Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2019 Oct 1;28(153):190044.
doi: 10.1183/16000617.0044-2019. Print 2019 Sep 30.

Comorbidities in idiopathic pulmonary fibrosis: an underestimated issue

Affiliations
Review

Comorbidities in idiopathic pulmonary fibrosis: an underestimated issue

Antonella Caminati et al. Eur Respir Rev. .

Abstract

Idiopathic pulmonary fibrosis (IPF) is a progressive and fibrosing lung disease with a poor prognosis. Between 60% and 70% of IPF patients die of IPF; the remaining causes of death may be due to comorbidities occurring in this ageing population. Interest in the role played by comorbidities in IPF has increased in the past few years. The optimal clinical management of IPF is multifaceted and not only involves antifibrotic treatment, but also vaccinations, oxygen supplementation, evaluation of nutritional status as well as psychological support and patient education. Symptom management, pulmonary rehabilitation, palliative care and treatment of comorbidities represent further areas of clinical intervention. This review analyses the major comorbidities observed in IPF, focusing on those that have the greatest impact on mortality and quality of life (QoL). The identification and treatment of comorbidities may help to improve patients' health-related QoL (i.e. sleep apnoea and depression), while some comorbidities (i.e. lung cancer, cardiovascular diseases and pulmonary hypertension) influence survival. It has been outlined that gathering comorbidities data improves the prediction of survival beyond the clinical and physiological parameters of IPF.

PubMed Disclaimer

Conflict of interest statement

Conflict of interest: A. Caminati reports personal fees from Roche and Boehringer Ingelheim, outside the submitted work. Conflict of interest: C. Lonati has nothing to disclose. Conflict of interest: R. Cassandro has nothing to disclose. Conflict of interest: D. Elia has nothing to disclose. Conflict of interest: G. Pelosi has nothing to disclose. Conflict of interest: O. Torre has nothing to disclose. Conflict of interest: M. Zompatori has nothing to disclose. Conflict of interest: E. Uslenghi has nothing to disclose. Conflict of interest: S. Harari reports grants and personal fees from Roche, Actelion and Boehringer Ingelheim, outside the submitted work.

Figures

FIGURE 1
FIGURE 1
Left lung cancer in a patient with idiopathic pulmonary fibrosis.
FIGURE 2
FIGURE 2
Right pulmonary embolism in a patient with idiopathic pulmonary fibrosis. a) Mediastinal window. b) Parenchymal window.

References

    1. Raghu G, Collard HR, Egan JJ, et al. . An official ATS/ERS/JRS/ALAT statement: idiopathic pulmonary fibrosis: evidence-based guidelines for diagnosis and management. Am J Respir Crit Care Med 2011; 183: 788–824. - PMC - PubMed
    1. Fernandez Perez ER, Daniels CE, Schroeder DR, et al. . Incidence, prevalence, and clinical course of idiopathic pulmonary fibrosis: a population-based study. Chest 2010; 137: 129–137. - PMC - PubMed
    1. Vancheri C, Failla M, Crimi N, et al. . Idiopathic pulmonary fibrosis: a disease with similarities and links to cancer biology. Eur Respir J 2010; 35: 496–504. - PubMed
    1. Olson AL, Swigris JJ, Lezotte DC, et al. . Mortality from pulmonary fibrosis increased in the United States from 1992 to 2003. Am J Respir Crit Care Med 2007; 176: 277–284. - PubMed
    1. Ley B, Collard HR, King TE Jr. Clinical course and prediction of survival in idiopathic pulmonary fibrosis. Am J Respir Crit Care Med 2011; 183: 431–440. - PubMed