|VALUE+ - Promoting Patient Involvement in EU Supported Health-related Projects|
|Duration||2008 - 2010|
European Commission, Directorate General for Public Health-supported project to improve the involvement of patient associations in health-related European studies and research.
Based on the WHO definition:
Health is a state of complete physical, mental and social well-being and not merely the absence of disease or infirmity,
we have in recent years seen a shift in health policy priorities towards considering a broad spectrum of citizen and patient needs. Globally, health system policy makers are now subscribing to the new paradigm of citizen or patient-centred services. If empowering the citizen is to imply more than just generic policy declarations, one needs to provide him with the means and tools to become a well-informed and self-assured patient, to involve him in decision processes in a way best suited to his level of understanding and knowledge, and to provide him with optimal medical services in situations when he does not want to, or is physically or mentally unable to be part of such processes. Value Plus will provide patient organisations with the tools to influence policy-making at EU-level and to participate in EC-funded projects of concern to their constituency. Empirica is supporting these efforts through the statistical analysis of past and ongoing EC-funded projects which show elements of patient involvement to derive insights on barriers and facilitators for greater patient involvement.
|EXPAND – Expanding Health Data Interoperability Services|
|Duration||2014 – 2015|
The aim of the EXPAND Thematic Network is to address the challenge of moving from a set of point-solution pilots to a large-scale deployment of cross-border facilities that support Member States (MS) in delivering their local eHealth plans and providing cross-border care. In particular, the objective of the Network is to launch a process through which it will be possible to harness the available resources and to act as a catalyst for their operational use on a large scale. While this process shall cater to cross border eHealth services in general, the initial focus of EXPAND shall be to secure the sustainability and expandability of the epSOS pilot services including the proper handover, up to the launch of the Connecting Europe Facility (CEF) which is planned to be operational in 2014.
In order to achieve its objectives, EXPAND brings together 20 national and regional health authorities and competence centers for semantic interoperability, Standards Developing Organizations (SDO), and a number of EU-supported initiatives such as EuroRec, SemanticHealthNet, PARENT and the EN13606 Association. The project is co-funded by the European Competitiveness and Innovation Programme (CIP).
|VPH-DARE@IT - VPH Dementia Research Enabled by IT - DareIT|
|Duration||2013 - 2017|
VPH-DARE@IT aims to provide a systematic, multifactorial and multiscale modelling approach to understanding dementia onset and progression; it will explore the lifestyle and environmental factors that predispose to its development, and will deliver more objective and accurate differential diagnosis than what is available thus far in Europe, by shortening the current average 20-month time lapse between the onset of cognitive and memory deficits and its specific clinical diagnosis.
|MD Paedigree - Model-Driven European Paediatric Digital Repository|
|Duration||2013 - 2017|
MD-Paedigree, which stands for Model-Driven European Paediatric Digital Repository, is a clinically-led VPH project which provides decision support to medical professionals wherever they treat their patients. Through disease simulations, sometimes requiring the availability of high performance and supercomputer resources, MD-Paedigree improves the diagnostic precision of paediatricians and offer child-specific treatment choices for Europe's children. Using MD-Paedigree, physicians will be able to select highly individualised treatment options, and receive on-the-spot support in predicting treatment outcome based on each patient's personal medical data. MD-Paedigree focuses on four paediatric disease areas: Cardiomyopathies, Obesity-related Cardiovascular Disease, Juvenile Idiopathic Arthritis, and Neurological & Neuromuscular Disease. The MD-Paedigree infostructure integrates the models with: knowledge discovery tools, semantic data representation, and integration and outcome analysis..
|PilotSmartCare - Joining up ICT and service processes for quality integrated care in Europe|
|Duration||2013 - 2016|
SmartCare develops and pilots integrated care pathways for older European citizens across organisations and locations, in particlar between social and health service providers. A key object of integration are existing home platforms, which monitor physiological parameters, environmental and behavioural patterns etc. In SmartCare these platforms are to be opened to cross-sectoral care teams, improving the ability of older people to better manage their chronic conditions at home and deal with their increasing frailty. The ICT platform will enable regionally customised integrated care models and care pathways (the SmartCare Pathways). The latter will be supported by workflow tools which will activate the most appropriate resources across the entire spectrum of services available for older people both for scheduled and emergency care.
