Subscribe to RSS
DOI: 10.1055/s-2007-959314
© Georg Thieme Verlag KG Stuttgart · New York
Dramatischer Anstieg von Clostridium-difficile-assoziierter Diarrhoe in Deutschland: Ist der neue Stamm PCR-Ribotyp 027 bereits angekommen?
Dramatic increase of diarrhea associated with Clostridium difficile in Germany: has the new strain PCR-ribotype 027 reached us?Publication History
eingereicht: 19.6.2006
akzeptiert: 30.11.2006
Publication Date:
25 January 2007 (online)
Zusammenfassung
In den letzten Jahren wurde in Nordamerika und Großbritannien ein drastischer Anstieg von Fällen nosokomialer Clostridium difficile-assoziierter Diarrhoe (CDAD) verzeichnet. Ebenso ist in Deutschland ein Anstieg der Patienten mit der Diagnose CDAD von 7,4 pro 100 000 stationärer Aufnahmen im Jahre 2000 auf 39,3 im Jahre 2004 festzustellen.
In Pittsburgh, USA wurde ein Anstieg der Inzidenz von CDAD-Fällen von 0,74 % im Jahre 1999 auf 1,2 % im Jahre 2000 beobachtet. Im gleichen Zeitraum stieg die Clostridium difficile (CD)-assoziierte Letalität von 0,5 % auf 2,0 %. Während eines Ausbruches (04/2001 - 03/2002) wurde ein neuer CD-Stamm für 87,5 % der schweren CDAD-Fälle verantwortlich gemacht. Seit März 2003 wurden in Kanada und in den USA gehäuft Ausbrüche durch diesen neuen CD-Stamm beobachtet, welcher mit einer besonders hohen Erkrankungsschwere und Letalität einhergeht. Darüber hinaus hat der Stamm auch bei jüngeren, ambulanten Patienten ohne Risikofaktoren zu Erkrankungen mit zum Teil sehr schweren Verläufen geführt.
Zeitgleich kam es auch in Großbritannien, den Niederlanden, Belgien und Frankreich zu mehreren Ausbrüchen, in denen dieser neue CD-Stamm nachgewiesen werden konnte.
In der Restriktions-Endonukleasen-Analyse wird er als Typ B1, in der PCR als Ribotyp 027, Toxintyp III und in der Pulsfeld-Gel-Elektrophorese als North American Profile 1 (NAP1) charakterisiert. Der Stamm besitzt durch ein zusätzliches binäres Toxin und durch auf ein Vielfaches erhöhte Spiegel der Toxine A und B eine erhöhte Virulenz. In Deutschland ist dieser Stamm bisher noch nicht nachgewiesen worden.
Diese Arbeit gibt einen Überblick über die bisherige Verbreitung des Erregers sowie Hinweise für die Diagnostik und Prävention.
Summary
There has been a dramatic increase of Clostridium difficile-associated diarrhea (CDAD) in North America and the UK over the last few years. A similar change in the epidemiology of CDAD has been noted in Germany where in 2004, of 100000 patients hospitalized in Germany, 39.3 were found to have CDAD, compared to 7,4 per 100 000 in 2000.
An increased incidence of CDAD was also observed in Pittsburgh, USA, from 0.74% in 1999 to 1,2% in 2000. At the same time, the mortality from CDAD rose from 0.48% to 2%. A new Clostridum difficile strain was responsible for 87.5% of severe CDAD cases during an outbreak in Pittsburgh between April 2001 and March 2002. Since March 2003 there has been an increasing number of nosocomial outbreaks due to a new Clostridium difficile strain in Canada and USA, a high proportion being severe and fatal cases of CDAD. Moreover, there have been community-acquired cases of severe CDAD in young patients without any specific risk factors for developing CDAD.
At the same time, outbreaks of CDAD involving the new Clostridium difficile strain have been reported from the UK, the Netherlands, Belgium and France. The new strain is characterized as type B1 by restriction enzyme analysis, as ribotype 027 and toxinotype III by PCR, and as North Amerikan Profile 1 (NAP 1) by pulsed-field gel electrophoresis. The extraordinary virulence of this strain is thought to be associated with an additional binary toxin and increased levels of toxins A and B.
This report provides information on the current epidemiological situation as well as recommendations for diagnosis and prevention.
