Which person is at the greatest risk for contracting hepatitis A?
A person who drank contaminated water
A person who had a blood transfusion
A newborn infant born to a mother with cirrhosis
A person who uses intravenous drugs regularly
The Correct Answer is A
Choice A reason: Hepatitis A is transmitted via the fecal-oral route, often through contaminated water or food. Ingesting water with hepatitis A virus leads to acute liver infection, as the virus replicates in hepatocytes, making this the highest risk scenario.
Choice B reason: Hepatitis A is not typically transmitted via blood transfusion, unlike hepatitis B or C. It spreads through contaminated food or water, so blood transfusion poses minimal risk for hepatitis A, making this choice incorrect.
Choice C reason: A newborn born to a mother with cirrhosis is not at high risk for hepatitis A, as it is not congenitally transmitted. Cirrhosis may result from hepatitis but does not directly increase hepatitis A risk, making this incorrect.
Choice D reason: Intravenous drug use is a risk factor for hepatitis B and C due to bloodborne transmission. Hepatitis A spreads via the fecal-oral route, not needles, so drug use poses lower risk compared to contaminated water, making this incorrect.
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Naxlex Comprehensive Predictor Exams
Related Questions
Correct Answer is C
Explanation
Choice A reason: Autosomal dominant disorders affect both genders equally, as they are not sex-linked. Heterozygous individuals express the disorder, not just males, due to the dominant allele on an autosome. The idea of females being carriers only applies to X-linked recessive disorders, making this choice scientifically inaccurate.
Choice B reason: Autosomal dominant disorders are caused by mutations on autosomes, not the Y chromosome, which is sex-linked and primarily affects males. These disorders do not typically skip generations, as the dominant allele is expressed in every affected individual, making this choice incorrect.
Choice C reason: In autosomal dominant disorders, a single mutated allele is sufficient for expression. An affected parent (heterozygous) has one normal and one mutated allele, leading to a 50% chance of passing the mutated allele to each child, causing the disorder. This genetic inheritance pattern makes this the correct choice.
Choice D reason: In autosomal dominant disorders, there is no "carrier" state as in recessive disorders, because heterozygous individuals express the disorder. The 50% probability applies to inheriting the disorder itself, not a carrier genotype, which is a concept relevant to autosomal recessive disorders, making this choice incorrect.
Correct Answer is C
Explanation
Choice A reason: Diarrhea is not a typical feature of autonomic dysreflexia, which involves sympathetic overactivity causing vasoconstriction. Bowel dysfunction may occur in spinal cord injury, but it is not specific to dysreflexia, making this incorrect.
Choice B reason: Tachycardia can occur in autonomic dysreflexia due to sympathetic stimulation, but it is less specific than headache, which is a hallmark symptom from severe hypertension, making this choice incorrect.
Choice C reason: Autonomic dysreflexia, often triggered by stimuli below the injury level, causes severe hypertension, leading to a pounding headache due to increased intracranial pressure. This is a hallmark symptom, making this the correct choice.
Choice D reason: Hypotension is not associated with autonomic dysreflexia, which causes hypertension from unopposed sympathetic responses. Hypotension may occur in spinal shock, not dysreflexia, making this choice incorrect.
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