Cefmetazole for bacteremia caused by ESBL-producing enterobacteriaceae comparing with carbapenems

被引:55
|
作者
Fukuchi, Takahiko [1 ,2 ]
Iwata, Kentaro [1 ,2 ]
Kobayashi, Saori [3 ]
Nakamura, Tatsuya [3 ]
Ohji, Goh [1 ,2 ,3 ]
机构
[1] Kobe Univ, Grad Sch Med, Div Infect Dis Therapeut, Chuo Ku, 7-5-2 Kusunokicho, Kobe, Hyogo 6500017, Japan
[2] Kobe Univ, Grad Sch Med, Dept Microbiol & Infect Dis, Chuo Ku, 7-5-2 Kusunokicho, Kobe, Hyogo 6500017, Japan
[3] Kobe Univ Hosp, Dept Clin Lab, Chuo Ku, 7-5-2 Kusunokicho, Kobe, Hyogo 6500017, Japan
来源
BMC INFECTIOUS DISEASES | 2016年 / 16卷
关键词
CMZ; Cefmetazole; CPs; Carbapenems; CRE; Carbapenems resistant enterobacteriaceae; ESBL; Extended spectrum beta-lactamase; SPECTRUM BETA-LACTAMASES; ESCHERICHIA-COLI; THERAPY; PYELONEPHRITIS; ANTIBIOTICS; RESISTANCE; ERTAPENEM; EFFICACY;
D O I
10.1186/s12879-016-1770-1
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Background: ESBL (Extended spectrum beta-lactamase) producing enterobacteriaceae are challenging organisms with little treatment options. Carbapenems are frequently used, but the emergence of carbapenem resistant enterobacteriaceae is a concerning issue, which may hinder the use of carbapenems. Although cephamycins such as cefoxitin, cefmetazole or cefotetan are effective against ESBL-producers in vitro, there are few clinical data demonstrating effects against bacteremia caused by these organisms. Methods: We performed a retrospective observational study on cases of bacteremia caused by ESBL-producers to investigate the efficacy of cefmetazole compared with carbapenems. We also evaluated whether the trend of antibiotic choice changed over years. Results: Sixty-nine patients (male 34, age 69.2 +/- 14.4), including two relapse cases, were reviewed for this analysis. The most common causative organisms were Escherichia coli (64, 93 %), followed by Klebsiella pneumoniae and K. oxytoca (2 each, 4 %). The group that received carbapenem therapy (43, 62 %) had increased severity in the Pittsburgh Bacteremic score than the group that received cefmetazole therapy, (1.5 +/- 1.5 vs 2.5 +/- 2.1, p = 0.048), while analysis of other factors didn't reveal any statistical differences. Five patients in the carbapenem group and one patient in the cefmetazole group died during the observation period (p = 0.24). CTX-M-9 were predominant in this series (59 %). Infectious disease physicians initially recommended carbapenems at the beginning of the current research period, which gradually changed over time favoring the use of cefmetazole instead (p = 0.002). Conclusion: Cefmetazole may be safely given to patients with bacteremia caused by ESBL-producers as a definitive therapy, if one can select out relatively stable patients.
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页数:6
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