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Transitions and touchpoints in idiopathic pulmonary fibrosis
  1. Jeffrey J Swigris
  1. Interstitial Lung Disease Program, National Jewish Health, Denver, Colorado, USA
  1. Correspondence to Dr Jeffrey J Swigris; swigrisj{at}njc.org

Abstract

Patients with idiopathic pulmonary fibrosis (IPF) face a poor prognosis and endure intrusive symptoms that impair quality of life. Many patients with IPF will require supplemental oxygen (O2) at some point in the course of their illness, and although it can improve blood oxygen and symptoms, O2 creates physical and emotional challenges for patients and their loved ones. Four events in the course of IPF—the first occurs at the time of diagnosis and the other three are related to O2—herald periods of transition for patients and their caregivers and mark touchpoints when they need extra care and support from practitioners.

  • interstitial fibrosis
  • long term oxygen therapy (itot)

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Footnotes

  • Contributors JJS is the sole contributor of the content of this manuscript and takes ultimate responsibility for it.

  • Funding .This work was supported in part by a generous gift from the Munn Foundation.

  • Competing interests None declared.

  • Patient consent Not required.

  • Provenance and peer review Not commissioned; externally peer reviewed.

  • Data sharing statement There are no data related to this perspective.

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