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  4. Risk factors and mechanisms of in vivo emergence of colistin resistance in carbapenem-resistant Klebsiella pneumoniae
 
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Risk factors and mechanisms of in vivo emergence of colistin resistance in carbapenem-resistant Klebsiella pneumoniae

Journal
International journal of antimicrobial agents
Journal Volume
57
Journal Issue
6
Date Issued
2021-06
Author(s)
Huang, Po-Han
Cheng, Yi-Hsiang
Chen, Wen-Yin
Juan, Chih-Han
Chou, Sheng-Hua
JIN-TOWN WANG  
Chuang, Chien
Wang, Fu-Der
Lin, Yi-Tsung
DOI
10.1016/j.ijantimicag.2021.106342
URI
https://scholars.lib.ntu.edu.tw/handle/123456789/638009
URL
https://api.elsevier.com/content/abstract/scopus_id/85105355671
Abstract
Colistin is one of the last-resort antibiotics for treating carbapenem-resistant Klebsiella pneumoniae (CRKP). However, colistin resistance in CRKP poses a global antimicrobial crisis, as therapeutic options are limited. We investigated risk factors for in vivo emergence of colistin resistance in CRKP and explored the underlying resistance mechanisms. We conducted this matched case-control study of patients with sequential CRKP clinical strains at a medical centre in Taiwan between October 2016 and June 2019. The case group included patients with an index colistin-resistant CRKP (ColR-CRKP) strain and a previous colistin-susceptible CRKP (ColS-CRKP) counterpart. The control group encompassed patients with both an index and previous ColS-CRKP strains. Cases and controls were matched according to the time at risk, and conditional logistic regression was used to evaluate potential risk factors. Alterations in genes associated with resistance were compared between ColR-CRKP and ColS-CRKP strains. We identified 24 CRKP cases with in vivo-emergent colistin resistance, matched in a 1:2 ratio with controls. Multivariate analysis showed that colistin exposure is the only independent risk factor predisposing to colistin resistance (adjusted odds ratio = 19.09, 95% confidence interval 1.26-290.45; P = 0.034). Alteration in the mgrB gene was the predominant mechanism for emergent colistin resistance (17/24; 71%). In conclusion, colistin use is a risk factor for in vivo emergence of colistin resistance in CRKP. Given the lack of a rapid and reliable method to detect colistin resistance in daily practice, physicians should be vigilant for the emergence of resistance during colistin treatment.
Subjects
Carbapenem; Colistin; Klebsiella pneumoniae; Resistance mechanism; Risk factors
SDGs

[SDGs]SDG3

Type
journal article

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