Latest database descriptions

The eight centers established between them collaboration in order to be able to collect and exchange information, to conduct clinical and epidemiological studies all together, to communicate and exchange data and results with other academic researchers, to construct partnership with pharmaceutical industries and to create a biocollection database linked to clinical data (for 3 of the 8 centers).

Objectives of the registry in terms of public health (monitoring, evaluation) - To provide data concerning specific incidences of cancer types in Guadeloupe in order to give those involved in public health care the necessary elements to adapt care provided and improve population health. - To contribute to the assessment of patient treatment throughout different phases (prevention, access to care, diagnostic and therapeutic treatment, follow-up) from registry data (stage, treatment modalities, mortality). - To give the registry an inter-regional, national and international dimension by comparing data with other départements in France, Caribbean countries with similar resources (Cuba, Barbados) and other worldwide regions to produce an etiological hypotheses. Objectives of the register in terms of research - to study the epidemiology of cancers in Guadeloupe and in French Overseas Départements in America (DFA) in collaboration with registers in Martinique and Guyana. - To identify specific public health problems from the register concerning regional malignancy in order to implement specific research protocols; - To investigate the territorial distribution of cancer (spatial heterogeneity) and possible association with areas containing the highest soil contamination of organochlorine pesticides and other environmental pollutants. - To identify other environmental, genetic or nutritional factors that may be involved in the onset of certain cancers in Guadeloupe.

General objective: To assess the impact of therapeutic practices on the outcome of patients with acute myocardial infarction Secondary objective: to assess the impact of genetic polymorphisms on treatment efficacy and/or tolerance - to research post-MI prognostic biomarkers for morbidity and mortality - historical comparisons with French cohorts formed 5 and 10 years ago (1995 USIC, 2000 USUC, coordination: N. Danchin). - International comparison with similar cohorts in other countries (in particular Israel: ACSIS cohort and United Kingdom: MINAP project).

The objectives of this survey are to:
- Collect all of the deaths of women associated with pregnancy, giving birth and post partum up to one year after giving birth, in France, including metropolitan France as well as Overseas départements.
- Identify deaths of a direct or indirect obstetric cause (maternal deaths in WHO terms, Internatioanl classification of diseases-1 revision) and characterize them;
- Classify and analyze the causes of mother mortality;
- Calculate the crude and corrected rates of mother mortality;
- Analyze in an in-depth manner the circumstances of maternal deaths and evaluate the quality of the obstetric care directly concerning the mother;
- Develop the analysis of the structural elements of the organization of obstetric care.