- 2007 Survey on Interruption of pregnancy (IVG)

Head :
Vilain Annick

Last update : 10/23/2013 | Version : 1 | ID : 1138

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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 2007 Survey on Interruption of pregnancy (IVG)
CNIL registration number, number and date of CPP agreement, AFSSAPS (French Health Products Safety Agency) authorisation Autorisation cnil du 12 avril 2007, portant le numéro 1222126
General Aspects
Health determinants Social and psychosocial factors
Keywords Interruption of pregnancy (IVG)
Scientific investigator(s) (Contact)
Name of the director Vilain
Surname Annick
Email annick.vilain@sante.gouv.fr
Organization DREES - Ministère chargé de la
Collaborations
Others Bases available at the Quetelet center
Funding
Funding status Public
Details Drees
Governance of the database
Sponsor(s) or organisation(s) responsible Direction de la recherche, des études, de l'évaluation et des statistiques (Drees)
Organisation status Public
Additional contact
Main features
Type of database
Type of database Study databases
Study databases (details) Not-repeated cross-sectional studies (except case control studies)
Database recruitment is carried out by an intermediary A selection of health institutions and services
Database recruitment is carried out as part of an interventional study No
Additional information regarding sample selection. 00 randomly selected establishments. The interventions reached the number of 13500 including the extensions. The survey method is a one-stage stratified sampling : all the establishments performing more than 1000 IVG a year, 40% of the establishments performing between 250 and 1000 IVG a year, 20% of the establishments performing less than 250 IVG a year.

All the doctors performing IVG into an establishment of the sample and all the doctors having a convention with one of the establishments included in the survey.

Eight regions and a department have wished to extend the survey field, in order to have a regional representativeness of their results. In these areas, the field of the survey will be extended to 8 full weeks for all the IVG, sometimes increasing the number of the randomly selected establishments.
Database objective
Main objective Describe the access and caring conditions at the interruption of pregnancy. Describe the care system and the social and demographic characteristics, especially concerning minors and medical interruption of pregnancy performed in clinic. Precise the financial caring procedures of the IVG, pregnancy history and the utilization of contraception for women having an IVG.
Inclusion criteria IVG performed in the establishments surveyed
Population type
Age Adolescence (13 to 18 years)
Adulthood (19 to 24 years)
Adulthood (25 to 44 years)
Population covered General population
Gender Woman
Geography area National
Detail of the geography area Metropolitan France. Data can be exploited at the local level only inside regions having been a part of an extension of the survey : Guadeloupe, Réunion, Corse, Centre, Provence-Alpes-Côte d'Azur, Nord-Pas de Calais, Alsace, Midi-Pyrénées, and the Rhône department
Data collection
Dates
Date of first collection (YYYY or MM/YYYY) 2007
Size of the database
Size of the database (number of individuals) [10 000-20 000[ individuals
Details of the number of individuals About 1300 IVG surveyed (for 200 000 annual IVG, according to the SAE, annual establishment statistics
Data
Database activity Data collection completed
Type of data collected Clinical data
Declarative data
Clinical data (detail) Direct physical measures
Declarative data (detail) Paper self-questionnaire
Presence of a biobank No
Health parameters studied Health event/morbidity
Health care consumption and services
Others
Care consumption (detail) Hospitalization
Medical/paramedical consultation
Medicines consumption
Other (detail) Social health inequalities
Procedures
Data collection method Auto questionnaire and questionnaire filled by the doctor from the medical record.
Participant monitoring No
Links to administrative sources No
Promotion and access
Promotion
Link to the document http://www.drees.sante.gouv.fr/methodologie-de-l-enquete-sur-les,10967.html
Link to the document http://www.drees.sante.gouv.fr/les-etablissements-et-les-professionnels-realisant-des-ivg,4464.html
Link to the document http://www.drees.sante.gouv.fr/l-enquete-aupres-des-structures-et-des-praticiens-realisant,6607.html
Access
Terms of data access (charter for data provision, format of data, availability delay) Anonymous file exploited by DREES, INED-INSERM only.
Access to aggregated data Access on specific project only
Access to individual data Access on specific project only

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