Update on Clostridium difficile infection

被引:51
作者
O'Donoghue, Caoilfhionn [1 ]
Kyne, Lorraine [1 ,2 ]
机构
[1] Mater Misericordiae Univ Hosp, Dept Med Older Person, Dublin 7, Ireland
[2] Univ Coll Dublin, Sch Med & Med Sci, Dublin 2, Ireland
关键词
Clostridium difficile; fidaxomicin; hypervirulent strains; monoclonal antibodies; INFLAMMATORY-BOWEL-DISEASE; POLYMERASE-CHAIN-REACTION; PROTON PUMP INHIBITORS; PCR RIBOTYPE 027; RISK-FACTOR; TOXINOTYPE-V; CLINICAL MICROBIOLOGY; EUROPEAN-SOCIETY; NORTH-AMERICA; DIARRHEA;
D O I
10.1097/MOG.0b013e3283411634
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Purpose of review This review summarizes the most recent epidemiological data and advances in research into the pathogenesis, diagnosis and treatment of Clostridium difficile infection (CDI). Recent findings The epidemiology of CDI has changed with the emergence of hypervirulent strains. CDI rates have increased in the community, in children and in patients with inflammatory bowel disease. Although the North American pulsed-field gel electrophoresis type 1, restriction endonuclease analysis group BI, PCR ribotype 027 (NAP1/BI/027) strain remains prevalent in North America, surveillance suggests that it is decreasing in Europe. A similar strain, PCR ribotype 078, is emerging which is associated with community-associated CDI and has been isolated in animals and food products. The Society for Healthcare Epidemiology of America and the Infectious Diseases Society of America have published new guidelines on the epidemiology, diagnosis, treatment, infection control and environmental management of C. difficile. Several novel therapies for CDI are at different stages of development. There have been promising trial results with fidaxomicin, a novel antibiotic for the treatment of CDI and monoclonal antibodies against toxins A and B, which have been shown to significantly reduce CDI recurrence rates. Summary Major advances have been made in our understanding of the spread and pathogenesis of C. difficile and new treatment options are becoming available.
引用
收藏
页码:38 / 47
页数:10
相关论文
共 120 条
[21]   Distribution of Clostridium difficile strains from a North American, European and Australian trial of treatment for C. difficile infections: 2005-2007 [J].
Cheknis, Adam K. ;
Sambol, Susan P. ;
Davidson, David M. ;
Nagaro, Kristin J. ;
Mancini, Maria C. ;
Hidalgo-Arroyo, G. Aida ;
Brazier, Jon S. ;
Johnson, Stuart ;
Gerding, Dale N. .
ANAEROBE, 2009, 15 (06) :230-233
[22]   Clostridium difficile ribotype 027 arrives in Hong Kong [J].
Cheng, Vincent C. C. ;
Yam, W. C. ;
Chan, Jasper F. W. ;
To, Kelvin K. W. ;
Ho, P. L. ;
Yuen, K. Y. .
INTERNATIONAL JOURNAL OF ANTIMICROBIAL AGENTS, 2009, 34 (05) :492-493
[23]   Clostridium difficile PCR ribotype 027: assessing the risks of further worldwide spread [J].
Clements, Archie C. A. ;
Magalhaes, Ricardo J. Soares ;
Tatem, Andrew J. ;
Paterson, David L. ;
Riley, Thomas V. .
LANCET INFECTIOUS DISEASES, 2010, 10 (06) :395-404
[24]   Clostridium difficile Strain NAP-1 Is Not Associated With Severe Disease in a Nonepidemic Setting [J].
Cloud, Jeffrey ;
Noddin, Laura ;
Pressman, Amanda ;
Hu, Mary ;
Kelly, Ciaran .
CLINICAL GASTROENTEROLOGY AND HEPATOLOGY, 2009, 7 (08) :868-873
[25]   Clinical Practice Guidelines for Clostridium difficile Infection in Adults: 2010 Update by the Society for Healthcare Epidemiology of America (SHEA) and the Infectious Diseases Society of America (IDSA) [J].
Cohen, Stuart H. ;
Gerding, Dale N. ;
Johnson, Stuart ;
Kelly, Ciaran P. ;
Loo, Vivian G. ;
McDonald, L. Clifford ;
Pepin, Jacques ;
Wilcox, Mark H. .
INFECTION CONTROL AND HOSPITAL EPIDEMIOLOGY, 2010, 31 (05) :431-455
[26]   European Society of Clinical Microbiology and Infectious Diseases (ESCMID): Data review and recommendations for diagnosing Clostridium difficile-infection (CDI) [J].
Crobach, M. J. T. ;
Dekkers, O. M. ;
Wilcox, M. H. ;
Kuijper, E. J. .
CLINICAL MICROBIOLOGY AND INFECTION, 2009, 15 (12) :1053-1066
[27]   Clostridium difficile-A continually evolving and problematic pathogen [J].
Dawson, Lisa F. ;
Valiente, Esmeralda ;
Wren, Brendan W. .
INFECTION GENETICS AND EVOLUTION, 2009, 9 (06) :1410-1417
[28]   Evaluation of a rapid molecular screening approach for the detection of toxigenic Clostridium difficile in general and subsequent identification of the tcdC Δ117 mutation in human stools [J].
de Boer, R. F. ;
Wijma, J. J. ;
Schuurman, T. ;
Moedt, J. ;
Dijk-Alberts, B. G. ;
Ott, A. ;
Kooistra-Smid, A. M. D. ;
van Duynhoven, Y. T. H. P. .
JOURNAL OF MICROBIOLOGICAL METHODS, 2010, 83 (01) :59-65
[29]   Clostridium difficile PCR ribotype 078 toxinotype V found in diarrhoeal pigs identical to isolates from affected humans [J].
Debast, Sylvia B. ;
van Leengoed, Leo A. M. G. ;
Goorhuis, Abraham ;
Harmanus, Celine ;
Kuijper, Ed J. ;
Bergwerff, Aldert A. .
ENVIRONMENTAL MICROBIOLOGY, 2009, 11 (02) :505-511
[30]   Use of gastric acid-suppressive agents and the risk of community-acquired Clostridium difficile-associated disease [J].
Dial, S ;
Delaney, JAC ;
Barkun, AN ;
Suissa, S .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2005, 294 (23) :2989-2995