Health Information Management: Integrating Information Technology ...
Health Information Management: Integrating Information Technology ...
Health Information Management: Integrating Information Technology ...
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30 STARTING POINTS<br />
successful initiatives was the FynCom project. Its participants aimed at<br />
developing a system that would enable GPs to send and receive lab results,<br />
specialist letters and prescriptions using the EDIFACT standard. One of<br />
the GPs, who was part of the project from its beginning, explains:<br />
In 1990 we got the ‘informatics scheme’. It was about how the<br />
politicians wished to develop health care ICT until the year 2000.<br />
The scheme consisted of 120 pages and on page 117 it said that<br />
perhaps one could imagine that in year 2000 primary and secondary<br />
health care organizations would be able to communicate with each<br />
other. We had tasted blood and agreed that we could not wait for that<br />
long.<br />
(Interview, GP, 1101)<br />
In 1994 the standards developed by the FynCom group were transferred<br />
into a new project called MedCom, whose aim it was to make the protocols<br />
work on a national level. At that time, the extended possibilities for data<br />
exchange implemented by means of a number of locally based pilot<br />
projects had become a major incitement for non-computerized GPs to start<br />
working with an EPR.<br />
New possibilities of sending and receiving data also meant that the<br />
content of the EPR was suddenly experienced by the GPs as very<br />
unorganized; it was basically one ever-expanding ‘toilet roll of text’. They<br />
needed some organizing principles in order to keep an overview of their<br />
notes. Simultaneously, as elsewhere in Europe, health authorities felt a<br />
growing need to monitor GP practices to be able to better control health<br />
care expenditure.<br />
In the late 1990s diagnostic codes were integrated in updated versions of<br />
the GPIS available on the market. The classification used was the<br />
International Classification of Primary Care (ICPC), which was developed<br />
to register not only end-diagnoses, but also, for instance, a patient’s<br />
reasons for encounter (the Dutch GPIS uses the same classification). At<br />
present day health authorities are searching for ways to use data from GPs<br />
databases for research purposes. This is no easy task. First, GPs easily feel<br />
that they become subject to external control, and many do not feel it is<br />
their job to register for ‘external’ purposes. Second, comprehensive policy<br />
aimed at protecting patient privacy is felt to stand in the way of such<br />
external use of data. The ministry of health has now put forward<br />
suggestions to reinterpret the strict rule that patients must give a written<br />
consent before anyone can exchange patient information.<br />
Recently, within the ministry of health, the problem-oriented medical<br />
record has been put on the agenda. The aim is to enable more detailed<br />
registration of chronic diseases and subsequent transfer of this data into<br />
clinical databases. A National Indicator Project launched to develop