Tick the drug belonging to glycopeptides:

Questions 52

ATI RN

ATI RN Test Bank

Cardiovascular Drugs Questions

Question 1 of 5

Tick the drug belonging to glycopeptides:

Correct Answer: A

Rationale: In pharmacology, understanding the classification of drugs is crucial for safe and effective medication administration. In the context of cardiovascular drugs, the correct answer is A) Vancomycin, which belongs to the glycopeptide class of antibiotics. Vancomycin is a potent antibiotic commonly used to treat serious bacterial infections such as methicillin-resistant Staphylococcus aureus (MRSA) and other Gram-positive bacterial infections. Its mechanism of action involves inhibiting bacterial cell wall synthesis by binding to the D-alanyl-D-alanine terminus of cell wall precursors, thereby disrupting cell wall formation and leading to bacterial cell death. Lincomycin (option B) is a lincosamide antibiotic that works by inhibiting bacterial protein synthesis. Neomycin (option C) is an aminoglycoside antibiotic that disrupts bacterial protein synthesis. Carbenicillin (option D) is a semisynthetic penicillin antibiotic. These antibiotics have different mechanisms of action and do not belong to the glycopeptide class like vancomycin. Educationally, knowing the classification of drugs is important for making informed decisions in clinical practice. Understanding the mechanisms of action of drugs helps healthcare professionals choose the most appropriate treatment for specific infections, thereby improving patient outcomes and reducing the risk of antibiotic resistance.

Question 2 of 5

Tick the drug, a benzimidazole derivative:

Correct Answer: B

Rationale: In this question about cardiovascular drugs, the correct answer is B) Mebendazole, a benzimidazole derivative. Benzimidazoles are a class of drugs commonly used to treat parasitic infections by disrupting the microtubule structure in the parasite. Mebendazole specifically acts by inhibiting microtubule formation, which leads to the paralysis and death of the parasites. Option A) Praziquantel is not a benzimidazole derivative; it is used to treat infections caused by schistosoma and tapeworms by disrupting the parasite's cell membrane. Option C) Suramin is a medication used in the treatment of African trypanosomiasis and onchocerciasis, but it does not belong to the benzimidazole class. Option D) Pyrantel is an anthelmintic medication that is used to treat intestinal worm infections. It works by causing paralysis of the worms but is not a benzimidazole derivative. Understanding the classification of drugs based on their chemical structure is crucial in pharmacology as it helps in predicting their mechanism of action, side effects, and potential drug interactions. Students should be familiar with different drug classes to make informed decisions in clinical practice when choosing the most appropriate treatment for patients.

Question 3 of 5

Which of the following actions most likely contributed to the thiazide-induced increase in renal excretion of potassium?

Correct Answer: B

Rationale: The thiazide-induced increase in renal excretion of potassium is most likely due to the blockade of the Na+/K+/2Cl− cotransporter. Thiazide diuretics inhibit the reabsorption of sodium in the distal convoluted tubule which leads to increased sodium and water excretion, as well as potassium excretion. By blocking the Na+/K+/2Cl− cotransporter, thiazides disrupt the normal electrolyte balance in the kidney, resulting in increased potassium excretion.

Question 4 of 5

Which of the following urine electrolyte profiles is most consistent with acetazolamide treatment?

Correct Answer: A

Rationale: Acetazolamide is a carbonic anhydrase inhibitor commonly used as a diuretic and in the treatment of glaucoma and altitude sickness. When analyzing its effects on urine electrolyte profiles, it is crucial to understand its mechanism of action. Acetazolamide works by inhibiting carbonic anhydrase in the proximal convoluted tubule of the nephron, leading to decreased bicarbonate reabsorption and subsequent alkaline diuresis. In the context of urine electrolyte profiles, the most consistent pattern with acetazolamide treatment is seen in Profile P, which typically demonstrates metabolic acidosis characterized by decreased bicarbonate levels and increased chloride levels due to the loss of bicarbonate in the urine. Profiles Q, R, and S are not consistent with acetazolamide treatment. Profile Q might show altered electrolyte levels, but not in a pattern typical of acetazolamide. Profile R might exhibit different electrolyte imbalances, such as hyperkalemia or hyponatremia, which are not characteristic of acetazolamide. Profile S may indicate dehydration or other conditions, but not the specific electrolyte changes associated with acetazolamide use. Understanding the effects of different cardiovascular drugs on electrolyte profiles is essential for healthcare professionals to make accurate clinical decisions and provide optimal patient care. This knowledge helps in interpreting lab results, monitoring drug efficacy, and managing potential side effects. A solid grasp of pharmacology and its implications on electrolyte balance is crucial in the field of cardiovascular medicine.

Question 5 of 5

Increased serum levels of which of the following may be associated with a decreased risk of atherosclerosis?

Correct Answer: D

Rationale: In the context of cardiovascular health and atherosclerosis, high-density lipoproteins (HDL) play a crucial role in reducing the risk of atherosclerosis. HDL is often referred to as "good cholesterol" because it helps remove excess cholesterol from the bloodstream and transport it to the liver for excretion. This process is known as reverse cholesterol transport, which ultimately leads to a decrease in the accumulation of plaque in the arteries, reducing the risk of atherosclerosis and cardiovascular disease. On the other hand, very low-density lipoproteins (VLDL), low-density lipoproteins (LDL), and intermediate-density lipoproteins (IDL) are considered "bad cholesterol" as they are associated with the buildup of cholesterol in the arteries, leading to atherosclerosis. VLDL carries triglycerides, LDL is known as the main carrier of cholesterol and is often deposited in arterial walls, and IDL is a precursor to LDL. Increased levels of these lipoproteins contribute to the development and progression of atherosclerosis by promoting the formation of plaque in the arteries. Educationally, understanding the role of different lipoproteins in cholesterol metabolism and their impact on cardiovascular health is essential for healthcare professionals, especially those working in cardiology or primary care. By grasping the functions of HDL versus VLDL, LDL, and IDL, clinicians can make informed decisions when managing patients at risk for atherosclerosis and cardiovascular disease. Promoting a high HDL level through lifestyle modifications and medications can be a key strategy in preventing atherosclerosis and its complications.

Access More Questions!

ATI RN Basic


$89/ 30 days

ATI RN Premium


$150/ 90 days

Similar Questions