The Role of Palliative Care in Reducing Symptoms and Improving Quality of Life for Patients with Idiopathic Pulmonary Fibrosis: A Review

Abstract Idiopathic pulmonary fibrosis (IPF) is a progressive fibrotic lung disease with a median survival of 3–4 years from time of initial diagnosis, similar to the time course of many malignancies. A hallmark of IPF is its unpredictable disease course, ranging from long periods of clinical stabil...

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Main Authors: Richard H. Zou, Daniel J. Kass, Kevin F. Gibson, Kathleen O. Lindell
Format: Article
Language:English
Published: Adis, Springer Healthcare 2020-01-01
Series:Pulmonary Therapy
Subjects:
Online Access:https://doi.org/10.1007/s41030-019-00108-2
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author Richard H. Zou
Daniel J. Kass
Kevin F. Gibson
Kathleen O. Lindell
author_facet Richard H. Zou
Daniel J. Kass
Kevin F. Gibson
Kathleen O. Lindell
author_sort Richard H. Zou
collection DOAJ
description Abstract Idiopathic pulmonary fibrosis (IPF) is a progressive fibrotic lung disease with a median survival of 3–4 years from time of initial diagnosis, similar to the time course of many malignancies. A hallmark of IPF is its unpredictable disease course, ranging from long periods of clinical stability to acute exacerbations with rapid decompensation. As the disease progresses, patients with chronic cough and progressive exertional dyspnea become oxygen dependent. They may experience significant distress due to concurrent depression, anxiety, and fatigue, which often lead to increased symptom burden and decreased quality of life. Despite these complications, palliative care is an underutilized, and often underappreciated, resource before end-of-life care in this population. While there is growing recognition about early palliative care in IPF, current data suggest referral patterns vary widely based on institutional practices. In addition to focusing on symptom management, there is emphasis on supplemental oxygen use, pulmonary rehabilitation, quality of life, and end-of-life care. Importantly, increased use of support groups and national foundation forums have served as venues for further disease education, communication, and advanced care planning outside of the hospital settings. The purpose of this review article is to discuss the clinical features of IPF, the role of palliative care in chronic disease management, current data supporting benefits of palliative care in IPF, its role in symptom management, and practices to help patients and their caregivers achieve their best quality of life.
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spelling doaj.art-e09e294f63ab456989c3fd9644e8d9cd2022-12-21T22:57:54ZengAdis, Springer HealthcarePulmonary Therapy2364-17542364-17462020-01-0161354610.1007/s41030-019-00108-2The Role of Palliative Care in Reducing Symptoms and Improving Quality of Life for Patients with Idiopathic Pulmonary Fibrosis: A ReviewRichard H. Zou0Daniel J. Kass1Kevin F. Gibson2Kathleen O. Lindell3Division of Pulmonary, Allergy, and Critical Care Medicine, Department of Medicine, University of PittsburghDivision of Pulmonary, Allergy, and Critical Care Medicine, Department of Medicine, University of PittsburghDivision of Pulmonary, Allergy, and Critical Care Medicine, Department of Medicine, University of PittsburghDivision of Pulmonary, Allergy, and Critical Care Medicine, Department of Medicine, University of PittsburghAbstract Idiopathic pulmonary fibrosis (IPF) is a progressive fibrotic lung disease with a median survival of 3–4 years from time of initial diagnosis, similar to the time course of many malignancies. A hallmark of IPF is its unpredictable disease course, ranging from long periods of clinical stability to acute exacerbations with rapid decompensation. As the disease progresses, patients with chronic cough and progressive exertional dyspnea become oxygen dependent. They may experience significant distress due to concurrent depression, anxiety, and fatigue, which often lead to increased symptom burden and decreased quality of life. Despite these complications, palliative care is an underutilized, and often underappreciated, resource before end-of-life care in this population. While there is growing recognition about early palliative care in IPF, current data suggest referral patterns vary widely based on institutional practices. In addition to focusing on symptom management, there is emphasis on supplemental oxygen use, pulmonary rehabilitation, quality of life, and end-of-life care. Importantly, increased use of support groups and national foundation forums have served as venues for further disease education, communication, and advanced care planning outside of the hospital settings. The purpose of this review article is to discuss the clinical features of IPF, the role of palliative care in chronic disease management, current data supporting benefits of palliative care in IPF, its role in symptom management, and practices to help patients and their caregivers achieve their best quality of life.https://doi.org/10.1007/s41030-019-00108-2Idiopathic pulmonary fibrosisPalliative careQuality of life
spellingShingle Richard H. Zou
Daniel J. Kass
Kevin F. Gibson
Kathleen O. Lindell
The Role of Palliative Care in Reducing Symptoms and Improving Quality of Life for Patients with Idiopathic Pulmonary Fibrosis: A Review
Pulmonary Therapy
Idiopathic pulmonary fibrosis
Palliative care
Quality of life
title The Role of Palliative Care in Reducing Symptoms and Improving Quality of Life for Patients with Idiopathic Pulmonary Fibrosis: A Review
title_full The Role of Palliative Care in Reducing Symptoms and Improving Quality of Life for Patients with Idiopathic Pulmonary Fibrosis: A Review
title_fullStr The Role of Palliative Care in Reducing Symptoms and Improving Quality of Life for Patients with Idiopathic Pulmonary Fibrosis: A Review
title_full_unstemmed The Role of Palliative Care in Reducing Symptoms and Improving Quality of Life for Patients with Idiopathic Pulmonary Fibrosis: A Review
title_short The Role of Palliative Care in Reducing Symptoms and Improving Quality of Life for Patients with Idiopathic Pulmonary Fibrosis: A Review
title_sort role of palliative care in reducing symptoms and improving quality of life for patients with idiopathic pulmonary fibrosis a review
topic Idiopathic pulmonary fibrosis
Palliative care
Quality of life
url https://doi.org/10.1007/s41030-019-00108-2
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