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Eurosurveillance, Volume 9, Issue 7, 01 July 2004
Euroroundup
Basic Surveillance Network, a European database for surveillance data on infectious diseases

Citation style for this article: Ternhag A, Tegnell A, Lesko B, Skaerlund K, Penttinen P. Basic Surveillance Network, a European database for surveillance data on infectious diseases. Euro Surveill. 2004;9(7):pii=472. Available online: http://www.eurosurveillance.org/ViewArticle.aspx?ArticleId=472

 

A Ternhag, A Tegnell, B Lesko, K Skaerlund, P Penttinen
Swedish Institute for Infectious Disease Control, Stockholm, Sweden

 


The Basic Surveillance Network was started in 2000 and is one of the networks on infectious diseases funded by the European Commission. The network collects and makes readily available basic surveillance data on infectious diseases from all the 'old' (pre-2004) European Union member states. The aim is to provide easy access to descriptive data that already exist in national databases, so that it is possible to monitor and compare incidence trends for infectious diseases in the EU member states.

The list of diseases covered by the network has recently been expanded from 10 initial 'pilot' diseases to over 40 diseases listed by the EU to be under surveillance. In the near future, the new member states will be invited to participate in the network.

Data are case-based and comprise date of onset of disease, age and sex. Only a very short list of disease specific additional variables, such as country of infection or immunisation status, is collected. Classification of cases ( possible, probable, confirmed) is specified according to EU case definitions.

The participants of the network have access to an internal web site were all the data is presented in tables and graphs. An open website is available for the public at https://www.eubsn.org./BSN/
 

Introduction
In September 1998, a proposal from the European Commission was adopted as a Decision of the European Parliament and Council (2119/98/EC) to set up a network for the epidemiological surveillance and control of communicable diseases in the European Community.
With this legal document as a background, several projects to develop designated surveillance networks (DSN) have been funded by the Commission and they are now operating at the European level (for diseases such as salmonellosis, legionellosis, tuberculosis and HIV/AIDS). Each one of them is collecting data at a detailed level and most of them have objectives beyond routine surveillance (surveillance that only includes information collected on a regular basis in a majority of European Union (EU) countries and by methods used by regular national surveillance systems). Some examples of these extended objectives used in different networks include: the collection of strains for the further study of resistance mechanisms; surveillance of antibiotic resistance; and to function as an early warning system for outbreaks in travellers [1-3]. To fulfil this type of detailed surveillance, a considerable input is often needed from the member states. Epidemiologists at the reporting institutes have to fill in manually questionnaires sent out by DSN at a regular basis. The different networks' case definitions may differ both from the one proposed by the EU and from the one used nationally. Age grouping can also vary between, for example, the World Health Organization and a DSN for the same disease.
A later EU decision listed some 40 diseases that should be under surveillance [4]. Today there is no single source of routine surveillance data for these diseases; many of them are not covered by a specific network and even when covered the data does not necessarily mirror the national surveillance data. An easy one-step access to simple descriptive data on numbers and incidences would be useful.
To conclude, there is a need for a surveillance network at the European level that handles rare diseases and also collects basic or 'generic' information on the other listed infectious diseases using the three-level system for case definitions (possible, probable, confirmed).
The Swedish Institute for Infectious Disease Control (SMI) applied for funding of a project to establish this network, and an agreement between the Commission and SMI was reached whereby SMI was to coordinate the formation of a Basic Surveillance Network (BSN). BSN was started in 2000.

Objectives
The key objective of the BSN project is to create a standard, passive system for sharing basic surveillance data, in order to detect and monitor incidence trends for infectious diseases in Europe. A long term objective is to promote activities that make national data more comparable than they are today. An example is the use of EU case definitions.

Method
One epidemiologist and one database manager have been identified at each national institute for infectious disease control in the (then) 15 EU member states plus Iceland, Norway and Switzerland. Together with these designated participants, a programme to fulfil the objectives has been developed. The following are the main principles of this programme that the participants have agreed on. The guiding principle has been to find a level of detail and frequency that is as low as possible, yet still useful:
· BSN collects data that already exist in national databases.
· Data are case-based, and include age, sex, report date. Classification of cases are specified (possible, probable, confirmed), based on the EU case definitions. If case-based data are unavailable, aggregated data will be collected.
· Only a short list of additional variables for each disease is collected [TABLE 1].
· The BSN database is updated on a monthly basis.
·Data collection: data are transferred from the national databases in a predefined format in xml or comma separated files. Before data are added to the common database, they are checked for consistency and adherence to the predefined format, and all exceptions found are clarified. The data are first published on the participating country's private web page,on the BSN internal website, where only the sending country can review them. During the first week of the following month, the new data are added to the common database.
· Aggregated data from the common database are accessible for all network members via the internal website. A module for standardised output to a public website has been created. To increase the interpretation of data, countries can add comments to the graphical presentation of the aggregated data, shown on the public website.

