Idiopathic pulmonary fibrosis: Now less idiopathic?
Idiopathic pulmonary fibrosis (IPF) is a progressive diffuse fibrosing lung disease that kills increasing numbers of individuals each year with levels of mortality that exceed those of many cancers.1 It is an important lung problem for many reasons including being the most common of the diffuse fibr...
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Published in | Respiratory medicine Vol. 103; no. 6; pp. 791 - 792 |
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Main Author | |
Format | Journal Article |
Language | English |
Published |
England
Elsevier Ltd
01.06.2009
Elsevier Limited |
Subjects | |
Online Access | Get full text |
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Summary: | Idiopathic pulmonary fibrosis (IPF) is a progressive diffuse fibrosing lung disease that kills increasing numbers of individuals each year with levels of mortality that exceed those of many cancers.1 It is an important lung problem for many reasons including being the most common of the diffuse fibrosing lung diseases and its awful prognosis. In two of these a higher incidence of gastro-oesophageal reflux was found in patients with IPF compared with normal individuals.7-9 In a third study, gastro-oesophageal reflux-induced oesophagitis was linked with pulmonary fibrosis.9 In a study of patients with end-stage IPF on a lung transplant waiting list, two thirds of were found to have gastro-oesophageal reflux.10 Interestingly, the typical symptoms (heartburn and regurgitation) could not distinguish between those with and without gastro-oesophageal reflux. |
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Bibliography: | SourceType-Other Sources-1 content type line 63 ObjectType-Editorial-2 ObjectType-Commentary-1 |
ISSN: | 0954-6111 1532-3064 |
DOI: | 10.1016/j.rmed.2009.03.014 |