Maternal Medicine - Endocrine, Haematology Flashcards

1
Q

What happens to:

TBG
Total T4 and T3
Free T4
TSH
in pregnancy
A

TBG - increased
Total T4 and T3 - no change
TSH - slight fall in first trimester

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2
Q

How many pregnancies are affected by hyperthyroidism and what proportion have a FHx of autoimmune disease/are due to Graves’ disease?

A

1 in 500
50% have FHx
90% due to Graves’

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3
Q

What is the mortality rate of a thyroid crisis (‘storm’)

A

25%

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4
Q

What is the rate of preterm labour in hyperthyroidism?

A

11-25%

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5
Q

What is the rate of stillbirth in hyperthyroidism?

A

8-15%

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6
Q

What is the rate of neonatal thyrotoxicosis in hyperthyroidism?

A

1-10%, usually transient

Most common if active disease in third trimester

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7
Q

How many pregnancies are complicated by hypothyroidism?

A

1%

Background 0.5% overt
2.5% subclinical

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8
Q

How many women with postpartum thyroiditis will develop hypothyroidism within 4 years?

A

20-30%

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9
Q

How many women with macroadenomas will have enlargement in pregnancy?

A

15%

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10
Q

How long after radioactive iodine should pregnancy be delayed?

A

6/12

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11
Q

What is the preferred medical treatment of hyperthyroidism in pregnancy?

A

PTU in T1 - lower teratogenicity

Consider change to carbimazole in T2 as ?PTU related hepatotoxicity in offspring

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12
Q

What is the recommendation with thyroxine dosing in pregnancy?

A

Increase by 25mcg when pregnancy confirmed
Monitor 4-6 weekly
Maintain TSH <2.5
Change to pre pregnancy dose post partum and check levels 4-6/52

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13
Q

What is the background risk of being a carrier for Haemophilia?

A

1 in 20,000

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14
Q

What is the % of population had Von Willerbrands?

A

1%

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15
Q

Which is the most common inherited bleeding disorder

A

Von willerbrands
1% of population
Chromosome 12 abnormality

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16
Q

What’s the role of vWF?

A

Stabilises factor VIII and helps platelets adhere to injured vessels
( factor 8 part of intrinsic pathway. 8a aides 9a’s conversion of 10 to 10a which changed prothrombin to thrombin.

17
Q

What is type 1 vWD?

A
Most common (75%)
Autosomal dominant 
Quantitative deficiency
Normal vWF
18
Q

Describe the different forms of type 2 vWD?

A

Autosomal dominant occasionally recessive
Qualitative deficiency
Abnormal vWF
2a low platelet function, no high molecular multimers
2b platelet increased affinity for Gp1b
2m low platelet function
2n normal platelet function.reduced factor 8 binding
(All but 2n have abnormal platelet function but normal factor 8 binding)

19
Q

What is type 3 vWD?

A

Auto recessive

Negligible vWF and reduced function of factor 8

20
Q

What happens to vWF and factor 8 levels in pregnancy ?

A

Increase
All increase apart from
factor 2 and protein C unchanged
Factors 11 and S decrease

21
Q

How do you diagnose vWD?

A

FBC- low platelets in type 2b, anaemia if bleeding
Clotting screen- APTT may be prolonged/ normal
VWF antigen - amount vWF present
VWF ristocetin-function of vWF
Factor 8 levels- may be low in all types
Collagen binding assay
Factor 8 binding -reduced in 2n
Rostocetin induced platelet agglutination- (RIPA) increased in 2b
Multimer analysis- none in 2a, normal or large in 2m

22
Q

What is the Management of vWF ante tally?

A

Joint Obstetric/haematology care
Von willerbrand screen 1st and third trimester
Anaesthetic review
vWF activity and factor 8 levels > 50 before invasive testing