Diagnosis and management of idiopathic pulmonary fibrosis: Thoracic Society of Australia and New Zealand and Lung Foundation Australia position statements summary

Introduction: Idiopathic pulmonary fibrosis (IPF) is a fibrosing interstitial lung disease associated with debilitating symptoms of dyspnoea and cough, resulting in respiratory failure, impaired quality of life and ultimately death. Diagnosing IPF can be challenging, as it often shares many features...

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Veröffentlicht in:	Medical journal of Australia 2018-02, Vol.208 (2), p.82-88
Hauptverfasser:	Jo, Helen E, Prasad, Jyotika D, Troy, Lauren K, Mahar, Annabelle, Bleasel, Jane, Ellis, Samantha J, Chambers, Daniel C, Holland, Anne E, Lake, Fiona R, Keir, Gregory, Goh, Nicole S, Wilsher, Margaret, Boer, Sally, Moodley, Yuben, Grainge, Christopher, Whitford, Helen M, Chapman, Sally A, Reynolds, Paul N, Beatson, David, Jones, Leonie J, Hopkins, Peter, Allan, Heather M, Glaspole, Ian, Corte, Tamera J
Format:	Artikel
Sprache:	eng
Schlagworte:	Anti-Inflammatory Agents, Non-Steroidal - therapeutic use Australia Bronchoalveolar Lavage - statistics & numerical data Disease Management Humans Idiopathic Pulmonary Fibrosis - diagnosis Idiopathic Pulmonary Fibrosis - therapy New Zealand Practice Guidelines as Topic Quality of Life Respiratory tract diseases
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