Latest database descriptions

Health, health care and insurance survey

April 09 2015

There are multiple purposes of the survey:
Firstly, ESPS (health and social protection survey) makes it possible to study the existing links on an individual level between the state of
health, access to health services, access to public and private insurance and the socio-economic status.
This makes it possible to conduct many analyses covering equity in the health system and to enlighten public efforts by participating in the evaluation of public policies, whether directly or indirectly linked to health.
ESPS is as such a reactive tool for researchers in the social sciences, making it possible to test new research hypotheses on French data.
ESPS is also an information tool for public health. It makes it possible to assess in an exploratory manner the prevalences of affections in the absence of specific instruments and complete sources, and this using detailed data on morbidity.
ESPS thus comprises a unique source of data on supplemental health insurance in France. Through its specific questioning pertaining to the supplemental contracts that the members of the households surveyed benefit from, it offers a panorama of the contracts that are actually in effect and as such of the distribution and of the changes in the levels of coverage in the population.

Identification of Molecular Markers of Sudden Death at Acute Phase of Myocardial Infarction

April 09 2015

General objective: To identify predisposing factors of ventricular fibrillation at the acute phase of myocardial infarct: to demonstrate that ventricular fibrillation at the acute phase of myocardial infarction follows a polygenic determinism.

Survey Observatory of Rare Diseases 2011

April 09 2015

The objective of the Observatory is to provide to all skateholders involved in the fight against rare diseases reliable data highlighting important issues to which patients and their families are confronted.
These data must allow not only to identify those issues but also to bring forward proposals to mitigate them.
This survey studied three topics:
- Misdiagnosis;
- Access to information;
- Financial support for healthcare, products and service delivery.

National Reference Centre for Von Willebrand Disease

April 09 2015

Epidemiology of different types and sub-types of von Willebrand Disease in France

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