Clostridium difficile infection in Europe: a hospital-based survey

被引:855
|
作者
Bauer, Martijn P. [1 ,2 ]
Notermans, Daan W. [2 ]
van Benthem, Birgit H. B. [2 ]
Brazier, Jon S. [3 ]
Wilcox, Mark H. [4 ,5 ]
Rupnik, Maja [6 ]
Monnet, Dominique L. [7 ]
van Dissel, Jaap T. [1 ]
Kuijper, Ed J. [1 ]
机构
[1] Leiden Univ, Med Ctr, Ctr Infect Dis, NL-2300 RC Leiden, Netherlands
[2] Natl Inst Publ Hlth & Environm, Ctr Infect Dis Control Netherlands, NL-3720 BA Bilthoven, Netherlands
[3] Microbiol Cardiff Univ Hosp Wales, Natl Publ Hlth Serv Wales, Anaerobe Reference Lab, Cardiff, S Glam, Wales
[4] Leeds Gen Infirm, Old Med Sch, Dept Microbiol, Leeds, W Yorkshire, England
[5] Univ Leeds, Leeds, W Yorkshire, England
[6] Ctr Microbiol, Inst Publ Hlth Maribor, Maribor, Slovenia
[7] European Ctr Dis Prevent & Control, Sci Advice Unit, Stockholm, Sweden
来源
LANCET | 2011年 / 377卷 / 9759期
关键词
NORTH-AMERICA; RISK-FACTORS; DISEASE; TOXIN; COLITIS; STRAIN; PCR; EPIDEMIOLOGY; EMERGENCE; SEVERITY;
D O I
10.1016/S0140-6736(10)61266-4
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background Little is known about the extent of Clostridium difficile infection in Europe. Our aim was to obtain a more complete overview of C difficile infection in Europe and build capacity for diagnosis and surveillance. Methods We set up a network of 106 laboratories in 34 European countries. In November, 2008, one to six hospitals per country, relative to population size, tested stool samples of patients with suspected C difficile infection or diarrhoea that developed 3 or more days after hospital admission. A case was defined when, subsequently, toxins were identified in stool samples. Detailed clinical data and stool isolates were collected for the first ten cases per hospital. After 3 months, clinical data were followed up. Findings The incidence of C difficile infection varied across hospitals (weighted mean 4.1 per 10 000 patient-days per hospital, range 0.0-36.3). Detailed information was obtained for 509 patients. For 389 of these patients, isolates were available for characterisation. 65 different PCR ribotypes were identified, of which 014/020 (61 patients [16%]), 001 (37 [9%]), and 078 (31 [8%]) were the most prevalent. The prevalence of PCR-ribotype 027 was 5%. Most patients had a previously identified risk profile of old age, comorbidity, and recent antibiotic use. At follow up, 101 (22%) of 455 patients had died, and C difficile infection played a part in 40 (40%) of deaths. After adjustment for potential confounders, an age of 65 years or older (adjusted odds ratio 3.26,95% CI 1.08-9.78; p=0.026), and infection by PCR-ribotypes 018 (6.19, 1.28-29.81; p=0.023) and 056 (13.01; 1.14-148.26; p=0.039) were significantly associated with complicated disease outcome. Interpretation PCR ribotypes other than 027 are prevalent in European hospitals. The data emphasise the importance of multicountry surveillance to detect and control C difficile infection in Europe.
引用
收藏
页码:63 / 73
页数:11
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