Description du projet
Advanced ICT for Risk Assessment and Patient Safety
Serious adverse effects resulting from the treatment with thalidomide prompted modern drug legislation more than 40 years ago. Post-marketing spontaneous reporting systems for suspected adverse drug reactions (ADRs) have been a cornerstone to detect safety signals in pharmacovigilance. It has become evident that adverse effects of drugs may be detected too late, when millions of persons have already been exposed.In this project, an alternative approach for the detection of ADR signals will be developed. Rather than relying on the physician's capability and willingness to recognize and report suspected ADRs, the system will systematically calculate the occurrence of disease (potentially ADRs) during specific drug use based on data available in electronic patient records. In this project, electronic health records (EHRs) of over 30 million patients from several European countries will be available. In an environment where rapid signal detection is feasible, rapid signal assessment is equally important. To rapidly assess signals, a number of resources will be used to substantiate the signals: causal reasoning based on information in the EHRs, semantic mining of the biomedical literature, and computational analysis of biological and chemical information (drugs, targets, anti-targets, SNPs, pathways, etc.).The overall objective of this project is the design, development and validation of a computerized system that exploits data from electronic healthcare records and biomedical databases for the early detection of adverse drug reactions. The EU-ADR system will generate signals using data and text mining, epidemiological and other computational techniques, and subsequently substantiate these signals in the light of current knowledge of biological mechanisms and in silico prediction capabilities. The system should be able to detect signals better and faster than spontaneous reporting systems and should allow for identification of subpopulations at higher risk for ADRs.
Champ scientifique
Appel à propositions
FP7-ICT-2007-1
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Régime de financement
CP - Collaborative project (generic)Coordinateur
3015 GD Rotterdam
Pays-Bas
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Participants (14)
8200 Aarhus
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15782 Santiago De Compostela
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08003 Barcelona
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08002 Barcelona
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33076 BORDEAUX CEDEX
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35138 Padova
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50141 Firenze
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Participation terminée
98124 Messina
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20126 MILANO
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3528AE Utrecht
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3810-193 Aveiro
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151 85 Sodertaelje
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NG7 2RD Nottingham
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WC1E 7HT London
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