| Literature DB >> 28528936 |
Yoshifusa Abe1, Işil Inan-Erdogan2, Kunihiko Fukuchi3, Hitomi Wakabayashi4, Yasuha Ogawa4, Satoshi Hibino5, Shunsuke Sakurai6, Kazuhiko Matsuhashi6, Yoshitaka Watanabe6, Kaori Hashimoto6, Kazuhisa Ugajin7, Kazuo Itabashi6.
Abstract
Although carbapenem is the recommended for urinary tract infection (UTI) caused by extended-spectrum beta-lactamase (ESBL)-producing organisms, non-carbapenems have been reported to be effective for adult patients with UTI caused by ESBL-producing organisms. The purpose of this study was to evaluate the efficacy of non-carbapenems for pediatric patients with UTI due to ESBL-producing Escherichia coli (E. coli) based on the microbiologic and clinical outcomes. Fifteen children, who were treated for first febrile UTI caused by ESBL-producing E. coli were enrolled in this study. Antimicrobial susceptibilities and ESBL production were determined according to the Clinical and Laboratory Standards Institute guidelines. To detect CTX-M genes, polymerase chain reaction was performed with specific primers for blaCTX-M detection. Of the 15 enrolled patients, 10 (66.7%) were boys and 5 (33.3%) were girls, with a median age of four months. VUR was detected in six patients (40%). For detection of blaCTX-M by PCR, CTX-M-3, CTX-M-8, CTX-M-14, and CTX-M-15 were detected in five, one, eight, and one patient, respectively. Overall, 14 of the 15 isolates (93.3%) were susceptible for fosfomycin (FOM), and all isolates were susceptible for cefmetazole (CMZ), flomoxef (FMOX), and imipenem/cilastatin (IPM/CS). Of the 15 patients, 12 (80%) clinically improved without the use of carbapenems. In conclusion, even if isolates of ESBL-producing E. coli are multidrug resistant based on MIC assessment, clinical susceptibility to non-carbapenems, such as CMZ, FMOX, and FOM, is possible. Accordingly, carbapenems may not be required all the time for treatment of pediatric UTI in clinical practice.Entities:
Keywords: Children; Extended-spectrum beta-lactamase; Upper urinary tract infection
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Year: 2017 PMID: 28528936 DOI: 10.1016/j.jiac.2017.04.006
Source DB: PubMed Journal: J Infect Chemother ISSN: 1341-321X Impact factor: 2.211