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Health-related quality of life in idiopathic pulmonary fibrosis: Data from the Australian IPF Registry

Citation

Glaspole, IN and Chapman, SA and Cooper, WA and Ellis, SJ and Goh, NS and Hopkins, PM and Macansh, S and Mahar, A and Moodley, YP and Paul, E and Reynolds, PN and Walters, EH and Zappala, CJ and Corte, TJ, Health-related quality of life in idiopathic pulmonary fibrosis: Data from the Australian IPF Registry, Respirology, 22, (5) pp. 950-956. ISSN 1323-7799 (2017) [Refereed Article]

Copyright Statement

Copyright 2017 Asian Pacific Society of Respirology

DOI: doi:10.1111/resp.12989

Abstract

Background and objective: Studies analysing the effect of worsening pulmonary physiological impairment in idiopathic pulmonary fibrosis (IPF) with respect to quality of life have been limited to single centres or highly selected trial populations. The aim of this study was to determine the principal determinants of baseline and longitudinal health‐related quality of life (HRQoL) in a large unselected IPF population.

Methods: We used the Australian IPF Registry to examine the relationship between HRQoL, measured using the St George Respiratory Questionnaire (SGRQ), and demographic features, physiological features, co‐morbidities and symptoms. Linear regression analysis was performed to identify predictors of baseline HRQoL, linear mixed model analysis to determine the effect of time and forced vital capacity (FVC) on SGRQ and Cox proportional hazards regression to examine the relationship between HRQoL and all‐cause mortality.

Results: Baseline data from 516 patients were available (347 males; mean (SD) age: 71.3  8.6 years). Univariate analysis showed significant associations between HRQoL and demographic, clinical and physiological features. However, multivariate analysis demonstrated independent associations only between SGRQ and dyspnoea (University of California San Diego Shortness of Breathlessness Questionnaire (UCSD‐SOBQ); R2 = 0.71, P < 0.0001), cough severity (visual analogue scale; R2 = 0.06, P < 0.0001) and depression (Hospital Anxiety and Depression Scale; R2 = 0.04, P < 0.0001). Linear mixed‐effects modelling of combined baseline and longitudinal data confirmed these associations, as well as for FVC% predicted (P = 0.005). Multivariate Cox proportionate‐proportional hazards regression analysis demonstrated no association between HRQoL and risk of mortality.

Conclusion: Cough, dyspnoea and depression are major symptomatic determinants of HRQoL in IPF. FVC decline is associated with worsening HRQoL.

Item Details

Item Type:Refereed Article
Keywords:cough, dyspnoea, forced vital capacity, pulmonary fibrosis, quality of life
Research Division:Medical and Health Sciences
Research Group:Cardiorespiratory Medicine and Haematology
Research Field:Respiratory Diseases
Objective Division:Health
Objective Group:Clinical Health (Organs, Diseases and Abnormal Conditions)
Objective Field:Cardiovascular System and Diseases
UTAS Author:Walters, EH (Professor Haydn Walters)
ID Code:125232
Year Published:2017
Web of Science® Times Cited:22
Deposited By:Medicine
Deposited On:2018-04-09
Last Modified:2018-09-11
Downloads:0

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