The drug of choice for herpes and cytomegalovirus treatment:

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ABVD chemotherapy drugs Questions

Question 1 of 5

The drug of choice for herpes and cytomegalovirus treatment:

Correct Answer: D

Rationale: The correct answer is D) Acyclovir. Acyclovir is an antiviral medication that is specifically effective against herpes simplex virus (HSV) and cytomegalovirus (CMV). It works by inhibiting the viral DNA polymerase, thus preventing viral replication and spread. This makes it the drug of choice for the treatment of both herpes and CMV infections. Option A) Saquinavir is a protease inhibitor used in the treatment of HIV, not herpes or CMV infections. Option B) Interferon alfa is used in various conditions like hepatitis B and C, certain cancers, and autoimmune diseases, but not for herpes or CMV treatment. Option C) Didanosine is a nucleoside reverse transcriptase inhibitor used in the treatment of HIV, not herpes or CMV infections. In an educational context, understanding the specific drugs used for different viral infections is crucial for healthcare providers to make accurate treatment decisions. Knowing the mechanism of action and spectrum of activity of each drug helps in selecting the most appropriate therapy for the patient's condition, thereby improving clinical outcomes. It is important for students to grasp these distinctions to ensure safe and effective patient care.

Question 2 of 5

Second generation anti-histaminics do not produce the following effect:

Correct Answer: D

Rationale: The correct answer is D) Anti-emetic effect. Second-generation antihistamines, such as loratadine or cetirizine, are primarily used to treat allergic conditions like allergic rhinitis and urticaria. They are not known for their anti-emetic effects. Option A) Anti-allergic action is correct because second-generation antihistamines are designed to alleviate allergy symptoms by blocking the action of histamine. Option B) May cause cardiac arrhythmia is incorrect. Second-generation antihistamines have a better safety profile compared to first-generation antihistamines and are less likely to cause cardiac side effects. Option C) Long-acting antihistaminic effect is correct as second-generation antihistamines have a longer duration of action compared to first-generation antihistamines. In an educational context, understanding the specific effects and uses of different generations of antihistamines is crucial for healthcare professionals to make informed decisions when prescribing medications. Knowing the differences between first and second-generation antihistamines can help in optimizing treatment plans and avoiding potential side effects.

Question 3 of 5

Sumatriptan is a selective agonist at:

Correct Answer: D

Rationale: In the context of ABVD chemotherapy drugs, it is crucial to understand the mechanism of action of various medications that may be used in conjunction with this regimen. Sumatriptan, a medication commonly used to treat migraines, is a selective agonist at 5-HT1D receptors. These receptors are found in the brain and play a role in vasoconstriction of intracranial blood vessels, which contributes to the relief of migraine symptoms. Option A, 5-HT2 receptors, is incorrect because sumatriptan does not primarily act on these receptors. 5-HT2 receptors are involved in various physiological processes, but not in the mechanism of action of sumatriptan. Option B, 5-HT3 receptors, is also incorrect. 5-HT3 receptors are mainly found in the gastrointestinal tract and are involved in the regulation of nausea and vomiting, not the mechanism of action of sumatriptan. Option C, 5-HT1A receptors, is not the correct answer either. While sumatriptan is a selective agonist at 5-HT1 receptors, it specifically targets the 5-HT1D subtype, not 5-HT1A. Understanding the specific receptor profile of medications like sumatriptan is essential for healthcare providers managing patients undergoing chemotherapy with ABVD regimen, as it helps optimize treatment outcomes and minimize potential drug interactions.

Question 4 of 5

The following enzyme can be inhibited by zileuton:

Correct Answer: C

Rationale: Zileuton is a leukotriene synthesis inhibitor used to treat asthma by blocking the 5-lipoxygenase enzyme, which plays a crucial role in the production of leukotrienes, potent mediators of inflammation. This inhibition reduces inflammation, bronchoconstriction, and mucous secretion in asthma patients. Option A, phosphodiesterase enzyme, is incorrect because zileuton does not target this enzyme. Phosphodiesterase inhibitors are used in the treatment of erectile dysfunction and pulmonary arterial hypertension. Option B, cyclooxygenase enzyme, is incorrect as zileuton does not inhibit this enzyme. Cyclooxygenase inhibitors, like aspirin and ibuprofen, target the synthesis of prostaglandins. Option D, phospholipase A2 enzyme, is also incorrect because zileuton does not inhibit this enzyme. Phospholipase A2 inhibitors are used in the treatment of inflammatory conditions like rheumatoid arthritis. Understanding the specific target of each drug is crucial in pharmacology to ensure proper treatment and avoid adverse effects. Educating healthcare professionals and students about drug mechanisms helps in making informed decisions for patient care.

Question 5 of 5

A 54-year-old woman with a history of left-sided breast cancer has been in remission for 5 years following paclitaxel therapy coupled with surgical resection. She has now noticed a new lump in her left breast close to where the original tumor was excised. A biopsy reveals recurring cancer. After talking with her physician, she decided to undergo more chemotherapy. Her physician prescribes a drug, which inhibits DNA topoisomerase. Which chemotherapy agent inhibits topoisomerase?

Correct Answer: D

Rationale: The correct answer is D) Irinotecan. Irinotecan inhibits DNA topoisomerase I, an enzyme essential for DNA replication and cell division. By inhibiting this enzyme, irinotecan interferes with cancer cell proliferation, making it an effective chemotherapy agent for treating various cancers, including breast cancer. Now, let's analyze why the other options are incorrect: A) Cisplatin: Cisplatin is a platinum-based chemotherapy drug that works by causing DNA cross-linking, leading to cell death. It does not inhibit topoisomerase. B) Docetaxel: Docetaxel is a taxane chemotherapy drug that acts by disrupting microtubule function in the cell, thereby inhibiting cell division. It does not inhibit topoisomerase. C) Erlotinib: Erlotinib is a tyrosine kinase inhibitor that targets the epidermal growth factor receptor (EGFR) pathway in cancer cells. It does not inhibit topoisomerase. Educational context: Understanding the mechanisms of action of different chemotherapy drugs is crucial in selecting the most appropriate treatment for cancer patients. Knowing which drugs target specific cellular pathways, like topoisomerase inhibition in the case of irinotecan, helps healthcare providers tailor treatment regimens for optimal outcomes. It is important for healthcare professionals to stay updated on the latest research and guidelines to provide evidence-based care to patients undergoing chemotherapy.

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