A pregnant woman is getting ready for a chorionic villus sampling procedure at 10 weeks.
The nurse has been educating her about the procedure.
Which of the following statements, if made by the client, would indicate that the teaching has been effective?
“Fetal lung maturity can be determined through a chorionic villus sampling.”
“I will have to have a non-stress test (NST) after the procedure to check the baby’s well-being.”
“The chorionic villus sampling is a non-invasive screening procedure.”
“Chorionic villus sampling can detect genetic abnormalities in the first trimester.”
The Correct Answer is D
Choice A rationale:
Fetal lung maturity is not assessed through chorionic villus sampling (CVS). It's primarily evaluated through amniocentesis, a different prenatal diagnostic procedure that involves sampling amniotic fluid.
CVS focuses on placental tissue, not lung development.
It's essential for clients to understand the specific purposes of each prenatal test to make informed decisions and have accurate expectations.
Choice B rationale:
While a non-stress test (NST) might be recommended after CVS in some cases, it's not a routine part of the procedure.
The decision to conduct an NST is based on individual risk factors and assessment by healthcare providers.
It's essential for clients to understand the potential need for additional testing but not assume it's always required.
Choice C rationale:
CVS is considered an invasive procedure, as it involves entering the uterus to collect placental tissue.
Non-invasive prenatal testing (NIPT) methods, which analyze fetal DNA in maternal blood, are available for screening purposes.
It's crucial for clients to differentiate between invasive and non-invasive prenatal testing options to make informed choices based on their preferences and risk factors.
Choice D rationale:
This statement accurately reflects the primary purpose of CVS.
It's a diagnostic procedure that can detect various genetic abnormalities, such as Down syndrome, cystic fibrosis, and TaySachs disease, during the first trimester of pregnancy.
Understanding the ability to detect genetic abnormalities early in pregnancy allows clients to make informed decisions about their pregnancy management and prepare for potential outcomes.
Nursing Test Bank
Naxlex Comprehensive Predictor Exams
Related Questions
Correct Answer is C
Explanation
Choice C rationale:
It is a misconception that fetal movement decreases as delivery approaches. While the nature of the movements may change— becoming less like kicks and more like rolls or twists due to less space in the uterus—the frequency of movements should remain consistent. In fact, increased fetal movement can be a sign of labor approaching. Therefore, a pregnant client who believes that fetal movements will decrease closer to delivery needs further instruction to ensure they are aware of this important health indicator.
Here's a detailed explanation of why the other choices are correct:
Choice A: This statement is correct. Fetal kick counts can be performed at home, providing a convenient and comfortable way to monitor fetal well-being.
Choice B: This statement is also correct. A decrease in fetal movement, defined as less than 3 kicks in an hour, is a potential concern and warrants contacting a healthcare provider for further evaluation.
Choice D: This statement is accurate as well. Daily fetal kick counts are generally recommended to establish a baseline of the baby's usual activity pattern and to detect any significant changes that might indicate a problem.
Correct Answer is C
Explanation
Choice A rationale:
This response is incorrect because newborn screening tests do not determine blood type. Blood type is typically determined through a separate blood test, such as an ABO and Rh typing test.
While knowing a baby's blood type is important for medical reasons, it's not the primary purpose of newborn screening.
Focusing solely on blood type could mislead parents about the broader scope of conditions that newborn screening aims to identify.
Choice B rationale:
This response is incorrect because newborn screening tests are not diagnostic tests. They are screening tests, which means they identify babies who may be at risk for certain diseases, but they do not confirm whether or not a baby actually has a disease.
Diagnostic tests are typically more specific and are performed after a screening test has indicated a potential problem.
It's crucial to clarify the distinction between screening and diagnosis to avoid causing undue alarm or confusion for parents.
Choice C rationale:
This is the correct response. It accurately explains that newborn screening tests are routine procedures that are performed to detect babies who may be at risk for developing certain diseases.
The emphasis on "risk" is important because it highlights that a positive screening result does not necessarily mean that a baby has a disease, but rather that further testing is needed to confirm the diagnosis.
This response also avoids making assumptions about the parents' carrier status, which is a sensitive topic that should be addressed with care and discretion.
Choice D rationale:
This response is incorrect because it assumes that the parents are carriers for a disease, which may not be the case.
Even if the parents are carriers, newborn screening tests are not designed to specifically determine whether a disease has been passed down from parent to child.
Making such assumptions could create unnecessary anxiety or confusion for parents, and it's important to provide information that is accurate and relevant to their specific situation.
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