Latest database descriptions

To improve the epidemiological and clinical description of ALS in France.

Register aims in terms of public healthcare (monitoring, assessment):
The aim of the register is to provide benchmarks for describing the dynamics of cancer progression (distribution, progression and impact of the disease according to the geography and demographics of the population) and to become involved in the evaluation of screening and prevention (by assessing the effectiveness of the programmes in place) and care assessment (analysing treatment paths used by patients; factors that determine diagnostic care management and distribution of good practice recommendations). It shall play a specialist role in aiding the assessment of public policies by the Regional Health Agency (ARS), in collaboration with other regional organisations (Poitou-Charentes Cancer Network, Regional Health Observatory and screening facilities). It shall participate in producing national (FRANCIM) and international (IARC) statistics.
Register aims in terms of research: Two research areas are preferred for continuing research conducted by the Public Health Team in Poitiers.
1) Assessing factors that affect access to screening facilities (access to screening facilities for sibship-based index cases) and assessing factors affecting access to care (patient satisfaction; access to technical surgical platforms and waiting periods for radiotherapy).
2) Automated classification of textual information contained in electronic anatomic pathology and cytopathology reports (collaboration with University of Rennes 1).

The aim of this registry is to promote research, therapeutic progress, information on family and medical training in the area of biliary atresia and related pathologies.

The main aim of RéAC is to improve the treatment conditions for cardiac arrest victims, as well as improve the chances of survival for patients.