Blood products and transfusions (3) Flashcards

1
Q

Blood compositon

A
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2
Q

What percent of blood is plasma?

A

55%

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3
Q

What percent of blood is formed elements?

A

45%

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4
Q

What is the makeup of plasma?

A
  • Proteins 7%
  • Water 92%
  • Other solutes 1%
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5
Q

What is the makeup of formed elements?

A
  • Platelets (140k-340k)
  • Leukocytes (5k-10k)
  • Erythrocytes (4.2-6.2 million)
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6
Q

What proteins are in plasma?

A
  • Albumin
  • Globulins
  • Fibrinogen
  • Prothrombin
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7
Q

What are the “other solutes” in plasma?

A
  • ions
  • nutrients
  • waste products
  • gases
  • regulatory substances
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8
Q

Rh factor percentage:

A
  • Rh+ = ~85%
  • Rh- = ~15%
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9
Q

What can cause a shift to the right on the oxyhemoglobin dissociation curve?

A
  • decreased pH (increased acid)
  • Increased CO2
  • increased temperature
  • increased 2,3 DPG
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10
Q

Blood Typing:

A
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11
Q

Blood compatibility (memorize)

A
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12
Q

Contents and use for whole blood:

A

Contents: all cells, platelets, clotting factors and plasma

Use: replace blood loss from hemorrhage

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13
Q

Contents and use for PRBCs:

A

Contents: red blood cells and some plasma

Use: replace blood cells in anemic patients

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14
Q

Contents and use for platelets:

A

Contents: thrombocytes and some plasma

Use: Replace platelets in a patient with thrombocytopenia

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15
Q

Contents and use for FFP:

A

Contents: plasma, a combination of fluid, clotting factors and protein

Use: replace volume in a burn patient or in hypovolemia secondary to low oncotic pressure

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16
Q

Contents and use for clotting factors:

A

Contents: specific clotting factors needed for coagulation

Use: replace factors missing due to inadequate production as in hemophilia

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17
Q

RBC and platelet specific gravities:

A

RBC: 1.08-10.9
Platelet: 1.03-1.04

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18
Q

Steps for separating a unit of whole blood:

A
  • The centrifuged product settle out into RBC, WBC and PRP
  • After separating PRP from the bag, PRP is centrifuged again for a longer time and is harder to spin
  • Platelets are heavier than plasma and will settle into the bottom of the bag
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19
Q

What is added to blood to help with storage?

What are their uses?

A

Citrate phosphate dextrose adenine

  • Citrate for chelation of calcium to prevent clotting
  • Phosphate as a buffer
  • Dextrose as a fuel source
  • Adenine as a substrate for the synthesis of ATP extending storage time from 21 to 35 days
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20
Q

What effect does blood storage have on oxygen delivery?

A

The longer blood is stored, the lower levels of 2,3 DPG are, which shift the oxyhemoglobin dissociation curve to the left and impairs oxygen delivery

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21
Q

PRBCs contain ____ unless they have been specifically ____.

A

Leukocytes; leukoreduced

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22
Q

How are PRBCs prepared?

A

By removing 200-250 ml of plasma from a unit of whole blood

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23
Q

Characteristics of PRBCs:

A
  • 1 unit = 200-350mL
  • Do not contain functional platelets or granulocytes
  • have the same O2 carrying capacity with whole blood
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24
Q

Why is PRBCs given to anemic patients?

A

Intended to increase the O2 carrying capacity in anemic patients who require an increase in their red cell mass without increasing their blood volume

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25
Q

How much does 1 unit of PRBCs increase hgb and hct?

A

1 unit = 1g/dL (10g/L) and hct by 3%

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26
Q

How is FFP prepared?

A

Removing plasma from whole blood within 8 hours of collection
- one bag is 200-250 mL

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27
Q

FFP is a good source of ____

A

antithrombin III

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28
Q

What is the dose for FFP?

A

10-15 mL/kg

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29
Q

Storage for FFP:

A
  • stored at -18C or below
  • expires 12 months after donation
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30
Q

1 unit of FFP increases ____

A

Level of each clotting factor by 2-3% in adults

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31
Q

FFP contains:

A

Water, carbohydrates, fats, minerals, proteins

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32
Q

How is cryo prepared?

