期刊
RESPIRATION
卷 93, 期 5, 页码 363-378出版社
KARGER
DOI: 10.1159/000464332
关键词
Idiopathic pulmonary fibrosis; Nintedanib; Pirfenidone; Pulmonary fibrosis; Interstitial lung disease
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 nonpharma-cologic 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. (C) 2017 S. Karger AG, Basel
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