Transfusion Medicine Flashcards

1
Q

what factor has the shortest half life?

A

factor VII

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2
Q

half life of factor VII?

A

6 hrs

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3
Q

how to reverse warfarin

A

PCC (FEIBA)
vitamin K (IV faster than PO)
plasma can be given if other options are not available

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4
Q

what is in PCCs

A

human-derived coagulation factor concentrates - contains factor 2, 7, 9 and 10, protein C and S

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5
Q

volume of one unit of cryo

A

10-15 mL

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6
Q

infusion time of cryo

A

15-30mins for total dose

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7
Q

sepsis occurs most frequently with which blood product and why

A

platelets, because they are stored at RT

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8
Q

what is TRALI

A

acute respiratory distress with hypoxia and bilateral chest infiltrates on x-ray - occurs within 6 hrs of transfusion

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9
Q

when can transfusion associated GVHD occur?

A
  • immunocompromised recipient

- immunocompetent recipient transfused a haplo identical product

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10
Q

who should receive irradiated blood?

A
  • Congenital immunodeficiency states
  • Intrauterine and neonatal exchange transfusions
  • Pre-term infants
  • Patients with lymphoma
  • Post-transplant (bone marrow or stem cell)
  • Treatment with purine analogues (e.g. fludarabine)
  • Directed donations from family members
  • HLA-matched platelets
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11
Q

most common antigen causing anti-platelet antibodies post transfusion?

A

HPA-1a

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12
Q

most common viral infection transmitted by blood product in canada

A

west nile virus (< 1 in 1 million)
hepatitis B (1 in 1.7 million)
chagas (1 in 4 million)

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13
Q

components of cryoprecipitate

A

fibrinogen
factor 8
factor 13
vWF

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14
Q

what is the correlation between ABO antigen expression and VWF

A

people with blood type O have approx 25% less factor 8 and VWF

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15
Q

dosing of pRBCs and how much hemoglobin should increase

A

10-20 cc/kg (15 cc/kg) should increase hemoglobin by 10

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16
Q

dosing of platelets and how much count should increase

A

10 cc/kg should increase platelets by 50-100

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17
Q

FFP dosing and how much coagulation factors should increase

A

10-15 cc/kg should increase coagulation factors 15-20%

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18
Q

dosing of cryo and how much fibrinogen should increase

A

1 unit/10kg should increase fibrinogen by 0.5

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19
Q

which viruses are destroyed by viral inactivation?

A

encapsulated viruses (inactivation affects lipid membrane) such as HIV, hep B/C, HTLV, EBV, CMV

20
Q

at what age do isohemagglutinins develop?

A

usually between 4-8 months

altho small amounts can be detected at birth

21
Q

what is a type and screen

A

determines the person’s ABO blood group, Rh status and screens for antibodies against minor antigens

22
Q

what is a cross match

A

mixing of the person’s serum with the washed RBCs that they were matched with to ensure they do not agglutinate

23
Q

most common blood type?

A

O (approx 46% in canada)

24
Q

least common blood type?

A

bombay (no AB or H antigen, <1%)

followed by AB (approx 3%)

25
common clinical scenarios that can have a positive DAT (name 3)
delayed hemolytic transfusion reaction AIHA HDFN
26
what is the indirect antiglobulin test?
the patient's serum is incubated with RBCs that are known to express a certain antigen on their cell surface, then incubated with anti-human globulin - observed to see if they agglutinate (used to screen pregnant women for antibodies that can cause HDFN)
27
patient has anaphylaxis to blood products. how do you investigate IgA deficiency?
IgA level | anti-IgA antibodies
28
special prep for platelets in patient with anaphylaxis related to IgA deficiency
apheresis platelets from IgA deficient donor
29
special prep for RBCs in patient with anaphylaxis related to IgA deficiency
wash to reduce IgA levels significantly
30
two uses of PCC
- to reverse warfarin-related bleeding | - to treat bleeding in hemophilia B if purified factor is not available
31
when would you use activated PCC (FEIBA)
in patient with hemophilia A and inhibitor who is bleeding
32
how common is selective IgA deficiency?
range from 1/100 to 1/1000 (in canada, less common in asians)
33
components of whole blood
RBC plasma buffy coat (which contains platelets)
34
storage limit of platelets
5 days
35
which antigens are important in SCD population
Rh and Kell
36
what is the formula used to identify patients who are refractory to platelet transfusions
Correct count increments = platelet count increase x BSA x 10^11 / total platelet transfused
37
how can you prevent platelet refractoriness?
use ABO compatible platelets
38
treatment of platelet refractoriness
try using HLA matched platelets, crossmatch the platelets, give fresh platelets, ABO matched platelets
39
cause of febrile transfusion reaction
cytokines that are generated / accumulated during storage of blood products
40
three benefits of leukoreduction
1. transmission of CMV 2. alloimmunization of HLA antigens 3. prevent febrile transfusion reactions
41
what products are leukoreduced?
RBC and platelets
42
why is blood irradiated?
to prevent transfusion associated GVHD
43
what products are irradiated?
RBCs platelets granulocytes non-frozen fresh plasma
44
indication for CMV negative blood
patients receiving intrauterine transfusion
45
indications for cryopreservation of RBCs
rare blood types (ie bombay phenotype)
46
when evaluating an antibody panel, which antibodies have a dosage effect? (ie, if the antigen is heterozygous, it may be a false negative)
``` Rh (other than D) Kidd Duffy MNS ("R you KidDing Me?") ```