Current best practice in rehabilitation in interstitial lung disease
- PMID: 28150539
- PMCID: PMC5933636
- DOI: 10.1177/1753465816676048
Current best practice in rehabilitation in interstitial lung disease
Abstract
Interstitial lung disease (ILD) is a group of chronic respiratory diseases characterized by dyspnoea on exertion and decline in health-related quality of life (HRQL). People with ILD experience significant exercise limitation with contributors that include ventilatory limitation, impaired gas exchange, decreased cardiac function and skeletal muscle dysfunction. Pulmonary rehabilitation (PR) is well established in patients with chronic obstructive pulmonary disease (COPD) as a means to overcome exercise limitation and improve activity-related dyspnoea. There is increasing evidence for similar effects of PR in people with ILD. This review discusses the evidence for PR in ILD, outlines the essential components of PR in this population, and highlights special considerations for exercise training in people with ILD. Possible future directions for PR research in people with ILD are explored.
Keywords: education; exercise limitation; exercise training; interstitial lung disease; pulmonary rehabilitation.
Conflict of interest statement
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References
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- American Thoracic Society and European Respiratory Society. (1999) Skeletal muscle dysfunction in chronic obstructive pulmonary disease. A statement of the American Thoracic Society and European Respiratory Society. Am J Respir Crit Care Med 159: S1–S40. - PubMed
-
- Agusti A., Roca J., Gea J., Wagner P., Xaubet A., Rodriguez-Roisin R. (1991) Mechanisms of gas-exchange impairment in idiopathic pulmonary fibrosis. Am Rev Respir Dis 143: 219–225. - PubMed
-
- Alakhras M., Decker P., Nadrous H., Collazo-Clavell M., Ryu J. (2007) Body mass index and mortality in patients with idiopathic pulmonary fibrosis. Chest 131: 1448–1453. - PubMed
-
- Araujo M., Baldi B., Freitas C., Albuquerque A., Marques da Silva C., Kairalla R., et al. (2016) Pulmonary rehabilitation in lymphangioleiomyomatosis: a controlled clinical trial. Eur Respir J 47: 1452–1460. - PubMed
-
- Arizono S., Taniguchi H., Sakamoto K., Kondoh Y., Kimura T., Kataoka K., et al. (2014) Endurance time is the most responsive exercise measurement in idiopathic pulmonary fibrosis. Respir Care 59: 1108–1115. - PubMed
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