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Abstract
The present study was undertaken to compare the efficacy and safety of a new regimen
of cefaclor (25 mg/kg BID) with amoxicillin-clavulanate and erythromycin TID at standard
doses for the treatment of pediatric patients with acute pharyngotonsillitis (APT).
A total of 673 children (age range, 2 to 12 years) with signs and symptoms of APT
were enrolled; 245 of these children who had a positive throat culture for group A
beta-hemolytic streptococci (GABHS) entered the study and were randomly assigned to
receive cefaclor 25 mg/kg BID, amoxicillin-clavulanate 15 mg/kg TID, or erythromycin
15 mg/kg TID. A 10-day antibiotic course was prescribed for each patient. Clinical
and bacteriologic responses were assessed at the end of treatment (day 10) and at
the follow-up visit (day 30). All GABHS strains isolated from throat cultures were
tested for in vitro sensitivity to the antibiotics used in the study. Side effects
(mainly nausea) were rare and mild in each group and did not require discontinuation
of therapy. No GABHS strain was resistant to cefaclor or to amoxicillin-clavulanate;
37.9% of the strains were resistant to erythromycin. The results indicated that cefaclor
given BID seems to be as effective as amoxicillin-clavulanate given TID (cure rate,
91.9% and 90.5%, respectively) and more effective than erythromycin given TID (cure
rate, 76.8%) for the treatment of patients with APT. Erythromycin resistance among
GABHS is an emerging problem in many geographic areas.
Keywords
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© 1998 Published by Elsevier Inc.