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Bas Rhin Ischaemic Heart Disease Register (Certified Register 2013-2016)

France, 1984
Reference ID
FRESH-PEF216-en
Producer(s)
Michel Velten, Marie Moitry
Metadata
DDI/XML JSON
Created on
Nov 15, 2025
Last modified
Nov 15, 2025
Page views
4
  • Study Description
  • Get Microdata
  • Identification
  • Scope
  • Coverage
  • Producers and sponsors
  • Study authorization
  • Sampling
  • Survey instrument
  • Data collection
  • Study activities
  • Quality standards
  • Data Access
  • Contacts
  • Metadata production
  • Identification

    Survey ID number

    FRESH-PEF216-en

    Title

    Bas Rhin Ischaemic Heart Disease Register (Certified Register 2013-2016)

    Country
    Name
    France
    Abstract

    The permanent monitoring of the Bas-Rhin population aged 35 to 74 and systematic, continuous recording of cases of myocardial infarction and coronary deaths allow for the continuous estimation - as well as development - of a certain number of epidemiological indicators concerning coronary disease: incidence rates, annual occurrence rates (incident and recurring events), death rates by myocardial infarction; coronary and presumed coronary death rates; fatality rate at 28 days - hospital and general coronary. These indicators can be supplied by gender, age and year. Although changes in trend are observed over time, it is possible to estimate the proportion attributable to the reduction in incidence of coronary events and the proportion attributable to the reduction in fatality. Joint analyses are performed on a regular basis with the other two French registries on ischaemic heart diseases, which use the same methodology. The register is a reference tool for validating epidemiological indicators for coronary disease, constructed from other data sources (estimation validation of indicators from the PMSI hospital database for myocardial infarction, validation of indicators for coronary mortality and sudden death from the CépiDc's national death statistics). Parallel to recording coronary disease, surveys on representative samples of the general population are carried out at regular intervals with a view to studying the level of cardiovascular risk factors and how they evolve. Development of descriptive studies completing the basic recording: since 2006, recording of all acute heart failure (myocardial infarction, acute coronary syndromes, unstable angina); periodic recording of out- and inpatient treatment for episodes of acute heart failure, etc. Thanks to the ischaemic heart disease register, several analytical epidemiology studies have been developed (ECTIM case-control and PRIME cohort). Use of data from the register to evaluate the merits of an approach measuring - on an ecological basis - the influence of lifestyle and socioeconomic status on the link between atmospheric pollution and myocardial infarction in the Urban Community of Strasbourg (CUS).

    Kind of Data

    ['Clinical data','Socio-demographic data']

    Unit of Analysis

    Individuals

    Scope

    Topics
    Topic Vocabulary URI
    Cardiology and vascular medicine health theme
    cim-11 http://id.who.int/icd/entity/1924438986
    Keywords
    mortality and fatality Ischaemic heart disease. Population registry. Epidemiological indicators: morbidity

    Coverage

    Geographic Coverage

    ['Grand Est']

    Universe

    {
    "level_sex_clusion_I": [
    "Male",
    "Female",
    "Other"
    ],
    "level_age_clusion_I": [
    "Adult (25 to 44 years)",
    "Middle Aged (45 to 64 years)",
    "Aged (65 to 79 years)"
    ],
    "level_type_clusion_I": [
    "Patients population"
    ],
    "level_type_clusion_other": "",
    "clusion_I": "",
    "clusion_E": ""
    }

    Producers and sponsors

    Primary investigators
    Name
    Michel Velten
    Marie Moitry
    Producers
    Name Role
    UNIVERSITE DE STRASBOURG sponsor
    Funding Agency/Sponsor
    Name
    INSTITUT NATIONAL DE LA SANTE ET DE LA RECHERCHE MEDICALE (INSERM)
    SANTE PUBLIQUE FRANCE

    Study authorization

    Agency
    Agency name
    CNIL

    Sampling

    Sample frame

    Unit Type

    ['Administrative database (employees, pupils, students, etc.) Medical-administrative database (patients, health insurance/mutual insurance) Disease and death registry']

    Sampling Procedure

    ['Other']

    Survey instrument

    Questionnaires

    Access on specific project only

    Methodology notes

    Observational Study

    Data collection

    Dates of Data Collection
    Start
    1984
    Time Method

    Morbidity registry

    Mode of data collection
    • Recording (audio, video, electrophysiological, imaging)

    Study activities

    Study activities
    Study activities
    Type
    primary evaluation
    Description
    Health event/morbidity Health event/mortality

    Quality standards

    Quality standards
    Standard
    ['Demographic variables: places of birth and residence: coding of municipalities (INSEE code) Clinical variables: clinician diagnoses coded according to the ICD 9 classification']

    Data Access

    Availability Status

    Restricted access

    Contacts

    Contacts
    Name Email
    Michel Velten michel.velten@unistra.fr
    Marie Moitry marie.moitry@chru-strasbourg.fr

    Metadata production

    DDI Document ID

    FRESH-PEF216-en

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