Schlüsselwörter
Clostridium difficile
-
Clostridium difficile-
assoziierte Diarrhoe - Prävention - Epidemiologie
Key words
Clostridium difficile - Clostridium difficile-associated diarrhoea - prevention - epidemiology
Literatur
- 1 Anonymous. Severe Clostridium difficile-associated disease in populations previously at low risk-four states, 2005. MMWR Morb Mortal Wkly Rep. 2005; 54 1201-1205
- 2 Anonymous. Clostridium difficile in England and Wales. Comm Dis Rep Weekly. 2000; 10 135
- 3 Anonymus. Outbreak of Clostridium difficile infection in a hospital in south east England. CDR weekly. 2005; 15
- 4 Bentley A H, Patel N B, Sidorczuk M. et al . Multicentre evaluation of a commercial test for the rapid diagnosis of Clostridium difficile-mediated antibiotic-associated diarrhoea. Eur J Clin Microbiol Infect Dis. 1998; 17 788-790
- 5 Block C. The effect of Perasafe and sodium dichloroisocyanurate (NaDCC) against spores of Clostridium difficile and Bacillus atrophaeus on stainless steel and polyvinyl chloride surfaces. J Hosp Infect. 2004; 57 144-148
- 6 Boyce J M. Using alcohol for hand antisepsis: dispelling old myths. Infect Control Hosp Epidemiol. 2000; 21 438-441
- 7 Cohen S H, Tang Y J, Silva J. Analysis of the pathogenicity locus in Clostridium difficile strains. J Infect Dis. 2000; 181 659-663
- 8 Dallal R M, Harbrecht B G, Boujoukas A J. et al . Fulminant Clostridium difficile: an underappreciated and increasing cause of death and complications. Ann Surg. 2002; 235 363-372
- 9 Delmee M. Laboratory diagnosis of Clostridium difficile disease. Clin Microbiol Infect. 2001; 7 411-416
- 10 Gaynes R, Rimland D, Killum E. et al . Outbreak of Clostridium difficile infection in a long-term care facility: association with gatifloxacin use. Clin Infect Dis. 2004; 38 640-645
- 11 George W L, Sutter V L, Citron D, Finegold S M. Selective and differential medium for isolation of Clostridium difficile. J Clin Microbiol. 1979; 9 214-219
- 12 Geric B, Rupnik M, Gerding D N, Grabnar M, Johnson S. Distribution of Clostridium difficile variant toxinotypes and strains with binary toxin genes among clinical isolates in an American hospital. J Med Microbiol. 2004; 53 887-894
- 13 Goncalves C, Decre D, Barbut F, Burghoffer B, Petit J C. Prevalence and characterization of a binary toxin (actin-specific ADP-ribosyltransferase) from Clostridium difficile. J Clin Microbiol. 2004; 42 1933-1939
- 14 Indra A, Huhulescu S, Hasenberger P. et al . First isolation of Clostridium difficile PCR ribotype 027 in Austria. Euro Surveill. 2006; 11 (9) E060914.3
- 15 Joseph R, Demeyer D, Vanrenterghem D. et al . First isolation of Clostridium difficile PCR ribotype027, toxinotype III in Belgium. Eurosurveillance weekly. 2005; 10 (10) E051020.4
- 16 Kuijper E J, Coignard B, Tull P. Emergence of Clostridium difficile-associated disease in North America and Europe. Clin Microbiol Infect. 2006; (Suppl 6) 12 2-18
- 17 Lai K K, Melvin Z S, Menard M J, Kotilainen H R, Baker S. Clostridium difficile-associated diarrhea: epidemiology, risk factors, and infection control. Infect Control Hosp Epidemiol. 1997; 18 628-632
- 18 Larson E, Bobo L, Bennett R. et al . Lack of care giver hand contamination with endemic bacterial pathogens in a nursing home. Am J Infect Control. 1992; 20 11-15
- 19 Loo V G, Poirier L, Miller M A. et al . A predominantly clonal multi-institutional outbreak of Clostridium difficile-associated diarrhea with high morbidity and mortality. N Engl J Med. 2005; 353 2442-2449
- 20 McDonald L C, Brazier J. Oral presentations at the Clostridium difficile workshop at ECDC,. Stockholm, Sweden, January 24th 2006
