3. Blood Transfusion Flashcards

1
Q

Why do we transfuse blood?

A

Bleeding

Poor making of blood

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2
Q

How do blood groups arise?

A

Arise from antigens, red cell antigens are expressed on cell surfaces (proteins, sugars, lipids). Can provoke antibodies

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3
Q

Explain ABO phenotypes

A

Each red blood cell contains genes that encode for glycosyltransferas. Glycans added to proteins or lipids on red cells. These mark the cells as a specific category e.g. A antibodies. They reject any other cell that does not reproduce the same category.

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4
Q

How do each blood groups distinguish between groups?

A

Blood group A has antibodies against B
Blood group B has antibodies against A
Blood group O has antibodies against A and B
Blood group AB has no antibodies

This is not the case for FFP donors. AB can donate to all where O can only donate to O

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5
Q

What happens if someone is given the wrong blood?

A

IgG binds to red blood cells more readily and will simply coat the blood cell so it is destroyed by the spleen. However if the IgM comes into contact with the blood it starts another pathway that leads to:

Blood clotting may occur throughout your body, shutting off the blood supply to vital organs or causing a stroke. Too much blood clotting can use up clotting factors and leave you at risk of excessive bleeding. Some of the products released from broken-down blood cells can cause kidney damage and possibly kidney failure.

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6
Q

What is the rhesus antigen?

A

Rhesus (RhD). Caused by the RHD and RHCE genes

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7
Q

What is anti-RHD?

A

RhD negative individuals make anti D if exposed to RhD positive cells.
This can lead to transfusion reactions or haemolytic disease of the newborn

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8
Q

How is blood taken?

A

Skin extensively cleaned, diversion pouch is used to take blood and then separates the blood into red, plasma and white cells.

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9
Q

What are the indications for red cell transfusions?

A

Correct severe acute anaemia, which might otherwise cause organ damage
To improve quality of like in patients with otherwise uncorectable anaemia
To prepare a patient for surgery or to speed up recovery
To reverse damage caused by a patients own red cells. Sickle cell disease

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10
Q

How are red blood cells stored and transfused

A

I unit is 440ml, transfuse over 2-4 hours, stored at 4 degrees

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11
Q

How do you quantify platelets?

A

1 dose platelets= 4 pooled or 1 apheresis donor.
Stored at 22 degrees, shelf life 7 days,
Transfuse over 20-30 minutes

You can Bypass groups as all platelets are screened for AB and Rhesus factors.

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12
Q

When would you need platelets?

A

Massive heamorrhage- keep platelet count above 75x109/l

Bone marrow failure-

Prophylaxis for surgery

Cardiopulmonary bypass- use only if bleeding

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13
Q

How do yiu quantify plasma?

A

1 unit from 1 unit of blood

Stored frozen, allow 30 mins to thaw

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14
Q

What are the indications for needing plasma components?

A

Massive heamorrhage
DIC with bleeding
Prophylactic

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15
Q

How do you deal with preventing blood mismatches

A

Make junior doctors take blood by the bedside and put the name on it there and then
Have two samples that concur to make sure it matches
Stop people just taking up blood and chucking it in

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16
Q

What is meant by group and screening

A

Make sure they know ABO and RhD types
Check against historical records
Screen for allo-antibodies in serum

17
Q

How do you test blood

A

Gell columns and automation to see if blood clots with other certain factors

Coombs test- direct vs indirect

Direct- tests the antibodies directly on the surface of red blood cells. This helps screen for autoimmune heamolytic anaemic,passive anti-D and heamolytic transfusion reactions

Indirect- takes cells from the mother and mixes them with known blood types. used for cross matching

18
Q

What is haemolytic disease of the new born?

A

When the mother and baby have different rhesus status and the maternal blood attacks the babies blood. Leads into anaemia and jaundice in the first term

This is very similar to neonatal alloimmune thrombocytopenia (NAIT) same but for platelets

19
Q

How is it treated?

A

Prevention using prophylactic anti-D

Sensitising events routine at 28 weeks

20
Q

How do you treat anti-D syndrome

A

Antibody totes
Doppler ultrasound
Intrauterine transfusions

21
Q

What other things do blood banks do?

A

Lecapherisis- bone marrow harvests
Donor lymphocyte infusions

Other banks- bone milk, tendons, heart valves, faecal, islet cells