Follow-up and nonpharmacological management of the idiopathic pulmonary fibrosis patient

Idiopathic pulmonary fibrosis (IPF) is a chronic, progressive, fatal form of diffuse interstitial lung disease. Management of IPF requires an orderly approach, with regular evaluations and implementation of both pharmacological and nonpharmacological treatments. Pulmonary rehabilitation can relieve...

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Bibliographic Details
Main Author: J.J. Egan
Format: Article
Language:English
Published: European Respiratory Society 2011-06-01
Series:European Respiratory Review
Subjects:
Online Access:http://err.ersjournals.com/content/20/120/114.full.pdf+html
Description
Summary:Idiopathic pulmonary fibrosis (IPF) is a chronic, progressive, fatal form of diffuse interstitial lung disease. Management of IPF requires an orderly approach, with regular evaluations and implementation of both pharmacological and nonpharmacological treatments. Pulmonary rehabilitation can relieve patients from the distressing symptoms of IPF and improve quality of life. Oxygen therapy is central to treatment of all patients. Lung transplantation enhances survival in selected patients. Mechanical ventilation may be used in patients with acute exacerbations, but the prognosis is poor in these cases. Palliative care focuses on symptom management, advance directives and end-of-life planning. Patient support groups may also play an important role.
ISSN:0905-9180
1600-0617