|ISAES - Interoperable e-Systems for Africa Enhanced by Satellites|
|Duration||2013 - 2014|
The ISAES-project will conduct a feasibility study focused mainly on interoperability aspects derived from to desgin, implement and operate a pan-African eHealth platform. This study is part of the first phase of the Satellite-enhanced eHealth for sub-Saharan Africa Programme (eHSA), which examines the critical success factors for the development of sustainable, satellite-enhanced eHealth and telemedicine services across SSA. Besides the studies on governance, regulatory issues and sustainability aspects, the interoperability of systems collaborating for the provision of eHEalth and telemedicine services has been identified as a major and ubiquitous challenge. In the context of this study the problem of interoperability is not only limited to technical standardizations but also takes issues of integrating cultural, financial, political and workflow systems into account. Finally the goals of this study are: (1) The identification of all domains linked to design, implementation and operation of the eHealth platform and its associated services, (2) the analyse of the current SSA situation, regarding ressources and degree of readiness and (3) the provision of a roadmap for future implementation.
|Epiria - Evaluation of Pertinence and Impact of Research Infrastructure Activity in FP7|
|Duration||2013 - 2014|
The aim of this evaluation study is to assess the pertinence, effectiveness and efficiency of the Research Infrastructure activities in FP7, and their impacts on scientific communities, research policy, innovation and society at large. The study is commissioned by DG CONNECT in the context of the Framework Contract SMART 2009/0042 Lot 2 and is being carried out by Technopolis Group in consortium with empirica.
|Regulatory impact analysis of the Swiss law on an electronic patient record|
|Client||Bundesamt für Gesundheit, Bern, Schweiz|
The electronic patient record is a core pillar of the eHealth Strategy Switzerland. By digitally supporting treatment processes the record aims to improve quality and efficiency of healthcare. Costs and benefits as well as potential incentives and risks associated with the introduction of the record have now been subjected to a regulatory impact analysis conducted by empirica in consortium with ecoplan ecoplan and commissioned by the Suisse Federal Office of Public Health
The results showed, that the aspired regulation and kick-off funding for the electronic patient record are likely to lead to its accelerated introduction and diffusion. Society as a whole as well as affected stakeholder groups - including general practitioners, hospitals and patients - will gain in the long term. In the short and medium term, however, a prolonged phase of investment needs to be overcome. The results were published by the Federal Office of Public Health
|Client||European Commission FP7-ICT-2009-6|
|Duration||3/2011 – 2/2015|
VPH-Share will develop the organisational fabric (the infostructure) and integrate optimised services to expose and share data and knowledge, jointly develop multiscale models for the composition of new VPH workflows and facilitate collaborations within VPH community.
Four flagship workflows (from @neurIST, euHeart, VPHOP, Virolab) provide existing data, tools and models, engage with the services developed by VPH-Share drive the development of the infostructure, and pilot its applications. Data sources are usually clinical data from individual patients - medical images and/or biomedical signals – sometimes with population information. The operations range from secure access and storage through annotation, data inference and assimilation, to complex image processing and physics-mathematical modelling, to data reduction and representation. The project focuses on bottleneck – the interface with the wealth of data from medical research infrastructures from clinical processes. VPH-Share will provide the essential services, as well as computational infrastructure, for the sharing of clinical and research data and facilitating the construction and operation of new VPH workflows, and collaborations between the members of the VPH community. Evaluating the effectiveness and fitness-for-purpose of the infostructure and developing a thorough exploitation strategy are activities, creating confidence in the communities. The consortium, through its optimal of medical, mathematical, engineering, software & hardware and industrial knowledge expertise from the EU and internationally, will make this effort a success, delivering European citizens clinically useful outcomes that will benefit society.
|Client||European Commission FP7, ICT for Health, Ageing Well, Inclusion and Governance|
|Duration||10/2011 – 3/2013|
DISCIPULUS aims at the grand challenge of the "Digital VPH Patient". The Digital Patient initiative will develop new ways of combining this rich patient information space into a highly visual, coherent, meaningful way, of generating new clinical information and ultimately of creating a "patient avatar" capable of supporting the medical professional by producing new clinical knowledge. The simulation and prediction of various treatment options could help clinicians to decide between options based on patient-specific information.
