ANTIBACTERIAL PROPERTIES OF INVESTIGATIONAL, NEW, AND COMMONLY USED ANTIBIOTICS AGAINST ISOLATES OF PSEUDOMONAS-CEPACIA IN MICHIGAN

被引:9
作者
BHAKTA, DR
LEADER, I
JACOBSON, R
ROBINSONDUNN, B
HONICKY, RE
KUMAR, A
机构
[1] MICHIGAN STATE UNIV,DEPT PEDIAT & HUMAN DEV,B240 LIFE SCI BLDG,E LANSING,MI 48824
[2] INGHAM MED CTR,MICROBIOL LAB,LANSING,MI
[3] MICHIGAN DEPT PUBL HLTH,MICROBIOL LAB,LANSING,MI 48909
关键词
PSEUDOMONAS-CEPACIA; CYSTIC FIBROSIS; ANTIBIOTICS; CEFTAZIDIME; PIPERACILLIN; MEZLOCILIN; CIPROFLOXACIN; CEFPIROME; DESACETYLCEFOTAXIME;
D O I
10.1159/000239020
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Microdilution antimicrobial susceptibility testing was performed with 73 isolates of Pseudomonas cepacia collected from the sputum of patients throughout Michigan with cystic fibrosis. Susceptibility testing was done using new and investigational antibiotics (loracarbef, cefixime, cefpirome, desacetylcefotaxime, cefpodoxime, cefmetazole, cefepime, cefprozil, and fleroxacin) and commonly used antibiotics (ceftazidime, mezlocillin, piperacillin, ciprofloxacin, tobramycin, and amikacin). Ceftazidime was the most active antibiotic, and 91.8% of isolates were susceptible to it with MIC50 and MIC90 values of less-than-or-equal-to 4 and 16 mug/ml, respectively. For mezlocillin, piperacillin, and ciprofloxacin 84.9, 89 and 39.7% of the isolates, respectively, were mostly moderately susceptible. Loracarbef, cefixime, cefprozil, cefmetazole, cefepime, fleroxacin, cefpodoxime, tobramycin, and amikacin did not show activity against P. cepacia. For cefpirome and desacetylcefotaxime 24.7 and 60.3% of the isolates, respectively, were moderately susceptible. Both MIC50 and MIC90 were > 32 mug/ml for cefpirome and 32 and > 64 mug/ml for desacetylcefotaxime.
引用
收藏
页码:319 / 323
页数:5
相关论文
共 7 条
[1]  
CHIN NX, 1984, DIAGNOSTIC MICROBI S, V2, P215
[2]   CEFTAZIDIME ALONE AND IN COMBINATION IN PATIENTS WITH CYSTIC-FIBROSIS - LACK OF EFFICACY IN TREATMENT OF SEVERE RESPIRATORY-INFECTIONS CAUSED BY PSEUDOMONAS-CEPACIA [J].
GOLD, R ;
JIN, E ;
LEVISON, H ;
ISLES, A ;
FLEMING, PC .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 1983, 12 :331-336
[3]   PSEUDOMONAS-CEPACIA - BIOLOGY, MECHANISMS OF VIRULENCE, EPIDEMIOLOGY [J].
GOLDMANN, DA ;
KLINGER, JD .
JOURNAL OF PEDIATRICS, 1986, 108 (05) :806-812
[4]   INVITRO ACTIVITY OF MULTIPLE ANTIMICROBIAL COMBINATIONS AGAINST PSEUDOMONAS-CEPACIA ISOLATES [J].
KUMAR, A ;
WOFFORDMCQUEEN, R ;
GORDON, RC .
CHEMOTHERAPY, 1989, 35 (04) :246-253
[5]   ANTIBIOTIC-RESISTANCE OF PSEUDOMONAS SPECIES [J].
PRINCE, A .
JOURNAL OF PEDIATRICS, 1986, 108 (05) :830-834
[6]  
THOMASSEN MJ, 1985, AM REV RESPIR DIS, V131, P791
[7]  
1990, NCCLS M2A2 NAT COMM