Pregnancy Flashcards

1
Q

Physiological changes in coagulation during pregnancy

A

Increase: fibrinogen, FVIII, VWF, VII, X
Stable: II, IX, XII
Slight fall: XI, XIII

Protein S falls (may be <40%), Protein C is stable
AT levels fall at time of delivery.

Acquired APC resistance due to high FV, FVIII and low protein S

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2
Q

Causes of anaemia in pregnancy

A
  1. Increased plasma volume
  2. Iron deficiency
  3. Folate deficiency
  4. AIHA - higher risk
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3
Q

Morphology changes in pregnancy

A
  1. May have increased MCV
  2. Neutrophilia
  3. Toxic changes
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4
Q

What are 5 reasons why VTE risk is higher in pregnancy?

A
  1. Increased clotting factors and fall in protein S
  2. Acquired APC resistance due to high factor V and VIIII levels
  3. Reduced fibrinolysis (increased PAI-2 from placenta)
  4. Compressive effect of placenta (2/3 DVTs occur in left leg)
  5. Operative delivery
  6. Inherited thrombophilia (seen in around 30%)
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5
Q

VWD in pregnancy

A

VWF and FVIII levels increase in pregnancy therefore may not have increased bleeding during pregnancy
BUT precipitous fall post partum ==> PPH
High molecular weight VWF does not increase therefore types 2A, 2B and 3 may have bleeding.
Replace with Biostate (dosing based on FVIII)

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6
Q

Haemophilia A and B in pregnancy

A

FVIII levels increase therefore haemophilia A is often not a problem
FIX levels are stable/don’t increase therefore haemophilia B carriers may need factor replacement when levels fall below 40%

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7
Q

Management of delivery in women who have haemophilia or severe VWD

A
  • Confirm disorder and severity
  • Preconception counselling
  • Close monitoring during pregnancy, particularly 3rd trimester to allow for delivery plan.
  • Assess risk to:
    1. Mother
    2. Fetus (sex determination is essential)
  • Avoid instrumental delivery if fetus might have VWD or haemophilia
  • Biostate given for VWD, avoid DDAVP
  • Avoid IM vitamin K to neonate if possible risk baby has haemophilia.
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8
Q

Methods to confirm fetal blood sample (5)

A
  1. MCV (fetal RBCs larger - occ unreliable if mother has macrocytosis or fetus has been transfused adult RBCs)
  2. BhCG - most reliable test, should be absent in fetal blood but high in maternal blood
  3. Apt and Downey (alkaline denaturation occurs with maternal blood but not fetal blood)
  4. Kleihauer Betke (acid denaturation of maternal cells but not fetal RBCs)
  5. I antigen - present on maternal cells but not fetal cells
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9
Q

Methods of intrauterine blood sampling

A
  1. Cordocentesis
  2. Intrahepatic vein sampling
  3. Cardiocentesis (high risk, last resort)
    * *give steroids, perform close to theatre, experienced person
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10
Q

5 Features of Gestational Thrombocytopenia

A
  1. Onset during late 2nd/3rd trimester
  2. Mild to moderate thrombocytopenia (usually >80, rarely <50)
  3. Not present prior to pregnancy
  4. Resolves post partum
  5. No risk of neonatal thrombocytopenia
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11
Q

Features of ITP in pregnancy

A
  1. Usually onset earlier in pregnancy, progressively worsens
  2. May be difficult to treat
  3. Thrombocytopenia often more severe than gestational thrombocytopenia
  4. 15% risk of neonatal thrombocytopenia (nadir 2-5 days, usually resolves by 2 weeks, low risk of ICH, doesn’t correlate with maternal platelet count)
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