Transfusion Medicine Flashcards

0
Q

what is the clinical management of anemia rules, when to transfuse and when not to transfuse?

A

ASA: “RBC transfusion if rarely indicated when the Hgb concentration is greater than 10 and is almost always indicated when its less than 6”

Hct<21% is too low, and 30% is high enough

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1
Q

What are the most common causes of transfusion related reactions? What groups of ppl are most susceptible to each?

A

Minor allergic reaction (0.5-4%) - usually an isolated event
-rxn to donor proteins
-itch, swell, rash -> benedryl, steroids?
-Try saline washed RBCs
Febrile Reaction (0.1-2%)
-recipient Abs to donor WBC HLA proteins
-F/C, nausea,resp. distress, myalgias, HA
-Tx w/acetaminophen
-Distinguish from hemolytic rxn w/neg direct coombs test
-Try leukocyte reduced products
- Immunosupressed pts should get this

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2
Q

explain the body’s compensatory mechanisms to anemia.

A
  • increased cardiac output (Decreased SVR -> Inc SV)
  • CO redistribution (Brain, Heart > muscles, skin, viscera)
    • Coronary flow incr by up to 500%
  • Incr O2 extraction (but not in the heart)
  • Change O2-Hb affinity (Hgb < 9 -> R shifted curve)

The heart can get more blood flow but cannot incr the amount of O2 extracted. The liver, kidneys and brain can do a better job at extracting O2 from blood. Heart has ER of 55 to 70% at baseline.

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3
Q

Who can receive blood from whom?

A

Of course you can always give A blood to persons with blood group A, B blood to a person with blood group B and so on. But in some cases you can receive blood with another type of blood group, or donate blood to a person with another kind of blood group.

The transfusion will work if a person who is going to receive blood has a blood group that doesn’t have any antibodies against the donor blood’s antigens. But if a person who is going to receive blood has antibodies matching the donor blood’s antigens, the red blood cells in the donated blood will clump.

O has no antigens, so it is the universal donor. Anyone can receive it bc there is no such thing as anti-O antibodies. But O can only receive O because it has anti-A and anti-B antibodies

AB has no antibodies so it can accept any type of blood and is the universal recipient. It has both A and B antigens.

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4
Q

Does FFP need to be ABO and Rh compatible?

A

FFP does not need to be cross-matched but should be ABO compatible. Group O FFP only should be transfused to group O recipients but O can receive A,B,AB,and O plasma. It is the universal recipient. This is opposite from PRBC compatibility. AB is the universal FFP donor but can only receive AB FFP.

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5
Q

What are the universal donors and recipients for pRBCs and FFP?

A

pRBCs - universal donor = O
- universal recipient = AB

FFP - universal donor = AB
- universal recipient = O

O has no antigens (receptors) and both A and B antibodies
AB has both A and B antigens (receptors) and no aantibodies

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6
Q

What is the difference between type and screen and type and cross?

A

Type and screen determines the pts ABO and Rh type. It also tests for about 25 specific antibodies that are clinically significant. Type and cross goes a step further to determine if there are any antibodies in the recipients serum that is going to react with the donors RBCs.

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7
Q

What is the difference between Rh+ and Rh- blood?

A

Rh + blood - D-antigens (85% of the population)
Rh - blood - anti-D antibody develops with exposure to Rh+

RH+ means that a person carries the RH atntigen. Rh- means that the person does not carry the RH antigen

The Rh factor assumes a special importance in maternal-fetal interactions. A mother who is Rh- can bear an Rh+ child if the father is Rh+ (either homozygous or heterozygous). Since there are no natural anti-Rh antibodies, this generally poses no special risk for the first pregnancy.

Many people also have a so called Rh factor on the red blood cell’s surface. This is also an antigen and those who have it are called Rh+. Those who haven’t are called Rh-. A person with Rh- blood does not have Rh antibodies naturally in the blood plasma (as one can have A or B antibodies, for instance). But a person with Rh- blood can develop Rh antibodies in the blood plasma if he or she receives blood from a person with Rh+ blood, whose Rh antigens can trigger the production of Rh antibodies. A person with Rh+ blood can receive blood from a person with Rh- blood without any problems

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8
Q

What are the 4 vitamin K dependent factors?

A

Factor II, VII, IX, X

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9
Q

What 4 factors are part of the extrinsic pathway?

A

Factors II, V, VII, X

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10
Q

Hemophilia A is characterized by what factor deficiency?

A

Factor VIII deficiency

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11
Q

What is the three step process for coagulation?

A

Activation, amplification and propogation

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12
Q

Factor IIa is also known as what?

A

Thrombin

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13
Q

Clotting factors are all inactive pro-enzymes that are all, with the exception of one factor, synthesized where? What is the exception?

A

All synthesized in the liver except for factor VIII

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14
Q

What is vWF deficiency characterized by?

A

poor platelet adhesion AND clinical hemophilia A

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15
Q

How does heparin effect coagulation?

A

It binds AT III (antithrombin III) and potentiates it. AT III inactivates thrombin, Factors XII, XI, X, IX