Transcription of Diagnosis of Idiopathic Pulmonary Fibrosis
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Diagnosis of Idiopathic Pulmonary Fibrosis
AMERICAN THORACIC SOCIETYDOCUMENTSD iagnosis of Idiopathic Pulmonary FibrosisAn Official ATS/ERS/JRS/ALAT Clinical Practice GuidelineGanesh Raghu, Martine Remy-Jardin, Jeffrey L. Myers, Luca Richeldi, Christopher J. Ryerson, David J. Lederer,Juergen Behr, Vincent Cottin, Sonye K. Danoff, Ferran Morell, Kevin R. Flaherty, Athol Wells, Fernando J. Martinez,Arata Azuma, Thomas J. Bice, Demosthenes Bouros, Kevin K. Brown, Harold R. Collard, Abhijit Duggal, Liam Galvin,Yoshikazu Inoue, R. Gisli Jenkins, Takeshi Johkoh, Ella A. Kazerooni, Masanori Kitaichi, Shandra L. Knight,George Mansour, Andrew G.
patients with IPF may present with an acute exacerbation as an initial manifestation (i.e., an unexplained worsening of dyspnea over a few weeks and new ground-glass opacification on HRCT scan with a background of lower lobe fibrotic lung disease) (10). Patients with IPF who are younger than 50 years old are rare; such patients may ...
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