TY - JOUR
T1 - Assessment of the impact of social deprivation, distance to hospital and time to diagnosis on survival in idiopathic pulmonary fibrosis
AU - Shankar, Rashmi
AU - Hadinnapola, Charaka M
AU - Clark, Allan B
AU - Adamali, Huzaifa
AU - Chaudhuri, Nazia
AU - Spencer, Lisa G
AU - Wilson, Andrew M
N1 - Publisher Copyright:
© 2024 The Authors
PY - 2024/4/25
Y1 - 2024/4/25
N2 - Idiopathic pulmonary fibrosis (IPF) is a progressive condition associated with a variable prognosis. The relationship between socioeconomic status or distance travelled to respiratory clinics and prognosis is unclear. To determine whether socioeconomic status, distance to hospital and time to referral affects survival in patients with IPF. In this retrospective cohort study, we used data collected from the British Thoracic Society Interstitial Lung Diseases Registry, between 2013 and 2021 (n = 2359) and calculated the quintile of Index of Multiple Deprivation 2019 score, time from initial symptoms to hospital attendance and distance as the linear distance between hospital and home post codes. Survival was assessed using Cox proportional hazards models. There was a significant association between increasing quintile of deprivation and duration of symptoms prior to hospital presentation, Gender Age Physiology (GAP) index and receipt of supplemental oxygen and antifibrotic therapies at presentation. The most deprived patients had worse overall survival compared to least deprived after adjusting for smoking status, GAP index, distance to hospital and time to referral (HR = 1.39 [1.11, 1.73]; p = 0.003). Patients living furthest from a respiratory clinic also had worse survival compared to those living closest (HR = 1.29 [1.01, 1.64]; p = 0.041). The most deprived patients with IPF have more severe disease at presentation and worse outcomes. Living far from hospital was also associated with poor outcomes. This suggests inequalities in access to healthcare and requires consideration in delivering effective and equitable care to patients with IPF. [Abstract copyright: Copyright © 2024 The Authors. Published by Elsevier Ltd.. All rights reserved.]
AB - Idiopathic pulmonary fibrosis (IPF) is a progressive condition associated with a variable prognosis. The relationship between socioeconomic status or distance travelled to respiratory clinics and prognosis is unclear. To determine whether socioeconomic status, distance to hospital and time to referral affects survival in patients with IPF. In this retrospective cohort study, we used data collected from the British Thoracic Society Interstitial Lung Diseases Registry, between 2013 and 2021 (n = 2359) and calculated the quintile of Index of Multiple Deprivation 2019 score, time from initial symptoms to hospital attendance and distance as the linear distance between hospital and home post codes. Survival was assessed using Cox proportional hazards models. There was a significant association between increasing quintile of deprivation and duration of symptoms prior to hospital presentation, Gender Age Physiology (GAP) index and receipt of supplemental oxygen and antifibrotic therapies at presentation. The most deprived patients had worse overall survival compared to least deprived after adjusting for smoking status, GAP index, distance to hospital and time to referral (HR = 1.39 [1.11, 1.73]; p = 0.003). Patients living furthest from a respiratory clinic also had worse survival compared to those living closest (HR = 1.29 [1.01, 1.64]; p = 0.041). The most deprived patients with IPF have more severe disease at presentation and worse outcomes. Living far from hospital was also associated with poor outcomes. This suggests inequalities in access to healthcare and requires consideration in delivering effective and equitable care to patients with IPF. [Abstract copyright: Copyright © 2024 The Authors. Published by Elsevier Ltd.. All rights reserved.]
KW - Idiopathic pulmonary fibrosis
KW - Travelling distance
KW - Socioeconomic status
KW - Access to care
KW - Social class
KW - Survival
UR - https://www.scopus.com/pages/publications/85192054234
UR - https://pure.ulster.ac.uk/en/publications/5bd51222-cf84-4a99-9005-bff330541671
U2 - 10.1016/j.rmed.2024.107612
DO - 10.1016/j.rmed.2024.107612
M3 - Article
C2 - 38677526
SN - 1532-3064
VL - 227
SP - 1
EP - 7
JO - Respiratory medicine
JF - Respiratory medicine
M1 - 107612
ER -