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Diagn Microbiol Infect Dis ; 87(3): 253-257, 2017 Mar.
Article in English | MEDLINE | ID: mdl-27939820

ABSTRACT

We described 27 polyclonal colistin-resistant Enterobacteriaceae (MIC 4-16 µg/mL) infections (12 pneumonia, 12 urinary tract infection (UTI), two Bacteremia, and one skin/soft tissue infection) in which 74% harbored KPC. The isolates were polyclonal, 6 STs were identified and the colistin resistance was due to chromosome mutations. Eight patients with UTI received monotherapy, and combination therapy was given to 19 patients. Overall mortality was 37%. In vitro synergy using time-kill assay was observed in 14 of 19 (74%) isolates tested; the synergistic effect was observed for almost all isolates for the combination of three drugs: colistin, amikacin, and tigecycline. The Kaplan-Meier survival curve showed no significant difference comparing combination therapy with 2, 3, or more drugs and risk factors associated with death were dialysis and shock. These findings reinforce the fact that colistin in combination with other classes of drugs can be useful in treating infections caused by colistin-resistant CRE.


Subject(s)
Amikacin/therapeutic use , Anti-Bacterial Agents/pharmacology , Colistin/therapeutic use , Drug Therapy, Combination , Enterobacteriaceae Infections/drug therapy , Enterobacteriaceae/drug effects , Minocycline/analogs & derivatives , Bacterial Proteins/genetics , Drug Resistance, Multiple, Bacterial/genetics , Drug Synergism , Enterobacteriaceae/genetics , Enterobacteriaceae/isolation & purification , Enterobacteriaceae Infections/microbiology , Enterobacteriaceae Infections/mortality , Female , Humans , Kaplan-Meier Estimate , Male , Microbial Sensitivity Tests , Middle Aged , Minocycline/therapeutic use , Pneumonia/drug therapy , Pneumonia/microbiology , Prospective Studies , Soft Tissue Infections/drug therapy , Soft Tissue Infections/microbiology , Tigecycline , Urinary Tract Infections/drug therapy , Urinary Tract Infections/microbiology , beta-Lactamases/genetics
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