The majority of community-acquired pneumonias (CAPs) are caused by typ
ical bacterial pathogens, i.e., S. pneumoniae, H. influenzae or M. cat
arrhalis. Atypical pneumonias, i.e., legionnaires' disease, C. pneumon
iae pneumonia and M. pneumoniae pneumonia are less common in frequency
than typical bacterial pathogens, but are of considerable public heal
th and therapeutic importance. The newest therapeutic considerations i
n CAP are related to monotherapy versus combination therapy, parentera
l versus oral therapy, minimizing the emergence of penicillin-resistan
t pneumococci and an appreciation that comorbid factors in antibiotic
selection are unimportant. Monotherapy using a respiratory quinolone o
r doxycycline covers both typical and atypical causes of CAPs and is e
qually efficacious and less expensive than double drug therapy. Except
in patients unable to take oral medications/those in CCUs, patients w
ith CAP may be started on i.v. antibiotic therapy, but should be switc
hed to oral therapy after 48 hours/clinical defervescence. The combina
tion of 2 days of i.v. therapy plus 12 days of oral therapy has been s
hown to be as effective as 14 days of i.v. therapy. The use of doxycyc
line or respiratory quinolones may forestall or eliminate the emergenc
e of highly penicillin-resistant pneumococci, and, for this reason, th
ese agents probably should be used preferentially over beta-lactam ant
ibiotics to treat CAPs. The status of the host's immune system, partic
ularly intact splenic function, and the underlying condition of the ca
rdiorespiratory system are the critical factors in predicting mortalit
y, morbidity, complications and hospital stay. However, antibiotic sel
ection is not affected by comorbidities, and antibiotics should not be
changed or added to the usual therapy of GAP because of comorbid fact
ors. Multiple drug therapy does not improve the outcome, which is a fu
nction of underlying host factors.