Lecture 9: Blood Component Therapy Flashcards

(54 cards)

1
Q

When is whole blood used?

A

actively bleeding patients
lost at least 25% of their blood volume
patients requiring exchange transfusion

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2
Q

What happens when whole blood is run out?

A

reconstituted whole blood may be used
(RBCs mixed with thawed type AB FFP from a different donor)

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3
Q

When are RBCs used?

A

oncology patients undergoing chemotherapy or radiation therapy
trauma patients
surgery patients
dialysis patients
premature infants
patients with sickle cell anemia

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4
Q

How does RBC transfusion affect the patient?

A

increases the patient’s hemoglobin approximately 1 g/dl and the hematocrit by 3 %

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5
Q

When are Leukocyte-Reduced RBCs used?

A

chronically transfused patients
patients having known febrile transfusion reactions

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6
Q

When is Leukoreduction (filtration) done?

A

72 hours from collection time

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7
Q

AABB Standards for Leukocyte-Reduced RBCs

A

85% of RBCs must remain
leukocytes must be reduced to less than 5x106 WBC/unit

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8
Q

What is added to Frozen RBCs

A

frozen by adding glycerol to prevent cell hydration and the formation of ice crystals that can cause cell lysis

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9
Q

What is done for frozen RBCs to be used?

A

Thawed
Glycerol Removed by washing the RBCs with a series of saline solutions
Must be used within 24 hours

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10
Q

What are washed RBCs used for?

A

Used for patients who have a reaction to plasma proteins
Used in infant or intrauterine transfusions

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11
Q

For washed RBCs, how much RBCs are lost?

A

10-20%

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12
Q

What are Irradiated RBCs used for?

A

prevents T cells proliferation using gamma radiation

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13
Q

What do T cells cause

A

caused graft-versus-host disease, with 90% of cases being fatal

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14
Q

What are platelets used for?

A

Use to control or prevent bleeding

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15
Q

When is the need for platelets indicated?

A

Indicated in patients with chemotherapy
post-bone marrow transplant patients
patients experiencing postoperative bleeding

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16
Q

Platelet concentrates

A

Contain approximately 5.5 x 1010 platelets/unit

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17
Q

Pooled platelets

A

choose one platelet bag of those to be pooled and empty content of other bags into it

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18
Q

What is the usual platelet order?

A

6-10 units

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19
Q

Plateletpheresis

A

HLA matched patients who receive numerous platelet transfusions can develop antibodies to the class I

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20
Q

What happens when HLA antigens are not matched?

A

platelets will not last for 5 days in the patient’s circulation

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21
Q

Purpose of FFP?

A

replace coagulation factors in the patient

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22
Q

When is the need for FFP indicated?

A

Bleeding patients who require factors II, V, VII, IX, and X
Abnormal coagulation due to massive transfusion
DIC when fibrinogen is > 100 mg/dL
Antithrombin III deficiencies
Patients on anticoagulants who are bleeding or require surgery

23
Q

Thawing process for FFP

A

in water bath at 30-37oC for 30-45 minutes in watertight container
agitators are preferred because the unit thaws faster

24
Q

Cryoprecipitated Antihemophilic Factor

A

It contains factor VIII, fibrinogen, Factor XIII, and von Willebrand factor

25
When is Cryoprecipitated Antihemophilic Factor used?
with factor XIII deficiency as a fibrin sealant
26
Pooled cryoprecipitate
pooled into one bag before transfusion thawed in a similar fashion to FFP before pooling
27
Fibrin glue
1-2 units of cryoprecipitate are mixed with thrombin and applied topically to the bleeding area
28
Granulocyte transfusions are considered?
rare and limited to septic infants
29
What is in a pheresis bag for Granulocyte Pheresis?
> 1.0 x 1010 granulocytes, platelets, and 20-50 ml of RBCs
30
How long does it take for cells to deteriorate in Granulocyte Pheresis?
2 hours
31
Labeling Current labeling requirements include
proper name unique number amount of blood collected amount and type of anticoagulant volume of component expiration date storage temperature ABO/D type reference to the “Circular of Information for the Use of Human Blood and Blood Components,” warning regarding infectious agents prescription requirements donor classification FDA license number if applicable
32
What are some additional labels that are needed?
Irradiated components- with facility name Autologous unit Circular of Information for the Ue of Human Blood and Blood Components” Pooled components: labels
33
Emergency Transfusions
Rapid loss of blood can result in hemorrhagic shock
34
Rapid blood loss symptoms
Hypotension, tachycardia, pallor, cyanosis, cold clammy skin, oliguria, decreased hematocrit, decreased (CVP), CNS depression, and metabolic shock
35
What is are the priority of acute blood loss?
Replace and maintain blood volume Make sure oxygen carrying capacity is adequate Maintain coagulation system integrity Correct metabolic colloid osmotic pressure
36
Massive transfusion
Replacement if a person’s entire blood volume (approximately 10 units) within 24 hours)
37
If time is not available to type the patient
type O, D negative blood is transfused into women of childbearing age Type O, D positive blood is transfused into me
38
What is one main difference with transfusing infants vs adults?
Smaller blood volume Transfusions are given in small volumes in multiple packs
39
Premature infants need transfusion to do what?
offset the effect of hemoglobin F in their system Since HbF doesn't give up O2 easily
40
Iatrogenic blood loss
blood taken from the neonate or infant for laboratory tests cause the neonate or infant to develop an anemia that may be severe enough to transfuse
41
Why use warmer bloods on infants?
Neonates and infants do not tolerate hypothermia liver’s inability to metabolite citrate anticoagulants and potassium
42
Liver transplant patients require large amounts of blood products because?
the liver produced many coagulation factors and cholesterol for RBC membranes
43
What type of transplants need ABO compatibility?
kidney, liver, and heart transplants
44
Progenitor cell transplants
Derived from bone marrow or umbilical cord blood
45
Wiskott–Aldrich syndrome (WAS
rare X-linked recessive disease
46
Wiskott–Aldrich syndrome (WAS) symtpoms
Eczema thrombocytopenia (low platelet count) immune deficiency bloody diarrhea
47
Fanconi Anemia
the result of a genetic defect in a cluster of proteins responsible for DNA repair
48
Fanconi Anemia symptoms
acute myelogenous leukemia (Most common) Bone marrow failure- about 90% 60-75% have congenital defects 75% have some form of endocrine problem
49
Therapeutic Hemapheresis
Replacement of blood from a patient to improve a patient’s health
50
Oncology
Chemotherapy drugs kill all cells that are undergoing mitosis
51
Action of chemotherapist drugs
Stopping DNA replication Interfering with mRNA production
52
Sickle Cell Anemia
abnormal hemoglobin (e.g., Hgb S) causes cells to be removed from circulation, resulting in a lowered hematocrit
53
Thalassemia
Decreased synthesis of the alpha and beta globin chains Hemolytic anemia results Transfusion support necessary
54
Aplastic Anemia
Blood transfusion support is usually needed until bone marrow transplant can occur