Transfusion Medicine Flashcards

1
Q

What is the purpose of trasfusing RBCs?

A

To increase O2 carrying capacity.

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2
Q

The most antigenic protein on the RBC surface is:

A

D antigen

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3
Q

a unit of packed RBCs (pRBCs), 250 ml, will increase Hb by ___ g/dL/

A

~1 g/dL

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4
Q

How long can you store pRBCs?

A

42 days

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5
Q

When is fresh frozen plasma (FFP) indicated?

A

Usually to replace clotting factors

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6
Q

1 unit of plasma, 200-250 ml, will increase clotting factors by ___%?

A

~20%

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7
Q

FFP must be stored at this temp.

A

-20 C

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8
Q

Does FFP have to be ABO compatible? Why or why not?

A

Yes, all the donor’s Abs are present!

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9
Q

What are the cryoprecipitates and what is their use? Do they need to be ABO compatible?

A

Cryoprecipitate is a source of fibrinogen, factors VIII, XIII, vWF. 15 mL (1 unit) of cryoprecip. will raise fibrinogen levels by 5-10 mg/dL.
Does not have to be ABO compatible. Although they do express ABO antigens, this just results in a shorter life, but does not impair their utility for treating an acute bleeding episode.

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10
Q

When is a platelet transfusion indicated?

A

To stop bleeding when a pt has a low platelet count (thrombocytopenia)
Rarely, to prevent bleeding when pt is thrombocytopenic

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11
Q

1 unit of platelets (300 mL) will increase platelet count by ~ ____K/uL (normal count is 150-450 K/uL).

A

~25K/uL

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12
Q

Can you refrigerate platelets?

Must they be ABO compatible?

A

No. Room temp storage life is only 4-5 days.

Does not need to be ABO compatible, no plasma/RBCs present.

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13
Q

What is the “O” antigen of RBCs?

A

The basic structural core of complex carbohydrates present on ALL RBCs. Everyone has the O antigen!

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14
Q

What is responsible for the variable blood types among humans?

A

Your genome encodes an enzyme, called ABO glycosyltransferase, which can attach a sixth sugar to the O antigen. Multiple alleles (variants) of the gene for this enzyme in the human gene pool. Fall into 3 classes, each transfers a different combination of A, A&B, B, or just O.

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15
Q

What is the genetic combination of alleles that yields an A, B, AB, or O blood type?

A
2 O alleles = type O
2 A alleles = type A
2 B alleles = type B
1 O + 1 A = type A
1 O + 1 B = type B
1 A + 1 B = type AB
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16
Q

What happens if a recipient is transfused with ABO-incompatible red cells?

A

They have Abs (IgM) to the antigens on the donor RBC surface.
Abs will fix complement > MAC complex > lysis
This is called an acute hemolytic transfusion reaction.
Can be fatal.

17
Q

What is the most antigenic protein on the red cell surface?

A

RhD

18
Q

Under what circumstances are pts determined to be RhD negative or D negative?

A

They have 2 deleted RhD alleles

19
Q

What is the most common RhD type? Pos/Neg

A

RhD neg

20
Q

Immunization of the mother during pregnancy to her fetus’s RhD can be prevented with:

A

administration of anti-Rh-gamma globulin

21
Q

Which RBC surface protein is the only antigen that we routinely characterize in both donor and potential recipients?

A

RhD

Over 80% of D (-) individuals transfused with D (+) red cells develop Abs

22
Q

What demographic NEVER is transfused with RhD positive blood if they are negative?

A

young girls and women of childbearing age

23
Q

Let’s say that your pt has an inherent lack of IgA, and receives a whole blood transfusion. What is a possible complication of them receiving another transfusion in the future?

A

If transfused after developing an Ab to IgA, they can have a severe, life threatening allergic reaction.

24
Q

What is a complication associated with multiple platelet transfusions?

A

Pts tend to become less responsive to platelet transfusions after 5-10 transfusions (i.e. their platelet counts stop going up much post transfusion).

25
Q

Is giving pRBCs indicated in an effort to expand blood volume?

A

No

26
Q

Does giving pRBCs promote wound healing?

A

No

27
Q

Is administering pRBCs indicated during or immediately after an acute MI? Why or why not?

A

Yes. Increased mortality at Hb < 10. Admin of pRBCs elevated Hb (O2 carrying capacity)

28
Q

What is an indication for plasma transfusion?

A

1) Replacing missing plasma proteins such as Factor VIII, or IX (hemophilias A & B), antithrombin III (rare pro-thrombotic condition), AdamTS13 deficiency (TTP)
Also, replacing multiple missing plasma proteins:
- Coumadin toxicity with bleeding

29
Q

What are 3 indications for platelet transfusion?

A

1) Treat ongoing hemorrhage in a thrombocytopenic pt (platelet count < 50K/uL)
2) Prevent hemorrhage in pts with severe thrombocytopenia (platelet cound <10K/uL)
3) Treat or prevent hemorrhage in pt with dysfunctional platelets (qualitative, not quantitative defect due to platelet inhibitory drugs and pts who have undergone cardiopulmonary bypass {more drugs})

30
Q

Name a few risks inherent to RBC transfusions.

A

Recipient immune response
Graft vs host disease
Volume overload
Transfusion transmitted infection

31
Q

List some pathological effects of an immune response to transfusion.

A

Acute hemolytic reaction
Production of an Ab to a minor red cell antigen
Urticarial reaction (hives) to transfused plasma
Febrile reaction to transfused leukocytes

32
Q

Why are sickle cell pts more at risk for an adverse event when transfused with RBCs?

A

~30% form Abs. Extended crossmatch should be standard of care. Includes:
ABO, Rh, RhCE, K compatibility

33
Q

What is a particular risk to immunocompromized pts receiving RBC transfusion?

A

Graft vs host disease. Always use leukoreduced or irradiated red cells for immunocompromized pts