Tracking dyspnea up to supplemental oxygen prescription among patients with pulmonary fibrosis

Abstract Background Dyspnea is the hallmark symptom of pulmonary fibrosis. Supplemental oxygen (O2) is prescribed to many patients with pulmonary fibrosis in hopes of alleviating dyspnea and improving physical functioning. We used response data from the University of California San Diego Shortness o...

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Main Authors: Amy L. Olson, Bridget Graney, Susan Baird, Tara Churney, Kaitlin Fier, Marjorie Korn, Mark McCormick, David Sprunger, Thomas Vierzba, Frederick S. Wamboldt, Jeffrey J. Swigris
Format: Article
Language:English
Published: BMC 2017-11-01
Series:BMC Pulmonary Medicine
Subjects:
Online Access:http://link.springer.com/article/10.1186/s12890-017-0497-0
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spelling doaj-10d3773c992b4596af282067e45b1c562020-11-25T00:47:13ZengBMCBMC Pulmonary Medicine1471-24662017-11-011711710.1186/s12890-017-0497-0Tracking dyspnea up to supplemental oxygen prescription among patients with pulmonary fibrosisAmy L. Olson0Bridget Graney1Susan Baird2Tara Churney3Kaitlin Fier4Marjorie Korn5Mark McCormick6David Sprunger7Thomas Vierzba8Frederick S. Wamboldt9Jeffrey J. Swigris10Interstitial Lung Disease Program, National Jewish HealthDivision of Pulmonary Sciences and Critical Care Medicine, University of Colorado Anschutz Medical CampusParticipation Program for Pulmonary Fibrosis (P3F)Interstitial Lung Disease Program, National Jewish HealthParticipation Program for Pulmonary Fibrosis (P3F)Participation Program for Pulmonary Fibrosis (P3F)Participation Program for Pulmonary Fibrosis (P3F)Interstitial Lung Disease Program, National Jewish HealthParticipation Program for Pulmonary Fibrosis (P3F)Participation Program for Pulmonary Fibrosis (P3F)Interstitial Lung Disease Program, National Jewish HealthAbstract Background Dyspnea is the hallmark symptom of pulmonary fibrosis. Supplemental oxygen (O2) is prescribed to many patients with pulmonary fibrosis in hopes of alleviating dyspnea and improving physical functioning. We used response data from the University of California San Diego Shortness of Breath Questionnaire (UCSD) which was administered monthly in the context of a longitudinal, observational study to plot a rich trajectory for dyspnea over time in patients with pulmonary fibrosis. We used other data from that study to identify clinical predictors of being prescribed O2 and to provide additional information for how UCSD scores could be used for clinical purposes. Methods We used linear mixed-effects models and multivariate Cox proportional hazards to model change in dyspnea scores over time and to identify significant predictors of time-to-O2-prescription among a pool of clinically-meaningful candidate variables. In the longitudinal study, all decisions, including whether or not to prescribe O2, were made by subjects’ treating physicians, not members of the research team. Results One-hundred ninety-four subjects with pulmonary fibrosis completed more than one UCSD or were prescribed O2 at some point during the follow-up period (N = 43). Twenty-eight of the 43 had analyzable, longitudinal data and contribute data to the longitudinal UCSD analyses. All 43 were included in the time-to-O2-prescription analyses. Subjects prescribed O2 had more severe dyspnea at enrollment (38.4 ± 19.6 vs. 22.6 ± 18.7, p < 0.0001) and a steeper increase in UCSD scores over time (slope = 1.18 ± 0.53 vs. 0.24 ± 0.09 points per month, p = 0.02) than subjects not prescribed O2. Controlling for baseline UCSD score and FVC%, subjects with a clinical summary diagnosis of idiopathic pulmonary fibrosis (IPF) were far more likely to be prescribed O2 than subjects with other forms of pulmonary fibrosis (hazard ratio = 4.85, (2.19, 10.74), p < 0.0001). Conclusions Baseline dyspnea and rise in dyspnea over time predict timing of O2 prescription. Accounting for disease severity, patients with IPF are more likely than patients with other forms of pulmonary fibrosis to be prescribed O2. UCSD scores provide clinically useful information; frequent administration could yield timely data on changes in disease status in patients with pulmonary fibrosis. Trial registration The longitudinal study is registered on ClinicalTrials.gov ( NCT01961362 ). Registered October 9, 2013.http://link.springer.com/article/10.1186/s12890-017-0497-0DyspneaHypoxiaLung diseases, interstitialOxygen inhalation therapyQuality of life
