[Epidemiology of interstitial lung diseases]
Autor: | Dominique, Valeyre, Olivia, Freynet, Geneviève, Dion, Diane, Bouvry, Isabella, Annesi-Maesano, Hilario, Nunes |
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Přispěvatelé: | Epidémiologie des maladies infectieuses et modélisation ( ESIM ), Université Pierre et Marie Curie - Paris 6 ( UPMC ) -Institut National de la Santé et de la Recherche Médicale ( INSERM ), Valeyre D, O Freynet, G Dion, Bouvry D, Annesi-Maesano I, Nunes H, Epidémiologie des maladies infectieuses et modélisation (ESIM), Université Pierre et Marie Curie - Paris 6 (UPMC)-Institut National de la Santé et de la Recherche Médicale (INSERM) |
Jazyk: | francouzština |
Rok vydání: | 2010 |
Předmět: |
MESH : Lung Diseases
Interstitial MESH: Humans MESH : Prevalence Incidence MESH: Idiopathic Pulmonary Fibrosis MESH: Sarcoidosis Pulmonary MESH : Humans [ SDV.SPEE ] Life Sciences [q-bio]/Santé publique et épidémiologie MESH : Idiopathic Pulmonary Fibrosis Idiopathic Pulmonary Fibrosis MESH : Incidence Sarcoidosis Pulmonary Prevalence Humans [SDV.SPEE]Life Sciences [q-bio]/Santé publique et épidémiologie MESH: Incidence Lung Diseases Interstitial MESH: Lung Diseases Interstitial MESH: Prevalence MESH : Sarcoidosis Pulmonary |
Zdroj: | La Presse Médicale La Presse Médicale, Elsevier Masson, 2010, 39 (1), pp.53-9. 〈10.1016/j.lpm.2009.09.015〉 La Presse Médicale, 2010, 39 (1), pp.53-9. ⟨10.1016/j.lpm.2009.09.015⟩ |
ISSN: | 0755-4982 2213-0276 |
Popis: | International audience; Diffuse interstitial lung diseases (DILD) cover more than 200 conditions classified in 4 groups: secondary DILD; sarcoidosis; particular DILDs and idiopathic interstitial pneumonias. Overall, these diseases have a prevalence of 60-80/100,000 and an incidence around 30/100,000. Sarcoidosis and idiopathic pulmonary fibrosis are the 2 most frequent diseases, accounting together for more than 50% of all cases, followed by DILD related to connective tissue disease and to immunologic lung diseases. The incidence of different causes of DILD depends on epidemiologic factors: age, sex, race, smoking habits, and history. Mortality is very elevated in idiopathic pulmonary fibrosis, linked in more than 80% of cases to the fibrosis itself, with a median survival between 24 and 36 months. The epidemiologic studies on DILD have substantial limitations, and new studies must be conducted, in particular in France where we lack epidemiologic data beyond one old study of sarcoidosis and one more recent study focused on farmer's lung in the Doubs. |
Databáze: | OpenAIRE |
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