A
  • Protein fraction taken off the top of the FFP when being thawed
  • then refrozen for up to 1 year
  • stored at -18C and below
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33
Q

What is in cryoprecipitate?

A
  • Factor VIII: C
  • Factor VIII: vWF
  • Factor XIII
  • Fibrinogen
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34
Q

How much does cryo increase fibrinogen?

A

Two units of cryo/10 kg of body weight increases fibrinogen concentration by 100 mg/dL (except for DIC or continued bleeding with massive transfusion)

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35
Q

Indications for the use of FFP:

A
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36
Q

Indications for use of cryo:

A
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37
Q

Indications for platelets transfusion:

A
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38
Q

How are platelets prepared?

A
  • Cytapheresis - by separating PRP from a unit of whole blood within 8 hours of collection and recentrifuged to remove plasma
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39
Q

How much does one unit of platelets increase levels?

A

one unit = increase platelets by 5-10,000

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40
Q

Why do you not want to give LR with blood products?

A

It has calcium in it so it can cause clotting

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41
Q

When would you use warming devices when administering blood products?

A
  • trauma patient receiving 4 or more units in 1 hour
  • 5 yo patient with a current temp of 98.1 receiving 2 units in 1 hour
  • a 90 yo patient with a temp of 97.5 receiving any unit
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42
Q

Preferred fluid for blood product administration:

A
  • Electrolyte-R pH 7.4 (normosol/plasmalyte)
  • Normal saline only used for priming blood tubing and flushing before and after
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43
Q

Indications for giving whole blood:

A

To maintain blood volume and O2 carrying capacity in acute or massive blood loss
- actively bleeding patient greater than 20% of body blood volume

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44
Q

Complications of blood transfusion:

A
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45
Q

Delayed complications of blood transfusion:

A
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46
Q

Mediators for a hemolytic transfusion reaction:

A

IgM A/b (usually ABO), complement

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47
Q

S/S for hemolytic transfusion reactions:

A

Fever (late), chills, hemoglobinemia, hypotension, dyspnea

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48
Q

Treatment and prevention for hemolytic transfusion reactions:

A

Decrease opportunities for error - treat ARF and DIC

49
Q

Nonhemolytic febrile transfusion reactions:

A
  • Mediators: A/b to HLA class I Ag
  • S/S: fever, chills
  • Treatment and prevention: antipyretics, leukocyte reduced
50
Q

What is the most common transfusion reaction?

A

Allergic transfusion reaction

51
Q

Mediators for allergic transfusion reactions:

A
  • Plasma proteins (mild reactions)
  • A/b to IgA (anaphylactic reactions)
52
Q

S/S of allergic transfusion reactions:

A

Urticaria, erythema, itching, anaphylaxis

53
Q

Treatment and prevention for allergic transfusion reactions:

A
  • Antihistamines
  • treat sx
  • transfuse IgA deficient components
54
Q

Noncardiogenic pulmonary transfusion reactions:

A

Mediators: donor/recipient WBC A/b
S/S: ARDS, fever, chill, cyanosis, hypotension, noncardiogenic pulmonary edema
Treatment and prevention: vigorous respiratory support (PEEP), steroids

55
Q

What is TRALI?

A

Acute lung injury that is temporally related to a blood transfusion - specifically it occurs within the first 6 hours following a transfusion

56
Q

Incidence and mortality for TRALI:

A

Incidence: unknown - but estimated to occur in 1:1300-5000 transfusions

Mortality: ranges from 5-25% with most patients recovering within 72 hours

57
Q

What is the criteria for TRALI?

A
  • Acute onset hypoxemia (cyanosis common)
  • P/F ratio <300 or SpO2 <90% on RA
  • Occurs within 6 hrs of transfusion
  • Bilat diffuse pulmonary infiltrates
  • No Left atrial hypertension (circulatory overload)
  • Fever common
  • Hypotension
58
Q

What percent of TRALI patients require mechanical ventilation?

59
Q

What might lungs of a patient with TRALI sound like?

A

Pulmonary crackles (and no signs of CHF/ volume overload)

60
Q

What are priority action if TRALI is suspected?

A
  • Stop transfusion
  • Support patient
  • If patient is intubated → obtain undiluted edema fluid ASAP (within 15 min) and plasma to see total protein
  • CBC/ CXR
  • Notify blood bank (request different unit and quarantine other units from same donor)
61
Q

What are some other issues that mimic transfusion reactions?

