Prevalence and incidence of interstitial lung diseases in a multi-ethnic county of Greater Paris

The objective of the study was to estimate the prevalence and incidence of interstitial lung diseases (ILDs) in Seine-Saint-Denis, a multi-ethnic county of Greater Paris, France.Patients with ILDs were identified between January and December 2012 by using several sources; all potentially involved me...

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Veröffentlicht in:The European respiratory journal Jg. 50; H. 2
Hauptverfasser: Duchemann, Boris, Annesi-Maesano, Isabella, Jacobe de Naurois, Camille, Sanyal, Shreosi, Brillet, Pierre-Yves, Brauner, Michel, Kambouchner, Marianne, Huynh, Sophie, Naccache, Jean Marc, Borie, Raphael, Piquet, Jacques, Mekinian, Arsène, Virally, Jerôme, Uzunhan, Yurdagul, Cadranel, Jacques, Crestani, Bruno, Fain, Olivier, Lhote, Francois, Dhote, Robin, Saidenberg-Kermanac'h, Nathalie, Rosental, Paul-André, Valeyre, Dominique, Nunes, Hilario
Format: Journal Article
Sprache:Englisch
Veröffentlicht: England 01.08.2017
Schlagworte:
Adolescent
Adult
Age Distribution
Aged
Aged, 80 and over
Connective Tissue Diseases - epidemiology
Ethnic Groups
Female
Humans
Idiopathic Pulmonary Fibrosis - epidemiology
Incidence
Logistic Models
Male
Middle Aged
Paris - epidemiology
Prevalence
Sarcoidosis, Pulmonary - epidemiology
Sex Distribution
Young Adult
ISSN:1399-3003, 1399-3003
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Zusammenfassung:The objective of the study was to estimate the prevalence and incidence of interstitial lung diseases (ILDs) in Seine-Saint-Denis, a multi-ethnic county of Greater Paris, France.Patients with ILDs were identified between January and December 2012 by using several sources; all potentially involved medical specialists from public and private hospitals, community-based pulmonologists and general practitioners, and the Social Security system. Diagnoses were validated centrally by an expert multidisciplinary discussion.1170 ILD cases were reported (crude overall prevalence: 97.9/10 and incidence: 19.4/10 /year). In the 848 reviewed cases, the most prevalent diagnoses were sarcoidosis (42.6%), connective tissue diseases associated ILDs (CTDs-ILDs) (16%), idiopathic pulmonary fibrosis (IPF) (11.6%), and occupational ILDs (5.0%), which corresponded to a crude prevalence of 30.2/10 for sarcoidosis, 12.1/10 for CTDs-ILDs and 8.2/10 for IPF. The prevalence of fibrotic idiopathic interstitial pneumonias, merging IPF, nonspecific interstitial pneumonia and cases registered with code J84.1 was 16.34/10 An adjusted multinomial model demonstrated an increased risk of sarcoidosis in North Africans and Afro-Caribbeans and of CTDs-ILDs in Afro-Caribbeans, compared to that in Europeans.This study, with a comprehensive recruitment and stringent diagnostic criteria, emphasises the importance of secondary ILDs, particularly CTDs-ILDs and the relatively low prevalence of IPF, and confirms that sarcoidosis is a rare disease in France.
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ISSN:1399-3003
1399-3003
DOI:10.1183/13993003.02419-2016