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Quality of Life and Healthcare Resource Use in a Real-world Patient Population with Idiopathic Pulmonary Fibrosis: The PROOF Registry

INTRODUCTION: The PROOF registry is a prospective, observational study that aimed to monitor disease progression in a real-world cohort of patients with idiopathic pulmonary fibrosis (IPF). Here, longitudinal quality-of-life (QoL) outcomes, healthcare resource use (HCRU), and the association between...

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Autores principales: Wuyts, Wim A., Dahlqvist, Caroline, Slabbynck, Hans, Schlesser, Marc, Gusbin, Natacha, Compere, Christophe, Maddens, Sofie, Rizzo, Shemra, Kirchgaessler, Klaus-Uwe, Bartley, Karen, Bondue, Benjamin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Healthcare 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9098727/
https://www.ncbi.nlm.nih.gov/pubmed/35429319
http://dx.doi.org/10.1007/s41030-022-00187-8
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author Wuyts, Wim A.
Dahlqvist, Caroline
Slabbynck, Hans
Schlesser, Marc
Gusbin, Natacha
Compere, Christophe
Maddens, Sofie
Rizzo, Shemra
Kirchgaessler, Klaus-Uwe
Bartley, Karen
Bondue, Benjamin
author_facet Wuyts, Wim A.
Dahlqvist, Caroline
Slabbynck, Hans
Schlesser, Marc
Gusbin, Natacha
Compere, Christophe
Maddens, Sofie
Rizzo, Shemra
Kirchgaessler, Klaus-Uwe
Bartley, Karen
Bondue, Benjamin
author_sort Wuyts, Wim A.
collection PubMed
description INTRODUCTION: The PROOF registry is a prospective, observational study that aimed to monitor disease progression in a real-world cohort of patients with idiopathic pulmonary fibrosis (IPF). Here, longitudinal quality-of-life (QoL) outcomes, healthcare resource use (HCRU), and the association between QoL and mortality in patients enrolled in the PROOF registry are presented. METHODS: QoL outcomes (St. George’s Respiratory Questionnaire [SGRQ], EuroQoL-5 dimensions-5 levels Health Questionnaire [EQ-5D-5L], EuroQoL-5 dimensions Health Questionnaire [EQ-5D] visual analogue scale [VAS] and cough VAS) and HCRU were collected for all patients. Associations between baseline QoL and mortality were assessed using univariate and multivariate analyses. During multivariate analyses, individual QoL measures were adjusted for the following covariates: age, sex, percent predicted forced vital capacity, percent predicted diffusing capacity of the lungs for carbon monoxide, smoking status, and supplementary oxygen use at registry inclusion. RESULTS: In total, 277 patients were enrolled in the PROOF registry. During the follow-up period, worsening in cough VAS score, SGRQ symptom score, and SGRQ activity score was observed, while EQ-5D VAS, SGRQ total score, and SGRQ impact score remained stable. During univariate analyses, EQ-5D VAS and all SGRQ sub-scores and total score at baseline were associated with mortality; however, during multivariate analyses, only the SGRQ total score, SGRQ impact score, and SGRQ symptom score at baseline were associated with mortality. During the follow-up period, 261 (94.2%) patients required an outpatient consultation (IPF- or non-IPF-related) and there were 182 hospitalizations in total, most of which were respiratory related (66.5%). CONCLUSIONS: The PROOF registry provided valuable, real-world data on the association between baseline QoL and mortality, and longitudinal HCRU and QoL outcomes in patients with IPF over 24 months and identified that SGRQ may be an independent prognostic factor in IPF. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s41030-022-00187-8.
