Health Telematics (AIM) Final Report
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Updated: Feb 1, 97 

IREP

Integrated Rehabilitation Programme

Project Code:   A2018
Project value:  3478 KECU
EC contribution:  1600 KECU
No of partners:  15
No of countries:  5
Duration:  30 months
Contact:
Ing. Sergio Copelli
TSD Tecnologie e Sistemi Datamont SRL
Via Taramelli 26
I-20124 Milano, Italy
Tel.: +39-2-62.70.80.54
Fax: +39-2-62.70.46.72

Overview

IREP was a new concept of technical services which support the European protocols for rehabilitation, including technical, medical and social issues. Its objectives were to define a uniform conceptual model of rehabilitation protocols and procedures and to build an information base of available rehabilitation protocols and expertise throughout Europe, to define a prototype of communication infrastructure and services interconnecting the rehabilitation centres and a prototype of a dedicated workstation for the use of rehabilitation professionals.

Purpose and objectives

The main objective of IREP is the creation of a European Information System to contribute to the modernisation and organisation of the Rehabilitation field.

Rehabilitation Medicine is a very new and unexplored experience in Europe. The field, instead of being perceived as a new beginning for the rehabilitation patient, is associated mostly as the last, desperate and rather conclusive step of patient's medical experience. Due to the combined disorganisation, unemployment and lack of communication among rehabilitators that characterise most European regions, patients do not reach their full therapeutic and restorative capabilities. This does not only confine the broader quality of life aspects for the patient but it creates a heavier burden on the society that has to support the quasi-rehabilitated patients in the ranks of unemployed and disabled citizens.

The aim of the IREP Consortium in addressing this area of work is to build a common European conceptual frame-work and to prototype effective and viable IT infrastructures and tools to support the rehabilitation of people with different types of physical handicaps.

The main outcomes of the project:

The technological scope of the project was very large because Rehabilitation is fairly new as an independent discipline and therefore it exhibits a large number of needs which must be addressed in a unified way: at one end the requirement of moving the rehabilitation process from the hospital to home in order to favour the integration of the handicapped inside his/her family and social context. At other end, the requirement, from the community of R&D specialists, for a high level of inter working between different Centres in different Countries for the definition of widely-accepted new rehabilitation protocols, for the harmonisation of existing ones and for sharing know-how and experiences.

The scientific baseline of IREP was an innovative approach to rehabilitation based on:

The project was planned over two phases, IREP 1 and IREP 2, with a total estimated effort of approximately 300 man months for each phase and with a duration of three years. The activity started with the definition of a formal model of the rehabilitation process which takes into account all possible actors, resources involved, medical practices, etc. This model has then been checked in some concrete application scenarios: Public Health, Patient Management and Research.

Significant categories of users have been identified: Patients, Families, Medical Teams, Volunteer Associations, Rehabilitation Specialists, IT Industry, Local Authorities and Social Services, Health care Planners, International Organisations (WHO, Rehabilitation International, etc.). For each category of users, the main requirements have also been set.

As a conclusion the general architecture of the IREP Information System has been defined. At the end of this step, the activity of prototyping and testing in a real site has been started. Due to the limited amount of time and resources, the Consortium decided to perform a limited experiment, with respect to the functionalities provided and the categories of users targeted.

IREP 1 was targeting the category of Medical Experts, that perform R&D in the Rehabilitation field. A sample of this category is represented in the Project. They provided a test site for the prototype and a general scientific validation to the overall approach. The first test site was at Ospedale Bambin Gesu' (Rome) in the domain of cardiac rehabilitation. This included a Base of harmonised protocols represented in a standard (to IREP) and homogeneous way. This protocol Base allowed the selection, customisation and tuning of the treatment for a specific patient with respect to a specific organisational environment and other parameters related to the specific case.

In parallel to this technological activity, a stream of medical activity contributing to populate the Information Base through the collection, harmonisation and validation of rehabilitation protocols currently in use in Europe was done. This stream of activity also played an important role for the creation of the consensus in the community of scientific experts.

The activity done in the phase 1 of the project was crucial for establishing the general framework and for testing through concrete experiments in real life environments the actual feasibility of the project goals.

The phase 2 of IREP extended the experience and the achievements of IREP 1 to implement a complete prototype of the IREP Information System: a full functional version was produced and a broader population of users addressed.

The categories of users addressed in this phase were:

Two main technological streams were addressed:

Telecommunication services for rehabilitation include:

Workstations for rehabilitation included a wide range of IT facilities:

This stream of activity requires strong investments and high technological competence, therefore it appeared to be mandatory to strengthen the contacts with related projects in AIM and in other CEC programmes in order to take advantage of the results achieved in these domains.

Results

General architecture of the IREP Telematic System has been defined.

Prototyping and testing in a real site. The test site was organised at the South & East Belfast Community Unit.

This first prototype of the IREP software makes contribution on three levels of rehabilitation: the clinical, the R&D and the administrative management levels. This prototype acquires and exploits a Base of harmonised protocols represented in an homogeneous way.

IREP has defined a model to describe in a formalised way the set of activities related to a certain pathology. The description is carried out on the basis of a meta model of generalised protocol which allows for each phase the definition of protocols and activities.

