Second-order pain is:

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Cardiovascular Drugs Pharmacology NCLEX Questions Questions

Question 1 of 5

Second-order pain is:

Correct Answer: B

Rationale: In the context of pharmacology, understanding pain pathways and types of pain is crucial for effective pain management using cardiovascular drugs. Second-order pain, as indicated by option B, is described as dull, burning pain. This type of pain is often associated with C-fibers, which are unmyelinated and slower in transmission compared to A-delta fibers. Dull, burning pain is typically less localized and can be more diffuse compared to sharp, well-localized pain, which is associated with A-delta fibers. Additionally, second-order pain is not effectively reduced by non-narcotic analgesics, as these drugs are more suited for milder, acute pain rather than the persistent, burning nature of second-order pain. Understanding the characteristics of different types of pain is essential for selecting appropriate pharmacological interventions for pain management in cardiovascular patients, ensuring optimal patient care and outcomes.

Question 2 of 5

Which of the following phenothiazine derivatives is a potent local anesthetic?

Correct Answer: C

Rationale: In this question, the correct answer is C) Chlorpromazine. Chlorpromazine belongs to the phenothiazine class of drugs, which are primarily known for their antipsychotic properties. However, chlorpromazine is unique among phenothiazines because it also possesses potent local anesthetic properties. This makes it a valuable drug for both psychiatric and anesthetic purposes. Now, let's explain why the other options are incorrect: A) Fluphenazine and B) Thioridazine are also phenothiazine derivatives, but they do not possess the same level of local anesthetic potency as chlorpromazine. Fluphenazine is primarily used as an antipsychotic medication, while thioridazine is known for its antipsychotic and antiemetic properties. D) None of the above is incorrect because chlorpromazine is indeed a potent local anesthetic among the given options. In an educational context, understanding the pharmacological properties of different drug classes is crucial for healthcare professionals, especially for pharmacology students and nurses preparing for exams like the NCLEX. Knowing the specific characteristics and uses of drugs within a class like phenothiazines can help healthcare providers make informed decisions regarding patient care and medication management.

Question 3 of 5

Which of the following CNS stimulants are the agents of selective effect?

Correct Answer: D

Rationale: In pharmacology, understanding the classification and mechanism of action of different drug categories is crucial for safe and effective patient care. In the context of CNS stimulants with selective effects, the correct answer is D) Actoprotectors. Actoprotectors are agents that enhance body resistance to physical and mental stress without causing generalized CNS stimulation. They selectively protect the body from stressors without exerting a non-specific stimulant effect on the CNS. Option A) Analeptics are CNS stimulants that act non-selectively to stimulate the brain centers, often leading to generalized CNS stimulation without a specific focus on enhancing resistance to stress. Option B) General tonics are substances that provide a general feeling of well-being and energy without a specific focus on CNS stimulation or stress protection. Option C) Psychostimulants are drugs that primarily act on the central nervous system to increase alertness, attention, and energy levels but do not necessarily provide selective protection against stressors. Educationally, understanding the nuances between different classes of CNS stimulants is vital for healthcare professionals to make informed decisions regarding drug therapy for patients. By grasping the specific effects and mechanisms of action of each drug category, practitioners can tailor treatment plans to individual patient needs, optimizing therapeutic outcomes while minimizing potential side effects and drug interactions. This knowledge is especially important in the field of cardiovascular pharmacology, where drug selection can significantly impact patient outcomes.

Question 4 of 5

Antianxiety agents have:

Correct Answer: D

Rationale: In the context of pharmacology, antianxiety agents, such as benzodiazepines, possess a variety of effects that contribute to their mechanism of action. The correct answer, option D, "All of the above," is correct because antianxiety agents exhibit sedative and hypnotic activity, muscle relaxing and anticonvulsant effects, as well as amnesic properties. Sedative and hypnotic activities help calm the central nervous system, promoting relaxation and sleep induction, which can be beneficial for patients experiencing anxiety. Muscle relaxing and anticonvulsant effects are important as they help alleviate physical symptoms of anxiety, such as muscle tension and seizures that may result from excessive neuronal firing during anxious states. Amnesic properties are crucial for patients who may undergo distressing or traumatic events, as they can help in blunting the memory of such events, aiding in the management of anxiety-related disorders. Options A, B, and C, when assessed individually, do not encompass the full range of effects exhibited by antianxiety agents. While sedative and hypnotic activities, muscle relaxing and anticonvulsant effects, and amnesic properties are indeed characteristics of antianxiety agents, it is the combination of all these effects that make option D the correct choice. Educationally, understanding the multifaceted effects of antianxiety agents is crucial for healthcare professionals, especially those prescribing or administering these medications. By grasping the diverse actions of these drugs, healthcare providers can make informed decisions regarding their use, ensuring optimal patient outcomes and safety.

Question 5 of 5

The limitation of sevoflurane is:

Correct Answer: B

Rationale: Rationale: The correct answer is B) Chemically unstable. Sevoflurane is a volatile anesthetic agent used for general anesthesia. One of its limitations is its chemical instability, as it can undergo chemical breakdown in the presence of carbon dioxide absorbents, leading to the formation of compound A, which is nephrotoxic. This is a crucial point to understand for safe administration of sevoflurane in clinical practice. Option A) High incidence of coughing and laryngospasm is incorrect because sevoflurane is actually known for its smooth induction and emergence, making it a preferred choice in anesthesia for its minimal airway irritation. Option C) Centrally mediated sympathetic activation leading to a rise of BP and HR is incorrect because sevoflurane is a cardiovascular stable anesthetic agent that typically causes minimal cardiovascular depression. Option D) Hepatotoxicity is incorrect since sevoflurane is not known to cause significant liver damage. It is primarily metabolized by the liver into inactive compounds and is considered safe for patients with hepatic impairment. Understanding the limitations and characteristics of different anesthetic agents is crucial for pharmacology students and healthcare professionals to ensure safe and effective patient care during surgical procedures. It is essential to grasp not only the benefits but also the potential drawbacks and contraindications of each medication to make informed clinical decisions.

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