Literature DB >> 27059622

Social/economic costs and health-related quality of life in patients with cystic fibrosis in Europe.

Karine Chevreul1,2,3, Morgane Michel4,5,6, Karen Berg Brigham4,7, Julio López-Bastida8,9, Renata Linertová9,10, Juan Oliva-Moreno9,11, Pedro Serrano-Aguilar9,12, Manuel Posada-de-la-Paz13, Domenica Taruscio14, Arrigo Schieppati15, Georgi Iskrov16,17, Márta Péntek18, Johann Matthias Graf von der Schulenburg19, Panos Kanavos20, Ulf Persson21, Giovani Fattore22.   

Abstract

OBJECTIVES: Our goal was to provide data on the economic burden and health-related quality of life (HRQOL) of patients with cystic fibrosis (CF) and their caregivers in Europe.
METHODS: A cross-sectional study was carried out on adults and children with CF in eight European countries. Patients completed an anonymous questionnaire regarding their socio-demographic characteristics, use of healthcare services and presence of a caregiver. Costs were calculated with a bottom-up approach using unit costs from each participating country, and HRQOL was assessed using EQ-5D. The principal caregiver also answered a questionnaire on their characteristics, HRQOL and burden.
RESULTS: A total of 905 patients with CF was included (399 adults and 506 children). The total average annual cost per patient varied from €21,144 in Bulgaria to €53,256 in Germany. Adults had higher direct healthcare costs than children, but children had much higher informal care costs (P < 0.0001). Total costs increased with patients' level of dependence. In adults, mean utility fell between 0.640 and 0.870, and the visual analogue scale ranged from 46.0 to 69.7. There was no difference in caregiver HRQOL regardless of whether they cared for an adult or a child. However, caregivers who looked after a child had a significantly higher burden (P = 0.0013).
CONCLUSIONS: Our study highlights the burden of CF in terms of costs and decreased HRQOL for both patients and their caregivers throughout Europe.

Entities:  

Keywords:  Costs and cost analysis; Cystic fibrosis; Economic burden; Health-related quality of life

Mesh:

Year:  2016        PMID: 27059622     DOI: 10.1007/s10198-016-0781-6

Source DB:  PubMed          Journal:  Eur J Health Econ        ISSN: 1618-7598


  23 in total

1.  Prevalence and prognostic factors of disability after childhood injury.

Authors:  Suzanne Polinder; Willem Jan Meerding; Hidde Toet; Saakje Mulder; Marie-Louise Essink-Bot; Ed F van Beeck
Journal:  Pediatrics       Date:  2005-12       Impact factor: 7.124

2.  Resource use, costs, and utility estimates for patients with cystic fibrosis with mild impairment in lung function: analysis of data collected alongside a 48-week multicenter clinical trial.

Authors:  Esi Morgan Dewitt; Chelsea A Grussemeyer; Joëlle Y Friedman; Michaela A Dinan; Li Lin; Kevin A Schulman; Shelby D Reed
Journal:  Value Health       Date:  2012-01-27       Impact factor: 5.725

3.  Parent-proxy EQ-5D ratings of children with attention-deficit hyperactivity disorder in the US and the UK.

Authors:  Louis S Matza; Kristina Secnik; Sally Mannix; F Randy Sallee
Journal:  Pharmacoeconomics       Date:  2005       Impact factor: 4.981

4.  Cost-of-illness methodology: a guide to current practices and procedures.

Authors:  T A Hodgson; M R Meiners
Journal:  Milbank Mem Fund Q Health Soc       Date:  1982

5.  Nationwide trends in the medical care costs of privately insured patients with cystic fibrosis (CF), 2001-2007.

Authors:  Becky A Briesacher; Alexandra L Quittner; Hassan Fouayzi; Jie Zhang; Andrine Swensen
Journal:  Pediatr Pulmonol       Date:  2011-04-04

6.  Health state utilities for childhood attention-deficit/hyperactivity disorder based on parent preferences in the United kingdom.

Authors:  Kristina Secnik; Louis S Matza; Suzi Cottrell; Eric Edgell; Dominic Tilden; Sally Mannix
Journal:  Med Decis Making       Date:  2005 Jan-Feb       Impact factor: 2.583

7.  Cost of illness of cystic fibrosis in Germany: results from a large cystic fibrosis centre.

Authors:  Mareike Heimeshoff; Helge Hollmeyer; Jonas Schreyögg; Oliver Tiemann; Doris Staab
Journal:  Pharmacoeconomics       Date:  2012-09-01       Impact factor: 4.981

8.  Quality of life and healthcare utilisation in cystic fibrosis: a multicentre study.

Authors:  Judy M Bradley; Steven W Blume; Maria-Magdalena Balp; David Honeybourne; J Stuart Elborn
Journal:  Eur Respir J       Date:  2012-07-26       Impact factor: 16.671

9.  Development and preliminary testing of the new five-level version of EQ-5D (EQ-5D-5L).

Authors:  M Herdman; C Gudex; A Lloyd; Mf Janssen; P Kind; D Parkin; G Bonsel; X Badia
Journal:  Qual Life Res       Date:  2011-04-09       Impact factor: 4.147

10.  Cost-effectiveness of a nurse-led telemonitoring intervention based on peak expiratory flow measurements in asthmatics: results of a randomised controlled trial.

Authors:  Daniëlle C M Willems; Manuela A Joore; Johannes J E Hendriks; Emiel F M Wouters; Johan L Severens
Journal:  Cost Eff Resour Alloc       Date:  2007-07-27
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1.  Spillover Effects on Caregivers' and Family Members' Utility: A Systematic Review of the Literature.

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2.  The Economic Burden of Cystic Fibrosis in Germany from a Payer Perspective.

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Journal:  Pharmacoeconomics       Date:  2019-08       Impact factor: 4.981

3.  Social/economic costs and health-related quality of life in patients with rare diseases in Europe.

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Review 5.  Valuing the "Burden" and Impact of Rare Diseases: A Scoping Review.

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6.  Economic Evaluation of Tobramycin Inhalation Powder for the Treatment of Chronic Pulmonary Pseudomonas aeruginosa Infection in Patients with Cystic Fibrosis.

Authors:  Srilekha Panguluri; Praveen Gunda; Laurie Debonnett; Kamal Hamed
Journal:  Clin Drug Investig       Date:  2017-08       Impact factor: 2.859

7.  Cost-effectiveness analysis of three algorithms for diagnosing primary ciliary dyskinesia: a simulation study.

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Review 9.  Cost-of-illness studies in rare diseases: a scoping review.

Authors:  Lidia García-Pérez; Renata Linertová; Cristina Valcárcel-Nazco; Manuel Posada; Inigo Gorostiza; Pedro Serrano-Aguilar
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10.  A systematic review of patient-reported outcome measures (PROMs) in cystic fibrosis.

Authors:  Irushi Ratnayake; Susannah Ahern; Rasa Ruseckaite
Journal:  BMJ Open       Date:  2020-10-01       Impact factor: 2.692

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