A
  • Sepsis
  • Hemoglobinuria (trauma, AKI, muscle damage)
62
Q

What are the causes of acute non-immunologic transfusion reactions?

A
  • Bacterial Contamination
  • Circulatory overload (TACO)
  • Hemolysis from physical/chemical means
63
Q

What mediators are involved in acute non-immunologic bacterial contamination of blood products?

A

Endotoxins produced by gram negative bacteria

64
Q

What are s/s of patient with bacterial contamination from blood products?

A
  • Fever
  • Shock
  • Hemoglobinuria
65
Q

What is the treatment of bacterial contamination from blood product?

A
  • IV ABX
  • Treat hypotension
  • Treat DIC
66
Q

What mediators are involved in transfusion associated circulatory overload (TACO)?

A

Fluid volume

67
Q

What are s/s or TACO?

A

*Cough
* Cyanosis
* Orthopnea
* Severe headache
* Peripheral edema
* Difficulty breathing

68
Q

How can TACO be prevented?

A
  • Give transfusion slowing in a small volume
69
Q

What causes physical/chemical hemolysis following a blood transfusion and what are the S/S?

A
  • Caused by exogenous destruction of RBCs
    *S/S: Hemoglobinuria
70
Q

What are the delayed immunologic reaction discussed in lecture?

A
  • Hemolytic transfusion reactions
  • Transfusion associated graft-vs host disease
  • Post transfusion purpura
70
Q

What is the treatment for physical/chemical hemolysis?

A

Document and rule out hemolysis d/t other causes

Treat DIC

71
Q

What type of blood transfusion reactions are the most common in the operating room?

A

Delayed complications

72
Q

What mediators are involved in hemolytic transfusion reactions?

73
Q

What are symptoms of hemolytic transfusion reactions?

A
  • Shortened RBC survival
  • Decreased Hgb
  • Fever
  • Jaundice
  • Hemoglobinuria
74
Q

How are hemolytic transfusion reactions treated/prevented?

A

Ig-negative blood for further transfusions

75
Q

What mediators area associated with transfusion related Graft-vs host disease?

A

Viable donor lymphocytes

(pancytopenia and hepatitis)

76
Q

What are S/S of transfusion graft vs host?

A
  • Fever
  • Skin rash
  • Desquamation (Skin peeling)
  • Anorexia
  • N/V/D
  • Hepatitis
  • Pancytopenia
77
Q

What is the treatment for transfusion associated graft vs host?

A

Gamma irradiation of cellular components

78
Q

What is the MOA of post-transfusion purpura?

A
  • Platelet specific antibody
79
Q

What are S/S of post transfusion purpura?

A
  • Thrombocytopenia
  • Clinical bleeding
80
Q

What is the treatment for post-transfusion purpura?

A
  • IV Ig
  • Plasma exchange
  • Corticosteroids
81
Q

How can we differentiate TRALI and TACO?

A

TACO→ no fever, HYPERtension, acute dyspnea, JVD can be changed, Rales and S3, diffuse b/l infiltrates, decreased EF, improvement with diuretics

TRALI→ fever, HYPOtension, acute dyspnea, JVD unchanged, Rales, diffuse b/l infiltrates, normal EF, No improvement with diuretics

82
Q

What is a delayed non-immunologic effect associated with blood transfusions?

A

Transfusion-induced Hemosiderosis (iron deposition)

83
Q

What is the MOA of transfusion-induced hemosiderosis? What are the s/s?

A

Iron overload

  • S/S: subclinical to death (usually people who are getting repeated transfusions)
84
Q

What is the treatment for transfusion induced hemosiderosis?

A
  • Decreased frequency of transfusion
  • Neocytes (young RBC that have longer life than RBC)
  • Iron chelation therapy
85
Q

What are the steps to follow if suspect blood transfusion reaction?

A
  • Discontinue the transfusion
  • Keep IV line open
  • Check all labels, forms, and Pt ID
  • Report to blood bank
  • Send requested blood samples
86
Q

What class of hemorrhage starts to affect BP?

A

Class 3 and 4 (BP starts to drop)

87
Q

What is the blood loss in mL for class 1-4?

