Pulmonary rehabilitation in restrictive thoracic disorders

Anne E. Holland, Nicolino Ambrosino

Research output: Chapter in Book/Report/Conference proceedingChapter (Book)Otherpeer-review

Abstract

The interstitial lung diseases (ILDs) are a group of over 200 debilitating conditions characterised by lung inflammation and/or fibrosis. Idiopathic pulmonary fibrosis (IPF), the most common and lethal of the ILDs, accounts for approximately one-third of the ILDs and has a median survival of 3 years from diagnosis [1]. However, the clinical course varies widely and some patients with IPF will experience long periods of stability, whilst others will have frequent exacerbations or a rapid decline [2]. Interstitial lung disease may also occur due to an underlying systemic disease process, such as connective tissue disease or sarcoidosis, or an occupational exposure, such as asbestosis or silicosis. The incidence of ILD is increasing globally, largely due to a rise in the number of people who are diagnosed with IPF. Idiopathic pulmonary fibrosis is a disease of older people, with an estimated prevalence of 19 per 100,000 in those aged 55–64 years, rising to 88 per 100,000 in those 75 and over [3]. Consequently there will be more people living with IPF as the population ages in developed nations.
Original languageEnglish
Title of host publicationTextbook of Pulmonary Rehabilitation
EditorsEnrico Clini, Anne E. Holland, Fabio Pitta, Thierry Troosters
Place of PublicationCham Switzerland
PublisherSpringer
Chapter28
Pages379-390
Number of pages12
Edition1st
ISBN (Print)978-3-319-65888-9
DOIs
Publication statusPublished - 8 Jan 2018
Externally publishedYes

Cite this

Holland, A. E., & Ambrosino, N. (2018). Pulmonary rehabilitation in restrictive thoracic disorders. In E. Clini, A. E. Holland, F. Pitta, & T. Troosters (Eds.), Textbook of Pulmonary Rehabilitation (1st ed., pp. 379-390). Springer. https://doi.org/10.1007/978-3-319-65888-9_28