ANTIBIOTIC-THERAPY AND ACUTE OUTCOME OF MENINGITIS DUE TO STREPTOCOCCUS-PNEUMONIAE CONSIDERED INTERMEDIATELY SUSCEPTIBLE TO BROAD-SPECTRUM CEPHALOSPORINS
Tq. Tan et al., ANTIBIOTIC-THERAPY AND ACUTE OUTCOME OF MENINGITIS DUE TO STREPTOCOCCUS-PNEUMONIAE CONSIDERED INTERMEDIATELY SUSCEPTIBLE TO BROAD-SPECTRUM CEPHALOSPORINS, Antimicrobial agents and chemotherapy, 38(5), 1994, pp. 918-923
Children with meningitis due to Streptococcus pneumoniae isolates that
are relatively or fully resistant to penicillin and have decreased su
sceptibility to broad-spectrum cephalosporins (MIC, greater than or eq
ual to 2.0 mu g/ml) who have failed treatment with broad-spectrum ceph
alosporins have been reported. The National Committee for Clinical Lab
oratory Standards has newly revised guidelines indicating that S. pneu
moniae isolates associated with meningitis for which the MICs are grea
ter than or equal to 0.5 mu g/ml should be considered resistant to bro
ad-spectrum cephalosporins. This recommendation is not clearly based o
n data related to clinical outcome and may be too conservative. We pre
sent data on five children who had S. pneumoniae meningitis due to iso
lates that were relatively or fully resistant to penicillin (MIC range
, 0.125 to 4.0 mu g/ml) and had cefotaxime or ceftriaxone MICs of 0.50
to 2.0 mu g/ml. Their clinical courses and outcomes were comparable t
o those of five children with S. pneumoniae meningitis due to strains
that were relatively or fully resistant to penicillin and were inhibit
ed by cefotaxime at concentrations of less than or equal to 0.25 mu g/
ml, as well as to those of 25 patients with S. pneumoniae meningitis d
ue to penicillin-susceptible isolates identified during the same perio
d. Children with meningitis due to S. pneumoniae with cefotaxime or ce
ftriaxone MICs of less than or equal to 1.0 mu g/ml may be adequately
treated with these antibiotics. Further clinical data are required bef
ore solid recommendations can be made regarding cephalosporin breakpoi
nts for S. pneumoniae.