Blood Transfusions Flashcards

(54 cards)

1
Q

Why do we transfuse blood?

A
  • Major bleeds

- Failure of production

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2
Q

How are blood groups established?

A
  • Arise from antigens= something that provokes an immune response
  • Red cell antigens are expressed on cell surface (proteins, sugars, lipids)
  • Can provoke antibodies
  • Glycans added to proteins or lipids on RBC
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3
Q

What does the ABO gene encode?

A

Glycosyltransferase

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4
Q

What do the A and B genes encode for?

A

Transferase enzymes

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5
Q

What is the A antigen?

A

N-acetyl-galactosamine

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6
Q

What is the B antigen?

A

Galactose

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7
Q

What is the O gene?

A

A non-functional allele

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8
Q

Describe the inheritance of blood groups.

A

A and B are co-dominant whilst O is recessive

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9
Q

What does blood group B have antibodies against?

A

A

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10
Q

What does blood group A have antibodies against?

A

B

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11
Q

What does blood group O have antibodies against?

A

A and B

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12
Q

What does blood group AB have antibodies against?

A

No antibodies

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13
Q

Who is universal red cell donor?

A

Blood group O

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14
Q

Who is the universal red cell recipient?

A

Blood group AB

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15
Q

Who is the universal FFP donor?

A

Blood group AB

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16
Q

Who is the universal FFP recipient?

A

Blood group O

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17
Q

What can RhD negative individuals do during pregnancy or transfusion?

A
  • They can make anti-D if exposed to RhD cells

- This can lead to transfusion reactions or haemolytic disease of the new-born

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18
Q

What screening do blood donors undergo?

A
  • Extensive ‘behavioural’ screening
  • Sex, age, travel, tattoo
  • Tested for ABO and Rh blood groups
  • Screened for HepB/C/E, HIV, syphilis
  • Variably screened for: HTLV1, malaria, West Nile virus, Zika virus…
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19
Q

What are the components and products of blood?

A

Plasma

  • Clotting or coagulation factors
  • Albumin
  • Antibodies

Buffy Coat

  • Platelets
  • White cells

Red Blood Cells

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20
Q

What are some indications fro RBC transfusion?

A
  • Severe acute anaemia
  • Uncorrectable anaemia
  • Surgery
  • Sickle cell disease
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21
Q

How are RBCs transfused?

A
  • Stored at 4oC
  • Transfuse over 2-4 hours
  • 1 unit increments ~5 g/L
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22
Q

How are platelets transfused?

A
  • 1 dose platelets (=4 pooled or 1 apheresis donor)
  • Increments 20-40 10^9/L
  • Stored at ~22oC, shelf life 7 days
  • Transfuse over 20-30 minutes
23
Q

When may platelets be transfused?

A
  • Massive haemorrhage
  • Bone marrow failure
  • Prophylaxis for surgery
  • Cardiopulmonary bypass
24
Q

What are the components of plasma?

A
  • Fresh frozen plasma

- Cryoprecipitate

25
What are the indications for FFP?
- Massive haemorrhage - DIC with bleeding - Prophylactic
26
How is FFP used?
- 1 unit from 1 unit of blood | - Stored frozen, allow 30 minutes to thaw
27
What are the lab tests for FFP?
PT and APTT
28
What is the lab test for cryoprecipitate?
Fibrinogen
29
How is cryoprecipitate stored?
Frozen, allow 20 minutes to thaw
30
How are patients grouped and screened?
- ABO and RhD type - Checked against historical records - Screen for allo-antibodies in serum
31
What is the direct Coombs test used for?
- Autoimmune haemolytic anaemia - Passive anti-D - Haemolytic transfusion reactions
32
What is the indirect Coombs test used for?
Cross matching
33
At what temperature do the ABO and Rh blood group systems usually react?
37C
34
What blood is usually available within minutes?
O- red cells (AB plasma)
35
What bloods are usually available uregently?
Type specific (ABO/RhD)
36
What bloods take time and are non-urgent?
- Full cross match to select the correct ABO/RhD type | - If allo-antibodies choose antigen negative blood
37
What is the definitive management for massive haemorrhage?
Rapid control of bleeding via intervention or surgery
38
Once a massive haemorrhage protocol has been activated what is there an immediate supply of?
- 6 units red cells - 4 units FFP - 1 unit platelets
39
What should decision to transfuse be based on?
The decision to transfuse should be based on a careful assessment of patient's clinical state and must be justified as essential to prevent major morbidity or mortality
40
How is prion disease transmittable?
By blood transfusion from early in the disease
41
How should transfusion reactions be managed?
- Stop transfusion - Check patient identity against component label - Consider: anaphylaxis, circulatory overload (TACO), acute haemolytic transfusion reaction (AHTR), bacterial infection, lung injury (TRALI) (other…)
42
Acute transfusion reaction: possible cause of pyrexia
FNHTR
43
Acute transfusion reaction: possible cause of urticaria
- Mild allergic reaction | - Anaphalaxis
44
Acute transfusion reaction: possible cause of dyspnoea
- TACO - TRALI - Anaphylaxis
45
Acute transfusion reaction: possible cause of shock
- IBCT - Anaphylaxis - TRALI - TAS
46
Acute transfusion reaction: treatment for pyrexia
- Antihistamine | - Other symptoms usually more concern (bronchospasm/shock)
47
Acute transfusion reaction: treatment of dyspnoea
- O2 - Diuretic - Ventilation - Adrenaline
48
Acute transfusion reaction: treatment of shock
- Adrenaline(IV)/Hydrocortisone/Antihistamine - IV fluid / ITU admission - Ventilation - Antibiotics, - FFP/platelets if DIC
49
What is sensitisation in rhesus disease?
Development of maternal anti D antibodies
50
Does IgG cross the placenta?
Yes
51
How does haemolytic disease of the new-born present at birth?
- Positive direct antiglobulin test - Jaundice - Anaemia
52
How is HDN prevented?
Using prophylactic anti-D at 28/40 weeks or during sensitising events
53
What is the treatment for HDN?
Careful monitoring - Antibody titres - Doppler ultrasound - Intrauterine transfusions
54
What is TRALI?
Transfusion related acute lung injury - Transfused anti-leucocyte Abs in donor plasma interact with patient’s WBC - Bilateral pulmonary infiltrate - Supportive management, ventilation