HDN Flashcards

1
Q

Describe the pathophysiology of HDN

A
  • HDN / HDNB / HDFNB (F= foetus)
  • jaundice: elevated (>300 uM) &/or rapid inc. (>8.5 uM/hr) serum bilirubin w/in 24hr or 14+ days post partum
  • Positive DAT: maternal Ab bound on Bb’s RBC
  • severe HDN -> kernicterus, hydrops fetalis
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2
Q

Which antibodies commonly cause HDN?

A

IgG Aby reactive @ IAT

  • Anti-c, -K, ABO
  • Rhesus, Kell, Duffy, MNS, Kidd, ABO
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3
Q

Summarise the serological testing required during the ante and post natal periods.

A
  • Ante-: @ first trimester visit: ABO & Rh(D) typing & Ab screen
  • Retest in 28 weeks for ABO & Rh(D) type and Ab screen if neg.
  • Post-:
    • Mum have ABO & Rh(D) and Ab screen (if not done already)
    • Bb: if mum is Rh(D) neg or has CSig. Ab = do ABO/Rh(D) group, DAT, Hb, Bilirubin, elution studies on baby
  • IF DAT positive => Ab screen
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4
Q

What are the requirements for blood products used in intrauterine transfusions?

A
  • <5 days old
  • ABO/Rh compatible w/ mum & foetus OR O neg cells
  • *K neg
  • Ag neg to maternal Ab (not want to give blood that’ll lyse bc from mum’s Aby)
  • CMV neg
  • Irradiated
  • HCT ≥70% (bc not want vol. overload)
  • XM compatible w/ maternal or infant plasma
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5
Q

2 test for determining foetal anaemia is baby @ risk of HDN (e.g. bc baby K+)

A
  • Quantification/titration
  • Middle cerebral artrey (MCA) Doppler ultrasound:
    • non-invasive
    • Velocity of blood flow in MCA
    • inc blood flow = anaemia
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6
Q

In which scenarios are CMV-negative blood products required for transfusion?

A
  • CMV-seroneg
  • at-risk patients:
    • Transplant recipients
    • immunosuppressive chemo
    • intrauterine transfusion
    • neonate
    • preg. women
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7
Q

In which scenarios are irradiated blood products required for transfusion?

A
  • HLA-matched transfusions
  • Intrauterine transfusion
  • Newborns
  • Immunodeficiency
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8
Q

What are CMV-negative blood componenets

A
  • negative to cytomegalovirus - carried from WBC
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9
Q

What is irradiated blood components & it’s purpose

A
  • RBC, plts treated w/ 25-50 Gy y-radiation
  • prevent transfusion-assoc graft-vs-host disease
    • prevent proliferation of donor T-lymphocytes
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10
Q

Describe why it is important to differentiate anti-D+C and anti-G in the management of HDN.

A
  • bc someone producing anit-G (OR anti-G +C) can receive Rh(D)Gg
  • BUT someone producing anti-D + C is not bc already produce/have immune anti-D
  • differentiate using G- or D- differnetiation
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11
Q

Describe how serological testing of the father is beneficial in management of HDN

A
  • perform XM w/ maternal plasma & paternal RBC
  • bc father may produce low incidence Ag => baby inherits => will sensitize mum
  • consider when there’s HDN w/ pos DAT but neg Aby screen for mum & ABO compatibility b/w mum & baby
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12
Q

Treatment options for HDNB

A
  • phototherapy

- Exchange transfusion: intrauterine

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13
Q

how can you determine if a person has acquired or immune anti-D?

A
  • probs prophylactic if anti-D quant is low

- immune: if quant. is stable or rising

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14
Q

Differentiate Rh(c) HDN w/ Rh(D) HDN

A
  • Rh(c): present similar to HDN to Rh(D) incompatibility

- note: there’s is no prophalactic anti-c

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15
Q

Describe the G Ag

A
  • An Ag on Rh blood group

- Present on C & D Ag = C+ and/or D+

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16
Q

How can you distinguish if a person has Anti-G or instead has 2 Aby, anti-C + D?

A
  • Anti-C + D: Anti-D stronger than Anti-C

* Anti-G: reaction to anti-C (D-C+ cells) stronger than anti-D (D+C- cells)

17
Q

interpret Rh(c) quant with risk of HDN

A

<7.5: unlikely risk to HDN
7.5-20: moderate risk to HDN
>20: High risk to HDN

18
Q

How does anti-K differ to anti-D HDN (features of Kell HDN)

A
  • previous history not indicate severity
  • poor correlation b/w Aby titre & disease severity
  • haemolysis not a dominant feature ≠ elevated bilirubin
    = anaemia from insuffiecient erythropoeisis due to dec production as anti-K binds to K Ag on erythroid progenitor cells
19
Q

ABO HDN

A
  • high titre of IgG in mum (can go through placenta)
  • elevated bilirubin w/o significant anaemia in foetal RBC: bc baby;s ABO Ag not fully developed
  • sensitised cells not lysed = DAT pos (not always)
  • spherocytes
20
Q

Describe the tests for foetomaternal haemorrhage

A
  • Acid elution / Kleihauer / - Betke test: Expose blood film to acid = denatures HbA (adult) => stain intact HbF (foetus) w/ erythrosine / eosine
  • Flow cytometry: detect D pos cells in maternal blood using Fluorescent-labelled anti-D Ab
21
Q

what needs to be done if mum has anti-K Aby

A
  • refer to specialist
  • phenotype/genotype father
  • > if father is K+ genotype baby’s DNA from maternal plasma
  • > if baby is K+, do MCA doppler& perform intrauterine transfusion if necessary