June 2012 pulmonary journal club
No abstract available. Article truncated at 150 words. Idiopathic Pulmonary Fibrosis (IPF) continues to be a devastating disease with no clinically significant treatment options. For years the treatment of IPF centered on a trial of prednisone followed by the addition of either cyclophosphamide or a...
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Arizona Thoracic Society
2012-06-01
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Online Access: | http://www.swjpcc.com/pulmonary-journal-club/2012/6/29/june-2012-pulmonary-journal-club.html?SSScrollPosition=159 |
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doaj-476e04a4064243889255d3c2ddbd9fa52020-11-24T21:56:58ZengArizona Thoracic SocietySouthwest Journal of Pulmonary and Critical Care2160-67732012-06-014222222June 2012 pulmonary journal clubMathew MNo abstract available. Article truncated at 150 words. Idiopathic Pulmonary Fibrosis (IPF) continues to be a devastating disease with no clinically significant treatment options. For years the treatment of IPF centered on a trial of prednisone followed by the addition of either cyclophosphamide or azathioprine as a ‘lets see if this helps’ approach. The 2011 ATS Consensus statement on IPF declared that the use of prednisone as monotherapy was not recommended. The consensus statement also yielded a weak recommendation for N-acetylcysteine (NAC) as monotherapy, and a weak recommendation of prednisone, azathioprine and NAC as combination therapy. This study is the first large multicenter, double-blind, placebo controlled trial looking at lung function in groups of patients treated with NAC monotherapy verses combination therapy (prednisone + azathioprine + NAC) versus placebo. The study was performed throughout 25 centers from 2009-2011. Inclusion criteria were a diagnosis of IPF, age 35-85, FVC > 50% and DLC0 > 30%. A total of 236 …http://www.swjpcc.com/pulmonary-journal-club/2012/6/29/june-2012-pulmonary-journal-club.html?SSScrollPosition=159azathioprineidiopathic pumonary fibrosisn-acetylcysteineprednisone |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Mathew M |
spellingShingle |
Mathew M June 2012 pulmonary journal club Southwest Journal of Pulmonary and Critical Care azathioprine idiopathic pumonary fibrosis n-acetylcysteine prednisone |
author_facet |
Mathew M |
author_sort |
Mathew M |
title |
June 2012 pulmonary journal club |
title_short |
June 2012 pulmonary journal club |
title_full |
June 2012 pulmonary journal club |
title_fullStr |
June 2012 pulmonary journal club |
title_full_unstemmed |
June 2012 pulmonary journal club |
title_sort |
june 2012 pulmonary journal club |
publisher |
Arizona Thoracic Society |
series |
Southwest Journal of Pulmonary and Critical Care |
issn |
2160-6773 |
publishDate |
2012-06-01 |
description |
No abstract available. Article truncated at 150 words. Idiopathic Pulmonary Fibrosis (IPF) continues to be a devastating disease with no clinically significant treatment options. For years the treatment of IPF centered on a trial of prednisone followed by the addition of either cyclophosphamide or azathioprine as a ‘lets see if this helps’ approach. The 2011 ATS Consensus statement on IPF declared that the use of prednisone as monotherapy was not recommended. The consensus statement also yielded a weak recommendation for N-acetylcysteine (NAC) as monotherapy, and a weak recommendation of prednisone, azathioprine and NAC as combination therapy. This study is the first large multicenter, double-blind, placebo controlled trial looking at lung function in groups of patients treated with NAC monotherapy verses combination therapy (prednisone + azathioprine + NAC) versus placebo. The study was performed throughout 25 centers from 2009-2011. Inclusion criteria were a diagnosis of IPF, age 35-85, FVC > 50% and DLC0 > 30%. A total of 236 … |
topic |
azathioprine idiopathic pumonary fibrosis n-acetylcysteine prednisone |
url |
http://www.swjpcc.com/pulmonary-journal-club/2012/6/29/june-2012-pulmonary-journal-club.html?SSScrollPosition=159 |
work_keys_str_mv |
AT mathewm june2012pulmonaryjournalclub |
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