Blood products and transfusion Flashcards

1
Q

What are the two main components of blood?

A

Cellular elements (RBCs, WBCs, platelets) and plasma.

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2
Q

What happens when blood is centrifuged?

A

Plasma rises to the top, solutes settle to the bottom, platelets in the middle.

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3
Q

What is the effect of high cholesterol on centrifuged blood?

A

Fat gel layer may form on top.

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4
Q

What are the blood types and Rh factor percentages?

A

Types: A, B, AB, O; Rh+ ~85%, Rh- ~15%.

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5
Q

Why is Rh status important in transfusion?

A

Rh incompatibility can lead to fetal issues in pregnancy and immune responses.

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6
Q

What is the universal donor and recipient?

A

Universal donor: O negative; Universal recipient: AB positive.

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7
Q

Why are females of childbearing age typically given O negative blood?

A

To prevent Rh sensitization and future fetal hemolytic disease.

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8
Q

What is the purpose of a type and screen?

A

Identifies ABO/Rh and screens for antibodies/antigens.

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9
Q

Why can type and screen take time?

A

Screening for hundreds of possible antibodies can delay processing.

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10
Q

Why is type and screen important for high-risk surgeries?

A

Prepares for potential transfusion and avoids emergency uncrossmatched transfusions.

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11
Q

What transfusion fluid was used in WWI/Vietnam?

A

Whole blood.

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12
Q

What replaced whole blood in the 1970s-1990s?

A

Component therapy (RBCs, FFP, etc.).

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13
Q

Why was normal saline originally used?

A

Rehydration for cholera, not designed for resuscitation.

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14
Q

What are the problems with crystalloid resuscitation?

A

Dilutes blood, causes inflammatory response, and disrupts microclots.

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15
Q

What are the four main blood components?

A

PRBCs, FFP, Cryoprecipitate, Platelets.

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16
Q

What is LTOWB?

A

Low Titer O Whole Blood – screened for minimal antibodies.

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17
Q

What does CPDA-1 do in blood storage?

A

Citrate chelates calcium, phosphate buffers, dextrose is fuel, adenine extends ATP production.

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18
Q

What happens to 2,3-DPG in stored blood?

A

Decreases over time, shifting O2 curve left and impairing oxygen delivery.

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19
Q

How are PRBCs prepared?

A

By removing 200-250mL plasma from whole blood.

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20
Q

What is the volume of PRBCs?

A

Typically 200-350mL.

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21
Q

What is the effect of PRBC transfusion?

A

Increases Hb by ~1g/dL and Hct by 3%.

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22
Q

Do PRBCs contain platelets or granulocytes?

A

No.

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23
Q

How is FFP prepared?

A

Plasma removed from WB within 8 hours, frozen at -18°C.

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24
Q

What is in FFP?

A

Water, carbs, fats, minerals, clotting proteins (stable and labile).

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25
Q

How much FFP is needed to raise clotting levels?

A

10–15 mL/kg raises factors by ~2-3%.

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26
Q

What is cryoprecipitate?

A

Protein-rich fraction from thawed FFP containing Factor VIII, vWF, fibrinogen, Factor XIII.

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27
Q

When is cryo used?

A

Massive transfusion, congenital bleeding disorders, fibrinogen replacement.

28
Q

How are platelets prepared?

A

From PRP or apheresis, then re-centrifuged.

29
Q

What is the volume of apheresis platelets?

A

250-300mL.

30
Q

How much does one unit of platelets increase PLT count?

A

5,000-10,000.

31
Q

How do pooled platelet units affect PLT count?

A

6-pack or 10-pack increases PLT by 60,000–100,000.

32
Q

Why should platelets not be warmed?

A

Causes aggregation; academic importance.

33
Q

What fluids are safe with blood transfusion?

A

Normal saline, Normosol, or PlasmaLyte.

34
Q

Why avoid Lactated Ringers with blood?

A

Contains calcium which can cause clotting.

35
Q

Why must blood be warmed?

A

To prevent hypothermia and coagulation impairment.

36
Q

What devices are used to warm blood?

A

Belmont, Level 1, Ranger, others.

37
Q

Why is whole blood advantageous?

A

Fewer additives, superior coagulation, easier logistics.

38
Q

How does whole blood compare to component therapy?

A

Less diluted, better platelet & factor levels, single product.

39
Q

What causes hypocalcemia during transfusion?

A

Citrate binds ionized calcium (iCa).

40
Q

What are signs of transfusion-induced hypocalcemia?

A

QT prolongation, seizures, ↓ cardiac output.

41
Q

When should calcium be replaced?

A

Every 4 units of blood; monitor iCa.

42
Q

Which calcium replacements are used?

A

Calcium chloride or gluconate.

43
Q

What are signs of hemolytic transfusion reactions?

A

Fever, chills, hypotension, dyspnea, hemoglobinuria.

44
Q

What mediates acute hemolytic reactions?

A

IgM antibodies and complement.

45
Q

What are symptoms of allergic transfusion reactions?

A

Itching, urticaria, erythema, anaphylaxis.

46
Q

What is TRALI?

A

Acute lung injury within 6 hours of transfusion, non-cardiogenic.

47
Q

What are TRALI signs?

A

Hypoxemia, bilateral infiltrates, no JVD, minimal diuretic response.

48
Q

What is TACO?

A

Volume overload causing pulmonary edema.

49
Q

How do TACO and TRALI differ?

A

TACO has HTN, JVD, responds to diuretics; TRALI does not.

50
Q

What causes delayed hemolytic reactions?

A

IgG antibodies.

51
Q

What is transfusion-associated GVHD?

A

Viable donor lymphocytes attack host; causes pancytopenia.

52
Q

How is GVHD prevented?

A

Irradiated cellular products.

53
Q

What is post-transfusion purpura?

A

Antibodies against platelets cause thrombocytopenia.

54
Q

What are signs of bacterial contamination in blood?

A

Fever, shock, hemoglobinuria.

55
Q

What causes it?

A

Gram-negative endotoxins; improper handling.

56
Q

What is transfusion-induced hemosiderosis?

A

Iron overload from repeated transfusions.

57
Q

How is hemosiderosis managed?

A

Chelation therapy or reduced transfusion frequency.

58
Q

What qualifies as an adult massive transfusion?

A

Replace total blood volume in 24h, 50% in 3h, or 4 units in 4h.

59
Q

What is the standard MTP ratio?

A

1:1:1 PRBCs : FFP : Platelets.

60
Q

Why is whole blood better in MTPs?

A

Higher hemostatic potential, fewer additives.

61
Q

What are key TEG parameters?

A

R-time, K-time, MA, Ly30.

62
Q

What does a prolonged R-time indicate?

A

Coagulation factor deficiency; give FFP.

63
Q

What does low MA mean?

A

Platelet dysfunction; give platelets.

64
Q

What does rapid clot lysis (Ly30) suggest?

A

Hyperfibrinolysis; give cryoprecipitate.

65
Q

What are initial steps after suspected transfusion reaction?

A

Stop transfusion, keep IV open, notify blood bank, send blood/urine samples.

66
Q

Why should you be cautious declaring a transfusion reaction?

A

It may delay further transfusions crucial for patient survival.