Blood Transfusions Flashcards

1
Q

Why should alternatives to transfusion be considered prior to each transfusion?

A

a) to conserve the blood supply

b) to increase patient safety by avoiding clinically non-essential exposure to donor blood.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

What is the first stage in processing blood after donation? What does this involve?

A

Leucodepletion –> whole blood is filtered before further processing to remove white cells

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

Why are WBCs removed during transfusion?

A

WBCs can carry infection or lead to transfusion reaction

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

After donation, what stage follows leucodepletion?

A

Blood is then separated into its components:
o RBCs
o Platelets
o Plasma

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

The plasma is then further separated.

What are the 3 forms in which plasma can then be given?

A
  1. Fresh frozen plasma (within 12 hours of donation)
  2. Cryoprecipitate
  3. Fractionation
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

What is cryoprecipitate?

A

This is manufactured from fresh, frozen plasma.

  1. Plasma is frozen and then defrosted at 4 degrees
  2. The bit of the plasma that melts at 4 degrees is collected –> this is the cryoprecipitate
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

What does cryoprecipitate contain?

A

Cryo is made from FFP which is frozen and repeatedly thawed in a laboratory to produce a source of concentrated clotting factors including Factor VIII, von Willebrand factor and fibrinogen.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

What is blood plasma fractionation?

A

The general processes of separating the various components of blood plasma:

 Clotting factors
 Albumin; may be given to patients with cirrhosis
 Immunoglobulins; may be given to immunocompromised
 Factor concentrates (FVIII, FIX, prothrombin complex)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

What is the most commonly transfused blood product?

A

RBCs

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

How long can RBCs be stored?

A

Stored at 4’C for up to 35 days from collection: most problems with blood will be due to incorrect storage

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

The plasma in RBC blood bags has been removed.

What is it replaced with? Why?

A

by a solution of electrolytes, glucose and adenine to keep the red cells healthy during storage

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

What is the usual transfusion time for RBCs?

A

1.30-3 hours

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

Haematocrit for RBC bags?

A

Haematocrit 60% (high volume of RBCs to total volume of blood)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

A 1 unit transfusion of RBCs is expected to raised Hb by what?

A

10 g/L

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

What are the 4 major indications for a RBC transfusion?

A
  1. Significant bleeding (based on volume of blood loss)
  2. Acute anaemia
  3. Acute anaemia with mild symptoms
  4. Chronic anaemia
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

When is RBC transfusion in acute anaemia given until?

A

Symptoms resolve

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
17
Q

When should you consider alternatives to transfusion in anaemia?

A

In treatable causes of anaemia:

  • Iron
  • B12
  • Folate
  • EPO treatment for patients with renal disease
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
18
Q

What is the overall purpose of RBC transfusion?

A

restore oxygen carrying capacity

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
19
Q

What is the adult therapeutic dose for platelets?

A

A pool of 4-6 donations, or a single apheresis donation

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
20
Q

What are the 2 methods of collection of platelets?

A
  1. Pooled platelets

2. Apheresis platelets

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
21
Q

Describe the ‘pooled platelets’ method of collection

A
  • 1 unit is produced from 1 unit of whole blood

- 4-6 of these units are pooled together (usually from 4 whole blood donors) in a single pack

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
22
Q

Describe the ‘apheresis’ method of platelet collection

A
  • Blood cycles through apheresis machine, platelets are removed, and all other constituents are returned to the donor (selective removal)
  • The amount of platelets collected with this procedure represents the equivalent of 4-6 units of random donor platelets
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
23
Q

What are the 2 major uses of platelet transfusion?

A
  1. Treatment of severe bleeding due to severe thrombocytopenia (low platelets) or platelet dysfunction
  2. Prevention of bleeding in in patients with thrombocytopenia/dysfunction, or prophylaxis for surgery
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
24
Q

What is thrombocytopenia?

A

Low platelets

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
25
Q

What would the platelet count need to be maintained above in:

a) massive haemorrhage/bleeding
b) critical site bleeding (CNS)

A

a) maintain platelet count >50x10^9/L

b) maintain >100x10^9/L

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
26
Q

What are the 3 major contraindications in platelet transfusion?

