W16 - Blood transfusion 2 Flashcards

1
Q

Adverse reactions to transfusion = time cut off for acute vs delayed

A

24 hours
<24 hours = acute
>24 hours = delayed

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2
Q

Name 5 types of ACUTE adverse reactions to transfusion

A
  1. Acute haemolytic (ABO incompatible)
  2. Allergic/anaphylaxis
  3. Infection (bacterial)
  4. Febrile no-haemolytic
  5. Respiratory
    => Transfusion associated circulatory overload (TACO)
    => Acute lung injury (TRALI)
    => Transfusion associated dyspnoea (TAD)
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3
Q

Name 5 types of DELAYED adverse reactions to transfusion

A
  1. Delayed haemolytic transfusion reaction (antibodies)
  2. Infection (viral, malaria, vCJD)
  3. TA GvHD
  4. Post transfusion purpura
  5. Iron overload
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4
Q

What 4 things should you measure as baseline when giving transfusion? How frequently should you measure?

A

1- Temp
2- HR
3- RR
4- BP
repeat after 15 minutes -> repeat hourly and at the end of transfusion

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5
Q

Febrile non-haemolytic transfusion reaction (FNHTR)

  • when does it occur?
  • what are the symptoms?
  • treatment?
A

Febrile non-haemolytic transfusion reaction (FNHTR)
- when does it occur = during/soon after transfusion (blood or platelets)

  • what are the symptoms = rise in temp of 1 degrees C, rigors
  • treatment = stop/slow transfusion + paracetamol
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6
Q

Cause of febrile non-haemolytic transfusion reaction (FNHTR)

A

due to donor white cells remaining in product during storage and releasing cytokines => now RARE due to leucodepletion of donor product

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7
Q

Allergic transfusion reaction:

  • when does it occur?
  • what are the symptoms?
  • treatment?
A

Allergic transfusion reaction:
- when does it occur = during/after transfusion (esp plasma)

  • what are the symptoms = mild urticarial rash with wheeze
  • treatment = stop/slow transfusions + IV antihistamines
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8
Q

Cause of allergic transfusion reactions

A

due to a plasma protein in donor, so it may NOT occur again depending on how common the allergen is
- commoner in recipients with other allergies and atopy

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9
Q

Acute haemolytic reaction (aka wrong blood):

  • when does it occur?
  • what are the symptoms?
  • treatment?
A

Acute haemolytic transfusion reaction (aka wrong blood):
- when does it occur = within 24 hours

  • what are the symptoms = signs of intravascular haemolysis:
  • restless
  • chest/loin pain
  • fever
  • vomiting
  • flushing
  • collapse/shock (BP low, HR high)
  • treatment = stop transfusion, check patient/component, take FBC, LFTs, clotting, repeat x-match and direct antiglobulin test (DAT), discuss w/ haematology
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10
Q

In terms of transfusion reactions, what is the #1 reason why they occur?

A

clerical error!

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11
Q

Bacterial contamination transfusion reaction:

  • when does it occur?
  • what are the symptoms?
  • treatment?
A

Bacterial contamination transfusion reaction:

  • when does it occur = within 24 hours
  • what are the symptoms =
  • restless
  • chest/loin pain
  • fever
  • vomiting
  • flushing
  • collapse/shock (BP low, HR high) due to endotoxin release
  • treatment = stop + abx + supportive
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12
Q

Which transfusion product is more likely to grow bacteria - red cells or platelets?

A

Platelets because they are stored at room temp whereas red cells are stored at 4 degrees C

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13
Q

Anaphylactic transfusion reaction:

  • when does it occur?
  • what are the symptoms?
  • treatment?
A

Anaphylactic transfusion reaction:
- when does it occur = soon after start of transfusion

  • what are the symptoms:
  • shock (low BP, high HR)
  • SOB +/- wheeze
  • laryngeal +/- facial oedema
  • treatment =
    1) stop blood transfusion
    2) adrenaline
    3) supportive care
    4) inhaled bronchodilator + glucagon + antihistamine + corticosteroids
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14
Q

Cause of anaphylactic transfusion reactions

in what disease are anaphylactic transfusion reactions more SEVERE?

A

IgE abs in patient => mast cell degranulation + vasoactive substance
*more severe in IgA deficiency

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15
Q

What is the most common pulmonary complication of transfusion reaction?

A

TACO

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16
Q

TACO:

  • when does it occur?
  • why does it occur?
  • what are the symptoms?
  • CXR findings?
A

TACO:
- when does it occur = ACUTE (within 6 hrs usually)

  • why does it occur = due to lack of attention to fluid balance, esp. in CF, renal impairment, hypoalbuminaemia, + fluid balance
  • what are the symptoms:
    1) SOB
    2) reduced O2 sat
    3) high HR
    4) high BP
  • CXR findings:
    1) fluid overload
    2) Cardiac Failure
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17
Q

TRALI:

  • when does it occur?
  • what are the symptoms?
  • CXR findings?
A

TRALI:
- when does it occur = ACUTE (during or within 6 hrs usually)

  • what are the symptoms:
    1) SOB
    2) reduced O2 sat
    3) high HR
    4) high BP
    **same as TACO)
  • CXR findings:
    1) bilateral pulmonary infiltrates not due to circulatory overload
18
Q

pathophysiology of TRALI

A

why does it occur = anti-WBC abs in donor => interact with patient WBCs => aggregates => stuck in pulmonary capillaries => lung damage

**sometimes abs not implicated

19
Q

Which infections cause (delayed) associated with transfusion reaction

A
  1. Malaria
  2. HIV 1/2, HEV, HBV, HCV, HLV 1/2, Parvovirus, CMV, WNV, Zika
  3. Variant CJD
20
Q

Pathophysiology of delayed haemolytic transfusion reaction

A

1-3% of all patients transfused develop an “immune” antibody to an RBC antigen they lack = ALLOMMUNISATION

if patient receives another transfusion with RBCS expressing the same antigens => abs cause RBC destruction = EXTRAVASCULAR HAEMOLYSIS (as IgG) so takes 5-10 days

21
Q

What investigation findings will suggest delayed haemolytic transfusion reaction?

