Blood transfusion Flashcards

1
Q

When do you use blood tranfusions?

A

If there is no other possbility

mainly in emergency situations

  • trauma + massive bleedings
  • very severe anaemia
  • clotting disorders etc.
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2
Q

What does the A gene in blood groups code for?

A

It codes for an enzyme adding galactosamine to fructose stem on cells

–> forms the A antigen

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3
Q

Which antigens and antibodies does a person with blood group A have?

A

A= A antigens and

Anti-B- antibodies –> can’t get blood that has B antigens (i.e. B+AB)

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4
Q

Which Antigens and Antibodies does someone with Blood group B has?

A

B

  • B-Antigen
  • Anti-A-antibody
  • –> can’t get blood with A antigen (i.e. A+AB)
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5
Q

Which Antigens and Antibodies does someone with blood group AB have?

A

AB

  • AB antigens
  • no anti-antibodies
  • –> can recieve any blood donation
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6
Q

Which antigens and antibodies does someone with blood group 0 have?

A

They have

  • no antigens
  • Anti -A- and Anti B antigens
  • –> can give blood to anyone
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7
Q

Why don’t the Anti- A and Anti-B antibodies in the plasma not affect the blood donation (0) given to patients with groups A or B?

A

Normally no full blood transfustion

  • only packed red cells and no plasma
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8
Q

What happens if you would give a blood transfusion of group B to someone with group A?

A

IgM anti-B antibodies would bind to blood cells by group B and set of a cytokine strom–>

  • lysis of erythrocytes
  • aggulation seen (IgM mediated)
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9
Q

Explain the process of blood group testing and matching blood

A

You need

  1. patients sample
  2. test with known anti-A/anti-B antibodies

–> Combine and look for reaction (if aggulation reaction –> not suitable for donation)

If necessary:

  • X match with donor blood + recipient
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10
Q

Explain the possible genotype for a RhD + and -ve person

A

+ ve: Dd or DD

-ve dd

–> recessive gene

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11
Q

Explain the possible genotype of someone having blood group A+B

A
  • A= AA or AO
  • B= BB or BO
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12
Q

What happens to RhD -ve people who are exposed to the RhD antigen?

A

They don’t have the RhD antibody from birth but can develop them furter in life–> can lead to problems in

  • another blood transfusion that is +ve (where you would react then)
  • in pregnancy with a -ve mother and a +ve foetus –> antigens would destroy the foetus blood cells
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13
Q

What happens when you transfuse a RhD -ve person who has developed Anti-D antigens a RhD +ve transfusion?

A

otherwise his anti-D would react with RhD posblood - causes delayed haemolytic transfusion reaction - anaemia; high bilirubin; jaundice etc

Reaction within 5-10 days

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14
Q

What is the significance of other antigens present on red blood cells other than A, B and RhD?

A

Only 8% of people develop antibodies against antigens they don’t have –> normally not matched for

If once antibodies have developed: must use corresponding antigen negative blood otherwise:

risk of delayed haemolytic reaction (can be severe)

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15
Q

Which tests are required to do before a transfusion?

A

ABO and RhD group, must do an ‘antibody screen’ of their plasma

–> for all the other possible antigens in blood/ on blood cells

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16
Q

In which 3 components is a standart blood sample normally devided?

A

Normally in

  • Red cell component
  • Platelets
  • Plasma
17
Q

When do you give red cells in a blood transfusion?

A

e..g in patients with trauma, hugh blood loss to restore oxygen carring capacity

18
Q

What does a FFP contain?

Who would recieve it?

A

FFP= Fresh Frozen plasma (frozen and thawed before use)

  • contains coagulation factors

Given to people with reduced blood coagulation (slowed PT+ APTH test)

reversal of warfarin for urgent surgery

Same blood group needed but no x-maching necessary

19
Q

What is cryoprecipitate?

Who needs it?

A

Part of plasma high in Fibrinogen and Facotr VIII

Given to patients with

  • massive bleeding and fibrinogen very low
  • Rarely hypofibrinogenaemia
20
Q

What are the characteristics of a platelet donation?

Who recieves it?

A

Shelf life of only 5 days with agitation

  • no x match required but choose same blood group (as otherwise lifespan of platelets shortened)
  • RhD sensitisation possible (because of contamination with red cells)

Given to patients with

  • thrombocytopaenia
  • Mainly in cancer/bone marrow failure
  • also in massive bleeding of DIC
  • reversing effects of anti-platelet drugs
21
Q

Which blood transfusion products are usually obtained via fractionated prodcuts?

A
  1. Single clotting factors
    • VIII, IX in haemophilia
    • Factor VIII in VWD (because is VWB factor is low, VIII is also low (VWB stabelises factor VIII)
  2. lImmunoglobulins
  3. Albumin
22
Q

Explain the transfusion of Immunoglobulins

A

Used for:

  • IM: Specific - tetanus; anti-D; rabies
  • IM: Normal globulin - broad mix in population (eg: HAV)
  • IVIg – pre-op in patients with ITP or AIHA
23
Q

How are blood donors tested?

What are the criteria?

A

Blood donors within high risk groups/risk behaviours are excluded

Blood is tested for infections (no 100% certainty):

  • Hepatitis B - HBsAg, PCR
  • Hepatitis C - anti-HCV, PCR
  • HIV - anti-HIV, PCR
  • HTLV - anti HTLV
  • Syphilis - TPHA (spirochete)
  • Hepatitis E - PCR
  • Some also tested for CMV (virus)

Questionnaire: e.g. malaria (exclude when recent travelling etc.)

vCreutzfeldt-Jacob disease also can be transmitted but very very rare

24
Q

How are platelet donations stored and what is their shelf life?

A

Stored at 22° (Room temperature and constantly agitated)

Shelf life: 5 days

(increased risk of infection due to warm storing temp)

25
Q

What is the storage and shelf life of FFP?

A

Fresh Frozen Plasma

(Same storage for Cryorecipitate)

  • collected (300ml) and frozen within 6h
  • Stored at -30°
  • Shelf Life: 2 years