Physical activity and activity space in patients with pulmonary fibrosis not prescribed supplemental oxygen

Abstract Background Patients with pulmonary fibrosis (PF) have impaired quality of life, and research suggests that dyspnea and physical activity are primary drivers. As PF progresses, some patients notice the disease “shrinks their worlds”. The objective of this study is to describe movement (both...

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Main Authors: Elisabeth Dowling Root, Bridget Graney, Susan Baird, Tara Churney, Kailtin Fier, Majorie Korn, Mark McCormic, David Sprunger, Tomas Vierzba, Frederick S. Wamboldt, Jeffery J. Swigris
Format: Article
Language:English
Published: BMC 2017-11-01
Series:BMC Pulmonary Medicine
Online Access:http://link.springer.com/article/10.1186/s12890-017-0495-2
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spelling doaj-cb93e50487b148618a40b981222907162020-11-24T23:02:36ZengBMCBMC Pulmonary Medicine1471-24662017-11-011711910.1186/s12890-017-0495-2Physical activity and activity space in patients with pulmonary fibrosis not prescribed supplemental oxygenElisabeth Dowling Root0Bridget Graney1Susan Baird2Tara Churney3Kailtin Fier4Majorie Korn5Mark McCormic6David Sprunger7Tomas Vierzba8Frederick S. Wamboldt9Jeffery J. Swigris10Department of Geography and Division of Epidemiology, The Ohio State UniversityDivision of Pulmonary Sciences and Critical Care Medicine, University of Colorado Anschutz Medical CampusInterstitial Lung Disease Program, National Jewish HealthParticipation Program for Pulmonary Fibrosis (P3F), National Jewish HealthParticipation Program for Pulmonary Fibrosis (P3F), National Jewish HealthParticipation Program for Pulmonary Fibrosis (P3F), National Jewish HealthParticipation Program for Pulmonary Fibrosis (P3F), National Jewish HealthParticipation Program for Pulmonary Fibrosis (P3F), National Jewish HealthParticipation Program for Pulmonary Fibrosis (P3F), National Jewish HealthParticipation Program for Pulmonary Fibrosis (P3F), National Jewish HealthParticipation Program for Pulmonary Fibrosis (P3F), National Jewish HealthAbstract Background Patients with pulmonary fibrosis (PF) have impaired quality of life, and research suggests that dyspnea and physical activity are primary drivers. As PF progresses, some patients notice the disease “shrinks their worlds”. The objective of this study is to describe movement (both physical activity and activity space) in a cohort of patients with PF of various etiologies who have not been prescribed supplemental oxygen (O2). Methods Subjects with PF not on supplemental O2 during the day were enrolled from across the U.S. from August 2013 to October 2015. At enrollment, each subject completed questionnaires and, for seven consecutive days, wore an accelerometer and GPS tracker. Results One hundred ninety-four subjects had a confirmed diagnosis of PF and complete, analyzable GPS data. The cohort was predominantly male (56%), Caucasian (95%) and had idiopathic pulmonary fibrosis (30%) or connective tissue disease related-PF (31%). Subjects walked a median 7497 (interquartile range [IQR] 5766-9261) steps per day. Steps per day were correlated with symptoms and several quality of life domains. In a model controlling for age, body mass index, wrist- (vs. waist) worn accelerometer and percent predicted diffusing capacity (DLCO%), fatigue (beta coefficient = −51.5 ± 11.7, p < 0.0001) was an independent predictor of steps per day (model R2=0.34). Conclusions Patients with PF, who have not been prescribed O2 for use during the day, have wide variability in their mobility. Day-to-day physical activity is related to several domains that impact quality of life, but GPS-derived activity space is not. Wearable data collection devices may be used to determine whether and how therapeutic interventions impact movement in PF patients. Trial registration NCT01961362 . Registered 9 October, 2013.http://link.springer.com/article/10.1186/s12890-017-0495-2
collection DOAJ
language English
format Article
sources DOAJ
author Elisabeth Dowling Root
Bridget Graney
Susan Baird
Tara Churney
Kailtin Fier
Majorie Korn
Mark McCormic
David Sprunger
Tomas Vierzba
Frederick S. Wamboldt
Jeffery J. Swigris
spellingShingle Elisabeth Dowling Root
Bridget Graney
Susan Baird
Tara Churney
Kailtin Fier
Majorie Korn
Mark McCormic
David Sprunger
Tomas Vierzba
Frederick S. Wamboldt
Jeffery J. Swigris
Physical activity and activity space in patients with pulmonary fibrosis not prescribed supplemental oxygen
BMC Pulmonary Medicine
author_facet Elisabeth Dowling Root
Bridget Graney
Susan Baird
Tara Churney
Kailtin Fier
Majorie Korn
Mark McCormic
David Sprunger
Tomas Vierzba
Frederick S. Wamboldt
Jeffery J. Swigris
author_sort Elisabeth Dowling Root
title Physical activity and activity space in patients with pulmonary fibrosis not prescribed supplemental oxygen
title_short Physical activity and activity space in patients with pulmonary fibrosis not prescribed supplemental oxygen
title_full Physical activity and activity space in patients with pulmonary fibrosis not prescribed supplemental oxygen
title_fullStr Physical activity and activity space in patients with pulmonary fibrosis not prescribed supplemental oxygen
title_full_unstemmed Physical activity and activity space in patients with pulmonary fibrosis not prescribed supplemental oxygen
title_sort physical activity and activity space in patients with pulmonary fibrosis not prescribed supplemental oxygen
publisher BMC
series BMC Pulmonary Medicine
issn 1471-2466
publishDate 2017-11-01
description Abstract Background Patients with pulmonary fibrosis (PF) have impaired quality of life, and research suggests that dyspnea and physical activity are primary drivers. As PF progresses, some patients notice the disease “shrinks their worlds”. The objective of this study is to describe movement (both physical activity and activity space) in a cohort of patients with PF of various etiologies who have not been prescribed supplemental oxygen (O2). Methods Subjects with PF not on supplemental O2 during the day were enrolled from across the U.S. from August 2013 to October 2015. At enrollment, each subject completed questionnaires and, for seven consecutive days, wore an accelerometer and GPS tracker. Results One hundred ninety-four subjects had a confirmed diagnosis of PF and complete, analyzable GPS data. The cohort was predominantly male (56%), Caucasian (95%) and had idiopathic pulmonary fibrosis (30%) or connective tissue disease related-PF (31%). Subjects walked a median 7497 (interquartile range [IQR] 5766-9261) steps per day. Steps per day were correlated with symptoms and several quality of life domains. In a model controlling for age, body mass index, wrist- (vs. waist) worn accelerometer and percent predicted diffusing capacity (DLCO%), fatigue (beta coefficient = −51.5 ± 11.7, p < 0.0001) was an independent predictor of steps per day (model R2=0.34). Conclusions Patients with PF, who have not been prescribed O2 for use during the day, have wide variability in their mobility. Day-to-day physical activity is related to several domains that impact quality of life, but GPS-derived activity space is not. Wearable data collection devices may be used to determine whether and how therapeutic interventions impact movement in PF patients. Trial registration NCT01961362 . Registered 9 October, 2013.
url http://link.springer.com/article/10.1186/s12890-017-0495-2
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