ATI RN
Pharmacology CNS Drugs Quizlet Questions
Question 1 of 5
A 60-year-old man presents to his primary care physician. During his interview, it is discovered that he is taking several outdated drugs for his medical condition. One of his medical conditions is hypertension, for which he takes a drug that prevents neurotransmitter uptake into vesicles. This prevents neurons from being able to concentrate and store certain neurotransmitters such as norepinephrine. Which of the following drugs is this?
Correct Answer: C
Rationale: The correct answer is C) Reserpine. Reserpine is a drug that inhibits the transport of neurotransmitters such as norepinephrine into storage vesicles, leading to decreased levels of norepinephrine in nerve terminals. This action ultimately results in decreased sympathetic outflow and lower blood pressure, making it effective for treating hypertension. A) Clonidine works by stimulating alpha-2 adrenergic receptors in the brainstem, leading to reduced sympathetic outflow and decreased blood pressure through central actions. B) Methyldopa works by being converted into alpha-methyl norepinephrine, which stimulates central alpha-2 adrenergic receptors, reducing sympathetic outflow. D) Scopolamine is an anticholinergic drug used primarily for motion sickness and nausea, not for hypertension. In an educational context, understanding how different classes of drugs work in the treatment of hypertension is crucial for healthcare professionals to make informed decisions when managing patients with cardiovascular conditions. Knowing the mechanisms of action of drugs like reserpine, clonidine, methyldopa, and scopolamine helps in selecting the most appropriate treatment based on the patient's condition and comorbidities.
Question 2 of 5
A 27-year-old hospital worker has access to the pharmacy when no other workers are around. He is able to find morphine and inject himself with supratherapeutic dose of morphine. He then collapses and is found dead by coworkers 24 h later. What is the most likely explanation for his death?
Correct Answer: D
Rationale: The correct answer is D) Respiratory depression and arrest. In this scenario, the individual injected himself with a supratherapeutic dose of morphine, which is an opioid. Opioids like morphine act on the central nervous system to depress respiratory drive. When taken in high doses, opioids can cause severe respiratory depression, leading to a decrease in the drive to breathe and ultimately respiratory arrest, resulting in death. Option A) Cardiac arrest is incorrect because the primary mechanism of death in opioid overdose is respiratory depression, not cardiac arrest. Option B) Cardiac ischemia is also incorrect as there is no indication in the scenario that the individual experienced a heart attack or ischemic event. Option C) Cardiomyopathy is not the cause of death in this case, as there is no mention of any pre-existing heart condition or heart muscle damage. Educationally, this question highlights the importance of understanding the pharmacological effects of opioids on the body, particularly the risk of respiratory depression associated with opioid overdose. It emphasizes the need for healthcare workers to be vigilant in preventing unauthorized access to controlled substances and to be aware of the potential risks associated with opioid misuse. This knowledge is crucial in clinical practice to ensure patient safety and prevent harm related to drug diversion and overdose.
Question 3 of 5
A 54-year-old man with seizure disorder and chronic neuropathic pain presents to his primary care physician for follow-up. Review of his laboratory studies indicates elevated liver function tests to four times the normal levels. Which of the following agents would be preferred to manage this patient?
Correct Answer: D
Rationale: In this scenario, the preferred agent to manage the patient with elevated liver function tests due to seizure disorder and chronic neuropathic pain would be option D) Pregabalin. Pregabalin is a medication used to treat neuropathic pain and seizures, and it is primarily excreted unchanged by the kidneys, making it a safer choice for patients with liver impairment as it does not require hepatic metabolism for elimination. Option A) Carbamazepine, option B) Phenobarbital, and option C) Phenytoin are all antiepileptic drugs that are metabolized in the liver. In the case of a patient with elevated liver function tests, using these medications can further burden the already compromised liver function and potentially worsen the condition. Carbamazepine, Phenobarbital, and Phenytoin are known to induce liver enzymes and can lead to hepatotoxicity in patients with liver dysfunction. Educationally, understanding the pharmacokinetics and pharmacodynamics of CNS drugs is crucial for healthcare professionals when managing patients with comorbidities such as liver impairment. It is essential to consider the organ functions of patients when selecting medications to minimize adverse effects and ensure optimal therapeutic outcomes. Pregabalin, with its renal excretion pathway, provides a safer alternative in this clinical scenario, highlighting the importance of individualized pharmacotherapy based on patient-specific factors.
Question 4 of 5
A 21-year-old male college student complains of difficulty falling asleep at night. He asks if there is anything “mild†he can take to help him get to sleep. Which of the following hypnotics mimics an endogenous hormone?
Correct Answer: D
Rationale: In this question, the correct answer is D) Ramelteon. Ramelteon is the only option that mimics an endogenous hormone, specifically melatonin, which regulates the sleep-wake cycle. Ramelteon acts on melatonin receptors in the brain to help regulate sleep patterns without causing the same risks of dependency or tolerance seen with traditional hypnotics. A) Diazepam and B) Lorazepam are benzodiazepines that act on GABA receptors to induce sedation and are not hormones. These drugs are not recommended for long-term use due to the risk of dependence and potential for cognitive impairment. C) Phenobarbital is a barbiturate with sedative properties but does not mimic an endogenous hormone like melatonin. Barbiturates are associated with a high risk of overdose and are not commonly used for sleep induction due to their safety profile. Educationally, understanding the mechanisms of action of different hypnotic drugs is crucial for healthcare professionals to make informed decisions when treating sleep disorders. Knowing the advantages of melatonin receptor agonists like ramelteon over traditional sedatives can help in selecting the most appropriate treatment for patients with insomnia.
Question 5 of 5
Which of the following statements is correct about the normal functioning of the nicotinic receptors in a 19-year-old man college student athlete from the college baseball team?
Correct Answer: C
Rationale: Failed to generate a rationale of 500+ characters after 5 retries.