To realise this vision, DISCIPULUS will develop a sound ICT research and innovation roadmap, informed by consultation and engagement of diverse groups from modellers and technology developers to end users, healthcare providers and regulators. The final goal is to deliver a single, universally useful, all-encompassing Roadmap. To prepare for this, DISCIPULUS will consolidate relevant RTD results by examining critically the state-of-play of both research and innovation throughout the VPH Community. It will document and map outputs central to the successful achievement of the Digital Patient. It will capture and quantify the needs of stakeholder communities, particularly those of clinicians and patients, which are key for the crafting of a successful, usable Digital Patient. A strong impact I anticipated on stressing EU leadership in VPH research, industrial exploitation, quality and sustainability of future healthcare.
|Client||EU CIP PSP Programme|
|Duration||2012 - 2015|
The main goal of the PALANTE project is to empower patients allowing them to make informed decisions about their health and take an active role in their care and collaborate effectively with their healthcare team thanks to the use of information and communication technologies. Patient empowerment reinforces healthcare quality and improves efficiency of healthcare systems and thus counters the trend of increasing healthcare costs. This is why patient empowerment is a priority area of EU policy.
Building on already existing e-health platforms and services in the 9 participating regions, the PALANTE project focuses on the implementation, scaling up and optimisation of 7 demonstration pilots based on the concept of secure and user friendly online access by citizens to their medical/health data. Two sites will allow an in-depth look into how patient access is already working. All pilot sites and on-going projects cover a wide range of services with different levels of complexity and a different number of patients, addressing different levels of empowerment. Altogether, 5 pilots address treatment of chronic diseases with applications of ICT integrated in chronic disease management support. Empirica is the partner leading evaluation in the project. It takes care of assessing the impact of eHealth in each site using a multi-method multi stakeholder approach.
|SemanticHealthNet - Semantic Interoperability for Health Network|
|Client||European Commission FP7-ICT-2011-7|
|Duration||2011 - 2014|
Semantic interoperability of EHR systems is a crucial prerequisite for enabling patient-centred care and advanced clinical and biomedical research. SemanticHealthNet will develop a scalable and sustainable pan-European organisational and governance process to achieve this objective across healthcare systems and institutions.
A clinical focus on chronic heart failure and cardiovascular prevention in the workplan shall define the semantic resources to be developed. The exemplars in cardiology and public health are specific enough to permit comprehensive development and validation of these resources, and yet typical enough for wider generalisation of the methodology and its governance. SemanticHealthNet will capture the needs articulated by clinicians and public health experts for evidence-based, patient-centred integrated care in these domains.. Existing European consensus in the management of chronic heart failure and cardiovascular prevention will then be integrated in EHR architectures, clinical data structures, terminologies and ontology by leading technical experts.
The consortium comprises more than 40 internationally recognised experts, including from USA and Canada, ensuring a global impact.
|Cross-border ePrescription guidelines|
|Client||European Commission DG Health and Consumer Affairs (DG SANCO) through its Executive Agency for Health and Consumers (EAHC)|
|Duration||09/2011 - 09/2013|
The recent European Union "Directive on the application of patients' rights in cross-border healthcare" stipulates in Article 11 the "Recognition of prescriptions issued in another Member State" for dispensation in any other Member State. (see: http://eur-lex.europa.eu/) It mandates the adoption of guidelines supporting Member States in developing and implementing the cross-border interoperability of ePrescriptions without prejudice to national rules.
The key goal of the cross-border ePrescription study (commissioned by DG SANCO through its Executive Agency for Health and Consumers ) is to produce a first draft of such guidelines on interoperable ePrescriptions. In the first phase of the study, empirica and its partners will analyse the present status of ePrescription in Member States of the European Union, identify already available guidelines at country level and related good practice, and explore the feasibility of such guidelines as well as the level of detail which may be appropriate to achieve the objective of a single market also for prescriptions on medicines and medical devices for patients. The ePrescription use case underlying the work in the study will be the epSOS (www.epsos.eu) cross-border use case.
Based on this analysis, and with input from European experts on policy, organisational, legal, technical and semantic interoperability challenges, during the second study phase guidelines will be drafted, validated, refined and delivered to the European Commission. Initial results are expected in the second half of 2012. Final results will be presented in the fall of 2013.
|ProeHealth: Enhancing eHealth Procurement|
|Client||European Commission, CIP ICT Policy Support Programme|
|Duration||12/2010 - 7/2012|
The ProeHealth study aims to improve the procurement of ICT solutions for healthcare by providing guidelines for the organisations involved in the procurement process. Both public and private healthcare organisations are included in this. The guidelines will be there to help them from the stage of planning procurement, as it arises that adopting an eHealth solutions is the most suitable approach, following up with instructions for transfer of planning to the procurement specification and finally the procurement process.
