Indicate the local anesthetic, which is mainly used for regional nerve block anesthesia:

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Pharmacology of Drugs Acting on Cardiovascular System Questions

Question 1 of 5

Indicate the local anesthetic, which is mainly used for regional nerve block anesthesia:

Correct Answer: B

Rationale: The correct answer is B: Tetracaine. Tetracaine is a long-acting local anesthetic commonly used for regional nerve block anesthesia due to its duration of action. It provides effective and prolonged pain relief in a specific area by blocking nerve conduction. Procaine (A) is a short-acting local anesthetic, making it less suitable for regional nerve block anesthesia. Bupivacaine (D) is a long-acting local anesthetic like tetracaine, but it is more commonly used for epidural or spinal anesthesia rather than regional nerve blocks. Therefore, tetracaine is the most appropriate choice for regional nerve block anesthesia among the options provided.

Question 2 of 5

Indicate the neuromuscular blocker, which causes tachycardia:

Correct Answer: C

Rationale: The correct answer is C (Pancuronium). Pancuronium is a non-depolarizing neuromuscular blocker that can cause tachycardia by blocking muscarinic receptors leading to the inhibition of the parasympathetic system. This results in the dominance of the sympathetic system, leading to tachycardia. Tubocurarine (A) and Atracurium (B) are also non-depolarizing neuromuscular blockers, but they do not directly cause tachycardia. Succinylcholine (D) is a depolarizing neuromuscular blocker that can cause bradycardia due to its effects on acetylcholine receptors at the neuromuscular junction.

Question 3 of 5

Characteristics of ephedrine include all of the following EXCEPT:

Correct Answer: D

Rationale: The correct answer is D because ephedrine actually increases arterial pressure by stimulating alpha-adrenergic receptors, leading to vasoconstriction. A is incorrect as ephedrine works by directly stimulating adrenergic receptors, not by releasing stored catecholamines. B is correct as ephedrine is indeed a mild CNS stimulant. C is incorrect as tachyphylaxis, or a rapid decrease in response with repeated administration, is not commonly associated with ephedrine.

Question 4 of 5

Which of the following beta receptor antagonists is preferable in patients with asthma diabetes or peripheral vascular diseases?

Correct Answer: B

Rationale: The correct answer is B: Metoprolol. Metoprolol is a cardioselective beta blocker, meaning it primarily targets beta-1 receptors in the heart and has minimal effect on beta-2 receptors in the lungs. This makes it preferable in patients with asthma as it reduces the risk of bronchoconstriction compared to non-selective beta blockers like Propranolol (choice A). Metoprolol also has a lower risk of masking hypoglycemic symptoms in diabetic patients compared to non-selective agents. Nadolol (choice C) and Timolol (choice D) are non-selective beta blockers and may worsen asthma and peripheral vascular diseases due to their effects on beta-2 receptors.

Question 5 of 5

Which of the following hypnotic benzodiazepines is more likely to cause “hangover” effects such as drowsiness dysphoria and mental or motor depression the following day?

Correct Answer: C

Rationale: In pharmacology, understanding the pharmacokinetics and pharmacodynamics of benzodiazepines is crucial to predict their effects. In this case, the correct answer is C) Flurazepam. Flurazepam is a long-acting benzodiazepine with active metabolites that can accumulate in the body, leading to prolonged sedative effects. Its half-life is longer compared to other benzodiazepines, contributing to the increased likelihood of "hangover" effects such as drowsiness, dysphoria, and mental or motor depression the next day. Now, let's analyze why the other options are incorrect: - A) Temazepam: Temazepam is an intermediate-acting benzodiazepine with a shorter half-life compared to Flurazepam. It is less likely to cause significant hangover effects due to its shorter duration of action. - B) Triazolam: Triazolam is a short-acting benzodiazepine, which is commonly used for insomnia due to its rapid onset of action and short duration. It is less likely to cause prolonged hangover effects compared to Flurazepam. - D) None of the above: This is incorrect as Flurazepam, as explained earlier, is more likely to cause hangover effects compared to the other options. Educationally, this question highlights the importance of considering the pharmacokinetic properties of drugs when predicting their side effects. Understanding the duration of action, metabolism, and potential for accumulation of drugs like benzodiazepines is crucial for healthcare professionals to make informed decisions regarding their use in clinical practice.

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