Red Blood Cell Isoimmunization Flashcards

1
Q

Whats the pathophysiology behind it?

Blood groups

A

Blood classified -ABO and rhesus genotype.
Rhesus genotype- 3 linked gene pairs. One allele is dominant ro the other: C/c, D/d, E/e. 1 allele from each parent in mendellian fashion.
Isoimmunization- D gene-
Dominant: DD, Dd express D antigen and are D rhesus +ve.
Homozygous recessive: dd : D rhesus -ve.
Immune system also recognises it as foreign.

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2
Q

How is sensitization happening?

A

Small # of fetal blood crosses placenta esp during delivery.

If babes- D rhesus +ve and mum D rhesus -ve- mother will mount an immune response( sensitisation) creating anti-D Abs.

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3
Q

Whats haemolysis/ rhesus haemolytic disease?

A

Immunity = permanent
If mother exposed to antigen again - subsequent pregnancy- ⬆️⬆️ Abs are rapidly created. Cross, bind to fetal blood cells- destroed in fetal reticuloendothelial system.
This can cause hawmolytic anaemia–> death

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4
Q

What similarly happens after blood transfusions?

A

Anti-c & anti-Kell( non-rhesus Ab) after transfusions.

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5
Q

What are some potentially sensitizing and events?

A
  1. Termination of pregnancy
  2. ERPC- evacuation of retained products of conception after miscarriage
  3. Ectopic pregnancy
  4. Vaginal bleeding
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6
Q

Whats red blood cell isoimmunization?

A

Occurs when the mother mounts an immune response against antigens on fetal red cells that enter her circulation.
Resulting Abs cross the plaventa and cause fetal red cell destruction.

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7
Q

How would you prevent a rhesus sensitisation?

A
  • production of maternal anti-D prevented by administration of exogenous anti-D . Any fetal Red cells that crossed- binds to their antigens and prevents recognition by maternal Abs.
    Anti-D given even if both parents rhesus -ve - cz possible non-paternity- care needed !

Anti-D is pointless if maternal anti-D present cz sensitization has occured.

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8
Q

In what other situations are Anti-D given? Antenatally?

A
  1. Antenatal: At 28weeks- anti-D (1500IU) given to ALL rhesus -ve women.
  2. 72hrs after sensitization event-benefit- within 10 days
    A. Miscarriage
    B. Threatened miscarriage after 12 weeks
    Or before if uterus intstrumented- ERPC
    C. E topic pregnancy
    D.termination of pregnancy
  3. After in utero procedures like amniocentesis and after
    4.external cephalic version
  4. Fetal death
  5. Antepartum haemorrhage.
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9
Q

Postnatally?

A

Neonates blood group checked and if rhesus +ve Anti-D given to mum within 72hrs of delivery.
Kleihauer test also performed- asses fetal cells in maternal circulation- 2rs of birth to detect larger fetomateenal haemorrhages- require larger doses of Anti-D.

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10
Q

When is the anti-D unnecessary?

A

If Neonate is rhesus -ve

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11
Q

How do we prevent the rhesus disease?

A

At 28 weeks check all women for Abs
Rhesus -ve women- given Anti-D at 28weeks, after bleeding or potentially sensitizing evet and after delivery if neonate us rhesus positive.

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12
Q

How often do we see the rhesus disease?

A

15% caucasian, fewer african and asian are rhesus -ve.
Anti-D- perinatal deaths
Anti-c, anti-E and anti-Kell- fetal anemia and post-natal jaundice.

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13
Q

What are some manifestations of the rhesus disease?

A

Abs will cross the placenta and cause haemolysis.
Mild-Neonatal jaundice -
If more- neonatal anaemia.- haemolytic
Severe- in utero anemia–> cardiac F, ascites, oedema (hydrops) —> fetal death.

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14
Q

How does rhesus disease worsens? .

A

With successive pregnancies as maternal Abs production increases

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15
Q

How do you identify isoimmunization?

A

Unsenitised women- screend at 28 weeks gestation.
Maternal Blood sampling for fetal cells- test for fetal rhesus- when father heterozygote.
Amniocentesis, but also has risks.
If anti-D levels are 10- investigate.
USS.

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16
Q

How do we manage isoimmunization?

A
  1. Identify women at risk of fetal haemolysis + anaemia
  2. Assesing how/if severly the fetus is anaemic
    3 blood transfusion in utero or delivery for affected fetus.
17
Q

How do u asses for fetal anemia?

A

Doopler USS- of peak velocity in systole (PVS) of fetal middle cerebral artery (MCA) - high sensitivity for significant anaemia at least before 36 weeks.
Very severe anaemia

18
Q

What happens if fetal anaemia suspected?

A

Fetal blood sampling- under USS guidance- needle in umbilical vein at the cord imsertion in the placents, or in intrahepatic vein.
Fetal loss:1%
After 28 weeks- done w/ facilities for immediate delivery if complications arise.

19
Q

Tests on neonates w/ rhesus -ve women-

A

FBC, blood film, bilirubin.