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Updated: Apr 27, 1999 |
This is the most recent structured information on this project. Complementary data can be found on previous documents | |
I4C-TripleC
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The
project I4C-TripleC intends to validate in three hospitals in Eastern Europe (in
Prague, Bratislava and Caslav) integrated workstations to support the continuity
of cardiac care. The workstation is the outcome of the project I4C: Integration
and Communication for the Continuity of Cardia Care, part of the 4th
Framework Programme in Health Telematics (HC1024). Validation will be supported
by an industry (Cardio Control) that collaborates in the I4C project;
co-ordination will be done by the co-ordinating partner of the I4C project
(Erasmus University Rotterdam) .
The
goals of I4C-TripleC will be reached by:
1.
Integrated access to cardiological patient data;
2.
Support of patient care, research and the assessment of the quality of
care;
3.
More comprehensive and more consistent recording of patient data and
biosignals, combined in a multimedia patient record.
The
purpose I4C-TripleC is to validate the workstation which is being developed in
the EU-project Integration and Communication for the Continuity od Cardiac Care
(I4C). The overall objective is to adapt the workstation to local clinical
circumstances as met in the three clinical settings, contribute to the extension
and assessment of the knowledge base for structured data entry and data
retrieval, and take care of the language adaptation, which is part of the
language module that will be implemented in I4C.
The work will be divided in three workpackages as described here.
Work Package 1. System
installation and technical adaptation of workstations
In
this work package, work will be undertaken on the system installation and the
technical adaptation of workstations and multimedia patient record to ensure the
continuity of care. The work package will facilitate data availability for the
different clinical users. The basis for this work package will be the existing
and operational prototype of the workstation.
The participating industry will investigate the technical requirements of the
clinical sites. Translation of documentation into the different languages has to
be done. Technical adaptations will be carried out.
Work Package 2. Adaptation
to user requirements for workstations
The
workstation as realised in I4C was adapted to typical clinical settings of
cardiological clinics related to the partners. In this project, an adaptation
should be made to the user requirements of clinics in three Eastern European
countries that were not part of the original consortium. This work in
I4C-TripleC will be as much as possible be implemented by industry, but co-ordinated
from the co-ordinating partner in the I4C project.
The existing user requirements of the workstation for cardiological applications
will be adapted, based on the analysis of the users' needs and the functional
requirements. The medical terminology will be translated to that of the clinical
partners.
Work Package 3. Evaluation
support and assessment of workstations
The
objectives of this work package are to collect and analyse evaluation results on
installations and user requirements adaptations, and to prepare and distribute
evaluation reports.
The assessment will be take place at clinics of the three clinical partners of
I4C-TripleC. The work is supported and a report is prepared by the work package
co-ordinator.
1.
Collect pre-installation evaluation data from associate clinical partners
2.
Collect post-installation evaluation data
3.
Prepare a final installation report
The
major results of the project will be:
1.
The clinical evaluation, together with the evaluations in the I4C
project, will lead to an improved version of the I4C workstation.
2.
The clinics in the Czeck and Slovak Republic will be able to
continue to work with the workstation which will lead to a better quality of
care.
3.
The project gives the
partners in the Czech and Slovak Republic the possibilty to work with latest
technology in health telematics (knowledge transfer).
-
Documentation user requirements (6/PD)
- Realisation of changes in user requirements (24/PD)
- Documentation of user requirements (9/PD)
- Realisation of requirements (24/PD)
- Verification report (24/PD)
Prof.dr.
Jan van Bemmel
Erasmus University Rotterdam
Dept. Of Medical Informatics
Dr. Molewaterplein 50
NL - 3015 GE Rotterdam
The Netherlands
Phone: +31 10 4087050
Fax: +31 10 4367117
Prof.dr.
Jana Zvarova.
Academy
of Sciences
Institute of Computer Sciences - EuroMISE
Pod vodarenskou vozi 2
Prague 8
Czech Republic
Phone: +420 2 6605 3097
Fax: +420 2 689 7013
E-mail: zvarova@euromise.cz
Jan
Peleska MD
Charles
University, General Faculty Hospital
U nemocnice 2
Prague 2
182 08
Prague
Czech Republic
Phone: +420 2 2496 2623
Fax: +420 2 29060913
Dr.
J. Hatala
Hana Grunfeldova MD
National Institute of Cardiovascular Diseases
Bratislava
83126
Slovak Republic
Hospital Caslav
Jenikovska 348
Caslav 286 01
Czech Republic
Phone: +420 322 2121
Prof.dr.
Nicos Maglaveras
Aristotelian
University
Laboratory of Medical Informatics
Box 323
54006 Thessaloniki
Greece
Phone: + 30 31 999272
Fax: + 30 31 999263
E-mail: nicmag@vergina.eng.auth.gr
Dick
van Luijk
Cardio Control
Patrijsweg 72
2289 EX Rijswijk
The Netherlands
Phone: +31 70 39 87 277
Fax: + 31 70 39 87 288
E-mail: cardio@euronet.nl
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