- 21 McDonald L C, Killgore G E, Thompson A. et al . An epidemic, toxin gene-variant strain of Clostridium difficile. N Engl J Med. 2005; 353 2433-2441
- 22 McDonald L C, Owings M, Jernigan D B. Clostridium difficile infection in patients discharged from US short-stay hospitals, 1996 - 2003. Emerg Infect Dis. 2006; 12 409-415
- 23 McEllistrem M C, Carman R J, Gerding D N, Genheimer C W, Zheng L. A hospital outbreak of Clostridium difficile disease associated with isolates carrying binary toxin genes. Clin Infect Dis. 2005; 40 265-272
- 24 McFarland L V, Mulligan M E, Kwok R Y, Stamm W E. Nosocomial acquisition of Clostridium difficile infection. N Engl J Med. 1989; 320 204-210
- 25 Muto C A, Pokrywka M, Shutt K. et al . A large outbreak of Clostridium difficile-associated disease with an unexpected proportion of deaths and colectomies at a teaching hospital following increased fluoroquinolone use. Infect Control Hosp Epidemiol. 2005; 26 273-280
- 26 Noren T. Outbreak from a high-toxin intruder: Clostridium difficile. Lancet. 2005; 366 1053-1054
- 27 Pear S M, Williamson T H, Bettin K M, Gerding D N, Galgiani J N. Decrease in nosocomial Clostridium difficile-associated diarrhea by restricting clindamycin use. Ann Intern Med. 1994; 120 272-277
- 28 Pepin J, Saheb N, Coulombe M A. et al . Emergence of fluoroquinolones as the predominant risk factor for Clostridium difficile-associated diarrhea: a cohort study during an epidemic in Quebec. Clin Infect Dis. 2005; 41 1254-1260
- 29 Pepin J, Valiquette L, Cossette B. Mortality attributable to nosocomial Clostridium difficile-associated disease during an epidemic caused by a hypervirulent strain in Quebec. Cmaj. 2005; 173 1037-1042
- 30 Perez J, Springthorpe V S, Sattar S A. Activity of selected oxidizing microbicides against the spores of Clostridium difficile: relevance to environmental control. Am J Infect Control. 2005; 33 320-325
- 31 Spigaglia P, Mastrantonio P. Molecular analysis of the pathogenicity locus and polymorphism in the putative negative regulator of toxin production (TcdC) among Clostridium difficile clinical isolates. J Clin Microbiol. 2002; 40 3470-3475
- 32 Tachon M, Cattoen C, Blanckaert K. et al . First cluster of C. difficile toxinotype III, PCR-ribotype 027 associated disease in France: preliminary report. Euro Surveill. 2006; 11 (5) E060504.1
- 33 Thomas C, Stevenson M, Riley T V. Antibiotics and hospital-acquired Clostridium difficile-associated diarrhoea: a systematic review. J Antimicrob Chemother. 2003; 51 1339-1350
- 34 van Steenbergen J, Debast S B, Van Kregten E. et al . Isolation of Clostridium difficile ribotype 027, toxinotype III in the Netherlands after increase in C. difficile-associated diarrhoea. Eurosurveillance weekly. 2005; 10 (7) E05714.1
- 35 Vonberg R, Schwab F, Gastmeier P. Clostridium difficile in discharged inpatients, Germany. Emerg Infect Dis. 2007; 13 179-180
- 36 Warny M, Pepin J, Fang A. et al . Toxin production by an emerging strain of Clostridium difficile associated with outbreaks of severe disease in North America and Europe. Lancet. 2005; 366 1079-1084
- 37 Wilcox M H, Fawley W N, Wigglesworth N. et al . Comparison of the effect of detergent versus hypochlorite cleaning on environmental contamination and incidence of Clostridium difficile infection. J Hosp Infect. 2003; 54 109-114
- 38 Wistrom J, Norrby S R, Myhre E B. et al . Frequency of antibiotic-associated diarrhoea in 2462 antibiotic-treated hospitalized patients: a prospective study. J Antimicrob Chemother. 2001; 47 43-50
Dr. med. Christiane Reichardt
Institut für Mirkobiologie, Arbeitsgruppe Krankenhaushygiene, Medizinische Hochschule Hannover
Carl-Neuberg-Straße 1
30625 Hannover
Phone: 0511/5329280
Fax: 0511/5328174
Email: reichardt.christiane@mh-hannover.de