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Published in: Orphanet Journal of Rare Diseases 1/2012

Open Access 01-12-2012 | Research

A national internet-linked based database for pediatric interstitial lung diseases: the French network

Authors: Nadia Nathan, Rola Abou Taam, Ralph Epaud, Christophe Delacourt, Antoine Deschildre, Philippe Reix, Raphaël Chiron, Ulrika de Pontbriand, Jacques Brouard, Michaël Fayon, Jean-Christophe Dubus, Lisa Giovannini-Chami, François Bremont, Katia Bessaci, Cyril Schweitzer, Marie-Laure Dalphin, Christophe Marguet, Véronique Houdouin, Françoise Troussier, Anne Sardet, Eglantine Hullo, Isabelle Gibertini, Malika Mahloul, Delphine Michon, Adrien Priouzeau, Laurie Galeron, Jean-François Vibert, Guillaume Thouvenin, Harriet Corvol, Jacques deBlic, Annick Clement, French RespiRare® Group

Published in: Orphanet Journal of Rare Diseases | Issue 1/2012

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Abstract

Background

Interstitial lung diseases (ILDs) in children represent a heterogeneous group of rare respiratory disorders that affect the lung parenchyma. After the launch of the French Reference Centre for Rare Lung Diseases (RespiRare®), we created a national network and a web-linked database to collect data on pediatric ILD.

Methods

Since 2008, the database has been set up in all RespiRare® centres. After patient's parents' oral consent is obtained, physicians enter the data of children with ILD: identity, social data and environmental data; specific aetiological diagnosis of the ILD if known, genetics, patient visits to the centre, and all medical examinations and tests done for the diagnosis and/or during follow up. Each participating centre has a free access to his own patients' data only, and cross-centre studies require mutual agreement. Physicians may use the system as a daily aid for patient care through a web-linked medical file, backed on this database.

Results

Data was collected for 205 cases of ILD. The M/F sex ratio was 0.9. Median age at diagnosis was 1.5 years old [0–16.9]. A specific aetiology was identified in 149 (72.7%) patients while 56 (27.3%) cases remain undiagnosed. Surfactant deficiencies and alveolar proteinosis, haemosiderosis, and sarcoidosis represent almost half of the diagnoses. Median length of follow-up is 2.9 years [0–17.2].

Conclusions

We introduce here the French network and the largest national database in pediatric ILDs. The diagnosis spectrum and the estimated incidence are consistent with other European databases. An important challenge will be to reduce the proportion of unclassified ILDs by a standardized diagnosis work-up. This database is a great opportunity to improve patient care and disease pathogenesis knowledge. A European network including physicians and European foundations is now emerging with the initial aim of devising a simplified European database/register as a first step to larger European studies.
Appendix
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Metadata
Title
A national internet-linked based database for pediatric interstitial lung diseases: the French network
Authors
Nadia Nathan
Rola Abou Taam
Ralph Epaud
Christophe Delacourt
Antoine Deschildre
Philippe Reix
Raphaël Chiron
Ulrika de Pontbriand
Jacques Brouard
Michaël Fayon
Jean-Christophe Dubus
Lisa Giovannini-Chami
François Bremont
Katia Bessaci
Cyril Schweitzer
Marie-Laure Dalphin
Christophe Marguet
Véronique Houdouin
Françoise Troussier
Anne Sardet
Eglantine Hullo
Isabelle Gibertini
Malika Mahloul
Delphine Michon
Adrien Priouzeau
Laurie Galeron
Jean-François Vibert
Guillaume Thouvenin
Harriet Corvol
Jacques deBlic
Annick Clement
French RespiRare® Group
Publication date
01-12-2012
Publisher
BioMed Central
Published in
Orphanet Journal of Rare Diseases / Issue 1/2012
Electronic ISSN: 1750-1172
DOI
https://doi.org/10.1186/1750-1172-7-40

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