; reacts with BOTH A and B
ABO Inheritance Pattern Codominant
Type O Prevalence Roughly half in all races
Type A Prevalence 40% in whites, roughly 30% for everyone else
Type B Prevalence 20% in Black/Asian, 10% in Hispanic/White
Type AB Prevalence 7% in Asian, roughly 3% for everyone else
Se gene Determines if ABH antigens are found in secretions
H gene Adds L-fucose to the terminal Galactose on an oligosaccharide chain on RBC surface
A-Antigen Gal-Nac
B-Antigen D-Gal
Bombay Phenotype hh Genotype. Cannot produce H antigen, will type as O despite genotype but IS INCOMPATIBLE WITH O. Anti-H is an IgM that reacts at 37C.
Maximum collection of blood for donation 10.5 mL per kg body weight
Minimum weight for donation 110 lbs or 50 kg
Minimum age for donation 16 or state law
Hgb needed for donation 12.5 g/dL females or 13.0 g/dL males
Hct needed for donation 38% females or 39% males
Temperature needed for donation Less than 99.5 F or 37.5 C
Blood pressure needed for donation Systolic: 90-180 mmHg; Diastolic: 50-100 mmHg
Time needed to wait between WB donations 2 weeks
What if the donor took medication that irreversibly alters PLT function within the last 48 hours? PLTs may be used as a pool but not the sole source
Hepatitis B Immunoglobin 1 year deferral
Possible exposure to HIV, hepatitis, or malaria 1 year deferral
Recipient of blood products 1 year deferral
Tattoo (unless at a state regulated facility) 1 year deferral
Skin puncture or mucous membrane exposure to blood or bodily fluid 1 year deferral
Living with or had sex with someone who is HIV, HBsAg or HBV NAT positive; is symptomatic for Hep C or any viral hepatitis; or is in high-risk category 1 year deferral
From the date of completion of treatment of syphilis, gonorrhoeae, or reactive STS 1 year deferral
Traveled to area endemic for malaria 1 year deferral
Spent more than 72 hrs in a correctional facility 1 year deferral
Immigrant from an area endemic for malaria 3 year deferral
Previously diagnosed with malaria but is now asymptomatic 3 year deferral
Viral hepatitis after age 11 Permanent or indefinite deferral
Confirmed HBsAg or HBV NAT positive test Permanent or indefinite deferral
Repeatedly reactive for anti-HBc or anti-HTLV Permanent or indefinite deferral
Sole donor after a recipient developed post-transfusion HIV, hepatitis, or HTLV Permanent or indefinite deferral
Previous infection with HTLV, HCV, T. cruzi, or HIV Permanent or indefinite deferral
Evidence of parenteral drug use Permanent or indefinite deferral
Family history of CJD Permanent or indefinite deferral
History of babesiosis Permanent or indefinite deferral
Expiration of units with ACD, CPD, or CPD2 21 days
Expiration of units with CPDA-1 35 days
Expiration of units with additives 42 days
Purpose of rejuvenating solutions Restores 2,3-DPG and ATP
Storage of units with rejuvenating solutions Frozen or at 1-6 C if used within 24 hours (must wash cells to remove solution!)