With respect to the management of the information concerning the patient, according to the IREP process model, through a number of logical steps taking into account the patient data, the organisation context and other aspects relevant for the medical decision, a customised version of a generalised pathology protocol can be prepared for the planning of the care on a specific patient which is affected by that pathology.

From that moment on, the complex logical structure of diagnostic and therapeutic activities defined for the pathology becomes the guide for the planning and for the execution of care activities on the patient providing also the basic structure to collect a number of synthetic information related to the patient and to the activities performed.

The environments in which the IREP system can be run may vary from simple cases in which a small number of physicians and rehabilitation specialists work on a limited number of patients affected by an homogeneous set of pathologies, to cases in which the health organisation is much more complex and the pathologies treated are spread over a wide spectrum.

As the targeted IREP services users include all categories of health operators, patients, researchers, administrators and other interested parties (from the phase of prevention to the phase of social integration), all other projects that aim at the same user population can be serviced by IREP process model and/or its network. IREP data base is structured in such a manner that allows continuos additions and expansions.

From the medical point of view IREP system can collect from the field of rehabilitation structured data and classifications, even semantic material which later can serve as a basis for the creation of an harmonising and even standardising process (rehabilitation procedures, e.g.).

IREP introduction in the Rehabilitation field is expected to reinforce systematisation in the working habits of rehabilitation workers and medical operators in general. The system introduces a methodological approach in health services delivery as well in file management and progress reporting; related changes are expected to be seen in the behaviour of health professionals that use the system.

For experts in the field of rehabilitation, the IREP data system rationalises their work. It is a tool for producing individual expert protocols and for combining the rehabilitation team's different protocols in a uniform protocol including the time-schedules. For the client the IREP software offers the advantage of receiving the printed plan of the rehabilitation process and its updated version easily available at any time along with the process.

For administrative purposes it is possible to plan the resources needed (specialists and equipment) better than earlier. Also the possibility to receive statistical data about the rehabilitation procedures can be useful for long-term planning of the employer and of governmental authorities.

IREP aims to build co-operation between providers of IT solutions so that a population needing rehabilitation interventions, rehabilitation operators and planners will benefit sooner from better services based on IT technology.

As a general objective, the exploitation of the results of IREP will allow the industrial participants:

List of Deliverables

Year 1

  • Overview of existing rehabilitation process in Europe (6/R/P)
  • IREP process model - first version (6/R/P)
  • IREP it infrastructure - user and functional requirements (6/R/R)
  • IREP SW/HW platform: guidelines and requirements (6/R/R)
  • DKB Data model specification (6/S/I)
  • Communication requirements (6/R/L)
  • Quality plan (6/R/L)
  • Multilingual rehabilitation protocols - First set (12/S/P)
  • IREP global architecture and design guidelines (12/R/L)
  • DKB specification and design (12/S/I)

    Year 2

  • DKB integration strategy (3/R/I)
  • Overall requirements of IREP workstations (3/R/L)
  • LINK to external data banks (3/T/L)
  • Running test bed - pathology group 1 (6/P/P)
  • Market evaluation (6/R/I)
  • Social impact evaluation (6/R/L)
  • IREP final global assessment (6/R/P)
  • Prototype DKB (6/P/L)
  • Access tools (6/P/L)
  • Network services (mail, directory, newsletter) (6/T/I)
  • Final report from scientific board (6/R/R)
  • Prototype communication infrastructure (6/P/R)
  • Draft network user manual (6/R/I)
  • Market survey (6/R/L)
  • Final report for Audit/concertation plans (9/R/R)

    List of Participants

    Dr. Roberto Dadda
    Database Informatica SPA.
    Viale Monza 257
    I-20126 Milano, Italy
    Tel.: +39-2-252.41
    Fax: +39-2-27.00.26.10
    Dr. Jan Ekberg
    Nat. Agency For Welfare & Health
    Siltasaarenkatu 18C 7th floor
    SF-00531 Helsinki, Finland
    Tel.: +358-0-39.67.20.91
    Fax: +358-0-71.44.69
    Dr. Nikos Damianakis
    Epsilon Software Ltd.
    377 Syngrou Avenue
    P. Faliro
    GR-17564 Athens, Greece
    Tel.: +30-1-942.17.07 / 942.56.71
    Fax: +30-1-942.77.19
    Prof. Francisco Del Pozo Guerrero
    Univ.Politecnica Madrid
    Tecnologica,Electronica y Bioengen.
    Ciudad Universitaria
    E-28040 Madrid, Spain
    Tel.: +34-1-336.73.07
    Fax: +34-1-336.72.16
    Dr. Francisco Vaz
    INESC - Dept. de Electronica
    P-3800 Aveiro, Portugal
    Tel.: +351-34-201.73
    Fax: +351-34-38.11.28
    Dr. David Puterflam
    Telesystemes Innovation
    33 rue de Vouille
    F-75015 Paris, France
    Tel.: +33-1-40.45.33.28
    Fax: +33-1-40.45.34.98
    Dr. Angelo Rossi Mori
    ITBM-CNR
    Viale Marx, 15
    I-00156 Roma, Italy
    Tel.: +39-6-827.71.01
    Fax: +39-6-82.22.03
    E-mail: mariano@color.irmkant.rm.cpr.it

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