Pneumonia is the leading cause of death from infection in the United States,
1 and timely empirical antibiotic therapy against the most likely pathogens is a cornerstone of care. However, causative pathogens are rarely identified,
2 leaving uncertainty in the choice of empirical antibiotic therapy. For patients hospitalized for community-onset pneumonia, this uncertainty has been magnified by the emergence of resistant organisms, chiefly methicillin-resistant
Staphylococcus aureus (MRSA) and
Pseudomonas aeruginosa. The concept of health care–associated pneumonia, intended to assist clinicians in risk assessment,
3 likely contributed to the overuse of broad-spectrum antibiotics.
4,5 Consequently, although fewer than 5% of hospitalized patients have resistant organisms detected, more than one-third receive broad-spectrum antibiotics.
6