Investigating significant health trends in idiopathic pulmonary fibrosis (INSIGHTS-IPF): rationale, aims and design of a nationwide prospective registry

Guidelines on the diagnosis and management of idiopathic pulmonary fibrosis (IPF), a rare manifestation of chronic progressive fibrosing interstitial pneumonia, have been updated by ATS/ERS/JRS/ALAT in 2011. In Europe, data are limited on the characteristics and management of such patients.

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Detalles Bibliográficos
Autores principales: Behr, Jürgen (Autor) , Hoeper, Marius M. (Autor) , Kreuter, Michael (Autor) , Klotsche, Jens (Autor) , Wirtz, Hubert (Autor) , Pittrow, David (Autor)
Formato: Article (Journal)
Lenguaje:inglés
Publicado: January 03, 2014
In: BMJ Open Respiratory Research
Year: 2014, Volumen: 1, Número: 1
ISSN:2052-4439
DOI:10.1136/bmjresp-2013-000010
Acceso en línea:Resolving-System, lizenzpflichtig, Volltext: https://doi.org/10.1136/bmjresp-2013-000010
Verlag, lizenzpflichtig, Volltext: https://bmjopenrespres.bmj.com/content/1/1/e000010
Enlace del recurso
Notas de Autor:Juergen Behr, Marius M. Hoeper, Michael Kreuter, Jens Klotsche, Hubert Wirtz, David Pittrow
Descripción
Sumario:Guidelines on the diagnosis and management of idiopathic pulmonary fibrosis (IPF), a rare manifestation of chronic progressive fibrosing interstitial pneumonia, have been updated by ATS/ERS/JRS/ALAT in 2011. In Europe, data are limited on the characteristics and management of such patients.
Notas:Gesehen am 20.10.2020
Descripción Física:Online Resource
ISSN:2052-4439
DOI:10.1136/bmjresp-2013-000010