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Antimicrobial Agents and Chemotherapy, January 1999, p. 16-20, Vol. 43, No. 1
Service ORL,
Received 20 May 1998/Returned for modification 18 August
1998/Accepted 19 October 1998
This multicenter, noncomparative, nonrandomized study evaluated the
clinical efficacy and safety of ceftriaxone for treating acute otitis
media in children following clinical failure of oral antibiotic
therapy. Middle-ear fluid samples were collected on day 0 and on day 3, 4, or 5 (day 3 to 5) and were used to test whether ceftriaxone therapy
can eradicate Streptococcus pneumoniae isolates with
increased resistance to penicillin (MIC
0066-4804/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
Eradication by Ceftriaxone of Streptococcus
pneumoniae Isolates with Increased Resistance to Penicillin in
Cases of Acute Otitis Media
1 mg/liter). At the
first visit, on day 0, middle-ear fluid was sampled for bacteriological
testing by tympanocentesis or otorrhea pus suction. Patients were
administered 50 mg of ceftriaxone/kg of body weight/day, injected
intramuscularly once daily, for 3 days. A second sample was collected
by tympanocentesis if a pneumococcus isolate for which the MIC of
penicillin was
1 mg/liter was detected in the day-0 sample and if the
middle-ear effusion persisted on day 3 to 5. This second sample was
tested for bacterial eradication. One hundred eighty-six children
aged 5 months to 5 years, 10 months, with acute otitis media clinical
failure were enrolled and treated in this trial. On day 10 to 12, 145 (83.8%) of the 173 patients evaluable for clinical efficacy were
clinically cured. Of the 59 patients infected by pneumococci, 36 had
isolates for which the MICs of penicillin were
1 mg/liter. Of those
patients, on day 10 to 12, 32 (88.9%) were clinically cured.
Middle-ear fluid samples collected by day 3 to 5 following the onset of
treatment with ceftriaxone were sterile for 24 of the 27 (88.9%)
patients who were infected as of day 0 by pneumococci for which the
MICs of penicillin were
1 mg/liter and who were evaluable for
bacteriological eradication. On day 10 to 12, 81.4% of S. pneumoniae-infected children and 87.5% of Haemophilus
influenzae-infected children were clinically cured. No
discontinuation of treatment due to adverse events, particularly due to
local reactions at the injection site, were reported. Only 11 adverse
events which had doubtful, probable, or possible links with the study
treatment were recorded. Both the bacteriologically assessed
eradication of pneumococci for which the MICs of penicillin were
1
mg/liter and the clinical cure rates demonstrate that ceftriaxone is of
value in the management of acute otitis media unresponsive to previous
oral antibiotic therapy.
*
Corresponding author. Mailing address: Service ORL,
Hôpital Bichat, 46, rue Henri Huchard, 75018 Paris, France.
Phone: (33) (0)1 40 25 77 51. Fax: (33) (0)1 42 28 61 82. E-mail:
pierre.gehanno{at}bch.ap-hop-paris.fr.
Antimicrobial Agents and Chemotherapy, January 1999, p. 16-20, Vol. 43, No. 1
0066-4804/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
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