Antenatal screening Flashcards

1
Q

What history points are required in the booking appointment

A
  • Obstetric history
  • Medical and surgical history
  • Medications and allergies
  • Mental health
  • Family history
  • Social history
  • History of domestic abuse or violence
  • Safety
  • History of FGM
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2
Q

What investigations are performed in the booking appointment

A

History
Weight
Height
Blood pressure

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3
Q

What are some important mental health questions asked in the booking appointment

A
  • Any new feelings that make you anxious or disturbed?
  • Suicide or self harm?
  • Feelings of incompetency as a mother?
  • Feeling estranged from the baby?
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4
Q

What are the criteria for oral glucose tolerance testing in pregnancy

A
  • BMI > 30
  • Previous macrosomic baby >4.5kg
  • Family history of diabetes (1st relative)
  • History of PCOS
  • Ethnic family origin from area of high diabetes prevalence
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5
Q

What are the main screening tests offered during pregnancy

A
  • Infection
  • Anaemia
  • Rhesus status
  • Haemoglobinopathy
  • Down’s, Edward’s and Patau’s syndrome
  • Foetal anomalies
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6
Q

What is involved in antenatal infection screening

A
  • Urine - Mid-stream urine sent
  • Blood - HIV, Syphilis, Hepatitis B
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7
Q

When is anaemia screening performed in pregnancy

A

FBC at booking scan and 28 weeks

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8
Q

What are the 2 conditions screened for in haemoglobinopathy screening

A

Sickle-cell disease
Thalassaemia

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9
Q

What is involved in haemoglobinopathy screening

A

Family origin questionnaire
Blood tests

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10
Q

When is rhesus antibody screening performed in pregnancy

A

Blood grouping at booking and 28 weeks

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11
Q

What is done if the mother is found to be rhesus D-negative

A
  • Offer anti-D to prevent maternal antibody formation
  • Routine prophylaxis at 28 weeks
  • Additional anti-D for potentially sensitising events
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12
Q

Describe the levels of trisomy screening in pregnancy

A
  1. Quadruple screening

If high risk on 1. then:

  1. NIPT

If high risk on 2. then:

  1. Invasive foetal genetic testing (CVS or amniocentesis)
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13
Q

What is used in the quadruple trisomy screen?

A

Crown-Rump length
Nuchal translucency
HCG levels
PAPP-A levels

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14
Q

What is nuchal translucency

A

The thickness of fluid behind a babies neck

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15
Q

When is quadruple trisomy screening done in pregnancy

A

11 - 13+6 weeks

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16
Q

What is a normal NT value (If CRL is 45-84mm)?

17
Q

What are some reasons why NT may not be measured?

A
  • User error (Very specific measurement)
  • Baby too small
  • Baby in an unsuitable position
18
Q

What are the risks of higher NT values

19
Q

When is 2nd trimester trisomy screening offered?

A

If booking was too late for 1st trimester screening

If NT was not obtained during 1st trimester

20
Q

What is screened for in 1st trimester trisomy screening

A

Trisomy 13 - Patau’s syndrome
Trisomy 18 - Edward’s syndrome
Trisomy 21 - Down’s syndrome

21
Q

What is screened for in 2nd semester trisomy screening

A

Trisomy 21 - Down’s syndrome

22
Q

What tests are done in 2nd trimester trisomy screening

A

HCG and AFP

23
Q

When is 2nd trimester trisomy screening performed

A

15-20 weeks

24
Q

What risk of trisomy is considered high risk

A

1/150 chance

25
Q

What is the risk scale on trisomy screening

A

1/5000 - 1/2

26
Q

What does NIPT stand for

A

Non-invasive prenatal testing

27
Q

What is involved in NIPT

A

Maternal blood sample to detect cell free foetal DNA from the placenta

28
Q

What are the 2 main forms of invasive foetal genetic testing

A

Chorionic villous sampling (CVS)
Amniocentesis

29
Q

When is CVS performed

A

11-14 weeks

30
Q

When is amniocentesis performed?

A

> 15 weeks

31
Q

What is the miscarriage rate of CVS

32
Q

What is the miscarriage rate of Amniocentesis

33
Q

Is local anaesthetic required in invasive foetal genetic testing

A

CVS - Local anaesthetic
Amniocentesis - No anaesthetic

34
Q

When is the mid-trimester anomaly screening performed?

A

18 - 20+6 weeks

35
Q

What are the benefits of the foetal anomaly screening programme (FASP)

A

Reduces mortality and morbidity and may allow in-utero management

36
Q

What 11 conditions are screened for on the FASP scan

A
  • Anencephaly
  • Open spina bifida
  • Cleft lip
  • Diaphragmatic hernia
  • Gastroschisis
  • Exomphalos
  • Serious cardiac abnormalities
  • Bilateral renal agenesis
  • Lethal skeletal dysplasia
  • Edward’s syndrome (T18)
  • Patau’s syndrome (T13)
37
Q

What is open spina bifida

A

A congenital condition in which there is failure of the neural tube to close, meaning the spinal cord comes outside of the foetal spine in a sac

38
Q

What is gastroschisis

A

A birth defect where there is a hole in the abdominal (belly) wall beside the belly button. This results in the baby’s intestines extending outside of the baby’s body. Sometimes other organs, such as the stomach and liver, can be found outside of the baby’s body.