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Idiopathic Pulmonary Fibrosis in Switzerland: Diagnosis and Treatment.

Authors :
Funke-Chambour M
Azzola A
Adler D
Barazzone-Argiroffo C
Benden C
Boehler A
Bridevaux PO
Brutsche M
Clarenbach CF
Hostettler K
Kleiner-Finger R
Nicod LP
Soccal PM
Tamm M
Geiser T
Lazor R
Source :
Respiration; international review of thoracic diseases [Respiration] 2017; Vol. 93 (5), pp. 363-378. Date of Electronic Publication: 2017 Mar 25.
Publication Year :
2017

Abstract

Idiopathic pulmonary fibrosis (IPF) is a severe progressive and irreversible lung disease. Novel antifibrotic drugs that slow disease progression are now available. However, many issues regarding patient management remain unanswered, such as the choice between available drugs, their use in particular subgroups and clinical situations, time of treatment onset, termination, combination or switch, or nonpharmacologic management. To guide Swiss respiratory physicians in this evolving field still characterized by numerous areas of uncertainty, the Swiss Working Group for interstitial and rare lung diseases of the Swiss Respiratory Society provides a position paper on the diagnosis and treatment of IPF.<br /> (© 2017 S. Karger AG, Basel.)

Details

Language :
English
ISSN :
1423-0356
Volume :
93
Issue :
5
Database :
MEDLINE
Journal :
Respiration; international review of thoracic diseases
Publication Type :
Academic Journal
Accession number :
28343230
Full Text :
https://doi.org/10.1159/000464332