Blood Transfusion 2 Flashcards

1
Q

What are the critical points in transfusion?

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2
Q

How do we classify adverse reactions to transfusions? What form them?

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3
Q

What is the risk of dying from a transfusion?

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1/135705

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4
Q

How can acute reaction be detected early?

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5
Q

Describe febrile non-haemolytic transfusion reaction (FNHTRY).

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6
Q

Describe wrong blood.

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7
Q

Make an ABO compatibility chart.

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8
Q

Describe bacterial contamination.

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9
Q

How do we prevent bacterial contamination?

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10
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11
Q

Describe anaphylaxis

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12
Q

What is the most common type of complication

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13
Q

Describe TACO

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14
Q

What is a TACO checklist?

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15
Q

Describe TRALI.

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16
Q

Describe infections.

17
Q

What transfusion transmitted infections are checked for?

18
Q

Which viruses should we be cautious of when transfusing?

19
Q

Describe delayed haemolytic transfusion reaction.

20
Q

How do patients with delayed haemolytics transfusion present? How should they be managed?

21
Q

Describe Transfusion Associated Graft-Versus-Host Disease (TaGVHD).

22
Q

Describe post transfusion purpura.

23
Q

Describe iron overload.

24
Q

Describe haemolytic disease of newborn.

25
Describe the Mechanism of RhD sensitisation during pregnancy.
1st pregnancy - red cells from foetus crossing over to mother so mother forms anti-D. Mother and foetus fine 2nd pregnancy - anti-D (IgG antibodies) crosses placenta and destroyed foetus
26
What are the clinical features of HDFN?
* Only IgG antibodies can cross the placenta. * If mother has high levels of IgG antibody - it can destroy fetal red cells, if they are positive for the corresponding antigen * Fetal anaemia (haemolytic) * Haemolytic disease of newborn (anaemia plus high bilirubin - which builds up after birth as no longer removed by placenta)
27
What is the Treatment of pregnancy when mother already has red cell antibody
All pregnant women have G&S at around 12 weeks (booking) and again at 28 weeks to check for RBC Antibodies. If antibody present: * check if father has the antigen (so baby could inherit it) * monitor level of antibody (high or rising - more likely to affect fetus) * Check ffDNA sample * If have antigen: Monitor fetus for anaemia – MCA Doppler ultrasound * Deliver baby early, as HDN gets a lot worse in last few weeks of pregnancy If necessary, intra-uterine transfusion can be given to fetus * Specialised centres, highly skilled - needle in umbilical vein * At delivery - monitor baby’s Hb and bilirubin for several days as HDN can get worse for few days * Can give exchange transfusion to baby if needed to increase bilirubin and increase Hb; plus phototherapy to decrease bilirubin Note: subsequent pregnancies usually worse
28
What is the most common and important antibody seen causing HDFN?
Anti-d
29
How can prevention on sensitisation be done?
always transfuse RhD negative females of child bearing potential with RhD negative blood. Can give intra-muscular injection of anti-D immunoglobulin, at times when mother is at risk of a fetomaternal bleed e.g. at delivery
30
What is the MOA of prophylactic anti-D immunoglobulin?
31
Name sensitising events and what the consequences could be.
1. Give anti-D at delivery if baby is RhD positive 2. Give anti-D Ig for ‘sensitising events’ during pregnancy, where FMH is likely to occur\*\* * spontaneous miscarriages if surgical evacuation needed and therapeutic terminations * amniocentesis and chorionic villous sampling * abdominal trauma (falls and car accidents)  * external cephalic version (turning the fetus)  * stillbirth or intrauterine death
32
What are the doses of anti-D given
33
What is the routine antenatal anti-D prophylaxis (RAADP)?
34
What are the other antibodies that affect HDN
_Anti-c and anti-Kell can cause severe HDN_ * usually less severe than anti-D * Kell causes reticulocytopenia in fetus as well as haemolysis _IgG Anti-A and anti-B antibodies from Group O mothers can cause mild HDN_ * usually not severe (phototherapy)
35
Describe Non-invasive fetal genotyping for mothers with antibodies
* NHSBT offers fetal genotyping - support for routine maternity and transfusion services both nationally and internationally. * A rapid, non-invasive, convenient and reliable service for prediction of fetal D, C, c, E and K status, using cell-free fetal DNA in maternal blood for women who have allo- antibodies. * Upon identification, mothers can then be informed and prepared for further careful monitoring during their pregnancy. * Also identifies pregnant women who have antigen-negative fetuses and who therefore are not at danger from HDFN
36
What is the use of ffDNA?