The question could be raised as to why such guidelines are necessary. The answer to this is that procuring eHealth solutions is a complex procurement process, quite different to other types of procurement. Experience shows that this complexity can lead to disappointing results. Often, expected benefits are not achieved or value for money is lacking. This leads to the conclusion that support is needed for those carrying out the procurement of eHealth solutions. Further proof for this hypothesis is the lack of any existing procurement guidelines which address eHealth components specifically.
|eHealth Innovation - Scaling up eHealth facilitated personalised health services: Developing a European roadmap for sustained eHealth Innovation|
|Client||European Commission DG INFSO and Media|
|Duration||5/2011 - 11/2013|
The focus of this Thematic Network is the re-architecting of healthcare services towards a patient centric cooperation of actors and the meaningful integration of information. A roadmap will be developed towards achieving personalised health services and a supportive eHealth infostructure, which would support virtual teams working efficiently and effectively at enabling and empowering patients to play greater roles in their own health and wellness. Special emphasis will be put on chronic disease management for an ageing population. eHealth Innovation will develop consensus among stakeholders and produce a roadmap towards making interoperable eHealth services deployed at large scale in Europe, thereby also supporting patients in managing their health. The resulting requirements for a supportive infostructure and for further innovation measures are further objectives.
In total, five workshops will be organised around thematic areas such as chronic disease management for an ageing population, personal health systems and the requirements for an EU-wide eHealth infostructure. The workshops will each produce validated reports and recommendations on their respective topics. The cumulated results will feed into a final validated roadmap.
Project website: www.ehealth-innovation.eu/
|ASSIST – Assessment and evaluation tools for Telemedicine|
|Client||esa – European Space Agency|
|Duration||1/2010 - 06/2011|
Healthcare is facing increasing quality and resource challenges and telemedicine is often regarded as part of the solution. Numerous pilots are underway, but will these telemedicine services really make healthcare more efficient? Will they increase access, quality, safety of care? And what added value can satellite communication bring to such services? These are questions the ASSIST study aims to address by developing comprehensive methods and easy to use toolkits for telemedicine assessment, which help pilot projects to objectively and rigorously evaluate their solution from an evidence-based multi-stakeholder perspective. ASSIST is funded through the ESA's General Studies Programme (GSP).
More information and project website: http://iap.esa.int/Useful-Resources/ASSIST
|INDEPENDENT - ICT Enabled Service Integration for Independent Living|
|Client||European Commission DG INFSO and Media, CIP Programme|
|Duration||1/2010 - 1/2013|
The project defines, delivers and pilots a digital infrastructure supporting coordinated cross-sector delivery of timely support to prevent older people from slipping out of safe independent living, maintaining quality of life. The infrastructure enables support services to overcome limitations of sectoral telehealth and telecare and empowers informal carers and the voluntary / third sector to participate in delivery of support, thus radically improving efficiency. The innovative new services are piloted at six sites across the Europe. The project brings together 20 organisations across 6 Member States representing all major stakeholders in the "value chain" of support to older people, from public authorities and social and health service providers to global industry players and specialist SMEs.
More information and project website: http://www.independent-project.eu/
|eCareBench - Coping with an ageing population - Learning from good eHealth and telecare practices|
|Client||European Commission DG INFSO and Media|
|Duration||8/2010 - 10/2011|
Against the background of the fact that the use of telemedicine services is still limited and the market for devices remains highly fragmented, despite the potential benefits and the technical maturity of many applications, the study explores the European space in terms of the deployment of ICT-enabled care services, to learn from successful examples, and to adapt policies and incentive structures. In an effort to address these needs, the study demonstrates the gains in promoting the de-ployment of home care services using ICT and facilitate the exchange of good practices. The study develops the following key outputs: a consistent, rigorous, and realistic conceptual and methodological design of the study, including clustering of models of long-term care, a choice of 10 national cases, and the structure of a scoreboard on innovation, a scoreboard on the openness to innovation of national models of long-term care in the area of ICT-enabled home care services, set up around a set of macro-categories related to the openness to innovation, a validation workshop of one day, informing relevant stakeholders and experts about, and collecting their views on the interim study findings, as well as more general views, especially on current and future developments in the area of the study and policy implications, a set of analysed good practices in innovative, ICT-enabled of home care services for older people with chronic diseases, covering all six macro-categories of the scoreboard, and several clusters of national long-term care models, a set of relevant, well grounded, and clear policy recommendations, supporting further policy developments at European level to promote the deployment of ICT-enabled home care services, their ongoing monitoring, and the exchange and transferability of good practices across Europe, and adequate promotion of the main findings of the study. The project covers all EU Member States with more intensive activities in 10 countries to be supported by experts and national correspondents from empirica's ENIR network (www.enir.org) in the different countries.
