Which of the following is a first-line drug for the treatment of active tuberculosis?
Amphotericin B
Isoniazid
Vancomycin
Fluconazole
The Correct Answer is B
Choice A reason: Amphotericin B is an antifungal drug used for systemic fungal infections like cryptococcosis. It binds to ergosterol in fungal cell membranes, causing cell death. It has no activity against Mycobacterium tuberculosis, the causative agent of tuberculosis, and is not used in tuberculosis treatment regimens.
Choice B reason: Isoniazid is a first-line drug for active tuberculosis. It inhibits mycolic acid synthesis, disrupting the cell wall of Mycobacterium tuberculosis, leading to bactericidal effects. It is highly effective in combination with other drugs like rifampin, ethambutol, and pyrazinamide, forming the cornerstone of tuberculosis therapy.
Choice C reason: Vancomycin is an antibiotic used for gram-positive bacterial infections, such as methicillin-resistant Staphylococcus aureus (MRSA). It inhibits cell wall synthesis but is ineffective against Mycobacterium tuberculosis, which has a unique mycolic acid-containing cell wall, requiring specific antitubercular drugs like isoniazid for treatment.
Choice D reason: Fluconazole is an antifungal drug that inhibits fungal cytochrome P450, disrupting ergosterol synthesis. It is used for infections like candidiasis but has no activity against Mycobacterium tuberculosis. Tuberculosis treatment requires bactericidal drugs targeting the mycobacterial cell wall, not antifungal agents like fluconazole.
Nursing Test Bank
Naxlex Comprehensive Predictor Exams
Related Questions
Correct Answer is A
Explanation
Choice A reason: Intravenous heparin has an immediate onset, as it rapidly enhances antithrombin activity, inhibiting thrombin and factor Xa, preventing clot formation. This quick action makes it ideal for acute conditions like pulmonary embolism, providing instant anticoagulation, with effects measurable by aPTT within minutes of administration.
Choice B reason: A 5- to 10-minute onset is too slow for IV heparin, which acts immediately upon entering the bloodstream. Subcutaneous heparin has a delayed onset (20-60 minutes), but IV delivery ensures rapid anticoagulant effects, making this timeframe incorrect for IV administration.
Choice C reason: A 20-minute onset is inaccurate for IV heparin. Its immediate binding to antithrombin provides instant anticoagulation, unlike oral anticoagulants like warfarin, which take days. The 20-minute timeframe may apply to subcutaneous heparin, not IV, which acts within seconds to minutes.
Choice D reason: A 1-hour onset is incorrect for IV heparin, which provides immediate anticoagulation by enhancing antithrombin’s inhibition of clotting factors. This rapid action is critical for acute thrombotic conditions. A 1-hour delay applies to drugs with slower absorption, not IV heparin’s direct action.
Correct Answer is A
Explanation
Choice A reason: Nystatin lozenges must dissolve slowly in the mouth to ensure prolonged contact with oral mucosa, effectively treating candidiasis by disrupting fungal cell membranes. Slow dissolution maximizes local antifungal activity, targeting Candida albicans in the oral cavity, a common complication of inhaled corticosteroid use.
Choice B reason: Rinsing the mouth with water before using an inhaler is appropriate for corticosteroids to prevent thrush but is irrelevant for nystatin lozenges. Nystatin treats existing oral candidiasis, and rinsing beforehand may reduce its contact time with affected mucosa, decreasing efficacy.
Choice C reason: Rinsing with mouthwash after an inhaler is not standard for nystatin or corticosteroid use. Mouthwash may contain alcohol, irritating oral mucosa or reducing nystatin’s antifungal effect. Rinsing with water after corticosteroids prevents thrush, but this instruction is misapplied to nystatin lozenges.
Choice D reason: Chewing nystatin lozenges is incorrect, as it reduces contact time with oral mucosa, decreasing antifungal efficacy. Swallowing the drug shifts its action to the gastrointestinal tract, ineffective for oral candidiasis. Slow dissolution ensures targeted treatment of Candida in the mouth, preventing recurrence.
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