Blood Groups & Transfusion Flashcards

1
Q

What forms blood groups?

A

Lipid bilayer with sugar residues and proteins on RBC surface
Sugar residues form type of blood group - ABO
Proteins form another type of blood group - rhesus
Genes determine what sugar and protein in produced and therefore the blood group

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2
Q

What are antigens?

A

over 300 - some less clinically important

RBC antigens stimulate antibody formation

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3
Q

What are antibodies?

A
  • Immunoglobulins in plasma which react specifically with an antigen
  • autoantibodies react with antigens on person’s own RBCs
  • alloantibodies produced by person against antigens which are not on own RBCs, either naturally occur in environment or part of an immune response
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4
Q

What does an antigen-antibody reaction result in?

A

Agglutination

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5
Q

What are the ABO blood groups?

A

A - has anti-b in plasma
B - has anti-a in plasma
O - has anti a and anti-b in plasma
AB - has no ABO antibody in plasma

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6
Q

What does having an anti-a in plasma mean?

A

Will be agglutinated by anti -a so will form an antigen-antibody reaction.

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7
Q

What is a phenotype and genotype?

A

Phenotype - antigens detectable on RBC membrane

Genotype - antigens encoded in the DNA, 1 copy from each parent

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8
Q

What are the phenotypes and genotypes for the blood groups?

A

Phenotype - A, B, AB, O

Genotype - AA AO, BB, BO, AB, OO

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9
Q

What are the relative blood group frequencies?

A

Most common is O, then A, then B, then AB

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10
Q

How do blood groups differ between ethnicities?

A

Africans - More O, A slightly more than B
European - more A than O
Asian - A and B same, slightly more AB then other ethnicities

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11
Q

Which antibodies are naturally occurring?

A

Anti-a and anti-b

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12
Q

Which blood groups can receive and donate from which other group and why?

A

Blood group A has A antigens with anti-B antibodies and therefore if they receive from B or AB which have B antigens the anti-B antibody would attack it meaning they can only receive from A and O. They can donate to AB and A only.
B type has anti-A antibodies so can only receive from B and O not A and AB. Can donate to B and AB.
AB has no antibodies so can receive from all groups. Can only donate to AB.
O has A and B antibodies so can only receive from O. Can donate to all.

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13
Q

Which is the universal recipient and donor?

A

AB is universal recipient as no antibodies.

O is universal donor as no antigens.

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14
Q

What is the rhesus blood group system?

A

3 pairs of proteins inherited as a triplet - D, C, E
Inherit one triplet from each parent
Alleles c and e are co-dominant

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15
Q

Which alleles are co-dominant?

A

A and B

C and E

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16
Q

What are the phenotypes for Rhesus blood group?

A

RhD positive - CcDDEe - CcDEe
RhD negative - Ccddee - Ccde
RhD negative - ccddee - cde
(rhesus negative has lower case d)

17
Q

How do you determine the phenotype for rhesus system?

A
  • serologically
  • put RBCs into wells each coated with one antibody and if antigen is present it will agglutinate with antibody and will not sink to the bottom so C/c/D/d/E/e positive or negative can be determined
18
Q

What are the approximate frequencies for Rhesus blood group?

A

More rhesus positive across all ethnicities by a significant amount

19
Q

What blood should rhesus positive and negative individuals receive?

A

Rhesus positive - rhesus positive or negative

Rhesus negative - rhesus negative, avoid positive

20
Q

How can a haemolytic disease and the foetus and newborn develop?

A

Rhesus positive father and rhesus negative mother produce a rhesus positive foetus
Rhesus negative mother carries positive fetus and during delivery blood can enter mother’s
Mother will produce anti-Rh antibodies in response to fetal antigens
During next pregnancy anti-Rh antibodies will cross placenta to Rhesus positive foetus and damage fetal RBCs
This all results in foetal anaemia and/or neonatal jaundice

21
Q

What are some ways to manage a haemolytic disease developing in the foetus/newborn?

A

Prophylaxis anti-D Ig the all negative mothers in third trimester

22
Q

What are some good clinical practice methods to avoid haemolytic disease?

A

Monitor adverse reactions
Patient identification
Sample labelling
Laboratory testing

23
Q

How are RBCs stored?

A

At 4 degrees, 35 day shelf life

24
Q

What are some indications for blood transfusion?

A

Blood loss - surgery, trauma, obstetric haemorrhage
Bone marrow failure - leukaemia, cancer, drugs
Haemolysis - malaria, sepsis, haemolytic disease of newborn
Inherited haemoglobin disorders - SC anaemia, thalassaemia
Anaemia due to iron, B12, folate deficiency - try and avoid transfusion and give haematinic replacement therapy instead

25
Q

What are some complications of transfusion?

A

Infectious - viral (HIV, HepE, HBV), bacterial, syphilis, parasites (malaria)
Non infectious - acute haemolytic transfusion reaction, delayed haemolytic transfusion reaction, allergic urticarial rash, transfusion related lung injury
Non immune - fluid overload, iron overload

26
Q

What are the most common reasons for ABO incompatibility?

A

Patient wrongly identified - unconscious, no wristband, human error, pre-transfusion sample from wrong patient

27
Q

What is an indirect antiglobulin test?

A

Used to detect IgG - alloantibodies formed after previous pregnancy or transfusion
- patients serum (containing IgG), incubate with reagent RBCs that will bind to IgG, incubate with antibodies to Ig, will agglutinate (positive indirect Coombs test)

28
Q

What should be monitored during a transfusion?

A

before - confirm patient identity, blood group, blood group of unit of blood
Pulse, bp, temperature

29
Q

How does a transfusion reaction present?

A

Signs - fever, hypotension, haemoglobinuria
Symptoms - restless, flushing, anxiety, abdominal pain, nausea, diarrhoea, pain at venupuncture site
STOP TRANSFUSION AND MAINTAIN VENOUS ACCESS WITH SALINE

30
Q

What types of antibodies are anti-a and b?

A

IgG and IgM

31
Q

What laboratory tests are done?

A

1 - Indirect positive coombes test where you mix all of patients plasma (containing antibodies) with blood type O (no antigens) mixed with all antigens to then see which ones agglutinate
2- Electronic crossmatching - check for any antibodies - if none then must be AB rhesus negative so can receive from all blood types
3 - serological crossmatching - if antibodies are present mix donor RBCs and patients plasma to check antibodies then do rhesus test with wells

32
Q

What is the indirect Coombes test?

A

Tests for autoimmune haemolytic anaemia where IgG antibodies attack RBC membrane proteins

33
Q

What can the effects of autoimmune haemolytic anaemia be?

A

jaundice

failure of haemoglobin to rise

34
Q

What can blood transfusions be used for?

A
blood loss - trauma, surgery, haemorrhage
bone marrow failure - leukaemia
haemolysis - malaria, sepsis
inherited haemoglobin disorders 
anaemia
35
Q

How do you investigate a transfusion reaction?

A

Take samples for FBC, renal and liver function tests, blood culutres, coagulation screen
Repeat compatibility testing pre and post transfusion
Direct antiglobulin test
Assess urine for haemoglobin
High dependency management - Renal support

36
Q

What is the difference between the direct and indirect Coombes test?

A

Direct - RBCs are already attached to IgG and get mixed with IgG antibodies to confirm attack on own RBCs
Indirect - use RBCs which are not attached to IgG and mix with IgG antibodies to see if IgG are present