A

Class 1: 750mL
Class 2: 750-1500mL
Class 3: 1500-2000mL
Class 4: >2000mL

88
Q

Which class of hemorrhage do you start giving blood products with crystalloids?

A

Class 3 and 4

89
Q

What is the purpose of MTP in adults?

A
  • Total blood volume is replaces within 24 hours
  • 50% of total blood volume replaced in 3 hours
  • Rapid bleeding rate= 4units RBC transfused w/in 4 hours or 150mL/min blood loss
90
Q

MTP in kids is >____ mL/kg transfusion.

91
Q

What blood products are used with MTP? What is the goal of MTP?

A

Balanced resuscitation→ 1:1:1 ratio of platelets: plasma: RBC

Goal is to get all the components back to whole blood

92
Q

What is blood component therapy?

A

Basically MTP (using multiple blood products to try to get back to whole blood ratios)

93
Q

Why is blood component therapy not as good as whole blood?

A

Blood component therapy= loss of coagulation factors and platelet function in reconstituted products→ can lead to increased anemia, thrombocytopenia, and coagulopathy

Requires multiple products= higher risk of infection from multiple donors

Products diluted with anticoagulants and additives

94
Q

Why is whole blood superior for hemostatic potential?

A
  • Less dilution from anticoagulants and additives than combination of 1:1:1
  • Higher platelet count in whole blood (200 vs 88)
  • Higher coagulation factor levels in whole blood (90% vs 65%)
95
Q

What products are given as 1st, 2nd, 3rd choice for low fibrinogen levels?

A

1) Cryo (2500mg)
2) Whole blood (1000mg)
3) FFP (400mg)

96
Q

How does stored whole blood (SWB) have to be stored/tested?

A
  • Cold: 2-6 degrees C
  • Storage: 21-35 days
  • Hemostatic capability: 14-21 days
  • Testing: same as blood components
97
Q

Which type of whole blood is the universal donor?

A

Low titer type O whole blood (LTOWB)

98
Q

What is the preferred resuscitation product?

A

Stored whole blood

99
Q

What is the protocol for trauma patients with unknown blood types?

A
  • Pre-transfusion blood sample (determine blood type
  • Additional transfusions require LTOWB or group O RBCs for 1month after initial transfusion
100
Q

What is the blood product of choice for males?
What is the blood product of choice for females of child bearing years?

A

Rh positive blood for males
Rh negative blood for females of child bearing years

101
Q

Why are there a limited number of centers in the US that provide whole blood transfusion for massive hemorrhage?

A

*Highly regulated process

102
Q

How long is LTOWB good for?

103
Q

What is the recommendation for WB in peds?

A

Few studies on WB In pediatric populations:

Age <15 or weight <40kg: Limit WB to 30mL/kg

104
Q

How much calcium gluconate has to be given to get the same effect as calcium chloride?

A

3x calcium gluconate = calcium chloride

105
Q

What are some clinical usages for calcium chloride?

A
  • Hypocalcemia
  • Long QTc
  • Decreased cardiac output
  • Coagulopathy
  • Seizures
106
Q

____% of trauma patients are hypocalcemic

107
Q

What is associated with sever hypocalcemia?

A
  • More coagulopathy
  • More blood transfused
  • Double mortality
108
Q

T/F: One unit of citrated blood product drops iCa?

A

True: Would be a good idea to replace calcium after one unit is transfused

109
Q

What is the lethal triad?

A
  • Hypothermia
  • Acidosis
  • Coagulopathy
110
Q

________ + _______ = decreased citrate metabolism

A

Hypothermia (caused by hemorrhage)
Liver injury

citrate is metabolized in the liver

111
Q

What are the different components of TEG?

A

R: reaction time
K: time to clot firmness
Angle: kinetics of clot development
MA: Maximum amplitude (Max clot strength)
LY30: Percent lysis 30 min after MA

112
Q

What does TEG stand for?

A

Thromboelastography

113
Q

What is the treatment for TEG-ACT >140?

114
Q

What is the treatment for TEG R-time >10?

115
Q

What is the treatment for TEG K-time >3?

116
Q

Treatment for TEG Angle <53?

A

Cryo +/- Platelets

117
Q

What is the treatment for TEG MA <50?

118
Q

What is the treatment for LY30 >3%