Blood Transfusion Flashcards

1
Q

How regularly can you donate blood?

A

Donor gives approx. 1pint (unit) max. every 4 months

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2
Q

 Blood shelf life is ….

A

5 weeks

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3
Q

How are A and B antigens on RBC formed

A

by adding one or other sugar residue onto a common glycoprotein and fucose stem on red cell membrane

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4
Q

How O group antigens on RBC formed

A

common glycoprotein and fucose stem on red cell membrane with no sugar

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5
Q

What is added onto a common glycoprotein and fucose stem on red cell membrane in A blood group and by what enzyme

A

N-ACETYL GALACTOSAMINE

n-acetyl galactosamine transferase)

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6
Q

What is added onto a common glycoprotein and fucose stem on red cell membrane in B blood group and by what enzyme

A

adds GALACTOSE (galactose transferase)

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7
Q
  • ‘A’ and ‘B’ genes are X
A

codominant

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8
Q

O gene is X

A

recessive

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9
Q
  • Person has antibodies against any antigen XXX own red cells
A

not present on

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10
Q

Which Ig causes haemolysis of red cells

A

IgM

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11
Q

What antibodies are found in the plasma of people with O blood group

A

both anti A and anti B

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12
Q

Which blood group can receive any blood

A

AB

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13
Q

Which blood group can give blood to anyone

A

O

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14
Q

What 2 antigens need to be matched for a blood transplant

A

RH and ABO

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15
Q

What are the Rh blood groups

A
RhD is the most important one 
RhD positive (if have D antigen) or RhD negative (if not)
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16
Q
  • Genes for RhD groups (notation and genotype)
A

D Codes for D antigen on red cell membrane
d Codes for no antigen and is recessive

  • dd= no D antigen RhD negative
  • Dd or DD= D antigen present RhD positive
17
Q

Proportion of people RhD positive and negative?

A
  • 85% of people are RhD positive, 15% negative
18
Q

Can People who lack the D antigen make anti-D antibodies, when?

A

Yes after RhD exposure through transfusion or if women fall pregnant with an RhD positive baby

19
Q

What type of Ig are anti D antibodies, what does this cause

A

IgG
Don’t fully activate the complement cascade Go as far as C3D stage, so you get antibody coated red cells and between 5-10 days later, these pass through the spleen and are destroyed by macrophages

20
Q

What does extravascular haemolysis cause

A

causes jaundice through the high bilirubin and the free haemoglobin damages kidney tubules

21
Q

What is HAEMOLYTIC DISEASE OF THE NEWBORN

A

If RhD neg mother has anti-D, and in the next pregnancy the foetus is RhD pos, the mother’s IgG anti-D anitbodies can cross the placenta causing haemolysis of foetal red cells if severe leads to hydrops fetalis, brain damage due to high bilirubin and even DEATH

22
Q

Why do we not give women who are child bearing age X type of blood

A

RhD positive blood to RhD negative women is never given to avoid haemolytic disease of the newborn

23
Q

What is used in an emergency to give blood

A

O neg

24
Q

RED CELLS:- Shelf life?

A

5 weeks

25
Q

RED CELLS: units/donor?

A

1

26
Q

RED CELLS: why do we not freeze?

A

Has a poor recovery when thawing

27
Q

FFP (fresh frozen plasma): storage conditions?

A

-30 degrees

28
Q

FFP (fresh frozen plasma): shelf life?

A
  • Shelf life 2 years
29
Q

FFP (fresh frozen plasma): unit/donor?

A
  • Shelf life 2 years
30
Q

FFP (fresh frozen plasma): time till use?

A
  • Must thaw approx. 20-30mins before use:

 Give ASAP- ideally within 1 hour or coagulation factors degenerate at RTP

31
Q

FFP (fresh frozen plasma): units/dose?

A
  • Dose 12-15ml/kg (usually 3 units)
32
Q

FFP (fresh frozen plasma): matching necessary?

A
  • Need to know blood group, but X-match not necessary (as contains ABO antibodies, which could cause some haemolysis but not very much so not fatal)
33
Q

FFP indications? (3)

A
  1. Patient bleeding AND abnormal coagulation test results (prothrombin time (PT)/activated partial thromboplastin time (APTT) abnormal) Monitor the response clinical and by coagulation tests
  2. Reversal of warfarin (anticoagulant that depletes factors II, VII, IX and X) e.g. for urgent surgery (if prothrombin complex concentrate (PCC) unavailable)
  3. Other conditions occasionally e.g. massive haemorrhage
34
Q

CRYOPRECIPITATE: storage conditions

A

same as FFP, -30

35
Q

CRYOPRECIPITATE: contains?

A

fibrinogen and factor VIII

36
Q

CRYOPRECIPITATE: indications?

A
  • If massive bleeding and fibrinogen very low

- Rarely it can be used for hypofibrinogenaemia

37
Q

Fractionated products that can be used for blood transfers? (3)

A
  • Factor VIII and IX:
  • Immunoglobulins:
  • Albumin:
38
Q

What disease has been transmitted via blood transfusion in the UK 4 times, what precaution is now taken to fix this?

A

Prion disease,

 All plasma pooled to make fractionated products now obtained from USA (UK plasma is sometimes used for FFP, but otherwise thrown away)
 All blood components have white cells filtered out (leucodepleted)- white cells are essential for uptake of vCJD prion into brain to cause disease