EuroREACH A Handbook to Access Health Care Data for Cross-country Comparisons of Efficiency and Quality

akronüüm: EUROREACH
algus: 2010-03-01
lõpp: 2013-02-28
 
programm: FP7 - Euroopa Liidu 7. raamprogramm
alaprogramm: HEALTH - Tervis
instrument: CSA-CA - Koordineerivad ja toetavad tegevused - koordineerivad tegevused
projektikonkurss: FP7-HEALTH-2009-single-stage
projekti number: 242099
kestus kuudes: 36
partnerite arv: 9
 
lühikokkuvõte: EuroREACH explores how coordination among recent innovations for better health care information systems and performance measurement at a national, European and international level can lead to improved access to data for cross-country, comparative research. This will be undertaken for a broad range of questions into the efficiency, quality and equity of health care services, following a patient-centred, disease-based approach. Better integrated health care in order to improve quality and cost-effectiveness of health services across providers and care settings is a major policy concern in the EU. EuroREACH comprises coordination activities for three types of initiatives to improve data access for research: 1. European and international initiatives and research projects; 2. National practice of innovative health information and performance management systems; 3. European and international data systems and new ways to link them to national sources and to qualitative structural indicators of health care systems for comparative analysis. Expert panels and two Sounding Board Conferences will support the project, by providing input and by reviewing progress. They will also be involved in broad dissemination. Results will include guidance for researchers to data access; policy lessons on good practice of national and international performance measurement and information system design, including questions of data linkages, data protection and mapping to international classifications and data framework. The outcome will be synthesised in a handbook entitled “EuroReach: Handbook to Access Health Care Data” that will serve as a generic guide to data access for researchers, other data users and stakeholders. It will also provide guidance to policy makers, discussing options for governing and reforming information systems. A final Conference will wrap up the project’s findings.
partneri jrk nr ja roll partneri nimi riik kontaktisik koduleht
1 koordinaator EUROPAISCHES ZENTRUM FUR WOHLFAHRTSPOLITIK UND SOZIALFORSCHUNG AT Flip Maas http://www.euro.centre.org
2 partner CEPS CENTRE D ETUDES DE POPULATIONS DE PAUVRETE ET DE POLITIQUES SOCIO-ECONOMIQUES LU Pierre Hausman http://www.ceps.lu
3 partner INSTITUT DE RECHERCHE ET DOCUMENTATION EN ECONOMIE DE LA SANTE FR Dominique Goldfarb http://www.irdes.fr
4 partner LONDON SCHOOL OF ECONOMICS AND POLITICAL SCIENCE UK Champa Heidbrink http://www.lse.ac.uk
5 partner MACCABI HEALTHCARE SERVICES IL Hadas Lewy
6 partner TERVEYDEN JA HYVINVOINNIN LAITOS FI Jaakko Penttinen http://www.thl.fi
7 partner TECHNISCHE UNIVERSITAET BERLIN DE Simone Ludwig http://www.tu-berlin.de
8 partner Tartu Ülikool EE Kadri Raav http://www.ut.ee
9 partner IMPERIAL COLLEGE OF SCIENCE, TECHNOLOGY AND MEDICINE UK Shaun Power http://www.imperial.ac.uk