Unique characteristics of community-onset healthcare-associated bloodstream infections: a multi-centre prospective surveillance study of bloodstream infections in Japan

被引:30
|
作者
Takeshita, N. [1 ]
Kawamura, I. [2 ]
Kurai, H. [2 ]
Araoka, H. [3 ]
Yoneyama, A. [3 ]
Fujita, T. [4 ,8 ]
Ainoda, Y. [4 ,9 ]
Hase, R. [5 ]
Hosokawa, N. [5 ]
Shimanuki, H. [6 ]
Sekiya, N. [7 ]
Ohmagari, N. [1 ]
机构
[1] Natl Ctr Global Hlth & Med, Dis Control & Prevent Ctr, Tokyo, Japan
[2] Shizuoka Canc Ctr Hosp, Div Infect Dis, Shizuoka, Japan
[3] Toranomon Gen Hosp, Dept Infect Dis, Tokyo, Japan
[4] Tokyo Womens Med Univ, Dept Infect Dis, Tokyo, Japan
[5] Kameda Med Ctr, Dept Infect Dis, Chiba, Japan
[6] Natl Ctr Global Hlth & Med, Ctr Clin Sci, Tokyo, Japan
[7] Komagome Hosp, Tokyo Metropolitan Canc & Infect Dis Ctr, Dept Clin Lab, Tokyo, Japan
[8] Natl Hosp Org, Hokkaido Canc Ctr, Dept Infect Dis, Sapporo, Hokkaido, Japan
[9] Ebara Hosp, Tokyo Metropolitan Hlth & Med Treatment Corp, Dept Infect Dis, Tokyo, Japan
关键词
Bacteraemia; Community-acquired; Healthcare-acquired; Community-onset healthcare-associated; Mortality; Japan; DEFINITION; BACTEREMIA; MORTALITY; OUTCOMES; LENGTH; STAY;
D O I
10.1016/j.jhin.2017.02.022
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
Background: Analysis of bloodstream infections (BSIs) is valuable for their diagnosis, treatment and prevention. However, limited data are available in Japan. Aim: To investigate the characteristics of patients with bacteraemia in Japan. Methods: This study was conducted in five hospitals from October 2012 to September 2013. Clinical, demographic, microbiological and outcome data for all blood-culturepositive cases were analysed. Findings: In total, 3206 cases of BSI were analysed: 551 community-onset healthcareassociated (CHA)-BSIs, 1891 hospital-acquired (HA)-BSIs and 764 community-acquired (CA)-BSIs. The seven-and 30-day mortality rates were higher in patients with CHA-and HA-BSIs than in patients with CA-BSIs. The odds ratios (ORs) for seven-day mortality were 2.56 [95% confidence interval (CI) 1.48-4.41] and 2.63 (95% CI 1.64-4.19) for CHA-and HABSIs, respectively. The ORs for 30-day mortality were 2.41 (95% CI 1.63-3.57) and 3.31 (95% CI 2.39-4.59) for CHA-and HA-BSIs, respectively. There were 499 cases (15.2%) of central-line-associated BSI and 163 cases (5.0%) of peripheral-line-associated BSI. Major pathogens included coagulase-negative staphylococci (N = 736, 23.0%), Escherichia coli (N = 581, 18.1%), Staphylococcus aureus (N = 294, 9.2%) and Klebsiella pneumoniae (N = 263, 8.2%). E. coli exhibited a higher 30-day mortality rate among patients with HABSIs (22.3%) compared with patients with CHA-BSIs (12.3%) and CA-BSIs (3.4%). K. pneumoniae exhibited higher 30-day mortality rates in patients with HA-BSIs (22.0%) and CHA-BSIs (22.7%) compared with patients with CA-BSIs (7.8%). Conclusion: CHA-and HA-BSIs had higher mortality rates than CA-BSIs. The prognoses of E. coli-and K. pneumonia-related BSIs differed according to the category of bacteraemia. (C) 2017 The Author(s). Published by Elsevier Ltd on behalf of The Healthcare Infection Society.
引用
收藏
页码:29 / 34
页数:6
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