ATI RN
Central Nervous System Stimulants and Related Drugs NCLEX Style Questions Questions
Question 1 of 5
Diethylstilbestrol (DES) should never be used in pregnant women because it is associated with all of the following EXCEPT:
Correct Answer: A
Rationale: DES, a synthetic estrogen, causes deep vein thrombosis (choice A), feminization of male offspring (choice B), and miscarriages (choice C) in pregnancy, linked to historical congenital anomalies (e.g., vaginal adenocarcinoma). Virilization of female offspring (choice D) isn't reported; DES mimics estrogen, not androgens. This exception highlights its teratogenic risks, banning its use in pregnancy.
Question 2 of 5
Which of the following statements regarding drugs of abuse is true?
Correct Answer: B
Rationale: The correct answer is B) LSD acts on various 5-HT receptors to produce its effects. This is true because LSD (lysergic acid diethylamide) is a hallucinogenic drug that primarily acts on serotonin (5-HT) receptors in the brain, particularly the 5-HT2A receptor subtype. By binding to these receptors, LSD alters sensory perception, mood, and thought processes, leading to its characteristic hallucinogenic effects. Option A is incorrect because Ketamine is not structurally related to psilocybin. Ketamine is a dissociative anesthetic that acts primarily on NMDA receptors in the brain, while psilocybin is the active compound in hallucinogenic mushrooms. Option C is incorrect because marijuana does not typically cause mydriasis (pupil dilation) and conjunctival injection (red eyes). These effects are more commonly associated with drugs like cocaine or amphetamines. Option D is incorrect because cocaine actually has a relatively short plasma half-life, typically around 1 hour. This rapid metabolism contributes to its short-lived effects and the cycle of craving and repeated dosing seen in cocaine abuse. In an educational context, understanding how different drugs interact with specific receptors in the brain can help healthcare professionals make informed decisions about patient care, especially in cases of substance abuse or overdose. Knowledge of the pharmacological actions of drugs of abuse is crucial for nurses, pharmacists, and other healthcare providers to effectively manage and treat patients with substance-related issues.
Question 3 of 5
Regarding ketamine, which statement is true?
Correct Answer: D
Rationale: In the context of Central Nervous System (CNS) stimulants and related drugs, understanding the pharmacology of ketamine is crucial for nursing practice. The correct answer, option D, stating that ketamine is contraindicated in sick sinus syndrome, is accurate because ketamine can exacerbate cardiac arrhythmias and should be avoided in patients with preexisting cardiac conduction abnormalities. Option A, stating that ketamine has a rapid onset of action, is incorrect as ketamine actually has a slower onset compared to other anesthetics. Option B, mentioning that ketamine is partially renally excreted, is also incorrect as ketamine is primarily metabolized in the liver. Option C, claiming that ketamine has no neurological side effects, is misleading as ketamine is known to cause side effects such as hallucinations and delirium. In an educational context, it is important for nursing students preparing for the NCLEX to understand the specific pharmacological properties and contraindications of CNS stimulants and related drugs like ketamine. By comprehensively reviewing each option and understanding why the correct answer is right while the others are wrong, students can enhance their critical thinking skills and improve their ability to answer similar questions on the exam.
Question 4 of 5
Regarding GABA, which statement is false?
Correct Answer: A
Rationale: Rationale: The correct answer is A) Receptor blockers have anticonvulsant activity. This statement is false because GABA receptor blockers actually reduce the inhibitory effects of GABA, leading to increased neuronal excitability, which is the opposite of what is needed for anticonvulsant activity. Option B) Is found in high concentrations in the basal ganglia is true. GABA is indeed found in high concentrations in the basal ganglia, which is involved in the regulation of voluntary motor movements. Option C) Concentrations in the basal ganglia are abnormally low in Huntington's chorea is true. In Huntington's disease, there is a decrease in GABA concentrations in the basal ganglia, contributing to the motor symptoms seen in this condition. Option D) Metabolism is inhibited by sodium valproate is true. Sodium valproate is known to inhibit the metabolism of GABA, leading to increased GABA levels and enhanced inhibitory neurotransmission. Educational context: Understanding the role of GABA in the central nervous system is crucial in the context of neurological disorders and pharmacology. GABA is the primary inhibitory neurotransmitter in the brain, playing a key role in maintaining the balance between excitation and inhibition. Knowledge of GABA function and dysfunction is essential for healthcare professionals, especially when considering the use of drugs that target the GABAergic system in the treatment of various conditions such as epilepsy, anxiety, and movement disorders.
Question 5 of 5
A 38-year-old woman presents to the ophthalmologist for a routine eye examination. She is given intraocular pilocarpine. She was supposed to be administered two drops in each to dilate the eyes for the examination. Unfortunately, the eyedrops were administered by a new technician who inadvertently administered 10 drops of pilocarpine in each eye. Which of the following agents should be immediately given to the patient?
Correct Answer: A
Rationale: In this scenario, the correct answer is A) Atropine. Pilocarpine is a parasympathomimetic drug that stimulates the muscarinic receptors in the eye, causing miosis (pupil constriction). Administering an excessive amount of pilocarpine can lead to excessive constriction of the pupil, resulting in symptoms like blurred vision, headache, brow ache, and potentially a decrease in vision. Atropine is an anticholinergic drug that acts by blocking the muscarinic receptors. By administering atropine, it can counteract the effects of pilocarpine overdose by dilating the pupil and alleviating the symptoms of excessive constriction. The other options (B) Carbachol, (C) Donepezil, and (D) Galantamine are not appropriate in this situation. Carbachol is also a parasympathomimetic drug like pilocarpine and would exacerbate the symptoms of pilocarpine overdose. Donepezil and Galantamine are both cholinesterase inhibitors used in the treatment of Alzheimer's disease and would not be effective in reversing the effects of pilocarpine overdose. From an educational perspective, understanding the pharmacology of these drugs is crucial for healthcare professionals to prevent medication errors and manage adverse drug reactions effectively. This case highlights the importance of drug knowledge, dosage calculation, and prompt intervention in clinical practice to ensure patient safety and optimal outcomes.