Evaluation of the enterovirus laboratory surveillance system in Denmark, 2010 to 2013

Author:

Condell Orla12,Midgley Sofie2,Christiansen Claus Bohn3,Chen Ming4,Chen Nielsen Xiaohui5,Ellermann-Eriksen Svend6,Mølvadgaard Mette7,Schønning Kristian8,Vermedal Hoegh Silje9,Andersen Peter Henrik10,Voldstedlund Marianne10,Fischer Thea Kølsen112

Affiliation:

1. European Program for Public Health Microbiology Training (EUPHEM), European Centre for Disease Prevention and Control, (ECDC), Stockholm, Sweden

2. Department of Microbiological Diagnostics and Virology, Statens Serum Insitut, Copenhagen S, Denmark

3. Department of Clinical Microbiology, Rigshospitalet, 2100 Copenhagen Ø, Denmark

4. Department of Clinical Microbiology, Sygehus Sønderjylland, Sønderborg, Denmark

5. Department of Clinical Microbiology, Slagelse Hospital, Slagelse, Denmark

6. Department of Clinical Microbiology, Aarhus University Hospital, Aarhus, Denmark

7. Department of Clinical Microbiology, Aalborg University Hospital, Aalborg, Denmark

8. Department of Clinical Microbiology, Hvidovre Hospital, Hvidovre, Denmark

9. Department of Clinical Microbiology, Odense Universitetshospital, Odense, Denmark

10. Department of Infectious Diseases Epidemiology, Statens Serum Institut, Copenhagen, Denmark

11. Center for Global Health and Department of Infectious Diseases, Clinical Institute, University of Southern Denmark, Odense

Abstract

The primary aim of the Danish enterovirus (EV) surveillance system is to document absence of poliovirus infection. The conflict in Syria has left many children unvaccinated and movement from areas with polio cases to Europe calls for increased awareness to detect and respond to virus-transmission in a timely manner. We evaluate the national EV laboratory surveillance, to generate recommendations for system strengthening. The system was analysed for completeness of viral typing analysis and clinical information and timeliness of specimen collection, laboratory results and reporting of clinical information. Of 23,720 specimens screened, 2,202 (9.3%) were EV-positive. Submission of cerebrospinal fluid and faecal specimens from primary diagnostic laboratories was 79.5% complete (845/1,063), and varied by laboratory and patient age. EV genotypes were determined in 68.5% (979/1,430) of laboratory-confirmed cases, clinical information was available for 63.1% (903/1,430). Primary diagnostic results were available after a median of 1.4 days, typing results after 17 days, detailed clinical information after 33 days. The large number of samples typed demonstrated continued monitoring of EV-circulation in Denmark. The system could be strengthened by increasing the collection of supplementary faecal specimens, improving communication with primary diagnostic laboratories, adapting the laboratory typing methodology and collecting clinical information with electronic forms.

Publisher

European Centre for Disease Control and Prevention (ECDC)

Subject

Virology,Public Health, Environmental and Occupational Health,Epidemiology

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