Over the past three decades, penicillin-resistant pneumococci have emerged
worldwide. In addition, penicillin-resistant strains have also decreased su
sceptibility to other beta-lactams (including cephalosporins) and these str
ains are often resistant to other antibiotic groups, making the treatment o
ptions much more difficult. Nevertheless, the present in vitro definitions
of resistance to penicillin and cephalosporins in pneumococci could not be
appropriated for all types of pneumococcal infections. Thus, current levels
of resistance to penicillin and cephalosporin seem to have little, if any,
clinical relevance in nonmeningeal infections (e.g., pneumonia or bacterem
ia). On the contrary, numerous clinical failures have been reported in pati
ents with pneumococcal meningitis caused by strains with MICs greater than
or equal to 0.12 mu g/ml, and penicillin should never be used in pneumococc
al meningitis except when the strain is known to be fully susceptible to th
is drug. Today, therapy for pneumococcal meningitis should mainly be select
ed on the basis of susceptibility to cephalosporins, and most patients may
currently be treated with high-dose cefotaxime (+/-) vancomycin, depending
on the levels of resistance in the patient's geographic area. In this revie
w, we present a practical approach, based on current levels of antibiotic r
esistance, for treating the most prevalent pneumococcal infections. However
, it should be emphasized that the most appropriate antibiotic therapy for
infections caused by resistant pneumococci remains controversial, and compa
rative, randomized studies are urgently needed to clarify the best antibiot
ic therapy for these infections.