Characteristics and incidence of Clostridium difficile-associated disease in The Netherlands, 2005

被引:102
作者
Paltansing, S.
van den Berg, R. J.
Guseinova, R. A.
Visser, C. E.
van der Vorm, E. R.
Kuijper, E. J.
机构
[1] Leiden Univ, Med Ctr, Natl Reference Lab Clostridium Difficile, Dept Med Microbiol, NL-2300 RC Leiden, Netherlands
[2] Free Med Univ, Dept Med Microbiol, Amsterdam, Netherlands
[3] Univ Amsterdam, Acad Med Ctr, Dept Med Microbiol, NL-1105 AZ Amsterdam, Netherlands
关键词
Clostridium difficile; epidemiology; Netherlands; PCR ribotypes; surveillance study; toxinotypes; BINARY TOXIN; ADP-RIBOSYLTRANSFERASE; DIAGNOSTIC METHODS; NORTH-AMERICA; RISK-FACTORS; STRAIN; PCR; DIARRHEA; GENE; EPIDEMIOLOGY;
D O I
10.1111/j.1469-0691.2007.01793.x
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
During a 2-month period in 2005, 13 laboratories participated in a surveillance study of Clostridium difficile-associated disease (CDAD) in 17 hospitals in The Netherlands. The median incidence rate of CDAD was 16/10 000 patient admissions (2.2/10 000 patient-days) and varied from 1 to 46/10 000 patient admissions according to hospital. In total, 81 patients with CDAD were reported; 49 (61%) patients had nosocomial CDAD, and 29 (36%) patients were admitted to hospital when already suffering from diarrhoea. Two (2%) deaths were attributable to CDAD; both of these patients were admitted with severe community-onset CDAD and were aged > 80 years. Among 64 toxinogenic isolates, ten (16%) belonged to PCR ribotype 027 and ten (16%) to PCR ribotype 014. Type 027 was identified in ten patients from one hospital during an unrecognised outbreak. Toxinotyping of the 64 isolates revealed the presence of six different toxinogenic types, with 41 (64%) isolates of toxinotype 0, ten (16%) isolates of toxinotype III, and nine (14%) isolates of toxinotype V. Of the 64 toxinogenic isolates, seven (11%) had a 39-bp deletion in the tcdC gene, 11 (17%) had an 18-bp deletion, and one (1%) had a deletion of c. 44 bp. Genes for binary toxin were present in 21 (33%) of the 64 toxinogenic isolates, mainly associated with toxinotypes III and V. It was concluded that the median CDAD incidence rate of 16/10 000 patient admissions in The Netherlands is considerably lower than that in Canada and the USA, and that the emerging type 027 can spread unnoticed. The high proportion (36%) of CDAD cases with a community onset has important implications for future studies of the epidemiology of CDAD.
引用
收藏
页码:1058 / 1064
页数:7
相关论文
共 30 条
[1]   Prospective study of Clostridium difficile infections in Europe with phenotypic and genotypic characterisation of the isolates [J].
Barbut, F. ;
Mastrantonio, P. ;
Delmee, M. ;
Brazier, J. ;
Kuijper, E. ;
Poxton, I. .
CLINICAL MICROBIOLOGY AND INFECTION, 2007, 13 (11) :1048-1057
[2]   A European survey of diagnostic methods and testing protocols for Clostridium difficile [J].
Barbut, F ;
Delmée, M ;
Brazier, JS ;
Petit, JC ;
Poxton, IR ;
Rupnik, M ;
Lalande, V ;
Schneider, C ;
Mastrantonio, P ;
Alonso, R ;
Kuipjer, E ;
Tvede, M .
CLINICAL MICROBIOLOGY AND INFECTION, 2003, 9 (10) :989-996
[3]   The new Clostridium difficile -: What does it mean? [J].
Bartlett, JG ;
Perl, TM .
NEW ENGLAND JOURNAL OF MEDICINE, 2005, 353 (23) :2503-2505
[4]   Comparison of PCR-ribotyping, arbitrarily primed PCR, and pulsed-field gel electrophoresis for typing Clostridium difficile [J].
Bidet, P ;
Lalande, V ;
Salauze, B ;
Burghoffer, B ;
Avesani, V ;
Delmée, M ;
Rossier, A ;
Barbut, F ;
Petit, JC .
JOURNAL OF CLINICAL MICROBIOLOGY, 2000, 38 (07) :2484-2487
[5]   Risk factors for Clostridium difficile infection [J].
Bignardi, GE .
JOURNAL OF HOSPITAL INFECTION, 1998, 40 (01) :1-15
[6]   SIMPLIFIED PROCEDURE FOR THE ROUTINE ISOLATION OF CLOSTRIDIUM-DIFFICILE FROM FECES [J].
BORRIELLO, SP ;
HONOUR, P .
JOURNAL OF CLINICAL PATHOLOGY, 1981, 34 (10) :1124-1127
[7]   The epidemiology and typing of Clostridium difficile [J].
Brazier, JS .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 1998, 41 :47-57
[8]  
Centers for Disease Control and Prevention (CDC), 2005, MMWR Morb Mortal Wkly Rep, V54, P1201
[9]  
Garcia A, 1997, J CLIN MICROBIOL, V35, P3007
[10]   Binary toxin-producing, large clostridial toxin-negative Clostridium difficile strains are enterotoxic but do not cause disease in hamsters [J].
Geric, B ;
Carman, RJ ;
Rupnik, M ;
Genheimer, CW ;
Sambol, SP ;
Lyerly, DM ;
Gerding, DN ;
Johnson, S .
JOURNAL OF INFECTIOUS DISEASES, 2006, 193 (08) :1143-1150