haemostasis 6: blood transfusion Flashcards

1
Q

what are the major blood groups?

A

ABO & RhD - A&B antigens on red cells formed by adding N-acetyl galactosamine / galactose sugar residue respectively onto a common glycoprotein and fucose stem on red cell membrane (O has neither A or B sugars - has stem only)

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2
Q

what is the pattern of inheritance for ABO?

A

A&B co-dominant, O recessive

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3
Q

A&B co-dominant, O recessive

A

whichever group is not present - IgM antibodies interact with corresponding antigen -> fully activates complement cascade -> haemolysis which is often fatal (in lab tests IgM cause agglutination with Abs - useful for testing blood group)

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4
Q

what is the pattern of inheritance for RhD?

A

autosomal dominant - D codes for D antigen on red cell membrane (d codes for no antigen) - 85% of people are RhD positive

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5
Q

what happens when RhD- people are given RhD+ blood?

A

IgG antibodies made - don’t activate whole complement cascade so response less severe than anti-ABabs

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6
Q

what happens if a pregnant woman produces antiRhD antibodies?

A

abs can cross placenta and cause haemolysis of foetal red cells -> anaemia -> after birth can cross blood-brain barrier and cause death

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7
Q

what other tests need to be done before transfusion re. antibodies in blood?

A

antibody screen - test patient plasma for other red cell antibodies (present in ~8% of population)

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8
Q

what happens to collected blood?

A

collected into bag with anticoagulant -> bag centrifuged -> each layer (red cells bottom, platelets middle, plasma top) squeezed into satellite bags -> cut free (closed system to avoid bacteria entering)

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9
Q

what happens to the plasma collected?

A

converted to: fresh frozen plasma (FFP) / cryoprecipitate - rich concentrated source of fibrinogen + FVIII / fractionation -> albumin / factors etc

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10
Q

how are red cells stored?

A

in a fridge (shelf life 5 weeks) - rarely frozen as it is less efficient but useful for rarer blood types as lasts longer

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11
Q

how is FFP stored?

A

frozen (shelf life around 2-3 years) -> thawed for ~30mins at body temp (can’t be heated as proteins will denature)

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12
Q

what are the indications for giving FFP?

A
  • if bleeding + abnormal PT/APTT tests

- reversal of warfarin eg for urgent surgery

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13
Q

how is cryoprecipitate stored?

A

frozen (made from FFP, shelf life around 2-3 years)

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14
Q

what are the indications for giving cryoprecipitate?

A

if massive bleeding and fibrinogen v low (genetic hypofibrinogenaemia rare)

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15
Q

how are platelets stored?

A

room temp & constantly agitated (shelf life 5 days as risk of baterial infection)

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16
Q

do you need to know the blood group of platelets?

A

yes - platelets have low levels of ABO on them so could be destroyed quickly & are stored in plasma with donor’s antibodies & can cause RhD sensitisation as there is some red cell contamination

17
Q

what are the indications for giving platelets?

A
  • patients with bone marrow failure
  • massive bleeding / acute DIC
  • low platelets + surgery needed
  • cardiac bypass for patient on antiplatelet drugs
18
Q

what are some of the products of blood fractionation?

A
  • factor VIII & IX (for haemophilia / VWD) - can be heat treated to kill viruses
  • immunoglobulins eg IVIg (soup of general antibodies) for pre-op patients with autoimmune conditions)
  • specific IM
  • albumin
  • useful in burns, plasma exchanges and more concentrated version for certain severe liver & kidney conditions
19
Q

what would exclude a person from becoming a potential donor?

A
  • infections eg hepB&C&E, HIV, syphilis
  • if they are at risk eg if they have had a heart attack
  • IV drug user
20
Q

what is prion disease?

A

neurodegenerative disease caused by prions (proteins) that cause incorrect folding of proteins
- vCJD disease in 4 people ever -> now all blood components have white cells filtered out