Clinical and Bacteriological Efficacy of Amikacin in The Treatment of Lower Urinary Tract Infection Caused by Extended-Spectrum Beta-Lactamase-Producing Escherichia Coli or Klebsiella Pneumoniae

dc.contributor.authorIpekci, Tumay
dc.contributor.authorSeyman, Derya
dc.contributor.authorBerk, Hande
dc.contributor.authorCelik, Orcun
dc.contributor.orcIDhttps://orcid.org/0000-0002-2755-0526en_US
dc.contributor.pubmedID25179392en_US
dc.contributor.researcherIDAAB-2986-2020en_US
dc.date.accessioned2023-12-13T11:07:40Z
dc.date.available2023-12-13T11:07:40Z
dc.date.issued2014
dc.description.abstractUrinary tract infections (UTIs) caused by extended-spectrum beta-lactamase (ESBL)-producing bacteria have become a growing problem limiting therapeutic options. The aim of this study was to investigate the clinical and microbiological efficacy of amikacin treatment in adult patients with lower UTIs due to ESBL-producing Escherichia coli (Ec) or Klebsiella pneumonia (Kp). We conducted a retrospective study of 36 outpatients aged >18 years with dysuria or problems with frequency or urgency in passing urine; pyuria and a positive urine culture (10(5) cfu/ml) for ESBL producing Ec or Kp which is also resistant to nitrofurantoin, fosfomycin, quinolones and trimethoprim/sulfamethoxazole, between January 2013 and February 2014. Patients received intramuscular amikacin 15 mg/kg/day for 10 days. Clinical success was defined as disappearance of symptoms. Bacteriological success was defined as sterile control urine cultures. 58.3% of patients were female. Age range was 18-89 years. All of the patients had at least one complicating factor. 77.8% of the isolates were E. coli. Clinical success rate was 97.2%. Overall bacteriological success rates were 91.7% on the 3 day of treatment, 97.1% at the end of the treatment and 94.1% on the 7-10 days after treatment. After 28-32 days following the treatment, reinfection was found in 12% whereas relapse was not determined. Nephrotoxicity was developed in one patient. The clinicians should keep in mind that amikacin treatment is an efficient and safe alternative treatment option before the carbapenem treatment especially in patients with lower UTIs caused by ESBL-producing Ec or Kp that are resistant to all oral antibiotics. (C) 2014, Japanese Society of Chemotherapy and The Japanese Association for Infectious Diseases. Published by Elsevier Ltd. All rights reserved.en_US
dc.identifier.endpage767en_US
dc.identifier.issn1341-321Xen_US
dc.identifier.issue12en_US
dc.identifier.scopus2-s2.0-84940102802en_US
dc.identifier.startpage762en_US
dc.identifier.urihttp://hdl.handle.net/11727/11081
dc.identifier.volume20en_US
dc.identifier.wos000345558800005en_US
dc.language.isoengen_US
dc.relation.isversionof10.1016/j.jiac.2014.08.007en_US
dc.relation.journalJOURNAL OF INFECTION AND CHEMOTHERAPYen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergien_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectESBL-producing Escherichia coli or Klebsiella pneumoniaen_US
dc.subjectLower urinary tract infectionen_US
dc.subjectAmikacinen_US
dc.titleClinical and Bacteriological Efficacy of Amikacin in The Treatment of Lower Urinary Tract Infection Caused by Extended-Spectrum Beta-Lactamase-Producing Escherichia Coli or Klebsiella Pneumoniaeen_US
dc.typearticleen_US

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