A
  1. Immune thrombocytopenic purpura
  2. Thrombotic thrombocytopenic purpura
  3. Heparin induced thrombocytopenia and thrombosis
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
27
Q

Transfusion time for platelet?

A

20-30mins/unit

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
28
Q

How are platelets stored?

A

Stored at 22’C on an agitator (risk of contamination by bacteria from donor’s are that can grow at storage temperature and be transmitted)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
29
Q

Shelf life of platelets?

A

5 days from collection

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
30
Q

What is fresh frozen plasma (FFP) comprised of?

A

Contains all clotting factors at physiological levels (these are most important)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
31
Q

Average units of FFP given during transfusion?

A

Give 4-6 for average adult, therapeutic dose is 12-15mL/kg (4 units of FFP for average adult)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
32
Q

Transfusion time of FFP?

A

30 mins/unit

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
33
Q

When is FFP thawed?

A

Immediately before use; 6 hours after thawing, the levels of the labile factors 5 and 8 begin to diminish

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
34
Q

What are the 3 major uses of FFP?

A
  1. Replace clotting factors in patients with multiple factor deficiencies (acquired coagulopathies)
  2. To treat significant bleeding in patients with abnormal clotting results
  3. To correct abnormal clotting results before invasive procedures
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
35
Q

What are 2 examples of multiple factor deficiencies (acquired coagulopathies)?

A
  1. Liver disease

2. Disseminated intravascular coagulation

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
36
Q

In which 3 situations would you NOT transfuse FFP?

A
  1. To treat single factor deficiencies where a factor concentrate is available e.g. haemophilia A
  2. To correct abnormal clotting in patients who are not bleeding/having procedures
  3. To reverse warfarin
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
37
Q

What clotting factors does warfarin inhibit (blood thinner)?

A

Warfarin inhibits clotting factors 2,7, 9 and 10 (people on warfarin are therefore deficient in these)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
38
Q

What is used to reverse warfarin instead of FFP?

A

Use Prothrombin complex concentrate instead –> This is a factor 9 (IX) complex, with a high concentration of vitamin K dependent factors 2, 9, 7, 10

39
Q

What is cryoprecipitate mainly used for?

A

High fibrinogen conc

40
Q

What does cryoprecipitate contain?

A

o Fibrinogen
o Von Willebrand factor
o Factors 8, 13

41
Q

Main use of cryoprecipitate transfusion?

A

Mainly used as a concentrated source of fibrinogen in acquired coagulopathies:

o Massive haemorrhage
o Disseminated intravascular coagulation (DIC)
o Liver failure

These patients will all have a LOW fibrinogen.

Therefore used in:

  1. Treatment of bleeding in patients with low fibrinogen: maintain fibrinogen >1.5g/L
  2. Prevention of bleeding in patients with low fibrinogen: maintain fibrinogen >1g/L

Do NOT use to correct low fibrinogen in patients that are not bleeding/having procedures

42
Q

How are Transfusion Transmitted Infections (TTI) mostly prevented?

A
  1. Donor questionnaire

2. Mandatory testing

43
Q

How is the transmission by transfusion of variant Creutzfeldt-Jakob disease (vCJD) prevented?

A

Leucodepletion (also import plasma from countries with low incidence of vCJD)

44
Q

How can blood components become contaminated after donation?

A
  • bacteria from the donor’s skin during collection
  • unrecognised bacteraemia in the donor
  • contamination from the environment

(The risk increases with storage after donation)

45
Q

What blood components are usually infected during donation? Why?

A

Platelets - stored at temperature of 22’C which favours the growth of bacteria

46
Q

What is febrile non-haemolytic transfusion reactions (FNHTR)

A

Complication of blood transfusion; due to build-up of cytokines or other biologically active molecules that accumulate during storage of blood components.

o Common
o Onset: during or soon after the transfusion
o Often a problem with platelets: 10-30% after a platelet transfusion and 1-2% after an RBC transfusion

47
Q

FNHTR is often caused by a problem with the…?

A

Platelets

48
Q

Onset of FNHTR?

A

during or soon after the transfusion

49
Q

Clinical features of FNHTR?