|NMS Physiome - Tools to develop the NeuroMusculoSkeletal Physiome|
|Client||Directorate General (DG) Information Society and Media of the European Commission|
|Duration||2010 - 2012|
NMS Physiome is a Virtual Physiological Human (VPH) cooperation of the worldwide largest research projects focusing on simulating the musculoskeletal apparatus, the Osteoporotic Virtual Physiological Human (VPHOP) integrated project, with the Center for Physics-based Simulation of Biological Structures (SIMBIOS) at Stanford University, USA.
|Client||Directorate General (DG) External Relations (RELEX) of the European Commission|
|Duration||20010 - 2011|
The overall goal of the EU-USA ARGOS eHealth Pilot Project is to contribute to establishing a "Transatlantic Observatory for Meeting Global Health Policy Challenges through ICT-Enabled Solutions" in order to develop and promote “Common Methods for Responding to Global eHealth Challenges in the EU and the US”.The Observatory will promote mutual understanding and learning among EU and US policy researchers and policy makers on the following general challenges with global dimension:
In the ARGOS eHealth project, the following specific target areas will be addressed:
Key outputs for each of the three topics are:
empirica leads one of three work packages, concerned with “Definition of a common approach measuring the adoption, usage and benefits-costs of eHealth”. This work will involve the USA Office of the National Coordinator (ONC) for Health IT, the National Institutes of Health (NIH), Harvard University, and the American Medical Informatics Association (AMIA) as coordinator on the USA side.
|Client||Directorate General (DG) Information Society and Media of the European Commission|
|Duration||2010 - 2011|
Smart Personal Health is a European Commission support action to promote awareness about issues and challenges of interoperability among personal health systems (PHS) and to other eHealth systems. The project will substantially assist the drafting of health policy by proposing recommendations for interoperability promotion to the European Commission, regional and national governments, stakeholder groups and industry.
|Client||DG Information Society, ICT for Health Unit|
|Duration||01/2009 - 08/2010|
The eHealth Strategies study will assess the progress made by EU-Member States in their efforts towards realising the goals of the European Union eHealth Action Plan. This strategy document, published by the European Commission in 2004, identified fields of required action to achieve eHealth interoperability in Europe. Building on the insights of the eHealth ERA project (final results brochure), which was also commissioned to empirica, the study team will describe, measure and assess:
At the end of the study, a summary European level progress report will be published. It will include
|Market sizing & five year forecast for the overall Healthcare ICT market across Europe|
|Client||COCIR (European Coordination Committee of the Radiological, Electromedical and Healthcare IT Industry)|
|Duration||07/2008 - 12/2008|
The overall goal of this study by empirica GmbH (Bonn, Germany) and data information intelligence GmbH (Leipzig, Germany), is to provide statistical insights on the current state of deployment of eHealth across Europe and to define an appropriate longer-term procedure for estimating and assessing the eHealth market and its potential, thereby supporting COCIR (European Coordination Committee of the Radiological, Electromedical and Healthcare IT Industry) and industry in their efforts towards developing the European and global market and realising the benefits of eHealth. The specific objectives are to:
The study aims to cover as many of the 27 EU Member States plus Norway and Iceland as feasible and where such data can be obtained within the temporal and budgetary limitations of the study.
