RDPLF - Registre de Dialyse Péritonéale de Langue Française

Head :
Verger Christian

Last update : 06/20/2012 | Version : 1 | ID : 3600

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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 Registre de Dialyse Péritonéale de Langue Française
Sign or acronym RDPLF
CNIL registration number, number and date of CPP agreement, AFSSAPS (French Health Products Safety Agency) authorisation --
General Aspects
Medical area Urology, andrology and nephrology
Health determinants Nutrition
Others (details) peritoneal dialysis, peritonitis, management of the anemia
Keywords dialysis, peritoneal dialysis, peritonitis, anemia, co-morbidities, quality of dialysis, nurse aspects, survival, nutrition
Scientific investigator(s) (Contact)
Name of the director Verger
Surname Christian
Address 30 rue Sere Depoin
Phone + 33 (0)6 08 76 59 91
Email c.verger@wanadoo.fr
Organization RDPLF
Collaborations
Funding
Funding status Private
Details Amgen, Baxter, Fresenius, Genzyme, HAC Pharma, Roche, SHIRE,
Governance of the database
Sponsor(s) or organisation(s) responsible Association RDPLF
Organisation status Private
Additional contact
Main features
Type of database
Type of database Morbidity registers
Database recruitment is carried out by an intermediary A selection of health institutions and services
Database recruitment is is made on the basis of: Another treatment or procedure
Database recruitment is carried out as part of an interventional study No
Additional information regarding sample selection. All patients with renal insufficiency treated via peritoneal dialysis in voluntary centers for participation; about 85% of French patients treated via peritoneal dialysis are followed
Database objective
Main objective Continuous analysis of the survival rates and complications of patients treated via peritoneal dialysis, assistance for participating centers in order to evaluate and compares themselves, prevent complications, manage the quality of dialysis, nutrition, anemia, surgical aspects linked to the peritoneal approach, assistance in publication. Information for patients.
Inclusion criteria All patients treated via peritoneal dialysis in French-speaking centers
Population type
Age 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 covered Sick population
Gender Male
Woman
Geography area International
Detail of the geography area France, Belgium, Switzerland, Tunisia, Morocco, Algeria
Data collection
Dates
Date of first collection (YYYY or MM/YYYY) 1986
Size of the database
Size of the database (number of individuals) Greater than 20 000 individuals
Details of the number of individuals France métropolitaine : 27108 DOM TOM : 1373
Data
Database activity Current data collection
Type of data collected Clinical data
Paraclinical data
Biological data
Clinical data (detail) Direct physical measures
Medical registration
Paraclinical data (detail) date of birth, date of treatments, therapeutic methods
Biological data (detail) urea, creatinine, CBC, albumin, bacteriology, ionogram,
Presence of a biobank No
Health parameters studied Health event/morbidity
Health event/mortality
Procedures
Data collection method collection on paper forms, updated at least every 3 months
Participant monitoring Yes
Details on monitoring of participants reminders by telephone and mail as soon as the delay in updating exceeds 3 months
Links to administrative sources No
Promotion and access
Promotion
Link to the document http://www.rdplf.org/publications.html
Link to the document
Description
Link to the document
Description
Access
Terms of data access (charter for data provision, format of data, availability delay) send back to the centers the statistical analysis of their own data, publication of the annual epidemiological data for the site, annual report can be downloaded from the site. Possibility open to everyone to use a portion of the database using pre-established personal queries on the site for depersonalized export of the database each evening.
The personalized publications and studies can be accessed by everyone, subject to approval by a committee of 12 nurses and doctors elected from within the centers (Commission on Good Practices).
Organization of a congress every 2 years bringing together 300 nephrologists and nurses
Access to aggregated data Access on specific project only
Access to individual data Access on specific project only

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