Which of the following types of patients are more vulnerable to drug toxicity?
Immunocompromised patients
Immunocompetent patients
Infants and elderly patients
Patients who have allergic reactions
The Correct Answer is A
A. Immunocompromised patients:
Immunocompromised patients, whose immune systems are weakened or impaired, are indeed more vulnerable to drug toxicity. This vulnerability can be due to factors such as decreased ability to metabolize and eliminate drugs, increased susceptibility to infections and opportunistic pathogens, and impaired organ function, particularly in the liver and kidneys, which are involved in drug metabolism and excretion.
B. Immunocompetent patients:
Immunocompetent patients have normal immune function and are generally less vulnerable to drug toxicity compared to immunocompromised individuals. However, susceptibility to drug toxicity can still vary depending on factors such as age, underlying health conditions, renal and hepatic function, and concurrent use of other medications.
C. Infants and elderly patients:
Infants and elderly patients are more vulnerable to drug toxicity due to factors such as immature or declining organ function, altered drug metabolism and elimination, and differences in body composition. In infants, organ systems are still developing, while in elderly patients, age-related changes can affect drug pharmacokinetics and increase the risk of adverse reactions.
D. Patients who have allergic reactions:
Patients who have allergic reactions may experience adverse drug reactions if they are exposed to the offending medication again. However, this does not necessarily make them more vulnerable to drug toxicity in general. Allergic reactions are specific immune responses and differ from drug toxicity, which can occur due to various mechanisms unrelated to allergies.
Nursing Test Bank
Naxlex Comprehensive Predictor Exams
Related Questions
Correct Answer is A
Explanation
A. Permanent, inheritable changes to DNA:
Mutations are alterations or changes in the DNA sequence of an organism's genome. These changes can be permanent and heritable, meaning they are passed on to offspring during reproduction. Mutations can occur spontaneously or be induced by various factors such as environmental agents, radiation, or errors in DNA replication or repair mechanisms. These changes can lead to variations in traits among individuals within a population and are essential for the process of evolution.
B. An organism that is capable of causing disease:
This definition refers to the term "pathogen." Pathogens are organisms, such as bacteria, viruses, fungi, or parasites, that are capable of causing disease in their hosts. Pathogens can infect humans, animals, plants, or other organisms and can lead to a wide range of diseases, from mild infections to life-threatening illnesses.
C. The severity of a disease that an organism is able to cause:
This definition refers to the term "virulence." Virulence is a measure of the severity or harmfulness of a pathogen, indicating its ability to cause disease in a host organism. Highly virulent pathogens are more likely to cause severe illness or death, while less virulent pathogens may cause milder symptoms or asymptomatic infections. Virulence factors, such as toxins, adhesion molecules, or evasion mechanisms, contribute to the pathogen's ability to cause disease.
D. A substance that can inhibit the growth of bacteria:
This definition refers to the term "antibiotic." Antibiotics are chemical substances produced by microorganisms, fungi, or synthesized in the laboratory that can inhibit the growth of or kill bacteria. Antibiotics are commonly used to treat bacterial infections and work by targeting specific bacterial structures or metabolic processes, thereby disrupting bacterial growth and survival. However, antibiotics are not mutations; instead, they are therapeutic agents used to combat bacterial infections.
Correct Answer is D
Explanation
A. Not affected:
This choice suggests that taking ciprofloxacin with antacids does not alter its absorption. However, this is not correct. When ciprofloxacin is taken with antacids containing certain ions (such as aluminum, magnesium, or calcium), the absorption of ciprofloxacin can indeed be affected due to the formation of insoluble complexes, leading to decreased absorption.
B. Delayed:
This choice implies that taking ciprofloxacin with antacids delays its absorption. While it's true that the interaction between ciprofloxacin and certain antacids can alter absorption, the main effect is not typically a delay in absorption but rather a decrease due to the formation of insoluble complexes. Therefore, while "delayed" may somewhat describe the effect, it doesn't fully capture the nature of the interaction.
C. Increased:
This choice suggests that taking ciprofloxacin with antacids increases its absorption. However, this is not accurate. Antacids containing aluminum, magnesium, or calcium can interfere with the absorption of ciprofloxacin by forming insoluble complexes with the drug, leading to decreased absorption rather than an increase.
D. Decreased:
This choice correctly identifies the effect of taking ciprofloxacin with antacids. When ciprofloxacin is taken concurrently with antacids containing aluminum, magnesium, or calcium, the absorption of ciprofloxacin is decreased. The ions in the antacids bind with ciprofloxacin in the gastrointestinal tract, forming insoluble complexes that are poorly absorbed, thereby reducing the effectiveness of the antibiotic.
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