Patients' outcomes and experience of health care can be improved through the systematic capture and use of information from their perspective. We are currently not using all the information we could gain fromPatients' outcomes and...
ver más
¿Tienes un proyecto y buscas un partner? Gracias a nuestro motor inteligente podemos recomendarte los mejores socios y ponerte en contacto con ellos. Te lo explicamos en este video
Proyectos interesantes
EUROREACH
EuroREACH A Handbook to Access Health Care Data for Cross co...
2M€
Cerrado
MANAGED OUTCOMES
Operations management and demand based approaches to healthc...
4M€
Cerrado
BAHCI
Bringing a health claim to information Measuring the impact...
173K€
Cerrado
ECHOUTCOME
European Consortium in Healthcare Outcomes and cost benefit...
1M€
Cerrado
IMPACT HTA
Improved Methods and Actionable Tools for Enhancing Health T...
5M€
Cerrado
BIMEDA
Big Medical Data Use in Primary Care an ethnographic socio...
195K€
Cerrado
Información proyecto H2O
Duración del proyecto: 60 meses
Fecha Inicio: 2020-09-30
Fecha Fin: 2025-09-30
Fecha límite de participación
Sin fecha límite de participación.
Descripción del proyecto
Patients' outcomes and experience of health care can be improved through the systematic capture and use of information from their perspective. We are currently not using all the information we could gain fromPatients' outcomes and experience of health care can be improved through the systematic capture and use of information from their perspective. We are currently not using all the information we could gain from Patient-Reported Outcomes (PROs) to accurately measure value from the patient perspective. This is due to the lack of standardisation, interoperability and implementation of PRO measurement schemes. We urgently need a European scale network of outcomes data collection, analysis and evidence sharing to inform clinical practice and healthcare decisions. To tackle these issues, this public-private consortium brings together scientists, clinicians and professionals to design and set up independent, patient-centred, Health Outcomes Observatories (H2Os). With input from patients, providers and health care decision makers (health ministries, health insurers, regional health authorities, public health agencies, medicines regulators, health technology assessment agencies), these Observatories will collect data and provide information not only for individual clinical care, but also for evaluation of new technologies and for healthcare decision making. We will establish ethically and legally sound national, or regional, H2Os and run these initially in four countries for three diseases. Based on a hybrid model of federated and centralised data collection, management and analysis, these Observatories will operate under a governance model that will guarantee that data are protected under jurisdictional data protection law. H2Os will be connected to a pan-European umbrella H2O to facilitate interoperability, guide reproducibility in other countries, and promote the benefit of measuring and using patient-centred outcomes at regional, national, European and global levels.