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Antibiotic susceptibilities and therapeutic options forUreaplasma urealyticuminfections in neonates

 

作者: K. WAITES,   D. CROUSE,   G. CASSELL,  

 

期刊: The Pediatric Infectious Disease Journal  (OVID Available online 1992)
卷期: Volume 11, issue 1  

页码: 23-29

 

ISSN:0891-3668

 

年代: 1992

 

出版商: OVID

 

关键词: Ureaplasma urealyticum;neonate;antibiotics;susceptibility testing;respiratory tract

 

数据来源: OVID

 

摘要:

The appreciation ofUreaplasma urealyticumas a human pathogen and documentation of antibiotic resistance have heightened interest in drug susceptibilities and treatment alternatives for patients infected with this organism. Neonates pose special problems when therapy must be considered because of potential toxicities, clinical unfamiliarity or lack of experience. Forty-three isolates ofU. urealyticumobtained from the lower respiratory tracts of neonates were tested against chloramphenicol, ciprofloxacin, clindamycin, erythromycin, doxycycline, and gentamicin by a microbroth dilution technique in 10B broth.In vitroresistance was observed in 1 or more strains for each of the drugs tested, except for erythromycin (minimal inhibitory concentration (MIC) range, 0.125 to 4 μg/ml, MIC90= 2 μg/ml). MIC90values for the remaining five antibiotics were: doxycycline, 2 μg/ml; chloramphenicol, 8 μg/ml; ciprofloxacin, 8 μg/ml; clindamycin, 16 μg/ml; and gentamicin, 32 μg/ml. The effect of pH and/or media components on MICs was evaluated by comparing MICs of American Type Culture Collection reference strainStaphylococcus aureus29213 obtained in Mueller-Hinton broth (pH 7.2 to 7.4) and 10B broth (pH 6.0). No appreciable effect was detected for ciprofloxacin, chloramphenicol or doxycycline, whereas gentamicin, erythromycin and clindamycin all had MICs elevated by one to several dilutions when tested in 10B broth. In some instances the difference was sufficient to alter the interpretation of the MIC. Clinical experience in treating neonatal ureaplasmal infections is reviewed along with recommendations for obtaining cultures, initiating and monitoring efficacy of therapy.

 

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