Characteristics of cefazolin inoculum effect-positive methicillin-susceptible staphylococcus aureus infection in a multicentre bacteraemia cohort

被引:29
|
作者
Song, K. -H. [1 ]
Jung, S. -I. [2 ]
Lee, S. [3 ,4 ]
Park, S. [3 ,4 ]
Kiem, S. M. [5 ]
Lee, S. H. [3 ,4 ]
Kwak, Y. G. [6 ]
Kim, Y. K. [7 ]
Jang, H. -C. [8 ]
Kim, Y. -S. [9 ]
Kim, H. -I. [10 ]
Kim, C. J. [11 ]
Park, K. -H. [2 ]
Kim, N. J. [12 ]
Oh, M. -D. [12 ]
Kim, H. B. [1 ]
机构
[1] Seoul Natl Univ, Dept Internal Med, Bundang Hosp, Seongnam, South Korea
[2] Chonnam Natl Univ, Dept Infect Dis, Sch Med, Gwangju, South Korea
[3] Pusan Natl Univ, Sch Med, Dept Internal Med, Busan, South Korea
[4] Pusan Natl Univ Hosp, Med Res Inst, Busan, South Korea
[5] Inje Univ, Coll Med, Dept Internal Med, Busan, South Korea
[6] Inje Univ, Ilsan Paik Hosp, Dept Internal Med, Goyang, South Korea
[7] Yonsei Univ, Sch Med, Dept Internal Med, Wonju, South Korea
[8] Chonnam Natl Univ, Hwasun Hosp, Dept Internal Med, Hwasun, Jeollanam Do, South Korea
[9] Chungnam Natl Univ, Sch Med, Chungnam Natl Univ Hosp, Div Infect Dis, Daejeon, South Korea
[10] Daegu Fatima Hosp, Dept Internal Med, Daegu, South Korea
[11] Ewha Womans Univ, Med Ctr, Seoul, South Korea
[12] Seoul Natl Univ Hosp, Dept Internal Med, Seoul, South Korea
关键词
BLOOD-STREAM INFECTIONS; A BETA-LACTAMASE; BLAZ GENE TYPES; TREATMENT FAILURE; ENDOCARDITIS; ASSOCIATION; RESISTANCE; CEPHALOSPORINS; PREVALENCE; MANAGEMENT;
D O I
10.1007/s10096-016-2799-1
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Cefazolin treatment failure has been observed in high-inoculum infections caused by methicillin-susceptible Staphylococcus aureus (MSSA) with a cefazolin inoculum effect (CIE). However, data on the characteristics and risk factors for the acquisition of CIE-positive MSSA infection are scarce. CIE positivity was measured as an MIC a 16 mu g/ml with a high inoculum (similar to 5 x 10(7) CFU/ml). The blaZ gene type was assessed through sequence analysis. The clinical characteristics and risk factors for the acquisition of CIE-positive MSSA infection were assessed. The association between the antimicrobial susceptibility profile and CIE positivity was evaluated. A total of 303 MSSA bacteraemia cases and their corresponding isolates were collected from ten hospitals: 61 (20.1 %) isolates showed a positive CIE; 254 (83.8 %) were positive for the blaZ gene. No significant association was found between CIE positivity and the site of infection. Metastatic cancer (aOR 2.86, 95 % CI, 1.10-7.48) and recent (a 1 month) close contact with a chronically ill patient (aOR 4.69, 95 % CI, 1.76-12.50) were identified as significant risk factors for CIE-positive MSSA infection through multivariate analyses. Resistances to clindamycin (OR 3.55, 95 % CI, 1.62-7.80) and erythromycin (OR 5.00, 95 % CI, 2.50-9.99) were associated with CIE positivity, presenting high specificity (92.9 %) and a negative predictive value (82.3 %). CIE-positive MSSA constituted approximately one-fifth of MSSA bacteraemia cases. Although CIE positivity was not clinically discernible, CIE positivity was associated with clindamycin or erythromycin susceptibility. Therefore, our findings suggest that cefazolin can be used in the treatment of high-inoculum MSSA infection if the isolates are susceptible to clindamycin or erythromycin.
引用
收藏
页码:285 / 294
页数:10
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