Azithromycin is an azalide antimicrobial agent active in vitro against
major pathogens responsible for infections of the respiratory tract,
skin and soft tissues in children. Pathogens that are generally suscep
tible to azithromycin include Haemophilus influenzae (including ampici
llin-resistant strains), Moraxella catarrhalis, Chlamydia pneumoniae,
Chlamydia trachomatis, Mycoplasma pneumoniae, Legionella spp., Strepto
coccus pyogenes and Streptococcus agalactiae. Azithromycin is also gen
erally active against erythromycin- and penicillin-susceptible Strepto
coccus pneumoniae and methicillin-susceptible Staphylococcus aureus. A
zithromycin is administered once daily, achieves clinically relevant c
oncentrations at sites of infection, is slowly eliminated from the bod
y and has few drug interactions. In children, azithromycin is usually
given as either a 3-day course of 10 mg/kg/day or a 5-day course with
10 mg/kg on the first day, followed by 5 mg/kg/day for a further 4 day
s. These standard regimens were as effective as amoxicillin/clavulanic
acid: clarithromycin, cefaclor and amoxicillin in the treatment child
ren with otitis media. Azithromycin was also as effective as either ph
enoxymethylpenicillin (penicillin V), erythromycin, clarithromycin or
cefaclor against streptococcal pharyngitis or tonsillitis in children,
but appears to result in moire recurrence of infection than phenoxyme
thylpenicillin in this indication, necessitating a dosage of 12 mg/kg/
day for 5 days. Community-acquired pneumonia, bronchitis and other res
piratory tract infections in children responded as well to azithromyci
n as to amoxicillin/clavulanic acid, cefaclor, erythromycin or josamyc
in, Azithromycin was similar or superior to ceftibuten in mixed genera
l practice populations of patients. However, symptoms of lower respira
tory tract infections resolved more rapidly with azithromycin than wit
h erythromycin, josamycin or cefaclor. Skin and soft tissue infections
responded as well iii azithromycin as to cefaclor, dicloxacillin or f
lucloxacillin, and oral azithromycin was as effective as ocular tetrac
ycline in treating trachoma. Although not as well tolerated as phenoxy
methylpenicillin in the treatment of streptococcal pharyngitis, azithr
omycin is at least as well tolerated as most other agents used to trea
t respiratory tract and other infections in children and was better to
lerated than amoxicillin/clavulanic acid. Adverse events that do occur
are mostly gastrointestinal and tend to be mild to moderate in severi
ty. Conclusions: Azithromycin is an effective and well tolerated alter
native to first-line agents in the treatment of respiratory tract, ski
n and soft tissue infections in children, offerring the convenience of
a short, once-daily regimen.