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Standardised surveillance of Clostridium difficile infection in European acute care hospitals: a pilot study, 2013
- Sofie M van Dorp1 , Pete Kinross2 , Petra Gastmeier3 , Michael Behnke3 , Axel Kola3 , Michel Delmée4 , Anastasia Pavelkovich5 , Silja Mentula6 , Frédéric Barbut7,8 , Agnes Hajdu9 , André Ingebretsen10 , Hanna Pituch11 , Ioana S Macovei12 , Milica Jovanović13 , Camilla Wiuff14 , Daniela Schmid15 , Katharina EP Olsen16 , Mark H Wilcox17,18 , Carl Suetens2 , Ed J Kuijper1 , for the European Clostridium difficile Infection Surveillance Network (ECDIS-Net) on behalf of all participants19
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View Affiliations Hide AffiliationsAffiliations: 1 Department of Medical Microbiology, Leiden University Medical Center, Leiden, the Netherlands 2 Surveillance and Response Support Unit, European Centre for Disease Prevention and Control, Stockholm, Sweden 3 Institut für Hygiene und Umweltmedizin, Charité Universitätsmedizin Berlin, Berlin, Germany 4 Microbiology Unit, Université Catholique de Louvain, Louvain-la-Neuve, Brussels, Belgium 5 Department of Microbiology, East-Tallinn Central Hospital, Tallinn, Estonia 6 Department of Infectious Disease Surveillance and Control, Bacteriology Unit, National Institute for Health and Welfare, Helsinki, Finland 7 National Reference Laboratory for Clostridium difficile, Pierre et Marie Curie University, Paris, France 8 Hôpital Saint-Antoine, Paris, France 9 Department of Hospital Epidemiology and Hygiene, National Center for Epidemiology, Budapest, Hungary 10 Departments of Infection Prevention and Microbiology, Oslo University Hospital Rikshospitalet, Oslo, Norway 11 Department of Medical Microbiology, Medical University of Warsaw, Warsaw, Poland 12 National Institute for Microbiology and Immunology, Laboratory of Anaerobic Bacteria, Cantacuzino Institute, Bucharest, Romania 13 Department of Microbiology, Clinical Center of Serbia, Belgrade, Serbia 14 Health Protection Scotland, Glasgow, United Kingdom 15 Austrian Agency for Health and Food Safety (AGES), Vienna, Austria 16 Department of Microbiology and Infection Control, Statens Serum Institut, Copenhagen, Denmark 17 Leeds Teaching Hospitals NHS Trust, Leeds, United Kingdom 18 University of Leeds, Leeds, United Kingdom 19 Other members of the ECDIS-Net project are listed at the end of the articleSofie M van Dorpsvandorp lumc.nl
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Citation style for this article: van Dorp Sofie M, Kinross Pete, Gastmeier Petra, Behnke Michael, Kola Axel, Delmée Michel, Pavelkovich Anastasia, Mentula Silja, Barbut Frédéric, Hajdu Agnes, Ingebretsen André, Pituch Hanna, Macovei Ioana S, Jovanović Milica, Wiuff Camilla, Schmid Daniela, Olsen Katharina EP, Wilcox Mark H, Suetens Carl, Kuijper Ed J, for the European Clostridium difficile Infection Surveillance Network (ECDIS-Net) on behalf of all participants. Standardised surveillance of Clostridium difficile infection in European acute care hospitals: a pilot study, 2013. Euro Surveill. 2016;21(29):pii=30293. https://doi.org/10.2807/1560-7917.ES.2016.21.29.30293 Received: 21 Jan 2016; Accepted: 18 Mar 2016
Abstract
Clostridium difficile infection (CDI) remains poorly controlled in many European countries, of which several have not yet implemented national CDI surveillance. In 2013, experts from the European CDI Surveillance Network project and from the European Centre for Disease Prevention and Control developed a protocol with three options of CDI surveillance for acute care hospitals: a ‘minimal’ option (aggregated hospital data), a ‘light’ option (including patient data for CDI cases) and an ‘enhanced’ option (including microbiological data on the first 10 CDI episodes per hospital). A total of 37 hospitals in 14 European countries tested these options for a three-month period (between 13 May and 1 November 2013). All 37 hospitals successfully completed the minimal surveillance option (for 1,152 patients). Clinical data were submitted for 94% (1,078/1,152) of the patients in the light option; information on CDI origin and outcome was complete for 94% (1,016/1,078) and 98% (294/300) of the patients in the light and enhanced options, respectively. The workload of the options was 1.1, 2.0 and 3.0 person-days per 10,000 hospital discharges, respectively. Enhanced surveillance was tested and was successful in 32 of the hospitals, showing that C. difficile PCR ribotype 027 was predominant (30% (79/267)). This study showed that standardised multicountry surveillance, with the option of integrating clinical and molecular data, is a feasible strategy for monitoring CDI in Europe.
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