Requirements for autologous donations No age limit, Hct +33%, Hgb +11 g/dL, no bacteremia, and collected >72 hours prior to need
Waiting period between donation of PLTs or WBCs At least 2 days apart and no more than 2 within one week (if donated RBCs, must wait 8 weeks)
Waiting period between donating 2 unit RBC apheresis 16 weeks
A 3 unit RBC donation must not decrease donor's Hct and Hgb below... Hct: not below 30%; Hgb: not below 10 g/dL
Guidelines for allogenic marrow donation HLA identical match lowers risk of GVHD; ABO compatibility NOT required
Tests performed on donor blood ABO, Rh (+ wk D if Rh neg), Antibody screens, Serologic tests, Tests for viral diseases
Serologic tests done on donor blood RPR for syphilis and antibody to T. cruzi
Viral disease tests done on donor blood Hepatitis C and B, HIV, Zika, HTLV, West Nile
Use for whole blood Massive volume loss in trauma or shock
How much does 1 pRBC raise the Hgb by? 1 g/dL
How much does 1 pRBC raise the Hct by? 3%
Changed in plasma in RBC storage over time NH4 and K+ rises while pH and Na+ lowers
Criteria for a unit of RBCs to be returned Unopened seal and less than 10 C
Purpose of washed RBCs To prevent anaphylactic shock in IgA deficient patients who have antibodies to IgA; Removes complement; Removes maternal anti-HPA-1a for neonatal transfusions
RBC storage 1-6 C for: 21 days (ACD, CPD, CPD2), 35 days (CPDA-1), 42 days (Additive), or 24 hours (open system)
Apheresis leukoreduced RBC QC >51 Hgb or >42.5 Hgb in 95% units tested
Frozen RBC storage 10 years at -65C in 40% glycerol or -120C in 20% glycerol; good for 24 hours once thawed and rinsed
Fresh Frozen Plasma or FFP24 storage 12 months at <-18C or 7 years <-65C
Cryoprecipitated AHF storage 12 months at <-18C
Purpose of Leukoreduced RBCs Prevents febrile nonhemolytic (FNH) reactions, HLA alloimmunization, and transmission of CMV
FFP Preparation Centrifuged from WB and frozen within 8 hours of collection
FFP Expiration 1 year if stored at <-18C, 7 years if at <-65C OR within 24 hours of thawing if 1-6C
Uses for FFP Multiple coagulation deficiencies, Factor XI deficiency, or deficiencies where there is no concentrate available
Ideal collection from FFP Males or never pregnant women to prevent TRALI
PF24 Plasma frozen to <-18 within 24 hours of collection
How Cryoprecipitate is made Precipitate formed when FFP from WB collection is thawed at 1-6C
What's in cryo? Fibrinogen, vWF, Factor VIII, Factor XIII, fibronectin, ristocetin cofactor activity
How long cryo is good for after collection <-18C for 1 year
How long cryo is good for once thawed 6 hours if closed system, 4 if open system
Most common uses for cryo Replace fibrinogen loss due to DIC or massive bleeding, or for dysfibrinogenemia with active bleeding
Use for Factor VII concentrates Treats moderate to severe Hemophilia A
Transfusion treatment for vWD Factor VIII concentrates containing vWF
Transfusion treatment for Hemophilia B Prothrombin complex concentrates (contains Vit K dependant factors, FII, FVII, FIX, FX) or Factor IX concentrates
Treatment for patients with Hemophilia A or B with inhibitor antibodies (causing FVIII to be bypassed) Recombinant activated Factor VIIa
Uses for DDAVP Synthetic hormone used for mild hemophilia A and type 1 vWD by increasing circulating vWF (releases from endothelial cells) and FVIII
PLT storage 5 days at RT with agitation
How long PLTs are good for once in open system 4 hours
PLT preparation from WB 1) Light spin to remove RBCs 2) Heavy spin to remove plasma and WBCs
Uses for PLTs Thrombocytopenia and platelet dysfunction
PLT transfusion is NOT recommended for... TTP, ITP, and Heparin Induced Thrombocytopenia (HIT)
Usual cause for dysfunction in PLT refractoriness HLA or platelet specific antibodies
How much 1 unit of PLTs raise PLT count by 5000 to 10,000 per uL
How much 1 APHERESIS unit of PLTs raise PLT count by 20,000 to 60,000 per uL
Why we keep small volume of plasma in PLT units To maintain pH above 6.2
Does Rh matter for PLTs? Only if Rh- women of childbearing age receive Rh+ unit due to residual RBCs. May need Rhogam.
Use for granulocyte pheresis Neutropenic patients with GN sepsis not responsive to antibiotics
Potential complications of granulocyte infusions if not IRR Transmission of CMV, GVHD, alloimmunization of HLA antibodies
Storage of granulocytes RT without agitation for 24 hours or ASAP
Do granulocytes need to be ABO compatible? YES. XM if >2mL RBCs.
Uses of IRR RBCs Prevents GVHD in: neonates, transfusions with relatives or HLA-matched donations, or congenital immunodeficiency
Outdate for IRR RBCs 28 days or original expiration, whichever comes first
Expiration of RT products when seal is broken (pooled or packed) 4 hours
Expiration of refrigerated products when seal is broken (pooled or packed) 24 hours
Created by: rachelkayw
 

 



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