Social/economic costs and health-related quality of life in patients with histiocytosis in Europe

Publikation: Beitrag in FachzeitschriftArtikelForschungPeer-Review

Autoren

  • BURQOL-RD Research Network

Externe Organisationen

  • Institute for rare diseases (IRD)
  • Medical University of Plovdiv
  • Hospital Universitario de Cruces
  • Universidad de Castilla-La Mancha
  • Red de Investigación en Servicios Sanitarios en Enfermedades Crónicas (REDISSEC)
  • Fundación Canaria de Investigación Sanitaria (FUNCANIS)
  • Servicio canario de la Salud
  • Instituto de Salud Carlos III (ISCIII)
  • Istituto di Ricerche Farmacologiche Mario Negri
  • Istituto Superiore di Sanita
  • Corvinus University of Budapest
  • London School of Economics and Political Science
  • Hopital Hotel-Dieu AP-HP
  • Institut national de la santé et de la recherche médicale (INSERM)
  • The Swedish Institute for Health Economics (IHE)
  • Università Commerciale Luigi Bocconi
  • Universite Paris 7
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Details

OriginalspracheEnglisch
Seiten (von - bis)67-78
Seitenumfang12
FachzeitschriftEuropean Journal of Health Economics
Jahrgang17
Frühes Online-Datum4 Apr. 2016
PublikationsstatusVeröffentlicht - Apr. 2016

Abstract

Objective: The aim of this study was to determine the economic burden from a societal perspective and the health-related quality of life (HRQOL) of patients with histiocytosis in Europe. Methods: We conducted a cross-sectional study of patients with histiocytosis from France, Germany, Italy, Spain, Bulgaria, the UK, and Sweden. Data on demographic characteristics, health resource utilisation, informal care, loss of labour productivity and HRQOL were collected from the questionnaires completed by patients or their caregivers. HRQOL was measured with the EuroQol 5-domain (EQ-5D) questionnaire. Results: A total of 134 patients (35 France, 32 Germany, 30 Italy, 24 Spain, 7 Bulgaria, 4 UK and 2 Sweden) completed the questionnaire. The average annual costs ranged from € 6832 to € 33,283 between countries, the year of reference being 2012. Estimated direct healthcare costs ranged from € 1698 to € 18,213; direct nonhealthcare costs ranged from € 2936 to € 17,622 and labour productivity losses ranged from € 1 to € 8855. The mean EQ-5D score for adult histiocytosis patients was estimated at between 0.32 and 0.85, and the mean EQ-5D visual analogue scale score was estimated at between 50.00 and 66.50. Conclusion: The main strengths of this study lie in our bottom-up approach to costing and in the evaluation of histiocytosis patients from a broad perspective (societal costs). This type of analysis is very scarce in international literature for rare diseases in comparison with other illnesses. We conclude that histiocytosis patients incur considerable societal costs and experience substantial deterioration in HRQOL.

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Social/economic costs and health-related quality of life in patients with histiocytosis in Europe. / BURQOL-RD Research Network.
in: European Journal of Health Economics, Jahrgang 17, 04.2016, S. 67-78.

