Clinical outcome of invasive infections in children caused by highly penicillin-resistant Streptococcus pneumoniae compared with infections caused bypenicillin-susceptible strains
D. Gomez-barreto et al., Clinical outcome of invasive infections in children caused by highly penicillin-resistant Streptococcus pneumoniae compared with infections caused bypenicillin-susceptible strains, ARCH MED R, 31(6), 2000, pp. 592-598
ing 1994-1998, we document the continuing emergence of drug-resistant Strep
tococcus pneumoniae strains at the Hospital Infantil de Mexico Federico Gom
ez in Mexico City.
Methods. We evaluate the clinical course of 49 invasive pneumococcal infect
ion outside the central nervous system (CNS) by a number of factors includi
ng the site, severity, and place where the infection was acquired, the unde
rlying health of die patient, and the adequacy of antimicrobial therapy.
Results. An underlying illness was present in 21 of 49 (43%) patients, 37 (
75%) patients had taken previous antimicrobial therapy, and 25% of the infe
ctions were nosocomially acquired. Overall, 25 of 49 (51%) of the pneumococ
cal strains tested were pencillin-resistant; strains with the highest resis
tance to penicillin were also resistant to cephalosporins. Twenty-two perce
nt of all strains were considered to be multidrug-resistant. Eleven of 25 p
enicillin-resistant strains were identified as multidrug-resistant, i.e., t
o erythromycin, TMP/SMX, and choramphenicol. Ten serotypes accounted for 88
% of the isolates, the most frequent serotypes being 23F, 14, 19V, 6A, and
6B. The overall case-fatality rate was 37% (18 of 49), with most deaths occ
urring within 3-5 days after antibiotic therapy was initiated. There was no
difference in the case fatality rate between children with penicillicin-no
nsusceptible and penicillin-susceptible pneumococcal infections; instead; c
ase-fatality rate correlated with severity of illness on admission and pres
ence of underlying disease.
Conclusions. Characterizing groups at risk for invasive pneumococcal diseas
e could aid in the development of preventive programs and increase the bene
fits from wide use of future conjugated vaccines. (C) 2001 IMSS. Published
by Elsevier Science Inc.