A

 Rise of temperature >1’C from baseline
 Rigors
 Tachycardia

50
Q

Treatment of FNHTR?

A

paracetamol, slow transfusion rate or mild or discard if temp rises >2^C or >39^C

51
Q

What is transfusion associated circulatory overload (TACO)?

A

Complication of blood transfusion; oedema develops primarily due to volume excess or circulatory overload

52
Q

Onset of TACO?

A

up to 24 hours after a transfusion

53
Q

Symptoms and signs of TACO?

A
Similar to LV failure.
Symptoms: 
	Sudden dyspnoea
	Orthopnoea
	Tachycardia
	Hypertension
	Hypoxemia

Signs:
 Raised BP
 Elevated jugular venous pulse

54
Q

Risk factors for TACO?

A
	Elderly patients
	Small children
	Patients with compromised LV function
	Large transfusion volume
	Increased rate of transfusion
55
Q

Prevention of TACO?

A

follow guidance on volume and rate of transfusion for each component

56
Q

Treatment of TACO?

A

O2, diuretics, monitor fluid balance

57
Q

What is the main cause of transfusion related deaths?

A

Pulmonary complications (e.g. TACO)

58
Q

Are TACo and FNHTR immunological or non-immunological complications of transfuion?

A

Non-immunological

59
Q

What is an acute haemolytic transfusion reaction?

A

Involve haemolysis of transfused red cells due to the presence of preformed antibodies against antigens that are expressed on the transfused RBC

60
Q

Most common cause of an acute haemolytic transfusion reaction?

A

ABO-incompatible transfusions

61
Q

Describe the haemolytic reaction if a patient with blood group A is transfused with blood group B blood

A

Patient is blood group A; has antigen-A on RBCs and have anti-B antibodies in blood

If patient transfused with blood group B; anti-B antibodies in patient blood will start to break new RBCs down and release free Hb in the circulation and activate complement system

62
Q

What does acute haemolytic transfusion reaction release into the blood?

A

Free Hb

63
Q

What are the 3 major deleterious effects of free Hb?

A
  1. Kidney damage
  2. Complement activation
  3. Nitric oxide depletion
64
Q

How can free Hb cause kidney damage?

A

tubular deposition of Hb causes oxidative damage to renal cells –> acute kidney injury

65
Q

How can complement activation due to free Hb cause:

a) fever, rigors, hypotension
b) bleeding?

A

a) endothelial cells –> cytokine shower
b) endothelial cells –> express pro-coagulant molecules –> clotting cascade is activated –> disseminated intravascular coagulation –> bleeding

66
Q

How can free Hb lead to NO depletion?

A

Free Hb binds to and inactivates nitric oxide leading to vasoconstriction, hypertension and angina

67
Q

Signs and symptoms of acute haemolytic transfusion reaction?

A
	Fever and chills
	Back pain
	Hypotension/shock
	Haemoglobinuria (may be first sign in anaesthetised patients)
	Increased bleeding (DIC)
	Chest pain
	Sense of impending death
68
Q

Onset of acute haemolytic transfusion reaction?

A

severe reactions may occur early in the transfusion (15 mins), but milder reactions may occur later, but usually before the end of transfusion

69
Q

Mortality rate of acute haemolytic transfusion reaction?

A

Fatal in 20-30% –> make sure you repeat cross-matching!

70
Q

What test is done to prevent adverse transfusion reactions?

A

Pre-transfusion testing

71
Q

What 3 aspects does pre-transfusion testing involve?

A
  1. Determine ABO group
  2. Determine Rh(D) group
  3. Test patient’s plasma for antibodies against other clinically significant blood group antigens (i.e. look for any other antibodies that you wouldn’t expect to find – blood group A patients should only have anti-B antibodies)
72
Q

During the plasma screen in pre-transfusion testing, what are the next stages if clinically significant non-ABO antibodies are detected?

A

antibody identification by testing the plasma against a panel of red cells containing all clinically significant blood groups –> find out what that antibody is reacting to

73
Q

What are potential causes of clinically significant non-ABO antibodies?