A

haemolysis screen:

  • raised:
    1) bilirubin
    2) LDH
    3) retics
  • reduced:
    1) Hb
  • DAT +
  • Haemoglobinuria (over few days)
  • U&Es - if renal failure
  • repeat G&S - for new abs
22
Q

Transfusion associated Graft-V-Host Disease (TaGVHD):

  • when does it occur?
  • what are the symptoms?
  • prognosis?
A

Transfusion associated Graft-V-Host Disease (TaGVHD):

  • when does it occur = usually 7-10 days post transfusion
  • what are the symptoms:
    1) severe diarrhoea
    2) liver failure
    3) skin desquamation
    4) BM failure
  • prognosis?
    rare, but always fatal (death weeks to months post transfusion)
23
Q

Pathophysiology of Transfusion associated Graft-V-Host Disease (TaGVHD)

A

Normally => donor’s blood contains lymphocytes => patient immune system recognises donor’s lymphocytes as foreign and destroys them

TaGVHD => susceptible patient (very immunosuppressed) = lymphocytes not destroyed => lymphocytes recognise patient tissue HLA ags as foreign => attack patient’s gut, liver, skin, BM

24
Q

How to prevent TaGVHD?

A

Irradiate blood components for very immunosuppressed or give HLA-matched components

25
Post transfusion purpura: - when does it occur? - what are the symptoms? - prognosis?
Post transfusion purpura: - when does it occur = 7-10 days post transfusion (blood or platelets) - what are the symptoms = purpura = pin prick red/purple blood spots - prognosis = resolves in 1-4 weeks but may cause life threatening bleeding
26
Post transfusion purpura: who does it affect? Treatment?
HPA-1 negative patients who were previously immunised by pregnancy or transfusion and have anti-HPA-1a antibody - treatment = IVIG
27
What is iron overload in transfusion? Treatment?
If lots of transfusions (\>50), over time iron can accumulate = cause organ damage (liver, heart, endocrine) - Treatment = iron chelation with transfusion once ferritin \>1000 (normally used in Thalassaemia/SCD)
28
How does RhD- mom make anti-D during 1st pregnancy?
If child is RhD + =\> during delivery, mom exposed to foetal RhD+ red cells =\> make anti-D (6 months later)
29
What happens to RhD- mom with anti-D in her 2nd pregnancy?
If foetus RhD + =\> maternal anti-D IgG crosses placenta =\> coats foetal RhD + cells =\> destroys them in foetal spleen and liver
30
Clinical features (4) of baby with haemolytic disease of the newborn (HDFN)
1. Anaemia signs (pale skin) 2. Hyperbilirubinaemia signs (jaundice) 3. Hepatosplenomegaly 4. If hydrops fetalis =\> severe oedema in organs
31
How and when are pregnant women assessed for red cell antibody?
Pregnant woman have G&S at around 12 weeks and again at 28 weeks to check for RBC abs
32
What (5) is done if a G&S screen for pregnant woman comes back possible for RBC antibodies (anti-D)?
1. Check if father has the antigen (and potentially baby has inherited it) 2. Monitor level fo abs (high/rising) 3. Check ffDNA sample 4. Monitor foetus for anaemia (MCA doppler US) 5. Deliver baby early as HDN gets worse in last few weeks
33
If foetus is very affected by anti-D, what sort of things (4) can be done?
1. intra-uterine transfusion to foetus 2. Deliver a few weeks early 3. At deliver - monitor baby's Hb + bilirubin for several days 4. Exchange transfusion to baby to lower bilirubin and increase Hb +/- phototherapy
34
What is the most important antibody for cause HDFN?
Anti-D
35
Can we prevent abs production by Rh - mom in her first pregnancy? If so, how?
YES RhD - females of childbearing age given IV anti-D or IM anti-D. NB: IM given closer to delivery when risk of fetomaternal blood loss
36
MOA of prophylactic anti-D Ig?
RhD + foetal red cells get coated with anti-D Ig =\> are removed by mom's spleen before they can sensitise the mom to produce anti-D abs
37
When do you have to give prophylactic anti-D Ig for it to be effective?
within 72 hours of the sensitising event (maternofoetal blood exchange) = does NOT work if mom previously sensitized and has anti-D
38
What are sensitising events in pregnancy?
Any time where maternal and foetal blood may exchange 1. Delivery 2. Spontaneous miscarriages 3. Amniocentesis or CVS 4. Abdominal trauma (falls/car accidents) 5. External cephalic version 6. Stillbirth or intrauterine death
39
What is the routine antenatal anti-D prophylaxis (RAADP)?
1% of pregnancies with no sensitising events lead to RhD - mom becoming sensitized THEREFORE all RhD - mom will receive routine anti-D prophylaxis in 3rd trimester (28w)
40
Other than anti-RhD antibodies, name other antibodies (3) that may develop and cause foetal distress?
1) anti-c 2) anti-kell (these 2 may cause severe HDN although rarer) 3) IgG anti-A and anti-B abs in Group O moms (this causes mild HDN)
41
Name 1 non-invasive foetal genotyping test How is it used?
Cell-free foetal DNA (ffDNA) =\> can check for foetal D, C, c, E, K status at 11 + 2 weeks gestation