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Pulmonary Rehabilitation
idiopathic pulmonary fibrosis (IPF), interstitial lung disease (ILD) and bronchiectasis. The guidance is not mandatory, and the commissioner should review the whole of the specification to ensure that it meets local needs and, once agreed with the Provider, it
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www.clinicaltrials.govwith Idiopathic Pulmonary Fibrosis (IPF) Co-ordinating Investigator : Trialsites: Multi-centre, multi-national Clinical phase: III Objective: The primary objective of this study is to assess the long-term safety of BIBF 1120 treatment in patients with Idiopathic Pulmonary Fibrosis who have completed one
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www.thoracic.orgidiopathic pulmonary fibrosis(IPF) if they have unexplained symptomatic or asymptomatic patterns of bilateral fibrosis on a chest radiograph or chest computed tomography (CT) scan, bibasilar inspiratory crackles, and an agetypicallyolderthan60years.Rarely,middle-aged adults (.40 yr and ,60 yr), especially
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www.jrs.or.jp以前は，idiopathic pulmonary fibrosis（IPF）という 疾患概念は，UIPとDIPの両方を含むものとされてき た．DIPは非常にまれな疾患のため，現在ではUIPと IPFは同義語として扱われている10）．さらにATS-ERS consensus statementでは，IPFは病理所見がUIPであ
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www.thoracic.orgTable 2. Comparison of Recommendations in the 2015 and 2011 Idiopathic Pulmonary Fibrosis Guidelines Agent 2015 Guideline 2011 Guideline New and revised recommendations Anticoagulation (warfarin) Strong recommendation against use* Conditional recommendation against use‡ Combination prednisone 1 azathioprine 1 N-acetylcysteine
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