A

previous transfusion, pregnancy

74
Q

What is the final test done before transfusion of RBCs (after pre-transfusion testing)?

A

Compatibility testing

75
Q

What does compatibility testing involve?

A

The crossmatching of selected donor blood of appropriate ABO and RhD type for a patient requiring a blood transfusion.

Patient’s plasma is mixed with aliquots of the donor red cells to see if a reaction (agglutination or haemolysis) occurs

76
Q

If there is no reaction during compatibility testing, what does this mean?

A

RBC units compatible –> no risk of acute haemolysis

77
Q

If there is a reaction during compatibility testing, what does this mean?

A

RBC units incompatible –> risk of acute haemolysis

78
Q

What is a delayed haemolytic reaction?

A

o Due to post-transfusion formation of new immune IgG antibodies against RBC antigens other than ABO.
o Occurs more than 24 hours after the transfusion
o Onset: 3-14 days following a transfusion of RBC

79
Q

Clinical features of a delayed haemolytic reaction?

A

 Fatigue
 Jaundice
 Fever

80
Q

Laboratory findings in delayed haemolytic reaction?

A

 Drop in Hb – extravascular haemolysis
 Increased LDH
 Increased indirect bilirubin

81
Q

How can the diagnosis of delayed haemolytic reaction be confirmed?

A

direct and indirect anti-globulin test should be positive

82
Q

What is a direct anti-globulin test?

A

Testing to see if the RBCs are bound to antibodies (they shouldn’t be):

o incubate red cells with anti-human globulin reagent (antibodies which can recognise human antibodies).
o If the red cells of the patients have antibodies bound to the surface, the reagent will bind to these and cause agglutination.
o This will give rise to a positive test

i.e. is the patient’s blood attacking the new blood?

83
Q

Patient’s can have allergic reactions to transfused blood.

What are these due to?

A

Due to hypersensitivity of the recipient to transfused ‘random’ proteins

84
Q

Clinical features of allergic reactions to transfused blood?

A
o	Rash
o	Urticaria
o	Pruritis
o	Rigors and fever
o	Periorbital oedema
85
Q

What are allergic reactions to transfused blood most often due to?

A

Common transfusion reaction (1%), more often after transfusion of components that contain PLASMA:
o FFP
o Cryoprecipitate
o Platelets

86
Q

Treatment of allergic reactions to transfused blood?

A

antihistamines, steroids, slow rate/discontinue transfusion

87
Q

Allergic reactions to transfused blood can lead to anaphylactic reactions.

These are severe and life-threatening.

What are the signs and symptoms?

A

 Laryngeal oedema
 Bronchospasm
 Hypotension
 Swelling

88
Q

Risk factors for anaphylactic reactions to transfused blood?

A

patients with IgA deficiency who have anti-IgA antibodies –> can become allergic to IgA in blood product they are receiving

89
Q

Treatment for anaphylactic reactions to transfused blood?

A

ABCDE, IM adrenaline, antihistamine IV, steroid IV, fluid

90
Q

What is transfusion related acute lung injury (TRALI)?

A

Complication of blood transfusion

  1. Antibody in blood product which attacks WBCs of patient
  2. WBCs become activated
  3. Activated WBCs lodge in pulmonary capillaries
  4. Release substances that cause endothelial damage and capillary leak
91
Q

Transfusion of what is most common with TRALI?

A

transfusion of plasma rich components (platelets, FFP)

92
Q

Diagnosis of TRALI?

A
o	Clinical and radiological diagnosis
o	Sudden onset of acute lung injury occurring within 6 hours of transfusion
o	Hypoxemia
o	New bilateral chest X-ray infiltrates
o	No evidence of volume overload
93
Q

How to differentiate between TACO and TRALI?

A

o With both, patients present with respiratory distress due to acute onset pulmonary oedema.
o With TRALI, patients also often have hypotension and fever, and can have transient leukopenia.
o With TACO, one would typically expect hypertension and a lack of fever and leukopenia.

94
Q

Why is plasma used in UK only from male donors?

A

Plasma from female donors is not currently used because it is more likely to contain antibodies that could cause a serious reaction when given to a patient; females are sensitised to antigens during pregnancy