collection DOAJ
language English
format Article
sources DOAJ
author Amy L. Olson
Bridget Graney
Susan Baird
Tara Churney
Kaitlin Fier
Marjorie Korn
Mark McCormick
David Sprunger
Thomas Vierzba
Frederick S. Wamboldt
Jeffrey J. Swigris
spellingShingle Amy L. Olson
Bridget Graney
Susan Baird
Tara Churney
Kaitlin Fier
Marjorie Korn
Mark McCormick
David Sprunger
Thomas Vierzba
Frederick S. Wamboldt
Jeffrey J. Swigris
Tracking dyspnea up to supplemental oxygen prescription among patients with pulmonary fibrosis
BMC Pulmonary Medicine
Dyspnea
Hypoxia
Lung diseases, interstitial
Oxygen inhalation therapy
Quality of life
author_facet Amy L. Olson
Bridget Graney
Susan Baird
Tara Churney
Kaitlin Fier
Marjorie Korn
Mark McCormick
David Sprunger
Thomas Vierzba
Frederick S. Wamboldt
Jeffrey J. Swigris
author_sort Amy L. Olson
title Tracking dyspnea up to supplemental oxygen prescription among patients with pulmonary fibrosis
title_short Tracking dyspnea up to supplemental oxygen prescription among patients with pulmonary fibrosis
title_full Tracking dyspnea up to supplemental oxygen prescription among patients with pulmonary fibrosis
title_fullStr Tracking dyspnea up to supplemental oxygen prescription among patients with pulmonary fibrosis
title_full_unstemmed Tracking dyspnea up to supplemental oxygen prescription among patients with pulmonary fibrosis
title_sort tracking dyspnea up to supplemental oxygen prescription among patients with pulmonary fibrosis
publisher BMC
series BMC Pulmonary Medicine
issn 1471-2466
publishDate 2017-11-01
description Abstract Background Dyspnea is the hallmark symptom of pulmonary fibrosis. Supplemental oxygen (O2) is prescribed to many patients with pulmonary fibrosis in hopes of alleviating dyspnea and improving physical functioning. We used response data from the University of California San Diego Shortness of Breath Questionnaire (UCSD) which was administered monthly in the context of a longitudinal, observational study to plot a rich trajectory for dyspnea over time in patients with pulmonary fibrosis. We used other data from that study to identify clinical predictors of being prescribed O2 and to provide additional information for how UCSD scores could be used for clinical purposes. Methods We used linear mixed-effects models and multivariate Cox proportional hazards to model change in dyspnea scores over time and to identify significant predictors of time-to-O2-prescription among a pool of clinically-meaningful candidate variables. In the longitudinal study, all decisions, including whether or not to prescribe O2, were made by subjects’ treating physicians, not members of the research team. Results One-hundred ninety-four subjects with pulmonary fibrosis completed more than one UCSD or were prescribed O2 at some point during the follow-up period (N = 43). Twenty-eight of the 43 had analyzable, longitudinal data and contribute data to the longitudinal UCSD analyses. All 43 were included in the time-to-O2-prescription analyses. Subjects prescribed O2 had more severe dyspnea at enrollment (38.4 ± 19.6 vs. 22.6 ± 18.7, p < 0.0001) and a steeper increase in UCSD scores over time (slope = 1.18 ± 0.53 vs. 0.24 ± 0.09 points per month, p = 0.02) than subjects not prescribed O2. Controlling for baseline UCSD score and FVC%, subjects with a clinical summary diagnosis of idiopathic pulmonary fibrosis (IPF) were far more likely to be prescribed O2 than subjects with other forms of pulmonary fibrosis (hazard ratio = 4.85, (2.19, 10.74), p < 0.0001). Conclusions Baseline dyspnea and rise in dyspnea over time predict timing of O2 prescription. Accounting for disease severity, patients with IPF are more likely than patients with other forms of pulmonary fibrosis to be prescribed O2. UCSD scores provide clinically useful information; frequent administration could yield timely data on changes in disease status in patients with pulmonary fibrosis. Trial registration The longitudinal study is registered on ClinicalTrials.gov ( NCT01961362 ). Registered October 9, 2013.
topic Dyspnea
Hypoxia
Lung diseases, interstitial
Oxygen inhalation therapy
Quality of life
url http://link.springer.com/article/10.1186/s12890-017-0497-0
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