A nurse is explaining the purpose of a Contraction Stress Test (CST) to a pregnant client.
What does the CST aim to assess?
Fetal well-being.
Maternal blood pressure.
Placental function.
Amniotic fluid volume.
The Correct Answer is A
A contraction stress test (CST) is performed near the end of pregnancy to determine how well the fetus will cope with the contractions of childbirth.
The aim is to induce contractions and monitor the fetus to check for heart rate abnormalities using a cardiotocograph.
A normal heartbeat is a good sign that the fetus will be healthy during labor.
Choice B is wrong because a CST does not measure maternal blood pressure.
Choice C is wrong because a CST does not assess placental function directly.
Choice D is wrong because a CST does not measure amniotic fluid volume.
Normal ranges for fetal heart rate are between 110 and 160 beats per minute.
Normal ranges for uterine contractions are between 2 and 5 contractions in 10 minutes, lasting less than 90 seconds each.
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Correct Answer is C
Explanation
This means that the baby’s heart rate did not slow down after the contractions induced by oxytocin, which is a sign of normal fetal well-being.
A negative CST is normal and desirable.
Choice A is wrong because no contractions were induced during the test.
This means that the test was inconclusive and could not assess the baby’s response to stress.
Choice B is wrong because late decelerations of the FHR were observed with at least 50% of contractions.
This means that the baby’s heart rate slowed down and stayed slow after the contractions, which is a sign of fetal distress and hypoxia.
A positive CST is abnormal and concerning.
Choice D is wrong because the client experienced mild uterine cramping during the test.
This is not a relevant factor for interpreting the CST results, which depend on the FHR patterns.
Uterine cramping can be a side effect of oxytocin administration or nipple stimulation.
Correct Answer is B
Explanation
This test can detect genetic disorders.
Chorionic villus sampling (CVS) is a prenatal test that involves taking a sample of tissue from the placenta to test for chromosomal abnormalities and certain other genetic problems.
The placenta is a structure in the uterus that provides blood and nutrients from the mother to the fetus.
Choice A is wrong because CVS does not provide information on neural tube defects, such as spina bifida.
For this reason, women who undergo CVS also need a follow-up blood test between 16 to 18 weeks of their pregnancy to screen for neural tube defects.
Choice C is wrong because CVS can detect chromosomal abnormalities, but not all chromosomal abnormalities are genetic disorders.
For example, Down syndrome is a chromosomal abnormality that occurs randomly and is not inherited from the parents.
Choice D is wrong because CVS cannot detect Rh sensitization, which is a condition where the mother’s immune system produces antibodies against the fetus’s blood cells.
Rh sensitization can be detected by a blood test that measures the level of antibodies in the mother’s blood.
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