Red Cell Antibodies Flashcards

1
Q

in IUFD where no sample can be obtained from the baby

A

prophylactic anti-D Ig within 72h of the diagnosis of IUfD, irrespective of the time of subsequent delivery

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2
Q

Do we give anti d in case of miscarrage

A

below 12 weeks no need for anti D (NICE)
*heavy recurrent bleeding and pain 250 anti-d - BCSH)

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3
Q

Indication of anti-d for non sensitized RH-ve women after birth?

A

500 IU within 72 hours w/ KBT

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4
Q

Routine antenatal Anti-D prophylaxis time & dose

A
  • at 28 and 34 (500lU)
  • or once At 28 (1500IU)
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5
Q

the most common encountered antibody during pregnancy

A

Anti-D

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6
Q

Do ART increases the risk of red cell alloimmunisation

A

No evidence

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7
Q

prevelence of positive antibody screens

A

1:80

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8
Q

prevelence of clinically significant alloantibodies other than anti-d

A

1-300

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9
Q

if at booking testing we find clinically significant antibody screen positive

A

we test for anti- DcK antibodies monthly until 28 weeks then from 28 w test twice weekly until delivery

after delivery test cord blood for : DAT, Hb, billirubin

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10
Q

if at booking testing we find clinically significant antibody screen positive other than DcK

A

repeat antibody screen at 28 w till delivery then test cord blood for DAT, Hb, bilirubin

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11
Q

if at booking testing we didn’t find clinically significant antibody screen positive

A

repeat antibody screen at 28 w till delivery

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12
Q

Cut-off for DcK antibodies

A

Anti-D: 4 iu/ml
Anti-c: 7.5 iu/ml
Anti-K: if positive

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13
Q

What may Anti-K do attacking the fetus

A

erythropoeisis suprression leading to severe fetal anemia (even in at low ab titre)

no hyperbilirubinemia

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14
Q

when to undertake genotyping for anti DcK

A

all at 16 weeks
Anti-K at 20 weeks

don’t do genotyping unless antibody reaches threshold

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15
Q

when to refer for FMU in case of Anti-DcK found

A
  1. rising AB above threshold
  2. U/S suggest of fetal anemia
  3. Hx of unexplained severe neonatl jaundice, anemia requires transfusion or exchange transfusion, to exclude HDFN as the cause
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