|Client||DG Information Society and Media of the European Commission|
|Duration||03/2008 - 03/2009|
This is the second study in a series of three linked studies to develop eHealth benchmarking at European level. The study will cover all 27 EU Member States plus Norway and Iceland as well as Canada and the USA. It will conduct background research and review existing measurement tools and systems for ICT for Health, as well as available eHealth statistics, in order to establish a framework for data compilation and to make progress towards the future establishment of an effective eHealth benchmarking system in Europe, collect the data on an agreed set of eHealth related phenomena from existing sources including professional bodies and regional and national ministries. The study will compile data from existing sources rather than generate original data and â€“ depending on the data availability â€“ provide a measurement for each of the agreed indicators in each country, identify, analyse and report good practice in developing and applying eHealth measurements and benchmarking frameworks for informing policy-making (in all 29+2 countries), and develop and deliver 29(+2) Country Briefs summarising key results for each of the European countries and plus Canada and the USA and make all study results available through a dedicated Online Knowledge Base. Thus this study will significantly enhance the capacity of the i2010 initiative to achieve its goals in relation to monitoring and benchmarking eHealth, a key aspect of information society developments in the old and the New Member States.
|epSOS - European Patients Smart Open Services, Open eHealth initiative for a European large scale pilot of patient summary and electronic prescription|
|Duration||2008 - 2013|
In 2004, Europeans made approximately 180 million trips of four nights or more outside their own country. Ensuring their access to seamless and safe healthcare has become a top priority for the European Commission. Information and communication technology plays a key role in this process as it facilitates the transfer of vital medical data across borders. So far, national health IT solutions have coexisted without any interaction. The EC funded Smart Open Services project will for the first time unite key Member States and industry players in a joint effort to get medical data and prescription information to any doctor in the Union - when and where it is needed, and in comprehensible form.
The EC Large Scale Pilot in eHealth aims to develop "Smart Open Services" providing patients travelling across Europe access to the same quality of care as in their home country. As its acronym "S.O.S" suggests, one focus is on getting medical data to doctors urgently when needed, another is on enabling patients travelling in another country of the EU to use a local pharmacy to obtain their prescription medicines ("e-prescription").
The Smart Open Services project has the potential to lay the groundwork for a future pan-European eHealth infrastructure which would revolutionise healthcare provision by reducing medical errors and avoiding unnecessary treatment.
|EHR-IMPACT - Economic impact of interoperable electronic health records and ePrescription in Europe|
|Duration||2008 - 2009|
This study for the European Commission will make a substantial contribution towards accelerating the implementation of the European eHealth Action Plan. Specifically, the study will actively support ongoing initiatives and implementation work on interoperable EHR and ePrescribing systems by illustrating and widely spreading new knowledge about their socio-economic impact and lessons learned from successful, beneficial applications.
The value added by eHealth will be measured in quantitative terms based on a small number of successful implementations covering a wide variety of types of applications, of healthcare provider organisations and health systems, and of local, regional or even national frameworks. Whereas the individual examples will provide insights on success factors and requirements, the aggregation of results will allow to draw macro level conclusions.
Best results have been obtained when involving local doctors, nurses and other stakeholders, experts and promoters who have a good integrative understanding of medical/clinical, health policy and ICT-related issues and who are aware of new developments and emerging technologies.
|VPHOP - Osteoporotic Virtual Physiological Human|
|Duration||2008 - 2012|
EU FP7 Large-scale integrating project: develop a multiscale modelling technology based on conventional diagnostic imaging methods that makes it possible, in a clinical setting, to predict for each patient the strength of his/her bones, how this strength is likely to change over time, and the probability that the he/she will overload his/her bones during daily life. With these three predictions, the evaluation of the absolute risk of bone fracture will be much more accurate than any prediction based on external and indirect determinants, as it is current clinical practice. These predictions will be used to: i) improve the diagnostic accuracy of the current clinical standards; ii) to provide the basis for an evidence-based prognosis with respect to the natural evolution of the disease, to pharmacological treatments, and/or to preventive interventional treatments aimed to selectively strengthen particularly weak regions of the skeleton. For patients at high risk of fracture, and for which the pharmacological treatment appears insufficient, the VPHOP system will also assist the interventional radiologist in planning the augmentation procedure. The various modelling technologies developed during the project will be validated not only in vitro, on animal models, or against retrospective clinical outcomes, but will also be assessed in term of clinical impact and safety on small cohorts of patients enrolled at four different clinical institutions, providing the factual basis for effective clinical and industrial exploitations.
|DebugIT - Detecting and Eliminating Bacteria UsinG Information Technology|
|Duration||2008 - 2011|
EU FP7 Large-scale integrating project: Based on advanced text, image and structured data mining of about 3m individual patient data from various hospitals new knowledge and decision support will be developed to improve patient safety in antibiotic use, to fight the fast emergence of resistances among pathogens, misuse and overuse of antibiotics.
