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Collateral damage of using colistin in hospitalized patients on emergence of colistin-resistant Escherichia coli and Klebsiella pneumoniae colonization and infection.
- Source :
-
Antimicrobial resistance and infection control [Antimicrob Resist Infect Control] 2018 Jul 17; Vol. 7, pp. 84. Date of Electronic Publication: 2018 Jul 17 (Print Publication: 2018). - Publication Year :
- 2018
-
Abstract
- Background: Colistin has been used for therapy of carbapenem-resistant Gram-negative infections in Thailand, especially carbapenem-resistant A. baumannii and P. aeruginosa , for more than 10 years. However, the prevalence of colistin-resistant A. baumannii or P. aeruginosa is still less than 5%. Colistin-resistant Enterobacteriaceae has been increasingly reported globally over the past few years and the use of colistin in food animals might be associated with an emergence of colistin resistance in Enterobacteriaceae. This study aimed to determine the effect of colistin exposure in hospitalized patients who received colistin on development of colistin-resistant (CoR) Escherichia coli (EC) or Klebsiella pneumoniae (KP) colonization and infection.<br />Methods: A prospective observational study was performed in adult hospitalized patients at Siriraj Hospital who received colistin for treatment of infections during December 2016 and November 2017. The surveillance culture samples were collected from the stool and the site of infection of each patient who received colistin at the study enrollment, days 3 and 7 after the study enrollment, and once a week thereafter for determination of CoR EC and CoR KP. CoR EC and CoR KP were also tested for a presence of mcr-1 gene.<br />Results: One hundred thirty-nine patients were included. Overall prevalence of CoR EC or CoR KP colonization was 47.5% among 139 subjects. Prevalence of CoR EC or CoR KP colonization was 17.3% of subjects at study enrollment, and 30.2% after study enrollment. Use of fluoroquinolones, aminoglycosides, and colistin was found to be significantly associated with CoR EC or CoR KP colonization. The mcr-1 gene was detected in 13.0% of CoR EC or CoR KP isolates, and in 27.3% of subjects with CoR EC or CoR KP colonization. CoR EC or CoR KP colonization persisted in 65.2% of the subjects at the end of the study. Five patients with CoR KP infections received combination antibiotics and they were alive at hospital discharge.<br />Conclusions: Prevalence of CoR EC or CoR KP colonization in hospitalized patients receiving colistin was high and it was associated with the use of colistin. Therefore, patients who receive colistin are at risk of developing CoR EC or CoR KP colonization and infection.<br />Competing Interests: The study protocol was approved by the Siriraj Institutional Review Board, and written informed consent was obtained from all subjects.Not applicable.The authors declare that they have no competing interestsSpringer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
- Subjects :
- Adult
Aged
Aged, 80 and over
Anti-Bacterial Agents adverse effects
Bacterial Proteins genetics
Bacterial Proteins metabolism
Colistin adverse effects
Communicable Diseases, Emerging drug therapy
Communicable Diseases, Emerging microbiology
Drug Resistance, Multiple, Bacterial
Escherichia coli growth & development
Escherichia coli Infections microbiology
Feces microbiology
Female
Hospitalization
Humans
Klebsiella Infections microbiology
Klebsiella pneumoniae growth & development
Male
Microbial Sensitivity Tests
Middle Aged
Prospective Studies
Thailand
Anti-Bacterial Agents therapeutic use
Colistin therapeutic use
Escherichia coli drug effects
Escherichia coli Infections drug therapy
Klebsiella Infections drug therapy
Klebsiella pneumoniae drug effects
Subjects
Details
- Language :
- English
- ISSN :
- 2047-2994
- Volume :
- 7
- Database :
- MEDLINE
- Journal :
- Antimicrobial resistance and infection control
- Publication Type :
- Academic Journal
- Accession number :
- 30026942
- Full Text :
- https://doi.org/10.1186/s13756-018-0375-4