W03_14 Principles of transfusion Flashcards

1
Q

what’s special about group AB individuals?

A

they are universal RBC recipient, and universal serum donor

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2
Q

what’s special about group O individuals?

A

they are universal RBC donor, and universal serum recipient

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3
Q

what do anti-A or anti-B agglutinins do?

A

potent activators of the complement cascade that causes hemolysis

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4
Q

how do people normally get blood minor group antibodies?

A

some sort of foreign blood exposure, like needlestick, transfusion, pregnancy, etc.

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5
Q

what’s delayed hemolytic transfusion reaction?

A

hemolysis occurring 4-11 days after transfusion, due to minor group incompatibility

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6
Q

what’s hemolytic disease of the newborn?

A

when a fetus has incompatible minor group matching with the mother, who had the antibodies from a previous exposure (i.e. first pregnancy), and sends them across the placenta to destroy fetal RBCs

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7
Q

why do you see RBC agglutination in major group incompatibility?

A

the antibodies are usually IgM molecules

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8
Q

why don’t you see RBC agglutination in minor group incompatibility?

A

the antibodies are usually IgG molecules

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9
Q

what’s Coombs’ test?

A

antiglobulin test - adding antibodies to some blood. if there are existing antibodies attached, then they will agglutinate

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10
Q

what’s the direct antiglobulin test?

A

mix antibodies directly with erythrocytes; shows that erythrocytes had antibody bound to them already

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11
Q

what’s the indirect antiglobulin test?

A

mix plasma with erythrocytes, then add the antiglobulin; shows that plasma had anti-erythrocyte antibodies

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12
Q

what’s the most important minor group antigen?

A

RhD (rhesus factor D). this is the most common cause of hemolytic disease of the newborn

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13
Q

note: RhD- patients are give RhD- blood only.

A

also note: RdD- mothers with RhD+ fetuses are given Ig against RhD to protect the baby

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14
Q

when do we match minor group negative blood other than RhD?

A

only when the person already has an antibody to it, since the reaction is not often severe

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15
Q

what’s the difference between the blood cross-match testing versus and antibody screen?

A

the cross-match tests the actual unit of blood to be given

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16
Q

in an emergency with no ideas of the type of patient blood, what’s the safest type of blood to give?

A

O-neg

17
Q

what molecule do we add to blood to prevent it from clotting?

A

citrate;

binds the calcium in the blood

18
Q

what are some additives we put into blood donations to keep the RBCs alive?

A

glucose;

also: adenine and phosphate

19
Q

how do we protect against contamination of donated blood units?

A

impossible for 100% sterility, so we try aseptic collection and storage, and keep refrigerated

20
Q

how do we deal with the issue of short supply?

A

pay donors;

advertise and promote altruism

21
Q

what’s the major issue with platelet donations?

A

they’re short-lived (short half life) and so are always in demand

22
Q

what is the important component of plasma donations?

A

coagulation factors (VIII, V, fibrinogen)

23
Q

how long can plasma be stored?

A

1 year @ < 18C

24
Q

what do we get from fractionated plasma products?

A

albumin, factor VIII, IX, XI, immunoglobulin; can be kept for years via lyophilization

25
Q

note: one vial of RhD antibody comes from 60,000 donors

A

okay

26
Q

what’s apheresis?

A

collection of a single blood component from a single donor, replacing the rest into the donor body