Activities
Annual meetings of all participating partners are held to discuss principles of operation and collaboration. Several temporary and one permanent working group have worked on various epidemiological and data management issues. Ten pilot diseases have been chosen for reports [TABLE 1]. They were selected to represent a wide range of different epidemiological characteristics, not in terms of public health priority, but primarily to test the feasibility of the collection and transfer protocols set up.
Data has been collected since 2000 and some countries have also reported historical data in monthly aggregated format since 1995. Historical data make the time series longer and facilitate detection of trends. There is a variation between the members of the network on how many diseases can ben reported to the network, and how often. Some can deliver data on all ten diseases, others on six or three, and others on none [see TABLE 2]. There are several reasons behind these differences. It may be that a specific disease is not under surveillance in the country, that the information is not stored in a computerised database, that the data are not stored at national but at county level or other reasons that make reporting impossible.
The designated participants of the network have access to an internal website where surveillance data are presented in various ways. The BSN focuses on numbers and incidence rates and their trends over time.



Discussion
One of the main benefits of the network is that once the monthly transfer of the standardised data is in place, incidence trends on more than 40 infectious diseases from all European countries are easily available within a short time delay. This is not currently possible to find, as most of the dedicated (disease specific) surveillance networks do not collect data on all national cases, but rather on a subset. This means that BSN will provide health professionals and the public with descriptive data on reported diseases. The network will not be a tool in itself to answer more complicated questions such as 'why has the incidence for hepatitis A in country X increased between 00-02?. It can, however, be a positive stimulus for professionals to initiate further investigative and analytical work, and furthermore provide them with information on incidence trends in other EU countries when they experience changes in their own countries.
There are numerous additional benefits that have been identified during the development of the network. Bringing database managers from the national institutes together for the first time made it possible to examine a number of questions from a new angle. Several of the countries were at different stages of developing new or updated versions of computerised reporting systems when the project started. The meeting of the database managers made it possible to exchange ideas and facilitated and improved the development of some of these systems.

Among epidemiologists, discussion on interpretation of data has been possible in a new forum, and detection of major shifts in trends and difference between different countries can be identified and analysed at a multinational level.
As with all surveillance networks, there are a number of inherent problems. When pooling incidence of diseases from individual countries based on data from their national surveillance systems, there are a number of obstacles to be faced regarding case definitions and other factors that will influence the number of cases reported. Although there are common case definitions for the infectious diseases under surveillance specified in Decision 2002/253/EC (19.3.2002), this only solves a small part of the problem. Other, more country specific factors, such as the tendency of people to seek medical care, different diagnostic methods in use, and the percentage of physicians sending in notifications probably have an impact on the numbers reported.
Another problem is that it takes time before data series become long enough to make trends in disease incidence obvious. Before this output can be produced, there is a risk that countries providing data and using the services will not perceive the output as valuable, and might therefore discontinue their data transfers. Despite such problems, BSN is becoming a useful part of the common surveillance system laid down by Decision 2119. Two main expansions of the network are planned for the future. The first, already is in progress, is to expand the number of diseases reported from the ten pilot diseases to all diseases included under Decision 2000/96/EC [TABLE 1]. The other is to invite the new members of the EU to join BSN. We foresee that with basic incidence rates for the member states published on a single website, BSN will continue to be a platform for collaboration and exchange of ideas.


References

1. Fisher IST. The Enter-net international surveillance networks - how it works. Euro Surveill 1999;4:52-5
2. Glissman S, Rönne T, Tozzi A. The EUVAC-NET project: creation and operation of a surveillance community network for vaccine preventable infectious diseases. Euro Surveill 2001;6:94-98.
3. Bronzwaer SLAM, Goettsch W, Olsson-Liljequist B, Wale MCJ, Vatopoulos AC, Sprenger MJW. European Antimicrobial Resistance Surveillance System (EARSS): objectives and organisation. Euro Surveill 1999;4:41-44
4. Commission Decision of 22 December 1999 on the communicable diseases to be progressively covered by the Community network under Decision No 2119/98/EC of the European Parliament and of the Council (2000/96/EC)

 



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