Publication | Open Access
A changing pattern of susceptibility of Xanthomonas maltophilia to antimicrobial agents: implications for therapy
200
Citations
29
References
1994
Year
Antimicrobial ChemotherapyDrug ResistanceActive AntibioticsAntimicrobial StewardshipAntimicrobial TherapyInfection ControlAntimicrobial ResistanceHealth SciencesAntimicrobial Drug DiscoveryAntibacterial AgentAntimicrobial PharmacokineticsAntimicrobial CompoundPharmacologyIntermediate SusceptibilityClinical MicrobiologyXanthomonas MaltophiliaAntimicrobial SusceptibilityAntibioticsDilution TechniqueMicrobiologyAntimicrobial AgentsAntimicrobial PharmacodynamicsMedicine
The in vitro susceptibilities of 130 Xanthomonas maltophilia isolates to 12 antibiotics--trimethoprim-sulfamethoxazole, minocycline, ticarcillin-clavulanate, ceftazidime, cefoperazone, cefoperazone-sulbactam, imipenem, ciprofloxacin, and the investigational quinolones PD 117558, PD 117596, PD 127391, and sparfloxacin--were determined by a microtiter broth dilution technique. Other than the investigational quinolones, the most active antibiotics were minocycline, trimethoprim-sulfamethoxazole, and ticarcillin-clavulanate, in order. However, the first two were not bactericidal, while about half of the isolates exhibited intermediate susceptibility to ticarcillin-clavulanate. Patterns of susceptibility to trimethoprim-sulfamethoxazole and ciprofloxacin relative to the years of isolation of these strains reflected the development of resistance to the antibiotic prophylaxis practices in the hospital. We recommend that a combination of antibiotics, such as trimethoprim-sulfamethoxazole, minocycline, and ticarcillin-clavulanate, at or close to the maximum tolerated doses be in the treatment of serious X. maltophilia infections.
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