In half a century of antibiotics use, new challenges have surfaced: the fast emergence of resistances among pathogens and the overuse of antibiotics. Antimicrobial resistance results in escalating healthcare costs, increased morbidity and mortality and the (re-)emergence of potentially untreatable pathogens. For infectious diseases DebugIT will
The DebugIT project, with its innovative approach, is a prime example of how ICT tools can be used to address the emerging challenges in healthcare. This project addresses several of the overriding call topics at once by tackling the problems around antibiotics and of antimicrobial resistance of infectious diseases in an international consortium uniting world class research facilities, SMEs and industry partners.
|HeartCycle - Compliance and effectiveness in heart failure (HF) and coronary heart disease (CHD) closed-loop management|
|Duration||2008 - 2011|
EU FP7 Large-scale integrating project: An advanced telemonitoring approach will be developed to close the loop between patients and professionals, giving appropriate access to monitoring, diagnosis and treatment results and reacting immediately, adapting personalized care plans and using automated decision support to derive therapy recommendations.
Each year Cardiovascular Disease (CVD) causes over 1.9 million deaths in the EU, causing direct health costs of €105 billion. Coronary Heart Disease (CHD), half of all CVD deaths, is the single most cause of death in Europe. Heart Failure (HF) – a CHD being the most frequent cause of hospitalization for people over 65 – has 10 million patients in the EU.
Current treatment of HF entails recommendations from clinicians on medication, diet and lifestyle. Patients only receive feedback at doctors visits, or when facing symptoms. Daily monitoring, close follow up, and help on treatment routine is lacking. Non-adherence to the treatment regime is a major cause of suboptimal clinical benefit.
|TEN4Health - Trans-European healthcare support network for Europe’s mobile citizen|
|Client||EU eTEN Programme|
|Duration||2007 - 2008|
Mobility of people is increasing, products and services can be bought in another Member State when the need arises, but obtaining healthcare outside their residence country is still problematic for many Europeans. And this in spite of the legal framework for healthcare provision across Member States having been set up already in 1971 by the EU and its Member States with the so-called E-forms and the later European Health Insurance Card (EHIC). However, knowledge about this is not wide spread, and the administrative processes accompanying cross-Member State provision of healthcare have not developed at the same pace as leisure travel and labour mobility.
To alleviate this situation, the TEN4Health project contributes towards improved healthcare provision for mobile European Union citizens. Initiated by leading public health insurance providers, the TEN4Health service package assures access of citizens to healthcare in participating Member States’ hospitals, based on a secure web service and its integration into developing European eHealth infrastructure networks.
|Good eHealth - Exchange of Good Practices in eHealth|
|Client||European Commission, DG Information Society and Media, Unit C4 - ICT for Health|
|Duration||2006 – 2008|
Despite the relatively slow implementation of eHealth in Europe, many eHealth developments have nevertheless been successfully implemented. These implementations constitute a source of valuable experience and of examples of good practices which to date have not yet been properly communicated for emulation and exploitation.
|eHealth for Safety - Impact of ICT on Patient Safety and Risk Management|
|Client||European Commission, DG Information Society and Media, Unit C4 - ICT for Health|
|Duration||2006 - 2007|
ICT can make a vital contribution to improving the safety of European patients by helping to reduce medical errors and other negative incidents, thereby saving lives, and enhancing efficiency, in particular in the field of risk management in healthcare. The eHealth for Safety study has the following overarching goals:
These goals translate into a three-phase approach, consisting of (1) baseline research, (2) empirical analysis, and the development of (3) a synthesis report as well as a roadmap for further research. Good practice case studies will form part of the study in order to demonstrate concrete applications of ICT tools to enhance patient safety.
|semanticHEALTH - Semantic Interoperability Deployment and Research Roadmap|
|Client||European Commission, DG Information Society and Media, 6th Framework Programme, IST. ICT for Health.|
|Duration||2006 - 2007|
The semantic aspects of interoperability have only recently been recognised as the major enabling factor for the safe and sensible communication of patient data. Health language is very large and diverse, and as such not equalled by other professional languages. This SemanticHEALTH SSA develops a European and global roadmap for deployment and research in health-ICT, focusing on semantic interoperability issues of e-Health systems and infrastructures. The roadmap will be based on consensus of the research community, and validated by stakeholders, industry and Member State health authorities. It
empirica is involved in semanticHEALTH as a subcontractor.