Blood transfusion Flashcards

1
Q

3 times when we give red cells

A

Symptomatic anaemia

If significant bleeding anticipated, activate major haemorrhage protocol

Exchange transfusion

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2
Q

what does FFP contain?

A

all clotting factors

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3
Q

when do we give FFP

A

Given for coagulopathy with associated bleeding

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4
Q

what does cryoprecipitate contain?

A

Contains Factor VIII, VWF and fibrinogen

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5
Q

how long does a grouping test take?

A

5-10mins

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6
Q

how long does a full crossmatch take?

A

30-40mins

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7
Q

when do you declare code red?

A

Definition is a sudden and continuing blood loss of > 2 litres

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8
Q

when is major haemorrhage protocol activated

A

systolic BP <90
unresponsive to fluid bolus
suspected or confirmed haemorrhage

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9
Q

how does blood grouping occur in the lab?

A

test pt’s red cells with anti-A, B and D. Agglutination shows that a particular ag is on the red cell, no antigen shows the antigen is absent.

Tets the pt’s plasma with A cells and B cells. Agglutination shows that a particular antibody is in the plasma or serum. No agglutination shows the ab is absent

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10
Q

Main indications for platelet transfusion

A

Prevention and treatment of haemorrhage in patients with thrombocytopenia or platelet function defects.

Platelet transfusions are not indicated in all causes of thrombocytopenia and may indeed be contraindicated in certain conditions.

The cause of the thrombocytopenia should be established before a decision about the use of platelet transfusion is made.

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11
Q

specific indications for platelet transfusion

A

Active bleeding and platelet counts <50 x 109/L

Invasive procedures with platelet counts <50 x 109/L

Coagulopathy or bleeding in a critical site (i.e. CNS, lungs) may require transfusion at higher levels

Prophylaxis in patients with platelet count < 10 x 109/L and failure of platelet production (BMT, MDS, etc)

Platelet count 10-20 x 109/L with failure of platelet production and additional risk factors (fever)

Active bleeding in association with a platelet qualitative defect

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12
Q

indications for FFP

A

Bleeding due to multiple factor deficiencies:

DIC with bleeding – (NB not indicated in absence of bleeding)

Massive transfusion/surgical bleeding (with abnormal clotting tests due to dilution or consumption of clotting factors)

Clotting factor deficiencies where no concentrate exists (eg Factor V)

Plasma exchange in TTP

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13
Q

CIs for FFP

A

FFP should not be used as a volume expander or a protein supplement

FFP does not reverse the effects of heparin and is not indicated in patients with prolongations of their aPTT or PT due to lupus anticoagulants.

FFP should not be used prophylactically for expected massive transfusion or following cardiac bypass.

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14
Q

how do we categorise transfusion reactions

A

Acute: during or within 24 hours of a blood transfusion

Delayed: occurring more than 24 hours after transfusion

Immune-mediated
Non immune-mediated

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15
Q

example of acute transfusion reactions

A
Acute haemolytic 
Febrile non-haemolytic
Urticarial
Anaphylactic 
TRALI
TACO
Acute hypotensive
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16
Q

example of delayed transfusion reaction

A
Delayed haemolytic
Post-transfusion purpura
GVHD
Transmission of infectious diseases
Iron overload
17
Q

what causes an acute haemolytic reaction?

A

alloantibodies against transfused red cells

18
Q

what causes febrile (non-haemolytic) reactions

A

Caused by antibodies in the patients’ plasma reacting against proteins in the donors’ blood

19
Q

how do we avoid febrile reactions?

A

leucodeplete blood

20
Q

how do we treat febrile reactions

A

stop the transfusion

give antipyretic and piriton

21
Q

signs and symptoms of an acute transfusion reaction

A
Increased temperature of  1°C to 2°C - fever
Urticaria
Rash
Pruritus
Pyrexia, rigors
Hypotension
Loin/Back pain
Increasing anxiety
Respiratory distress
Dark urine
Severe Tachycardia
Unexpected bleeding (DIC)
Feeling of impending doom
22
Q

what does TRALI stand for?

A

Transfusion Related Acute Lung Injury

23
Q

how do we manage TRALI

A
admit to ICU
aggressive ventilatory support
haemodynamic support 
no diuretics- underlying pathology involves microvascular injury rather than fluid overload
steroids uncertain