A nurse is teaching about neural tube defects to a group of pregnant females. Which of the following disease processes should the nurse include as an example of a neural tube defect?
Cerebral palsy.
Muscular dystrophy.
Spina bifida.
Hydrocephalus.
The Correct Answer is C
Choice A reason: Cerebral palsy results from brain injury, often perinatally, affecting movement and posture, not from neural tube closure failure. It involves motor cortex damage, not structural defects of the neural tube, which forms early in embryonic development, making it unrelated to neural tube defects.
Choice B reason: Muscular dystrophy is a genetic disorder causing progressive muscle degeneration, not a neural tube defect. It affects muscle fibers, not the embryonic neural tube, which forms the brain and spinal cord, distinguishing it from conditions like spina bifida.
Choice C reason: Spina bifida is a neural tube defect where the embryonic neural tube fails to close, causing spinal cord and vertebral defects. This congenital malformation can lead to neurological impairments, like paralysis, due to exposed or malformed spinal structures, a hallmark of neural tube defects.
Choice D reason: Hydrocephalus involves cerebrospinal fluid accumulation in the brain, often secondary to other conditions, but is not a primary neural tube defect. It results from impaired fluid dynamics, not failure of neural tube closure, distinguishing it from spina bifida’s embryonic origin.
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Related Questions
Correct Answer is A
Explanation
Choice A reason: Newborn screening for phenylketonuria involves a heel stick blood test within 24-48 hours post-birth to detect elevated phenylalanine levels. Early testing ensures timely diagnosis, preventing intellectual disability from untreated phenylketonuria, a genetic disorder impairing phenylalanine metabolism, requiring immediate dietary intervention.
Choice B reason: Lack of manifestations does not exempt newborns from phenylketonuria screening, as symptoms appear later. Screening is universal, as early detection prevents severe neurological damage from phenylalanine accumulation, making this statement incorrect for standard newborn care protocols.
Choice C reason: Testing one week after birth delays phenylketonuria screening, risking untreated phenylalanine buildup, which causes irreversible brain damage. Screening occurs within 24-48 hours to ensure early intervention, making this timing incorrect for effective management of this metabolic disorder.
Choice D reason: Fasting for 6 hours is not required for phenylketonuria screening. The heel stick test is performed regardless of feeding status, as phenylalanine levels are detectable early. Fasting risks hypoglycemia in newborns, making this an unnecessary and harmful requirement.
Correct Answer is A
Explanation
Choice A reason: Placing the child in isolation is the priority to prevent the spread of bacterial meningitis, a highly contagious infection transmitted via respiratory droplets. Droplet precautions, including a private room, protect healthcare workers and patients, reducing nosocomial transmission of pathogens like Neisseria meningitidis.
Choice B reason: Obtaining blood cultures is critical to identify the causative organism in bacterial meningitis, guiding antibiotic therapy. However, it is secondary to isolation, as delaying containment risks spreading the infection, which can cause severe neurological complications or death in exposed individuals.
Choice C reason: Administering IV antibiotics is urgent in bacterial meningitis to treat the infection, but isolation takes precedence to prevent transmission. Antibiotics reduce bacterial load but do not immediately eliminate contagiousness, making isolation the first step to ensure public health safety.
Choice D reason: Preparing for a lumbar puncture confirms the diagnosis by analyzing cerebrospinal fluid, but it is not the priority over isolation. Delaying isolation risks spreading the contagious infection, whereas the lumbar puncture, while diagnostic, does not address immediate transmission concerns.
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