Blood Transfusion 1 Flashcards
What are the important blood groups?
ABO and RhD
What are the blood components?
red cells, fresh frozen plasma, platelets, cryoprecipitate
What is the process of blood donation?
selection of donors, testing of donations, processing blood into components
What are the 4 rights of blood?
Giving the right blood to the right patient at the right time for the right reason
What antibodies are present in Group A blood?
Anti B
What antibodies are present in Group B blood?
Anti A
What antibodies are present in Group AB blood?
None (universal receiver)
What antibodies are present on Group O blood?
Anti A and Anti B (Universal Donor)
What does ABO/ RhD incompatibility cause?
Intravascular Haemolysis
What is RhD?
Red cells which carry the RhD antigen are ‘RhD positive’
These patients can receive RhD negative (just a waste!) or RhD positive red cells
What can’t you give RhD negative patients?
RhD negative patients lack the RhD antigen
These patients can make immune anti-D if exposed to RhD positive red cells
Immune anti-D antibodies are IgG, which do not cause direct agglutination of RBCs so not immediate haemolysis & death, but delayed haemolytic transfusion reaction
How much of the population is RhD positive/ negative?
85% of the population are RhD-positive and 15% RhD-negative
What happens if there is no RhD negative blood to transfuse?
RhD-negative blood is often in short supply so it may be necessary to use RhD-positive blood for the transfusion of RhD-negative patients.
Why do pregnant women care about Rhesus Status?
Immune Anti-D made by a Rh negative mother exposed to Rh positive blood, can cause haemolytic disease of the newborn or severe fetal anaemia and heart-failure (hydrops fetalis) in RhD-negative females of child bearing potential.
How do you test patients ABO and RhD group?
use known anti-A and anti-B and anti-D reagents against patient’s RBCs
And “reverse group”: known A and B group RBCs against patient’s plasma (IgM antibodies)
Positive = agglutination (clumping)
Negative =
Red cells stay suspended
The BLOOD GROUP is done before every transfusion, even if it has been done many times before
What are the results of column agglutination?
Positive = agglutination (cells stay at the top)
Negative = No agglutination, cells pass through the beads (or gel) to the bottom
Agglutination with anti-B and A1 cells
No reaction with anti-A and anti-D or with B cells
These techniques can be ‘automated’ or ‘manual’: room temp, 10 mins
What do we do about the other RBC antigens?
Can’t test all other RBC antigens (100s)
But about 1-3% of patients have immune RBC antibodies to one or more RBC antigen
Must identify clinically significant RBC antibodies and transfuse RBCs that are negative for that antigen to prevent a DELAYED HAEMOLYTIC TRANSFUSION REACTION
How do you do an antibody screen on a patients blood plasma?
Use 2 or 3 reagent red cells containing all the important red cell antigens between them
Screen by incubating the patient’s plasma and screening cells using IAT** technique
**INDIRECT ANTIGLOBULIN TECHNIQUE (bridges red cells coated by IgG, which can’t themselves bridge 2 red cells – to form a visible clump. Takes 30 mins’ incubation at 37°C)
Group and Save
The ANTIBODY SCREEN is done before every transfusion, even if it has been done before, because can make new antibodies.
How has the screening process been automated?
Bar coded samples (id correct throughout – no mix up)
Computer interfaces
Robotic sample and reagent handling
Liquid level sensors (? failed to add reagent)
Reading of results by image analysis
Interpretation of results
Download to patient record
How do you issue blood?
DONOR RBCs ARE LABELLED WITH
ABO & D TYPE
THEY ARE ALSO LABELLED WITH
OTHER Rh ANTIGENS AND K
Select the correct ABO and D type from stock fridge
Select antigen negative blood if RBC antibody detected in antibody screen and ID panel
Select K negative blood for females of childbearing potential
What is a full serological crossmatch?
Indirect antiglobulin technique:
Patient plasma incubated with donor red cells at 370C for 30-40 mins, will pick up antibody antigen reaction that could cause destroy the red cells and cause extravascular haemolysis. Add antiglobulin.
IgG antibodies can bind to RBC antigens but do not crosslink so AHG reagent is added