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dc.contributor.authorTaruscio, Domenica
dc.contributor.authorMollo, Emanuela
dc.contributor.authorGainotti, Sabina
dc.contributor.authorPosada De la Paz, Manuel 
dc.contributor.authorBianchi, Fabrizio
dc.contributor.authorVittozzi, Luciano
dc.identifier.citationArch Public Health. 2014 Oct 13;72(1):35.
dc.description.abstractBACKGROUND: The European Union acknowledges the relevance of registries as key instruments for developing rare disease (RD) clinical research, improving patient care and health service (HS) planning and funded the EPIRARE project to improve standardization and data comparability among patient registries and to support new registries and data collections. METHODS: A reference list of patient registry-based indicators has been prepared building on the work of previous EU projects and on the platform stakeholders' information needs resulting from the EPIRARE surveys and consultations. The variables necessary to compute these indicators have been analysed for their scope and use and then organized in data domains. RESULTS: The reference indicators span from disease surveillance, to socio-economic burden, HS monitoring, research and product development, policy equity and effectiveness. The variables necessary to compute these reference indicators have been selected and, with the exception of more sophisticated indicators for research and clinical care quality, they can be collected as data elements common (CDE) to all rare diseases. They have been organized in data domains characterized by their contents and main goal and a limited set of mandatory data elements has been defined, which allows case notification independently of the physician or the health service. CONCLUSIONS: The definition of a set of CDE for the European platform for RD patient registration is the first step in the promotion of the use of common tools for the collection of comparable data. The proposed organization of the CDE contributes to the completeness of case ascertainment, with the possible involvement of patients and patient associations in the registration process.
dc.description.sponsorshipThis work is part of the activities of the project titled “Building Consensus and synergies for the EU Registration of Rare Disease Patients” (EPIRARE), funded by the European Commission within the framework of the Health Project, Work Plan 2010 (Grant n. 20101202).
dc.publisherBioMed Central (BMC) 
dc.subjectCommon data elements
dc.subjectEuropean platform
dc.subjectRare diseases
dc.subjectPatient registration
dc.titleThe EPIRARE proposal of a set of indicators and common data elements for the European platform for rare disease registration
dc.typejournal article
dc.rights.licenseAtribución 4.0 Internacional*
dc.contributor.funderUnión Europea. Comisión Europea 
dc.identifier.journalArchives of Public Health
dc.repisalud.centroISCIII::Instituto de Investigación de Enfermedades Raras
dc.rights.accessRightsopen accesses_ES

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