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

Head :
Moitry Marie, Laboratoire d’épidémiologie et de santé publique
Velten Michel, Laboratoire d'épidémiologie et de santé publique

Last update : 05/29/2018 | Version : 1 | ID : 216

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Métadonnées
Identification
General Aspects
Scientific investigator(s) (Contact)
Collaborations
Funding
Governance of the database
Additional contact
Type of database
Database objective
Population type
Dates
Size of the database
Data
Procedures
Promotion
Access
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General
Identification
Detailed name Bas Rhin Ischaemic Heart Disease Register (Certified Register 2013-2016)
CNIL registration number, number and date of CPP agreement, AFSSAPS (French Health Products Safety Agency) authorisation CNIL no. 997139
General Aspects
Medical area Cardiology
Pathology (details) Epidemiology, public health
Keywords mortality and fatality, Ischaemic heart disease. Population registry. Epidemiological indicators: morbidity
Scientific investigator(s) (Contact)
Name of the director Moitry
Surname Marie
Address Université de Strasbourg - Faculté de médecine – 4, rue Kirschleger 67085 STRASBOURG cedex
Phone 03 68 85 31 95
Email mmoitry@unistra.fr
Unit Laboratoire d’épidémiologie et de santé publique
Organization Université de Strasbourg
Name of the director Velten
Surname Michel
Address Université de Strasbourg - Faculté de médecine - 4, rue Kirschleger 67085 STRASBOURG cedex
Phone 03 68 85 31 95
Email michel.velten@unistra.fr
Unit Laboratoire d'épidémiologie et de santé publique
Organization Université de Strasbourg - Faculté de
Collaborations
Funding
Funding status Public
Details National Institute for Healthcare and Medical Research - INSERM Institute for Public Health Surveillance - InVS
Governance of the database
Sponsor(s) or organisation(s) responsible Université de Strasbourg - Faculté de médecine
Organisation status Public
Additional contact
Main features
Type of database
Type of database Morbidity registers
Additional information regarding sample selection. Selection of subjects having the required inclusion criteria.Several sources are used to identify cases: - Teaching hospitals (ER, cardiac surgery, intensive care, cardiology departments, etc.) - General hospitals (ER, intensive care, cardiology departments, etc.) - Private clinics with cardiology department- SAMU, ASUM, SOS Médecins emergency services - Hospitals and departments not specialising in cardiology or intensive care - Retirement homes, medium- and long-term stays- Other hospitals (rural)- Regional-level departments for health and social affairs (DDASSs) - Private-practice GPs, cardiologists and other consultants if required - Cardiac rehabilitation centres
Database objective
Main objective 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).
Inclusion criteria Monitoring of population living in the Bas-Rhin aged 35 to 74 inclusive. Recording of the following pathologies:

1) Myocardial infarction: events reported by clinicians as a myocardial
infarction (or equivalent term).
2) Death:
- certain coronary deaths (myocardial infarction or other coronary clinical history) or
probable coronary (subjects died without apparent cause, but with a history of coronary disease)
- sudden deaths occurring in less than 24 hours without other evident cause of death and
without a history of coronary disease
- deaths with insufficient data (the cause of death could not be established)

Since 2006, in the same age range, additional recording of events reported by the clinician: acute coronary syndrome, unstable angina, clinical complications with aggravation of coronary disease.
Population type
Age Adulthood (25 to 44 years)
Adulthood (45 to 64 years)
Elderly (65 to 79 years)
Population covered Sick population
Pathology IX - Diseases of the circulatory system
Gender Male
Woman
Geography area Departmental
French regions covered by the database Alsace Champagne-Ardenne Lorraine
Detail of the geography area Bas-Rhin region
Data collection
Dates
Date of first collection (YYYY or MM/YYYY) 1984
Size of the database
Size of the database (number of individuals) [10 000-20 000[ individuals
Details of the number of individuals 1997-2008: 13 620
Data
Database activity Current data collection
Type of data collected Clinical data
Administrative data
Clinical data (detail) Direct physical measures
Administrative data (detail) identification data, place of birth (INSEE coding), place of residence (INSEE coding)
Presence of a biobank No
Health parameters studied Health event/morbidity
Health event/mortality
Procedures
Data collection method Active From 1984 to 1994, recording under the MONICA-WHO project. Recording has begun again since 1997.
Classifications used Demographic variables: places of birth and residence: coding of municipalities (INSEE code) Clinical variables: clinician diagnoses coded according to the ICD 9 classification
Participant monitoring Yes
Details on monitoring of participants Vital status: survival at 28 days for all recorded events is systematically researched
Links to administrative sources Yes
Linked administrative sources (detail) PMSI
Promotion and access
Promotion
Link to the document http://tinyurl.com/PUBMED-RCIBR
Access
Terms of data access (charter for data provision, format of data, availability delay) Publications, oral communications, annual reports, leaflets/monographs
Access to aggregated data Access on specific project only
Access to individual data Access on specific project only

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