Epidemiological investigation of fluoroquinolone resistance in infections due to extended-spectrum β-lactamase-producing Escherichia coli and Klebsiella pneumoniae

被引:183
作者
Lautenbach, E
Strom, BL
Bilker, WB
Patel, JB
Edelstein, PH
Fishman, NO
机构
[1] Univ Penn, Sch Med, Ctr Clin Epidemiol & Biostat, Med Ctr, Philadelphia, PA 19104 USA
[2] Univ Penn, Med Ctr, Dept Med, Div Infect Dis, Philadelphia, PA 19104 USA
[3] Univ Penn, Med Ctr, Dept Med, Div Gen Internal Med, Philadelphia, PA 19104 USA
[4] Univ Penn, Med Ctr, Ctr Clin Epidemiol, Philadelphia, PA 19104 USA
[5] Univ Penn, Med Ctr, Dept Biostat & Epidemiol, Philadelphia, PA 19104 USA
[6] Univ Penn, Med Ctr, Dept Pathol & Lab Med, Philadelphia, PA 19104 USA
基金
美国国家卫生研究院;
关键词
D O I
10.1086/322667
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The incidence of infections due to extended-spectrum beta -lactamase (ESBL)-producing Escherichia coli and Klebsiella pneumoniae (ESBL-EK) has increased markedly in recent years. Treatment is difficult because of frequent multidrug resistance. Although fluoroquinolones offer effective therapy for ESBL-EK infections, their usefulness is threatened by increasing fluoroquinolone resistance. To identify risk factors for fluoroquinolone resistance in ESBL-EK infections, a case-control study of all patients with ESBL-EK infections from 1 June 1997 through 30 September 1998 was conducted. Of 77 ESBL-EK infections, 43 (55.8%) were resistant to fluoroquinolones. Independent risk factors for fluoroquinolone resistance were fluoroquinolone use (odds ratio [OR], 11.20; 95% confidence interval [CI], 1.99-63.19), aminoglycoside use (OR, 5.83; 95% CI, 1.12-30.43), and long-term care facility residence (OR, 3.39; 95% CI, 1.06-10.83). The genotypes of fluoroquinolone-resistant ESBL-EK isolates were closely related. Efforts should be directed at modification of these risk factors to preserve the utility of fluoroquinolones in the treatment of ESBL-EK infections.
引用
收藏
页码:1288 / 1294
页数:7
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