Eurosurveillance, Volume
11, Issue
37,
14 September 2006
Emergence of Clostridium difficile toxinotype III, PCR-ribotype 027-associated disease, France, 2006
B Coignard (b.coignard@invs.sante.fr)1, F Barbut2, K Blanckaert3, JM Thiolet1, I Poujol1, A Carbonne3, JC Petit4, JC Desenclos1
1Département Maladies Infectieuses, Institut de Veille Sanitaire, Saint-Maurice, France
2Unité d’Hygiène et de Lutte contre les Infections Nosocomiales, Hôpital Saint-Antoine, Paris, France
3Centre de Coordination de la Lutte contre les Infections Nosocomiales (CClin) Paris-Nord, Paris, France
4Service de Microbiologie, Hôpital Saint-Antoine, Paris, France
On 27 March 2006, the Institut de Veille Sanitaire (InVS) was alerted to a cluster of Clostridium difficile associated disease (CDAD) in a healthcare facility (HCF) in northern France through its national nosocomial infection notification system [1]. This first cluster involved 41 patients (median age 82 years) who developed CDAD between 24 January 2006 and 24 May 2006, of whom 14 (34%) died. However, none of these deaths were found to be attributable to the CDAD. Of 23 strains isolated from these patients and sent to a central laboratory for typing, 17 (74%) were found to be the toxinotype III, PCR-ribotype 027 epidemic strain which had also been isolated from severe CDAD outbreaks in North America and Europe [2]. This cluster has now been controlled.
The InVS alerted all French healthcare facilities about this first 027 cluster through regional infection control coordinating centres (CClin). After the notification,other CDAD clusters were notified to the InVS. In northern France, as of 12 September 2006 and including the first described outbreak, 16 healthcare facilities and two nursing homes have notified severe CDAD cases or CDAD clusters to the InVS. A total of 266 cases have been reported which occurred from January to September 2006, mostly among elderly patients hospitalised in acute care or rehabilitation departments. Two healthcare facilities accounted for 143 (54%) of all cases. Among these 266 patients, 71 (27%) deaths were registered, 15 (6%) of which were attributable to CDAD according to mortality review results. As CDAD diagnosis relies on enzyme immunoassays, stool culture was not systematically available. Of the 114 C. difficile strains isolated from these 266 patients and typed, 81 (71%) were found to be the 027 strain. The 027 strain was isolated in 11 healthcare facilities and one nursing home. In other French regions, 13 healthcare facilities notified CDAD clusters to the InVs but none of these were associated with the 027 strain.
Control measures
Local infection control units implemented control measures for each cluster, assisted by the CClin when necessary. Control measures included standard and contact precautions, use of solutions containing hypochlorite for environmental cleaning, meticulous hand hygiene, and closure of wards in five facilities. Audits of antimicrobial prescriptions also were recommended. By 12 September 2006, seven episodes had been controlled and 11 were still considered as active (that is, new cases in these clusters had been notified within the past month).
Discussion
Our data confirm the emergence and spread of the 027 strain of C. difficile in northern France since January 2006. Clusters can be controlled if they are detected early and if strict control measures, which apply for any type of CDAD, are implemented. However, this strain has a particular epidemic potential and inter-hospital transmission is likely to occur when transferring patients, a similar situation to that which was observed in a regional outbreak of Acinetobacter baumannii infection in France in 2003 [3]. The emergence of C. difficile 027 in northern France could be linked to similar clusters in northern Europe, although our investigations did not find any evidence (such as the transfer of an index patient across borders) to support this hypothesis.
National recommendations for surveillance, prevention and control of CDAD were disseminated in France in May 2006 [4]. A national laboratory network consisting of the Anaerobe National Reference Centre and five regional laboratories has been set up in order to characterise isolated strains. Current efforts are being focused on reinforcing recommendations in all healthcare facilities and nursing homes, in order to detect and control clusters early and limit the spread of the 027 strain. Surveillance for CDAD will be instituted at national level in 2007.
More information can be found (in French) at the web page for the Réseau d’alerte, d’investigation et de surveillance des infections nosocomiales (Raisin): http://www.invs.sante.fr/raisin.
References:
- Tachon M, Cattoen C, Blanckaert K, Poujol I, Carbonne A, Barbut F, Petit JC, Coignard B. First cluster of C. difficile toxinotype III, PCR-ribotype 027 associated disease in France: preliminary report. Euro Surveill 2006;11(5):E060204. http://www.eurosurveillance.org/ew/2006/060504.asp#1
- Kuijper EJ, Coignard B, Tüll P, on behalf of the ESCMID Study Group for Clostridium difficile (ESGCD), EU Member States and the European Centre for Disease Prevention and Control. Emergence of Clostridium difficile-associated disease in North America and Europe. Clin Microbiol Infect 2006;12 (suppl. 6):2-18. http://www.blackwell-synergy.com/toc/clm/12/s6
- Naas T, Coignard B, Carbonne A, Blanckaert K, Bajolet O, Bernet C, Verdeil X, Astagneau P, Desenclos JC, Nordmann P, on behalf of the French Nosocomial Infection Early Warning, Investigation and Surveillance Network. VEB-1 extended-spectrum ß-lactamase–producing Acinetobacter baumannii, France. Emerg Infect Dis 2006; 12: 1214-22. http://www.cdc.gov/ncidod/EID/vol12no08/05-1547.htm
- Réseau d’alerte, d’investigation et de surveillance des infections nosocomiales (Raisin). Conduite à tenir : diagnostic, investigation, surveillance, et principes de prévention et de maîtrise des infections à Clostridium difficile. Institut de Veille Sanitaire, 2006, 42 p. http://www.invs.sante.fr/publications/2006/guide_raisin/index.html
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