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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Bibliographic Details
Main Author: Mathew M
Format: Article
Language:English
Published: Arizona Thoracic Society 2012-06-01
Series:Southwest Journal of Pulmonary and Critical Care
Subjects:
Online Access:http://www.swjpcc.com/pulmonary-journal-club/2012/6/29/june-2012-pulmonary-journal-club.html?SSScrollPosition=159
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spelling 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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