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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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Bibliographic Details
Main Authors: Behr, Jürgen (Author) , Hoeper, Marius M. (Author) , Kreuter, Michael (Author) , Klotsche, Jens (Author) , Wirtz, Hubert (Author) , Pittrow, David (Author)
Format: Article (Journal)
Language:English
Published: January 03, 2014
In: BMJ Open Respiratory Research
Year: 2014, Volume: 1, Issue: 1
ISSN:2052-4439
DOI:10.1136/bmjresp-2013-000010
Online Access:Resolving-System, lizenzpflichtig, Volltext: https://doi.org/10.1136/bmjresp-2013-000010
Verlag, lizenzpflichtig, Volltext: https://bmjopenrespres.bmj.com/content/1/1/e000010
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Author Notes:Juergen Behr, Marius M. Hoeper, Michael Kreuter, Jens Klotsche, Hubert Wirtz, David Pittrow
Description
Summary: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.
Item Description:Gesehen am 20.10.2020
Physical Description:Online Resource
ISSN:2052-4439
DOI:10.1136/bmjresp-2013-000010

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