Among Gram-positive pathogens, Staphylococcus aureus is the leading cause o
f death from nosocomial pneumonia, The bacterium developed progressive resi
stance to beta -lactams, and methicillin-resistant strains emerged in the 1
980s, In consequence, vancomycin has become the drug of choice for treatmen
t of this infection over the last decade, based on susceptibility tests and
the serum antimicrobial levels recorded, However, half of the patients tre
ated with vancomycin have died. In contrast, in patients receiving beta -la
ctams for pneumonia caused by methicillin-sensitive S, aureus, survival is
the rule. These observations, together with the emergence of isolates with
reduced susceptibility to glycopeptides, raised concern about the use of va
ncomycin as standard therapy for pneumonia caused by Gram-positive cocci. M
aintaining tissue levels above minimal inhibitory concentration is vital to
successful clinical outcome, Optimizing treatment focusing on this goal an
d new antimicrobials provide new opportunities to improve survival.