Difficulty: Medium
Correct Answer: Cephalothin
Explanation:
Introduction / Context:
β-lactamase–producing Staphylococcus aureus inactivates many β-lactam antibiotics by hydrolyzing their β-lactam ring. This question tests recognition of agents that remain effective versus those predictably inactivated, guiding rational therapy choices for staphylococcal infections.
Given Data / Assumptions:
Concept / Approach:
Drugs with inherent resistance to staphylococcal β-lactamase (e.g., isoxazolyl penicillins) or drugs that are not β-lactams (e.g., vancomycin) retain activity. Adding a β-lactamase inhibitor protects susceptible β-lactams. Early cephalosporins like cephalothin are hydrolyzed by staphylococcal β-lactamases and thus unreliable.
Step-by-Step Solution:
Verification / Alternative check:
Empiric and definitive therapy guidelines for methicillin-susceptible S. aureus favor β-lactamase–stable agents (e.g., nafcillin, oxacillin) or cefazolin rather than cephalothin; for β-lactamase production more broadly, non-β-lactams like vancomycin remain effective when indicated.
Why Other Options Are Wrong:
Common Pitfalls:
Assuming all cephalosporins uniformly resist β-lactamases; in reality, susceptibility varies by generation and enzyme spectrum.
Final Answer:
Cephalothin
Discussion & Comments