A patient with coronary artery disease asks the nurse about the "good cholesterol" laboratory values. The nurse knows that "good cholesterol" refers to which lipids?
Triglycerides
High-density lipoproteins (HDLs)
Very-low-density lipoproteins (VLDLs)
Low-density lipoproteins (LDLs)
The Correct Answer is B
Choice A reason: Triglycerides are not "good cholesterol." They are lipids stored in adipose tissue or transported in blood, associated with cardiovascular risk when elevated. Unlike HDLs, triglycerides do not remove cholesterol from arteries, making them a risk factor, not a protective lipid in coronary artery disease.
Choice B reason: High-density lipoproteins (HDLs) are known as "good cholesterol" because they transport cholesterol from peripheral tissues to the liver for excretion, reducing arterial plaque buildup. Higher HDL levels are protective against coronary artery disease, making this the correct answer for the patient’s question.
Choice C reason: Very-low-density lipoproteins (VLDLs) transport triglycerides, contributing to atherosclerosis when elevated. They are not considered "good cholesterol," as they do not facilitate cholesterol removal like HDLs. VLDLs are associated with increased cardiovascular risk, unlike the protective role of HDLs.
Choice D reason: Low-density lipoproteins (LDLs) are "bad cholesterol," as they deposit cholesterol in arterial walls, promoting atherosclerosis and coronary artery disease. Unlike HDLs, which remove cholesterol, LDLs increase cardiovascular risk, making this an incorrect choice for "good cholesterol" in laboratory values.
Nursing Test Bank
Naxlex Comprehensive Predictor Exams
Related Questions
Correct Answer is C
Explanation
Choice A reason: Itraconazole is a systemic antifungal used for infections like histoplasmosis. It inhibits ergosterol synthesis but is not typically used topically for athlete’s foot due to its oral or intravenous administration. Its systemic use carries risks like hepatotoxicity, making it unsuitable for localized dermatophyte infections.
Choice B reason: Ketoconazole is available as a topical cream but is less commonly used for athlete’s foot compared to terbinafine. It inhibits fungal ergosterol synthesis and is effective for cutaneous infections, but its topical use is more associated with seborrheic dermatitis or candidiasis, not primarily tinea pedis.
Choice C reason: Terbinafine is a topical antifungal commonly used for athlete’s foot (tinea pedis). It inhibits squalene epoxidase, disrupting fungal cell membrane synthesis, leading to fungal death. Its topical application effectively treats dermatophyte infections like Trichophyton, making it a first-line choice for localized fungal infections.
Choice D reason: Amphotericin B is a systemic antifungal used for severe fungal infections. It binds to ergosterol, causing fungal cell lysis, but is not used topically for athlete’s foot due to its toxicity and intravenous administration. It is reserved for life-threatening systemic infections, not cutaneous conditions.
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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