Haem: Blood Tranfusions Pt.4 Flashcards

1
Q

Describe the storage and shelf-life of platelets.

A

Stored at 22 degrees for 7 days

NOTE: they are screened for bacteria before release

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2
Q

What are clincial features of anaphylactic reaction to blood products.

A

Severe and life-threatening reaction that starts soon after start of transfusion

  • Occurs within seconds/minutes
  • Drop in BP
  • Rise in HR
  • Very breathless with a wheeze
  • Laryngeal or facial oedema

NOTE: most allergic reactions to blood products are not this severe

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3
Q

What is the mechanism of anaphylactic reaction to blood products?

A

Caused by IgE-mediated mast cell degranulation

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4
Q

Which patient group is more likely to have severe allergic reactions to blood products?

A

IgA deficient patients - anti-IgA antibodies may develop in response to exposure to IgA in donor’s blood

Most likely to occur with plasma transfusion

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5
Q

What are the signs of transfusion associated circulatory overload (TACO)? When does it present?

A

Signs are due to pulmonary oedema/fluid overload

  • SoB
  • Low oxygen saturations
  • High HR
  • High BP
  • Raised JVP

Usually caused by a lack of attention to fluid balance (especially in cardiac failure, hypoalbuminaemia, extremes of age)

Presents within 6 hours of transfusion

NOTE: this is the most common pulmonary complication to transfuson

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6
Q

What are the CXR features of TACO?

A

Fluid overload

Cardiac failure

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7
Q

What are the main clinical features of TRALI?

A

Looks like ARDS

  • SoB
  • Drop in oxygen saturation
  • Rise in HR
  • Rise in BP
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8
Q

What CXR features would you expect to see in TRALI?

A

Bilateral pulmonary infiltrates within 6 hours of transfusion, NOT due to circulatory overload and other causes.

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9
Q

Outline the mechanism of TRALI.

A
  • Anti-WBC antibodies (HLA or neutrophil) in donor blood interact with WBC in the patient
  • Results in release of neutrophil proteolytic enzymes and toxic oxygen metabolites in the pulmonary vasculature
  • This leads to lung damage

Mechanism actually not fully understood

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10
Q

What are the main differences between TACO and TRALI?

A

JVP - raised in TACO, not in TRALI
Furosemide - response in TACO, not in TRALI

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11
Q

How can TRALI be avoided?

A

Using male donors (haven’t been pregnant) who haven’t had a transplant or transfusion so they will not have produced antibodies against HLA

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12
Q

What is alloimmunisation?

A
  • The process of developing antibodies against an antigen
  • 1-3% of people receiving transfusions will develop antibodies against an RBC antigen that they lack
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13
Q

What are the consequences of alloimmunisation with regards to blood transfusions?

A

Delayed haemolytic transfusion reaction
- Repeat transfusion with blood containing the antigen will lead to extravascular haemolysis

  • This is IgG mediated so will take 5-10 days
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14
Q

What are the typical blood test results you expect to see during a haemolytic episode?

A
  • High bilirubin
  • Low haemoglobin
  • High reticulocytes
  • High LDH
  • Positive DAT
  • Haemoglobinuria (for a few days until haemolysis stops)

NOTE: U&E should be tested to check for renal failure. Also group and screen should be repeated to check for the development of new antibodies

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15
Q

In which patient groups is CMV dangerous?

A
  • Very immunosuppressed (e.g. SCT)
  • Pregnant women
  • Neonates

Usually removed by routine leukodepletion

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16
Q

What is the dangerous effect of parvovirus infection?

A

Causes temporary red cell aplasia

17
Q

Which patients are most affected by parvovirus infection?

A
  • Foetuses
  • Patients with haemolytic anaemia (e.g. sickle cell disease)
18
Q

What precaution can be made by blood donation services to prevent transmission of vCJD?

A

Blood services exclude people who have had transfusions in the past as donors.

19
Q

Describe the mechanism of transfusion-associated GvHD

A
  • Donor blood will contain some lymphocytes that are capable of dividing
  • Normally, the patient’s immune system will recognise and destroy these foreign lymphocytes
  • In the very immunosuppressed patients, the donor lymphocytes are not destroyed
  • They begin to recognise patient HLA as foreign and begins attacking it
  • This damages the gut, liver, skin and bone marrow

NOTE: this is always fatal

20
Q

What are the clinical manifestations of transfusion-associated Graft-versus-Host disease?

A
  • Severe diarrhoea
  • Liver failure
  • Skin desquamation
  • Bone marrow failure

Death then occurs within weeks to months