18.05.08 Maternal serum screening and Down syndrome screening Flashcards

1
Q

Give a definition of screening

A

UKNSC: is a process of identifying apparently healthy people who may be at increased risk of a disease or condition.

They can then be offered information, further tests and appropriate treatment to reduce their risk and or any complications arising from the disease or condition.

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2
Q

What is the aim of the NHS foetal anomaly screening programme?

A

The NHS Fetal Anomaly Screening Programme offers screening to all pregnant women in England to assess the risk of trisomy 21 and a number of fetal anomalies.

FASP aims to ensure that there is equal access to uniform and quality-assured screening, and that women are provided with high quality information so they can make an informed choice about their screening options and pregnancy. FASP is overseen by the UK NSC and is part of Public Health England.

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3
Q

What is the associated between advanced maternal age and Down syndrome risk?

A

Risk of Down syndrome pregnancies advances with age. Use as the sole criteria for risk gives a detection rate of 30% for a 5% false positive rate.

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4
Q

When can screening for Down syndrome be undertaken?

A

From 10-20/40

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5
Q

Define prevalance

A

Prevalence – The number of individuals in a population with the target condition

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6
Q

Define sensitivity and specificity

A

Sensitivity – A screen’s ability to refer individuals (for further tests) who do have the target condition. (proportion of +ves which are correctly ID’d as such)

Specificity – A screen’s ability to NOT to refer individuals who do NOT have the target condition (Proportion of –ves which are correctly ID’d as such)

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7
Q

Define detection rate and screen positive rate

A

Detection Rate (DR) – The proportion of affected individuals with a positive screening result.

Screen Positive Rate (SPR) - The proportion of individuals who will be given a high risk result following screening

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8
Q

Define false positive rate and false negative rate

A

False Positive Rate (FPR) - The proportion of unaffected individuals with a positive screening result. It is the complement of specificity ie: Specificity=100-FPR

False negative Rate (FNR) – The proportion of women who are given a lower risk result but have an affected pregnancy. It is the complement to the sensitivity.

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9
Q

What is the nuchal translucency? When is it measured?

A

Measured between 11+2 and 14+1 weeks, sonographer takes an US measurement (in mm) of the NT

NT is the maximum thickness of the subcutaneous translucency between the fetal skin and the soft tissue overlying the cervical spine (fluid under the skin at back of the fetal neck).

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10
Q

What size of NT is associated with aneuploidy?

A

A NT of ≥3.5mm is strongly associated with aneuploidy (+21,18,13, 45,X and triploidy in order of highest to lowest prevalence). NT of ≥3.5mm with a normal karyotype can be associated with a range of structural malformations (often Cardiac), and or genetic syndromes.

If the NT is >3.5mm between 11 and 14 weeks (found in ~1% of pregnancies) the pregnancy will be considered at an increased risk and a diagnostic test will be offered. Increased NT reflects foetal heart

failure and is strongly associated with a chromosomal abnormality.

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11
Q

What are multiples of the mean?

A

Measures levels of serum analytes (markers) that have passed from fetus into mother’s blood

Multiples of the Median (MoM) are calculated for each serum marker

MoM – the serum marker concentration for a pregnant woman, divided by the median concentration value for unaffected pregnancies of the same gestational age

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12
Q

Why is the MoM used instead of mean?

A

The median is used instead of the mean because it is not skewed by very high or very low values

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13
Q

Which markers are used in the combined screen? When is this performed and what is the detection rate?

A

Combined Screening - β-hCG, PAPP-A+ NT - The recommended test

Serum screening is performed between 10+0 and 14+1 (ideally at 11+2).

DR ~87% for 5% FPR
DR 90% for SPR of 2.2%

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14
Q

Which markers are used in the quadruple screen? When is this performed and what is the detection rate

A

Quadruple Screening – AFP, β-hCG, uE3+ Inhibin A

Performed at 14+2 to 20 weeks gestation (second trimester)

The recommended test for women who present too late for combined screening and in some trusts where combined screening has not yet been introduced

DR ~81% for 5% FPR

DR 75% for 3% SPR

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15
Q

Other than the Quad and combined screening tests, what other serum screening strategies exist?

A

1) Integrated Test - PAPP-A, β -hCG and NT measurement in 1st trimester followed by AFP, uE3 and inhibin A in second trimester (DR ~96% for 5% FPR)
2) Serum Integrated Test - PAPP-A and β -hCG at 11+0-13+6 wks followed by AFP, uE3 and inhibin A at 5-20 wks (Integrated test without NT) (DR ~88% for 5% FPR)
3) Contigency test
4. Stepwise sequential

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16
Q

Which factors affect serum screening? How are they taken into consideration.

A
  1. BMI, decreased levels in heavier women, increased in lighter
    2) Ethnicity: higher in Afro-Caribbean women than in Caucasian women
    3) IVF: Free β-hCG and hCG levels tend to be about 10% higher and uE3 levels about 10% lower in women (age must be considered of donor egg if used).
    4) Diabetes
    5) Smokers
    6) Twin pregnancies (Quad test recommented)

MoM values are adjusted

17
Q

What conditions are not screened for in the quad test.

A

Trisomy 13 and 18 (only detected in combined test)

18
Q

What is an absent nasal bone indicative of?

A

Absent Nasal Bone: ~60-70% +21 fetuses have absent/hypoplasia of nasal bone, also seen in ~50% +13 and ~60% +18 (figures vary depending on which study).

19
Q

Women who are found to be ‘low risk’ through testing in either the 1st or 2nd trimesters, or who have declined screening for DS should not be referred for further assessment of chromosomal abnormalities even if normal variants (whether single or multiple) are seen at the 18+0- 20+6 weeks foetal anomaly screening scan. What are these normal variants.

A

Choroid plexus cyst(s)

Dilated cisterna magna

Echogenic foci of the heart

2 vessel cord

20
Q

Which normal variants detected on ultrasound should be reported, even if the woman has decline DS or has been previously determined to be low risk.

A

Referral for further assessment/chromsomes
Nuchal fold (>6mm)
Ventriculomegaly (atrium >10mm)
Echogenic bowel (with bowel density equivalent to bone)
Renal pelvic dilation (Anteroposterior diameter measurement >7mm)
Small measurements compared to dating scan (significantly less than 5th centile on national charts)

21
Q

What is the miscarriage risk associated with CVS sampling? AF sampling? Foetal blood sampling?

A

CVS: 1-2%
AF: 0.5-1%
FBS: 2-2.5%

22
Q

What are the potential technologies that may impact on current screening programmes/

A

NIPT

Proteomics: an be used to identify and characterize proteins in maternal serum from patients at high-risk for +21, 18 and 13 on the basis of ultrasound and maternal serum triple tests. Maternal serum protein profiling using proteomics (SELDI-TOF MS, SDS-PAGE, MALDI-TOF) in early second trimester of pregnancy may allow non-invasive diagnostic testing for the most common trisomies and may complement ultrasound-based methods to more accurately determine pregnancies with fetal aneuploidies

23
Q

Other than in DS, what other conditions may be indicated by decreased alpha-fetoprotein levels?

A

Hydatidiform molar pregnancies

Foetal demise

24
Q

Which conditions are assoicated with a rise in AFP?

A

Neural tube defects

Gastrointestinal defects.

Cystic hygroma.

Renal abnormalities

Abdominal wall detected pregnancies

25
Q

Other than in DS, what other conditions may be indicated by decreased unconjugated oestriol uE3?

A

+13 and +18 pregnancies.

Anencephaly.

Congenital adrenal hyperplasia.