کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
3346775 | 1407783 | 2016 | 6 صفحه PDF | دانلود رایگان |
• The OXA-232 CRE infections share many associated factors with ESBL Enterobacteriaceae.
• The previous use of β-lactam/β-lactamase antibiotics was associated to OXA-232 CRE infections.
• In absence of ESBL, OXA-232 CRE infections may be treated with 3rd generation cephalosporin.
We describe the outcomes and factors associated with OXA-232 producing carbapenem-resistant Enterobacteriaceae infections. A case–control-control study was performed; each case of infection by a carbapenem-resistant/OXA-232 (OXA-232-cases, n = 27) was matched by isolation site, species, and date, with 2 cases of infection by carbapenem-susceptible/third-generation cephalosporin-susceptible (TGCS-controls, n = 54) and 2 cases by carbapenem-susceptible/ESBL producing Enterobacteriaceae (ESBL-controls, n = 54); 66% were urinary tract and 18.5% intra-abdominal infections. In the multivariable analysis with ESBL-controls, previous use β-lactam/β-lactamase antibiotics (OR 6.2; 95% CI 1.6–23.8) and, third-generation cephalosporins (OR 0.2; 95% CI 0.05–0.8) were associated with OXA-232 infection; with TGSC-controls previous use of β-lactam/β-lactamase antibiotics (OR 3.7; 95% 1.1–12.0) was associated. Among the OXA-232-cases, 29% received imipenem/cilastatin or meropenem, 11.1% ceftriaxone, 22.2% a carbapenem-based combination and 33.3% other antimicrobials as treatment. Previous β-lactam/β-lactamase antibiotics are associated with OXA-232 infections, and some may be treated with other active carbapenems or, in the absence of ESBL, third-generation cephalosporins.
Journal: Diagnostic Microbiology and Infectious Disease - Volume 86, Issue 2, October 2016, Pages 243–248