Publikation: Beitrag in FachzeitschriftArtikelForschungPeer-Review

BURQOL-RD Research Network. Social/economic costs and health-related quality of life in patients with histiocytosis in Europe. European Journal of Health Economics. 2016 Apr;17:67-78. Epub 2016 Apr 4. doi: 10.1007/s10198-016-0790-5
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title = "Social/economic costs and health-related quality of life in patients with histiocytosis in Europe",
abstract = "Objective: The aim of this study was to determine the economic burden from a societal perspective and the health-related quality of life (HRQOL) of patients with histiocytosis in Europe. Methods: We conducted a cross-sectional study of patients with histiocytosis from France, Germany, Italy, Spain, Bulgaria, the UK, and Sweden. Data on demographic characteristics, health resource utilisation, informal care, loss of labour productivity and HRQOL were collected from the questionnaires completed by patients or their caregivers. HRQOL was measured with the EuroQol 5-domain (EQ-5D) questionnaire. Results: A total of 134 patients (35 France, 32 Germany, 30 Italy, 24 Spain, 7 Bulgaria, 4 UK and 2 Sweden) completed the questionnaire. The average annual costs ranged from € 6832 to € 33,283 between countries, the year of reference being 2012. Estimated direct healthcare costs ranged from € 1698 to € 18,213; direct nonhealthcare costs ranged from € 2936 to € 17,622 and labour productivity losses ranged from € 1 to € 8855. The mean EQ-5D score for adult histiocytosis patients was estimated at between 0.32 and 0.85, and the mean EQ-5D visual analogue scale score was estimated at between 50.00 and 66.50. Conclusion: The main strengths of this study lie in our bottom-up approach to costing and in the evaluation of histiocytosis patients from a broad perspective (societal costs). This type of analysis is very scarce in international literature for rare diseases in comparison with other illnesses. We conclude that histiocytosis patients incur considerable societal costs and experience substantial deterioration in HRQOL.",
keywords = "Cost-of-illness, Europe, Health-related quality of life, Histiocytosis, Social cost",
author = "{BURQOL-RD Research Network} and Georgi Iskrov and Itziar Astigarraga and Rumen Stefanov and Julio L{\'o}pez-Bastida and Renata Linertov{\'a} and Juan Oliva-Moreno and Pedro Serrano-Aguilar and Manuel Posada-de-la-Paz and Arrigo Schieppati and Domenica Taruscio and M{\'a}rta P{\'e}ntek and {von der Schulenburg}, {Johann Matthias Graf} and Panos Kanavos and Karine Chevreul and Ulf Persson and Giovanni Fattore",
note = "Funding Information: Supported by the Social Economic Burden and Health-Related Quality of Life in Patients with Rare Diseases in Europe Project, which has received funding from the European Union in the framework of the Health Programme [grant A101205]. The Executive Agency of the European Union is not responsible for any use that may be made of the information contained here. ",
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TY - JOUR

T1 - Social/economic costs and health-related quality of life in patients with histiocytosis in Europe

AU - BURQOL-RD Research Network

AU - Iskrov, Georgi

AU - Astigarraga, Itziar

AU - Stefanov, Rumen

AU - López-Bastida, Julio

AU - Linertová, Renata

AU - Oliva-Moreno, Juan

AU - Serrano-Aguilar, Pedro

AU - Posada-de-la-Paz, Manuel

AU - Schieppati, Arrigo

AU - Taruscio, Domenica

AU - Péntek, Márta

AU - von der Schulenburg, Johann Matthias Graf

AU - Kanavos, Panos

AU - Chevreul, Karine

AU - Persson, Ulf

AU - Fattore, Giovanni

N1 - Funding Information: Supported by the Social Economic Burden and Health-Related Quality of Life in Patients with Rare Diseases in Europe Project, which has received funding from the European Union in the framework of the Health Programme [grant A101205]. The Executive Agency of the European Union is not responsible for any use that may be made of the information contained here.

PY - 2016/4

Y1 - 2016/4

N2 - Objective: The aim of this study was to determine the economic burden from a societal perspective and the health-related quality of life (HRQOL) of patients with histiocytosis in Europe. Methods: We conducted a cross-sectional study of patients with histiocytosis from France, Germany, Italy, Spain, Bulgaria, the UK, and Sweden. Data on demographic characteristics, health resource utilisation, informal care, loss of labour productivity and HRQOL were collected from the questionnaires completed by patients or their caregivers. HRQOL was measured with the EuroQol 5-domain (EQ-5D) questionnaire. Results: A total of 134 patients (35 France, 32 Germany, 30 Italy, 24 Spain, 7 Bulgaria, 4 UK and 2 Sweden) completed the questionnaire. The average annual costs ranged from € 6832 to € 33,283 between countries, the year of reference being 2012. Estimated direct healthcare costs ranged from € 1698 to € 18,213; direct nonhealthcare costs ranged from € 2936 to € 17,622 and labour productivity losses ranged from € 1 to € 8855. The mean EQ-5D score for adult histiocytosis patients was estimated at between 0.32 and 0.85, and the mean EQ-5D visual analogue scale score was estimated at between 50.00 and 66.50. Conclusion: The main strengths of this study lie in our bottom-up approach to costing and in the evaluation of histiocytosis patients from a broad perspective (societal costs). This type of analysis is very scarce in international literature for rare diseases in comparison with other illnesses. We conclude that histiocytosis patients incur considerable societal costs and experience substantial deterioration in HRQOL.

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KW - Health-related quality of life

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