A nurse is explaining the purpose of a nuchal translucency (NT) ultrasound to a pregnant client.
What does this ultrasound measure?
Fetal growth and development.
Blood flow in the umbilical cord.
Chromosomal abnormalities like Down syndrome.
Structural abnormalities in the baby's organs.
The Correct Answer is C
This is because a nuchal translucency ultrasound measures the amount of fluid behind the baby’s neck in the first trimester of pregnancy, which can indicate the risk of having a chromosomal condition like Down syndrome.
Some possible explanations for the other choices are:
Choice A is wrong because fetal growth and development are not directly related to the nuchal translucency measurement.
Fetal growth and development are assessed by other parameters such as crown-rump length, biparietal diameter, abdominal circumference, etc.
Choice B is wrong because blood flow in the umbilical cord is not measured by the nuchal translucency ultrasound.
Blood flow in the umbilical cord is assessed by Doppler ultrasound, which evaluates the resistance and velocity of blood flow in the umbilical artery and vein.
Choice D is wrong because structural abnormalities in the baby’s organs are not detected by the nuchal translucency ultrasound.
Structural abnormalities in the baby’s organs are diagnosed by a detailed anatomy scan, which is usually performed in the second trimester of pregnancy.
The normal range for nuchal translucency is between 1 mm and 3 mm.
A measurement above 3 mm is considered increased and may indicate a higher risk of chromosomal or genetic conditions.
However, a nuchal translucency ultrasound is a screening test and not a diagnostic test, so it does not confirm or rule out any condition.
It only provides a probability based on statistical calculations.
Therefore, further testing may be recommended if the nuchal translucency measurement is increased or if other risk factors are present.
Nursing Test Bank
Naxlex Comprehensive Predictor Exams
Related Questions
Correct Answer is B
Explanation
AFP is a screening tool that can indicate the possibility of certain fetal anomalies, such as neural tube defects, abdominal wall defects, or chromosomal abnormalities.
However, AFP results are not diagnostic and cannot confirm the presence or absence of these conditions.
Therefore, further tests, such as ultrasound or amniocentesis, are needed to verify the results.
Choice A is wrong because AFP results are not diagnostic for fetal anomalies.
They only indicate a risk level that needs to be confirmed by other tests.
Choice C is wrong because AFP results can detect not only neural tube defects, but also other fetal anomalies, such as abdominal wall defects or chromosomal abnormalities.
Choice D is wrong because AFP results are not affected by maternal race and ethnicity.
They are affected by maternal age, weight, diabetes, multiple gestation, and gestational age.
Correct Answer is D
Explanation
The correct answer is choice D. The client has a history of placenta previa.
Placenta previa is a condition where the placenta covers all or part of the cervix, blocking the baby’s exit from the uterus.
This can cause severe bleeding during pregnancy and delivery and increase the risk of complications for both the mother and the baby.
Therefore, the nurse should report this condition to the provider before performing an amniocentesis.
Choice A is wrong because having Rh-negative blood type is not a contraindication for amniocentesis.
However, the client may need an injection of Rh immunoglobulin after the procedure to prevent Rh sensitization.
Choice B is wrong because having a history of preterm labor is not a contraindication for amniocentesis.
However, the client may need to be monitored closely for signs of preterm labor after the procedure.
Choice C is wrong because having a history of gestational diabetes is not a contraindication for amniocentesis.
However, the client may need to have their blood glucose levels checked before and after the procedure.
Amniocentesis is a diagnostic procedure that involves removing and testing a small sample of amniotic fluid from the uterus for genetic or chromosomal conditions, such as Down syndrome, Edwards syndrome or Patau syndrome.
It can also be used to diagnose fetal infections, treat excess amniotic fluid, or test fetal lung maturity
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