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spelling pubmed-90987272022-05-14 Quality of Life and Healthcare Resource Use in a Real-world Patient Population with Idiopathic Pulmonary Fibrosis: The PROOF Registry Wuyts, Wim A. Dahlqvist, Caroline Slabbynck, Hans Schlesser, Marc Gusbin, Natacha Compere, Christophe Maddens, Sofie Rizzo, Shemra Kirchgaessler, Klaus-Uwe Bartley, Karen Bondue, Benjamin Pulm Ther Original Research INTRODUCTION: The PROOF registry is a prospective, observational study that aimed to monitor disease progression in a real-world cohort of patients with idiopathic pulmonary fibrosis (IPF). Here, longitudinal quality-of-life (QoL) outcomes, healthcare resource use (HCRU), and the association between QoL and mortality in patients enrolled in the PROOF registry are presented. METHODS: QoL outcomes (St. George’s Respiratory Questionnaire [SGRQ], EuroQoL-5 dimensions-5 levels Health Questionnaire [EQ-5D-5L], EuroQoL-5 dimensions Health Questionnaire [EQ-5D] visual analogue scale [VAS] and cough VAS) and HCRU were collected for all patients. Associations between baseline QoL and mortality were assessed using univariate and multivariate analyses. During multivariate analyses, individual QoL measures were adjusted for the following covariates: age, sex, percent predicted forced vital capacity, percent predicted diffusing capacity of the lungs for carbon monoxide, smoking status, and supplementary oxygen use at registry inclusion. RESULTS: In total, 277 patients were enrolled in the PROOF registry. During the follow-up period, worsening in cough VAS score, SGRQ symptom score, and SGRQ activity score was observed, while EQ-5D VAS, SGRQ total score, and SGRQ impact score remained stable. During univariate analyses, EQ-5D VAS and all SGRQ sub-scores and total score at baseline were associated with mortality; however, during multivariate analyses, only the SGRQ total score, SGRQ impact score, and SGRQ symptom score at baseline were associated with mortality. During the follow-up period, 261 (94.2%) patients required an outpatient consultation (IPF- or non-IPF-related) and there were 182 hospitalizations in total, most of which were respiratory related (66.5%). CONCLUSIONS: The PROOF registry provided valuable, real-world data on the association between baseline QoL and mortality, and longitudinal HCRU and QoL outcomes in patients with IPF over 24 months and identified that SGRQ may be an independent prognostic factor in IPF. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s41030-022-00187-8. Springer Healthcare 2022-04-16 /pmc/articles/PMC9098727/ /pubmed/35429319 http://dx.doi.org/10.1007/s41030-022-00187-8 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by-nc/4.0/Open AccessThis article is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License, which permits any non-commercial use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) .
spellingShingle Original Research
Wuyts, Wim A.
Dahlqvist, Caroline
Slabbynck, Hans
Schlesser, Marc
Gusbin, Natacha
Compere, Christophe
Maddens, Sofie
Rizzo, Shemra
Kirchgaessler, Klaus-Uwe
Bartley, Karen
Bondue, Benjamin
Quality of Life and Healthcare Resource Use in a Real-world Patient Population with Idiopathic Pulmonary Fibrosis: The PROOF Registry
title Quality of Life and Healthcare Resource Use in a Real-world Patient Population with Idiopathic Pulmonary Fibrosis: The PROOF Registry
title_full Quality of Life and Healthcare Resource Use in a Real-world Patient Population with Idiopathic Pulmonary Fibrosis: The PROOF Registry
title_fullStr Quality of Life and Healthcare Resource Use in a Real-world Patient Population with Idiopathic Pulmonary Fibrosis: The PROOF Registry
title_full_unstemmed Quality of Life and Healthcare Resource Use in a Real-world Patient Population with Idiopathic Pulmonary Fibrosis: The PROOF Registry
title_short Quality of Life and Healthcare Resource Use in a Real-world Patient Population with Idiopathic Pulmonary Fibrosis: The PROOF Registry
title_sort quality of life and healthcare resource use in a real-world patient population with idiopathic pulmonary fibrosis: the proof registry
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9098727/
https://www.ncbi.nlm.nih.gov/pubmed/35429319
http://dx.doi.org/10.1007/s41030-022-00187-8
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