Blood Transfusions Flashcards

1
Q

what is activating complement

A

are able to cause potentially fatal haemolysis (destruction of red cells) if incompatible blood is transfused.

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2
Q

Blood group A (rbc type,antibodies in plasma and antigens in rbc)

A

rbc = a
antibodies in plasma= anti b
antigens in rbc= a antigen

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3
Q

Blood group B

A

rbc type= b
antibodies in plasma= anti a
antigens in rbc= b antigen

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4
Q

Blood group AB

A

rbc type= ab
antibodies in plasma= none
antigens in rbc= a and b antigens

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5
Q

Blood Group O

A

rbc type= o
antibodies in plasma= anti a and anti b
antigens in rbc= none

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6
Q

how are a and b antigens formed of red cells

A

by adding one or other sugar residue onto a common glycoprotein and fucose stem (H antigen) on the red cell membrane.

Group O has neither A or B sugars – H stem only

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7
Q

What does the A gene do

A

Codes for an enzyme that adds N-acetyl galactosamine to the common H antigen

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8
Q

What does the B gene do

A

Codes for the enzyme which adds galactose

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9
Q

Are A and B genes co dominant

A

Yes

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10
Q

Is O recessive or dominant

A

Recessive

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11
Q

What are the possible genes for blood group A

A

AA or OA

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12
Q

Possible genes for blood group B

A

BB or OB

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13
Q

Why is it safe to give blood group O to anyone in an emergency

A

As group O has no ABO antigens

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14
Q

RhD negative

A

dd

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15
Q

RhD positive

A

DD or Dd ( is d gene codes for no antigen and is recessive)

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16
Q

Can people who lack the RhD antigen make anti D antibodies

A

Yes, after they are exposed to the RhD antigen, either by transfusion of RhD positive blood or in women if they are pregnant with an RhD positive foetus. Anti-D antibodies are IgG class antibodies

17
Q

Implications of anti D antibodies on future transfusions

A

1) future transfusions; patient must in future have RhD negative blood (otherwise their anti-D would react with RhD positive blood - causesdelayed haemolytic transfusion reaction– with anaemia; high bilirubin (from breakdown of red cells); jaundice etc.).

18
Q

Implications of anti-D antibodies on HDN

A

haemolytic disease of the newborn-if RhD neg mother has anti-D, then in the next pregnancy, if fetus is RhD positive: mother’s IgG anti-D antibodies can cross the placenta (only IgG class antibodies can do this) – attach to the RhD positive red cells of the foetus and cause haemolysis of foetal red cells - if severe:hydrops fetalisand death. If less severe, the baby survives but after birth, the high bilirubin levels can cause brain damage or death.

19
Q

How to avoid sensitisation of RhD negative patients

A
  • Transfuse blood of same RhD group

- Group O negative blood

20
Q

Steps needed to provide ABO and Rh compatible b

Pod

A

Test ABO and RhD blood groups of patients red cells and an antibody screen on the patients plasma ( group and screen),

21
Q

How is an antibody screen performed

A
  • Patient plasma is incubated with 2 or 3 different fully typed’screening’ red cells, which are known to possess all the blood group antigens which matter clinically.
    * If the antibody screen is negative, any donor blood which is ABO & RhD compatible can be given.
    * If the antibody screen is positive, the antibody must be identified with the use of a large panel of red cells. Donor units of blood that lack the corresponding blood group antigen are then chosen for cross matching with the recipient’s plasma prior to transfusion.
22
Q

Compatibility testing before transfusing patients

A

. Patient blood sample (plasma + cells).
• ABO group (test patient’s red cells with known anti-A and anti-B reagents).
• RhD group (test patient’s red cells with known anti-D and reagent).
• Select donor blood of the same ABO & RhD group.
• Antibody screen +/- antibody panel, to identify antibody/ies.
2​.Cross-match:patient’s serum mixed with chosen donor red cells - should not react: if reacts (agglutinates) = incompatible.
Blood with X antigens will agglutinate with an anti-X reagent.

23
Q

Why may blood donors be excluded

A

if they have any disease that might make blood donation hazardous for them, e.g. cardiovascular/ neurological disease, or if their blood would be hazardous for the recipient (risk of viral, bacterial or parasitic infections, certain diseases or drugs).
Donor education and self-exclusion of individuals who are at high risk of having contracted blood-borne infectious diseases are essential to ensure that individuals who are in an early infectious stage, in whom the infection is not yet detectable by any test (i.e. in the’window period’of infection) do not donate.

24
Q

Infection testing done on all blood samples

A

HIV, hep B , hep C , hep E , HTLV and Syphillis

25
Q

Infection testing done on some samples

A

CMV, T.cruzil, Malaria. Blood test to exclude vCJD is not yet available

26
Q

How is blood separated

A

450 ml of blood is collected from donor into a sterile plastic bad containing an anti-coagulants and centrifuged. Not efficient to use whole blood as patients only need one component. Eg. When giving anemic patients red cell transfusion, they don’t need the excess fluid contained in the plasma part as this puts them at risk of fluid overload.

So whole blood is centrifuged into three parts:
Red cells bottom
Platelets middle
Plasma top
( then squeeze each layer into satellite bags and cut free)

27
Q

What could red cells given be used to treat

A

Anaemia without volume deficiency

28
Q

What could platelets given be used to treat

A

Platelet deficiency

29
Q

What could FFP given be used to treat

A

Any coagulation factor decline

30
Q

What could cyroprecipitate given be used to treat

A

Factor 8, VWF , 13 deficiency, fibrinogen , fibronectin ( made from FFP)