Effective Oral Combination Treatment for Extended-Spectrum Beta-Lactamase-Producing .

Microb Drug Resist

Department of Pediatrics and Neonatology, Faculty of Medicine, Hashemite University, Zarqa, Jordan.

Published: October 2019

Extended-spectrum beta-lactamase-producing (ESBL-EC) is increasing worldwide. The drugs of choice for treatment of ESBLs are parenteral carbapenems. The aim of this study was to evaluate the and efficacy of a new combination of oral cephalosporins and amoxicillin/clavulanate in treatment of ESBL-EC. A total of 150 ESBL-EC samples were collected over 1 year from two referral centers. Synergistic studies of cephalosporins and amoxicillin/clavulanate were performed using disk approximation and disk replacement methods. Combination treatment was assessed on 20 ESBL-EC urinary tract infection (UTI) patients. ESBL-EC isolates were confirmed in 150 patients with a mean age of 46.67 years, 75.2% of them being women. Antibiotic susceptibility testing of isolates indicated high resistance rate to oral antibiotics. The frequency of positive synergy and mean distance of synergy between cephalosporins and amoxicillin/clavulanate was significantly higher with cefotaxime and cefixime compared with cefpodoxime, cefdinir, and ceftazidime using disk approximation and disk replacement methods ( < 0.05). Addition of amoxicillin/clavulanate enhanced the susceptibility rate with cefixime from 8.6% to 86.3%, significantly higher than with other cephalosporins ( < 0.0005). Cefixime and amoxicillin/clavulanate synergy was not affected by age, gender, hospital, department, sample type, or bacterial load. Eighteen of 20 ESBL-EC-positive UTI patients had a positive synergy test and complete clinical and microbiological resolution after completion of cefixime and amoxicillin/clavulanate oral treatment course. Cefixime and amoxicillin/clavulanate combination therapy could be an effective oral outpatient treatment option for ESBL-EC. synergistic testing is simple and predictive of successful treatment.

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http://dx.doi.org/10.1089/mdr.2019.0065DOI Listing

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