The Living with Pulmonary Fibrosis questionnaire in progressive fibrosing interstitial lung disease

The Living with Idiopathic Pulmonary Fibrosis (L-IPF) questionnaire was developed with substantial input from patients with idiopathic pulmonary fibrosis (IPF) to assess symptoms and health-related quality of life (HRQoL). Because IPF is the prototypical chronic fibrosing interstitial lung disease (...

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Main Authors: Jeffrey Swigris, Katelyn Cutts, Natalia Male, Michael Baldwin, Klaus B. Rohr, Donald M. Bushnell
Format: Article
Language:English
Published: European Respiratory Society 2021-05-01
Series:ERJ Open Research
Online Access:http://openres.ersjournals.com/content/7/2/00145-2020.full
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spelling doaj-2628793232a245ae81c74f7c7f901f902021-07-05T08:43:40ZengEuropean Respiratory SocietyERJ Open Research2312-05412021-05-017210.1183/23120541.00145-202000145-2020The Living with Pulmonary Fibrosis questionnaire in progressive fibrosing interstitial lung diseaseJeffrey Swigris0Katelyn Cutts1Natalia Male2Michael Baldwin3Klaus B. Rohr4Donald M. Bushnell5 National Jewish Health, Denver, CO, USA Evidera, Bethesda, MD, USA Boehringer Ingelheim International GmbH, Ingelheim am Rhein, Germany Boehringer Ingelheim International GmbH, Ingelheim am Rhein, Germany Boehringer Ingelheim International GmbH, Ingelheim am Rhein, Germany Evidera, Bethesda, MD, USA The Living with Idiopathic Pulmonary Fibrosis (L-IPF) questionnaire was developed with substantial input from patients with idiopathic pulmonary fibrosis (IPF) to assess symptoms and health-related quality of life (HRQoL). Because IPF is the prototypical chronic fibrosing interstitial lung disease (ILD) with a progressive phenotype, we expanded applicability of the L-IPF by deleting the word “idiopathic”, creating the L-PF (Living with Pulmonary Fibrosis) questionnaire, and then assessed its relevance among patients with progressive fibrosing ILDs in one-to-one interviews. Patients in the USA and Germany with any progressive fibrosing ILD other than IPF were asked about their disease and symptoms, completed the 44-item L-PF questionnaire (comprising two modules that assess symptoms and impacts of disease) and then answered a series of debriefing questions. Interviews were recorded, transcribed and coded for qualitative content analysis. 20 patients were interviewed, but time constraints meant not all were asked about all items. The most frequent diagnoses were rheumatoid arthritis-associated ILD (25%) and mixed connective tissue disease-associated ILD (20%). Almost all patients endorsed the symptoms assessed by the L-PF: shortness of breath (19 out of 20 patients), cough (19 out of 20) and fatigue (18 out of 20). Most patients endorsed impacts of progressive fibrosing ILD on activities of daily living, physical well-being, sleep, emotional well-being, and social aspects of their lives. Most patients had an overall positive impression of the Symptoms module and understood items as intended. All seven patients asked understood the items of the Impacts module. The L-PF contains concepts relevant and important to patients with progressive fibrosing ILD, and items are understood as intended.http://openres.ersjournals.com/content/7/2/00145-2020.full
collection DOAJ
language English
format Article
sources DOAJ
author Jeffrey Swigris
Katelyn Cutts
Natalia Male
Michael Baldwin
Klaus B. Rohr
Donald M. Bushnell
spellingShingle Jeffrey Swigris
Katelyn Cutts
Natalia Male
Michael Baldwin
Klaus B. Rohr
Donald M. Bushnell
The Living with Pulmonary Fibrosis questionnaire in progressive fibrosing interstitial lung disease
ERJ Open Research
author_facet Jeffrey Swigris
Katelyn Cutts
Natalia Male
Michael Baldwin
Klaus B. Rohr
Donald M. Bushnell
author_sort Jeffrey Swigris
title The Living with Pulmonary Fibrosis questionnaire in progressive fibrosing interstitial lung disease
title_short The Living with Pulmonary Fibrosis questionnaire in progressive fibrosing interstitial lung disease
title_full The Living with Pulmonary Fibrosis questionnaire in progressive fibrosing interstitial lung disease
title_fullStr The Living with Pulmonary Fibrosis questionnaire in progressive fibrosing interstitial lung disease
title_full_unstemmed The Living with Pulmonary Fibrosis questionnaire in progressive fibrosing interstitial lung disease
title_sort living with pulmonary fibrosis questionnaire in progressive fibrosing interstitial lung disease
publisher European Respiratory Society
series ERJ Open Research
issn 2312-0541
publishDate 2021-05-01
description The Living with Idiopathic Pulmonary Fibrosis (L-IPF) questionnaire was developed with substantial input from patients with idiopathic pulmonary fibrosis (IPF) to assess symptoms and health-related quality of life (HRQoL). Because IPF is the prototypical chronic fibrosing interstitial lung disease (ILD) with a progressive phenotype, we expanded applicability of the L-IPF by deleting the word “idiopathic”, creating the L-PF (Living with Pulmonary Fibrosis) questionnaire, and then assessed its relevance among patients with progressive fibrosing ILDs in one-to-one interviews. Patients in the USA and Germany with any progressive fibrosing ILD other than IPF were asked about their disease and symptoms, completed the 44-item L-PF questionnaire (comprising two modules that assess symptoms and impacts of disease) and then answered a series of debriefing questions. Interviews were recorded, transcribed and coded for qualitative content analysis. 20 patients were interviewed, but time constraints meant not all were asked about all items. The most frequent diagnoses were rheumatoid arthritis-associated ILD (25%) and mixed connective tissue disease-associated ILD (20%). Almost all patients endorsed the symptoms assessed by the L-PF: shortness of breath (19 out of 20 patients), cough (19 out of 20) and fatigue (18 out of 20). Most patients endorsed impacts of progressive fibrosing ILD on activities of daily living, physical well-being, sleep, emotional well-being, and social aspects of their lives. Most patients had an overall positive impression of the Symptoms module and understood items as intended. All seven patients asked understood the items of the Impacts module. The L-PF contains concepts relevant and important to patients with progressive fibrosing ILD, and items are understood as intended.
url http://openres.ersjournals.com/content/7/2/00145-2020.full
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