SNSPE - National Surveillance System for Childhood Lead Poisoning

Head :
Lecoffre Camille

Last update : 07/03/2015 | Version : 1 | ID : 7542

print
Print
xml
XML

Export to XML

Please choose the format :

pdf
PDF
xml
CSV (Excel)

Export to CSV

What sections do you want to export ?

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
Select all | Invert selection | No selection

Which version do you want to export ?

send
Send
General
Identification
Detailed name National Surveillance System for Childhood Lead Poisoning
Sign or acronym SNSPE
CNIL registration number, number and date of CPP agreement, AFSSAPS (French Health Products Safety Agency) authorisation CNIL approval no. 903398
General Aspects
Medical area Biology
Pediatrics
Pathology (details) housing
Health determinants Intoxication
Lifestyle and behavior
Pollution
Social and psychosocial factors
Keywords lead poisoning, blood lead level, dilapidated housing, obligatory notification, surveillance system, lead, children, poisoning
Scientific investigator(s) (Contact)
Name of the director Lecoffre
Surname Camille
Address 12, rue du val d’Osne – 94410 Saint Maurice
Phone + 33 (0)1 41 79 69 68
Email c.lecoffre@invs.sante.fr
Organization Institut de veille sanitaire
Collaborations
Funding
Funding status Public
Details InVS
Governance of the database
Sponsor(s) or organisation(s) responsible INVS - Institut de Veille Sanitaire
Organisation status Public
Additional contact
Main features
Type of database
Type of database Morbidity registers
Additional information regarding sample selection. Surveillance system designed to screen for lead poisoning in children (without knowing population toxicity). Recorded blood lead level testing (initial screening and follow-up) ordered in children (younger than 18) following exposure risk factor research (individual identification or screening campaigns), regardless of the result. Includes cases of lead poisoning reported to the ARS/DDASS (blood lead level higher than 100 μg/L) and cases identified during toxicity surveys.
Database objective
Main objective Monitoring:
1/ Description of lead poisoning screening activities for children;
2/ Identification of lead poisoning cases and description of the characteristics;
3/ Description of medical and environmental management of children with lead poisoning.
Inclusion criteria Children younger than 18 years old with blood lead toxicity.
Population type
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)
Population covered General population
Gender Male
Woman
Geography area National
Detail of the geography area France
Data collection
Dates
Date of first collection (YYYY or MM/YYYY) 1992
Size of the database
Size of the database (number of individuals) Greater than 20 000 individuals
Details of the number of individuals Over 95,000 children with a total of >150,000 records.
Data
Database activity Current data collection
Type of data collected Clinical data
Declarative data
Biological data
Administrative data
Clinical data (detail) Medical registration
Details of collected clinical data Presence of clinical symptoms, anaemia, iron deficiency.
Declarative data (detail) Face to face interview
Details of collected declarative data Questionnaire completed by prescribing physician (interviewing parents) and the laboratory.
Biological data (detail) Blood lead level results, (+/- haemoglobin).
Administrative data (detail) Identification data, place of residence.
Presence of a biobank No
Health parameters studied Health event/morbidity
Others
Other (detail) Lead poisoning screening, obligatory notification of cases.
Procedures
Data collection method The prescribing physician must complete a monitoring form and send it to the laboratory with the order for all blood lead level requests for minors. This includes the date and sampling method, as well as the assay result on the form. A copy is forwarded to the inter-regional poison control centre (CAPTV), and the form is returned to the prescribing physician. Forms are recorded on computer in each CAPTV and then digitally transmitted to InVS that constructs the national anonymous database. This system is supplemented by new lead poisoning case reports (first blood lead level higher than100 μg/L) by the ARS to InVS. Duplications are deleted. Data retrieved from the SNSPE are anonymous individual data for individuals younger than 18, when blood samples are taken.
Classifications used -
Quality procedure(s) used Duplicate processing (2 data sources for lead poisoning cases only): section detected automatically by national software application and another section by manual research. Control and recording at CAPTV and InVS application level. Variable data quality: completeness varies according to region and every passing year (improved completeness in the blood lead level number). Some variables are poorly recorded (medical treatments and environmental measures implemented between blood lead levels).
Participant monitoring Yes
Details on monitoring of participants National recommendations included blood lead level follow-up for poisoning or exposure risk factors.The same monitoring form is completed for successive blood lead levels by the physician to clarify the medical treatment and environmental procedures implemented to avoid exposure.
Links to administrative sources No
Promotion and access
Promotion
Link to the document http://opac.invs.sante.fr/index.php?lvl
Link to the document http://www.invs.sante.fr/fr../layout/set/print/Publications-et-outils/Rapports-et-syntheses/Environnement-et-sante/2010/Depistage-du-saturnisme-chez-l-enfant-en-France-de-2005-a-2007
Link to the document http://opac.invs.sante.fr/index.php?lvl
Link to the document http://opac.invs.sante.fr/index.php?lvl
Link to the document http://opac.invs.sante.fr/index.php?lvl
Link to the document http://www.invs.sante.fr/Dossiers-thematiques/Environnement-et-sante/Saturnisme-chez-l-enfant
Link to the document https://www.formulaires.modernisation.gouv.fr/gf/cerfa_12378.do
Access
Terms of data access (charter for data provision, format of data, availability delay) Access to results:
On the InVS website: publications and dashboards (aggregate data per year, department and municipality if the number is sufficiently high).

Access to data:
The requesting body may access indirect personal data if authorised by the CNIL.
Send request to InVS.

Source must be mentioned.
Last year of available data: n-2

Partners - FAQ - Contact - Site map - Legal notices - Administration - Updated on December 15 2020 - Version 4.10.05

View Edit Create here