Tick the drug which belongs to nucleoside reverse transcriptase inhibitors:

Questions 52

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ATI Cardiovascular Drugs Quizlet Questions

Question 1 of 5

Tick the drug which belongs to nucleoside reverse transcriptase inhibitors:

Correct Answer: A

Rationale: The correct answer is A: Didanosine. Nucleoside reverse transcriptase inhibitors (NRTIs) are a class of antiretroviral drugs used to treat HIV/AIDS. Didanosine is an NRTI that inhibits the reverse transcriptase enzyme, crucial for HIV replication. Gancyclovir is a nucleoside analog used to treat viral infections but not specifically NRTIs. Nevirapine is a non-nucleoside reverse transcriptase inhibitor. Vidarabine is a nucleoside analog antiviral drug, but it is not classified as an NRTI. Overall, only Didanosine belongs to the NRTI class of drugs.

Question 2 of 5

A 59-year-old woman presented with an abrupt onset of palpitations accompanied by a vague complaint of feeling ill. Subsequent Holter monitoring revealed atrial fibrillation with a ventricular response up to 152 bpm. The patient's past history included primary hyperparathyroidism and intermittent claudication for 3 years, apparently due to peripheral occlusive arteriosclerosis. Which of the following drugs would be appropriate for the chronic control of the patient's arrhythmia?

Correct Answer: B

Rationale: The correct answer is B: Propranolol. Propranolol is a beta-blocker that can be used for rate control in atrial fibrillation. It works by blocking the effects of adrenaline on the heart, slowing the heart rate and reducing the force of contraction. In this case, the patient has atrial fibrillation with a rapid ventricular response, and propranolol can help slow the heart rate to a more appropriate level. A: Digoxin is primarily used for rate control in patients with heart failure, not as the first-line agent for atrial fibrillation with a rapid ventricular response. C: Verapamil is a calcium channel blocker that can also be used for rate control in atrial fibrillation, but beta-blockers are generally preferred in patients with concomitant peripheral artery disease. D: Lidocaine is a local anesthetic and antiarrhythmic agent used for ventricular arrhythmias, not appropriate for atrial fibrillation.

Question 3 of 5

The mechanism of action of cyclosporine involves

Correct Answer: B

Rationale: In understanding the mechanism of action of cyclosporine, it is crucial to comprehend its interaction with cyclophilin. Option B, "Binding to cyclophilin to cause inhibition of a cytoplasmic phosphatase," is the correct answer. Cyclosporine forms a complex with cyclophilin, which then inhibits calcineurin, a cytoplasmic phosphatase. This inhibition ultimately leads to the suppression of T-cell activation and the immune response. Option A, "Activation of calcineurin," is incorrect because cyclosporine actually inhibits calcineurin rather than activating it. Option C, "Blockade of interleukin-2 receptors," is not the primary mechanism of action of cyclosporine. While cyclosporine does influence interleukin-2 production indirectly by inhibiting T-cell activation, its primary mode of action is through calcineurin inhibition. Option D, "Inhibition of phospholipase A2," is also incorrect as this is not a function of cyclosporine. In an educational context, understanding the mechanism of action of cardiovascular drugs like cyclosporine is essential for nursing and medical students. Knowing how these drugs work at a molecular level helps in grasping their therapeutic effects and potential side effects. This knowledge is vital for safe medication administration and patient care in clinical practice.

Question 4 of 5

Antianginal drugs afford the following benefit/benefits

Correct Answer: D

Rationale: The correct answer is D) Both (a) and (b) - Terminate anginal attacks and decrease the frequency of anginal attacks. The rationale behind this is that antianginal drugs work in different ways to achieve these benefits. Some medications like nitroglycerin help terminate acute anginal episodes by dilating blood vessels, increasing blood flow, and reducing the workload on the heart. Others like beta-blockers or calcium channel blockers help decrease the frequency of anginal attacks by reducing myocardial oxygen demand, improving oxygen supply to the heart, and controlling heart rate and blood pressure. Option A) Terminate anginal attacks is correct, as mentioned above, some antianginal drugs are fast-acting and can provide immediate relief during an anginal episode. Option B) Decrease the frequency of anginal attacks is also correct because long-term use of antianginal medications can help prevent or reduce the frequency of anginal episodes by improving overall heart function and reducing the workload on the heart. Option C) Retard the progression of coronary artery disease is incorrect because while some antianginal drugs can help manage symptoms and improve quality of life for patients with coronary artery disease, they do not directly slow down or reverse the progression of the underlying disease process. In an educational context, understanding the benefits of antianginal drugs is crucial for healthcare professionals caring for patients with angina or coronary artery disease. By knowing how these medications work and the specific benefits they offer, healthcare providers can make informed decisions about treatment options, educate patients on medication use and expected outcomes, and ultimately improve patient outcomes and quality of life.

Question 5 of 5

While treating auricular fibrillation, digitalization is necessary prior to quinidine because

Correct Answer: A

Rationale: In the treatment of atrial fibrillation, digitalization is necessary prior to quinidine because it prevents a paradoxical increase in ventricular rate. Digitalis glycosides like digoxin help to control the ventricular response by reducing the conduction through the atrioventricular (AV) node, thereby preventing rapid ventricular rates commonly seen in atrial fibrillation. By slowing down the ventricular response, digitalization provides a more stable hemodynamic state before initiating quinidine therapy. Option B, stating that quinidine is only effective in the presence of digitalis, is incorrect. Quinidine is effective on its own in treating atrial fibrillation and does not require digitalis for its efficacy. Option C, suggesting that digitalization reduces the dose and side effects of quinidine, is also incorrect. Digitalization does not directly impact the dose or side effects of quinidine. Option D, stating that digitalization antagonizes the extracardiac effects of quinidine, is also incorrect. The primary reason for digitalization prior to quinidine is related to the control of ventricular rate in atrial fibrillation rather than the extracardiac effects of quinidine. In an educational context, understanding the rationale behind the specific order of medications in treating atrial fibrillation is crucial for healthcare professionals. By grasping the importance of digitalization before quinidine, providers can optimize patient care and outcomes in managing cardiac arrhythmias effectively.

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