Cargando…

Treatment patterns, resource use and costs of idiopathic pulmonary fibrosis in Spain – results of a Delphi Panel

BACKGROUND: Idiopathic pulmonary fibrosis (IPF) is a form of chronic fibrosing interstitial pneumonia characterized by progressive worsening of dyspnea and lung function, with a poor prognosis. The objective of this study was to determine treatment patterns, resource use and costs of managing Spanis...

Descripción completa

Detalles Bibliográficos
Autores principales: Morell, Ferran, Esser, Dirk, Lim, Jonathan, Stowasser, Susanne, Villacampa, Alba, Nieves, Diana, Brosa, Max
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4710031/
https://www.ncbi.nlm.nih.gov/pubmed/26758510
http://dx.doi.org/10.1186/s12890-016-0168-6
_version_ 1782409764833067008
author Morell, Ferran
Esser, Dirk
Lim, Jonathan
Stowasser, Susanne
Villacampa, Alba
Nieves, Diana
Brosa, Max
author_facet Morell, Ferran
Esser, Dirk
Lim, Jonathan
Stowasser, Susanne
Villacampa, Alba
Nieves, Diana
Brosa, Max
author_sort Morell, Ferran
collection PubMed
description BACKGROUND: Idiopathic pulmonary fibrosis (IPF) is a form of chronic fibrosing interstitial pneumonia characterized by progressive worsening of dyspnea and lung function, with a poor prognosis. The objective of this study was to determine treatment patterns, resource use and costs of managing Spanish patients with IPF. METHODS: A three-round Delphi consensus panel of 15 clinical experts was held between December 2012 and June 2013 using questionnaires to describe the management of patients with IPF. A cost analysis based on Delphi panel estimates was made from the Spanish National Health System (NHS) perspective, including the direct costs of IPF diagnosis and management. Unit costs were applied to Delphi panel estimates of health resource use. Univariate sensitivity analyses were made to evaluate uncertainties in parameters. RESULTS: The Delphi panel estimated that 20, 60 and 20 % of IPF patients presented with stable disease, slow and rapid disease progression, respectively. The estimated annual cost per patient with stable disease, slow and rapid disease progression was €11,484, €20,978 and €57,759, respectively. This corresponds to a weighted average annual cost of €26,435 with itemized costs of €1,184 (4.5), €7,147 (27.0), €5,950 (22.5), €11,666 (44.1) and €488 (1.9 %) for the diagnosis of IPF, treatment, monitoring, management of acute exacerbations and end-of-life care, respectively. The parameter that varied the annual cost per patient the most was resource use associated with acute exacerbations. CONCLUSIONS: The management of patients with IPF in Spain, especially patients with rapid disease progression, has a high economic impact on the NHS. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12890-016-0168-6) contains supplementary material, which is available to authorized users.
format Online
Article
Text
id pubmed-4710031
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-47100312016-01-13 Treatment patterns, resource use and costs of idiopathic pulmonary fibrosis in Spain – results of a Delphi Panel Morell, Ferran Esser, Dirk Lim, Jonathan Stowasser, Susanne Villacampa, Alba Nieves, Diana Brosa, Max BMC Pulm Med Research Article BACKGROUND: Idiopathic pulmonary fibrosis (IPF) is a form of chronic fibrosing interstitial pneumonia characterized by progressive worsening of dyspnea and lung function, with a poor prognosis. The objective of this study was to determine treatment patterns, resource use and costs of managing Spanish patients with IPF. METHODS: A three-round Delphi consensus panel of 15 clinical experts was held between December 2012 and June 2013 using questionnaires to describe the management of patients with IPF. A cost analysis based on Delphi panel estimates was made from the Spanish National Health System (NHS) perspective, including the direct costs of IPF diagnosis and management. Unit costs were applied to Delphi panel estimates of health resource use. Univariate sensitivity analyses were made to evaluate uncertainties in parameters. RESULTS: The Delphi panel estimated that 20, 60 and 20 % of IPF patients presented with stable disease, slow and rapid disease progression, respectively. The estimated annual cost per patient with stable disease, slow and rapid disease progression was €11,484, €20,978 and €57,759, respectively. This corresponds to a weighted average annual cost of €26,435 with itemized costs of €1,184 (4.5), €7,147 (27.0), €5,950 (22.5), €11,666 (44.1) and €488 (1.9 %) for the diagnosis of IPF, treatment, monitoring, management of acute exacerbations and end-of-life care, respectively. The parameter that varied the annual cost per patient the most was resource use associated with acute exacerbations. CONCLUSIONS: The management of patients with IPF in Spain, especially patients with rapid disease progression, has a high economic impact on the NHS. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12890-016-0168-6) contains supplementary material, which is available to authorized users. BioMed Central 2016-01-12 /pmc/articles/PMC4710031/ /pubmed/26758510 http://dx.doi.org/10.1186/s12890-016-0168-6 Text en © Morell et al. 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Morell, Ferran
Esser, Dirk
Lim, Jonathan
Stowasser, Susanne
Villacampa, Alba
Nieves, Diana
Brosa, Max
Treatment patterns, resource use and costs of idiopathic pulmonary fibrosis in Spain – results of a Delphi Panel
title Treatment patterns, resource use and costs of idiopathic pulmonary fibrosis in Spain – results of a Delphi Panel
title_full Treatment patterns, resource use and costs of idiopathic pulmonary fibrosis in Spain – results of a Delphi Panel
title_fullStr Treatment patterns, resource use and costs of idiopathic pulmonary fibrosis in Spain – results of a Delphi Panel
title_full_unstemmed Treatment patterns, resource use and costs of idiopathic pulmonary fibrosis in Spain – results of a Delphi Panel
title_short Treatment patterns, resource use and costs of idiopathic pulmonary fibrosis in Spain – results of a Delphi Panel
title_sort treatment patterns, resource use and costs of idiopathic pulmonary fibrosis in spain – results of a delphi panel
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4710031/
https://www.ncbi.nlm.nih.gov/pubmed/26758510
http://dx.doi.org/10.1186/s12890-016-0168-6
work_keys_str_mv AT morellferran treatmentpatternsresourceuseandcostsofidiopathicpulmonaryfibrosisinspainresultsofadelphipanel
AT esserdirk treatmentpatternsresourceuseandcostsofidiopathicpulmonaryfibrosisinspainresultsofadelphipanel
AT limjonathan treatmentpatternsresourceuseandcostsofidiopathicpulmonaryfibrosisinspainresultsofadelphipanel
AT stowassersusanne treatmentpatternsresourceuseandcostsofidiopathicpulmonaryfibrosisinspainresultsofadelphipanel
AT villacampaalba treatmentpatternsresourceuseandcostsofidiopathicpulmonaryfibrosisinspainresultsofadelphipanel
AT nievesdiana treatmentpatternsresourceuseandcostsofidiopathicpulmonaryfibrosisinspainresultsofadelphipanel
AT brosamax treatmentpatternsresourceuseandcostsofidiopathicpulmonaryfibrosisinspainresultsofadelphipanel