Entred 2007-2010 - National Representative Sample of people with diabetes 2007-2010 
Responsable(s) :
Fosse-Edorh Sandrine
Date de modification : 01/07/2019 | Version : 1 | ID : 7786
| Général | |
| Identification | |
| Nom détaillé | National Representative Sample of people with diabetes 2007-2010 |
| Sigle ou acronyme | Entred 2007-2010 |
| Numéro d'enregistrement (ID-RCB ou EUDRACT, CNIL, CPP, etc.) | 907172 |
| Thématiques générales | |
| Domaine médical |
Endocrinology and metabolism |
| Déterminants de santé |
Lifestyle and behavior |
| Mots-clés | type 1 diabetes, vascular risk, socioeconomic level, socioeconomic status, educational measures, quality of care, cost, type 2 diabetes, characteristics, complication, hospitalisation, mortality |
| Responsable(s) scientifique(s) | |
| Nom du responsable | Fosse-Edorh |
| Prénom | Sandrine |
| Adresse | 12 rue du Val d’Osne 94415 Saint Maurice Cedex |
| Téléphone | + 33 (0)1 55 12 53 14 |
| s.fosse@invs.sante.fr | |
| Organisme | INVS - Institut de Veille |
| Collaborations | |
| Financements | |
| Financements |
Public |
| Précisions | InVS, CnamTS, RSI, HAS, INPES. |
| Gouvernance de la base de données | |
| Organisation(s) responsable(s) ou promoteur | INVS - Institut de Veille Sanitaire |
| Statut de l’organisation |
Secteur Public |
| Contact(s) supplémentaire(s) | |
| Caractéristiques | |
| Type de base de données | |
| Type de base de données |
Study databases |
| Base de données issues d'enquêtes, précisions |
Not-repeated cross-sectional studies (except case control studies) |
| Origine du recrutement des participants |
An administrative base or a register |
| Le recrutement dans la base de données s'effectue dans le cadre d'une étude interventionnelle |
No |
| Informations complémentaires concernant la constitution de l'échantillon | Sample is based on a random selection of personal keys in the Local Health Insurance databases. The sample consists of individuals with these keys who have received at least three reimbursements for oral antidiabetic medications and/or insulin over the last twelve months. |
| Objectif de la base de données | |
| Objectif principal | To describe the characteristics of people pharmacologically treated for diabetes, their health with regards to diabetes, the quality of care received, treatment plan and self-management education; their quality of life, experiences and requirements in terms of education and information, as well as the cost of diabetes. |
| Critères d'inclusion | Beneficiaries of the French general scheme of health insurance (CNAMTS) (excluding local mutualist sections) and the Independent Scheme for employees (RSI); residing in mainland France or overseas départements (DOM); and who have received at least three reimbursements for oral antidiabetic medications and/or insulin over the last twelve months. |
| Type de population | |
| Age |
Newborns (birth to 28 days) Infant (28 days to 2 years) Early childhood (2 to 5 years) Childhood (6 to 13 years) Adolescence (13 to 18 years) Adulthood (19 to 24 years) Adulthood (25 to 44 years) Adulthood (45 to 64 years) Elderly (65 to 79 years) Great age (80 years and more) |
| Population concernée |
Sick population |
| Sexe |
Male Woman |
| Champ géographique |
National |
| Détail du champ géographique | France |
| Collecte | |
| Dates | |
| Année du premier recueil | 08/2006 |
| Année du dernier recueil | 07/2009 |
| Taille de la base de données | |
| Taille de la base de données (en nombre d'individus) |
[10 000-20 000[ individuals |
| Détail du nombre d'individus | 8,000 people in metropolitan France, 800 people from overseas départements and 850 children. |
| Données | |
| Activité de la base |
Data collection completed |
| Type de données recueillies |
Clinical data Declarative data Biological data Administrative data |
| Données cliniques, précisions |
Direct physical measures |
| Détail des données cliniques recueillies | Medical questionnaire sent to attending physicians. |
| Données déclaratives, précisions |
Paper self-questionnaire Phone interview |
| Détail des données déclaratives recueillies | Self-administered patient questionnaire and phone questionnaire administered by National Health Insurance medical officers. |
| Données biologiques, précisions | Medical questionnaire sent to physicians. |
| Données administratives, précisions | Medical consumption, hospitalisation data and mortality data. |
| Existence d’une biothèque |
No |
| Paramètres de santé étudiés |
Health event/morbidity Health event/mortality Health care consumption and services Quality of life/health perception |
| Consommation de soins, précisions |
Hospitalization Medical/paramedical consultation Medicines consumption |
| Modalités | |
| Mode de recueil des données | Data collected by self-administered questionnaire, phone questionnaire and physician questionnaire, combined with passive medical and administrative data collection (medical consumption and hospitalisation) and mortality data (vital status and cause of death). |
| Nomenclatures employées | CIM 10. |
| Suivi des participants |
Yes |
| Détail du suivi | Passive medical and administrative data collection (medical consumption and hospitalisation) for two years and mortality data (vital status and cause of death). |
| Appariement avec des sources administratives |
Yes |
| Sources administratives appariées, précisions | Local medical consumption data, PMSI, RNIPP and CépiDC. |
| Valorisation et accès | |
| Valorisation et accès | |
| Lien vers le document | principales publications.docx |
| Accès | |
| Charte d'accès aux données (convention de mise à disposition, format de données et délais de mise à disposition) |
The results are published as reports, summaries and articles. Complete bibliography on the ENTRED website..
Data are available to external teams after project is submitted to an assessment committee. |
