Social/economic costs and health-related quality of life in patients with juvenile idiopathic arthritis in Europe

Publikation: Beitrag in FachzeitschriftArtikelForschungPeer-Review

Autoren

  • BURQOL-RD Research Network

Externe Organisationen

  • 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
  • London School of Economics and Political Science
  • Istituto Superiore di Sanita
  • Istituto di Ricerche Farmacologiche Mario Negri
  • Institute for rare diseases (IRD)
  • Medical University of Plovdiv
  • Corvinus University of Budapest
  • Federación Española de Enfermedades Raras (FEDER)
  • The Swedish Institute for Health Economics (IHE)
  • AP-HP Assistance Publique - Hopitaux de Paris
  • Institut national de la santé et de la recherche médicale (INSERM)
  • Università Commerciale Luigi Bocconi
  • Université Paris VII
  • Instituto de Salud Carlos III (ISCIII)
Forschungs-netzwerk anzeigen

Details

OriginalspracheEnglisch
Seiten (von - bis)79-87
Seitenumfang9
FachzeitschriftEuropean Journal of Health Economics
Jahrgang17
Ausgabenummer1
Frühes Online-Datum16 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 juvenile idiopathic arthritis (JIA) in Europe. Methods: We conducted a cross-sectional study of patients with JIA from Germany, Italy, Spain, France, the United Kingdom, Bulgaria, and Sweden. Data on demographic characteristics, healthcare resource utilization, informal care, labor productivity losses, and HRQOL were collected from the questionnaires completed by patients or their caregivers. HRQOL was measured with the EuroQol 5-domain (EQ-5D-5L) questionnaire. Results: A total of 162 patients (67 Germany, 34 Sweden, 33 Italy, 23 United Kingdom, 4 France, and 1 Bulgaria) completed the questionnaire. Excluding Bulgarian results, due to small sample size, country-specific annual health care costs ranged from €18,913 to €36,396 (reference year: 2012). Estimated direct healthcare costs ranged from €11,068 to €22,138; direct non-healthcare costs ranged from €7837 to €14,155 and labor productivity losses ranged from €0 to €8715. Costs are also shown to differ between children and adults. The mean EQ-5D index score for JIA patients was estimated at between 0.44 and 0.88, and the mean EQ-5D visual analogue scale score was estimated at between 62 and 79. Conclusions: JIA patients incur considerable societal costs and experience substantial deterioration in HRQOL in some countries. Compared with previous studies, our results show a remarkable increase in annual healthcare costs for JIA patients. Reasons for the increase are the inclusion of non-professional caregiver costs, a wider use of biologics, and longer hospital stays.

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Social/economic costs and health-related quality of life in patients with juvenile idiopathic arthritis in Europe. / BURQOL-RD Research Network.
in: European Journal of Health Economics, Jahrgang 17, Nr. 1, 04.2016, S. 79-87.

Publikation: Beitrag in FachzeitschriftArtikelForschungPeer-Review

BURQOL-RD Research Network. Social/economic costs and health-related quality of life in patients with juvenile idiopathic arthritis in Europe. European Journal of Health Economics. 2016 Apr;17(1):79-87. Epub 2016 Apr 16. doi: 10.1007/s10198-016-0786-1
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title = "Social/economic costs and health-related quality of life in patients with juvenile idiopathic arthritis 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 juvenile idiopathic arthritis (JIA) in Europe. Methods: We conducted a cross-sectional study of patients with JIA from Germany, Italy, Spain, France, the United Kingdom, Bulgaria, and Sweden. Data on demographic characteristics, healthcare resource utilization, informal care, labor productivity losses, and HRQOL were collected from the questionnaires completed by patients or their caregivers. HRQOL was measured with the EuroQol 5-domain (EQ-5D-5L) questionnaire. Results: A total of 162 patients (67 Germany, 34 Sweden, 33 Italy, 23 United Kingdom, 4 France, and 1 Bulgaria) completed the questionnaire. Excluding Bulgarian results, due to small sample size, country-specific annual health care costs ranged from €18,913 to €36,396 (reference year: 2012). Estimated direct healthcare costs ranged from €11,068 to €22,138; direct non-healthcare costs ranged from €7837 to €14,155 and labor productivity losses ranged from €0 to €8715. Costs are also shown to differ between children and adults. The mean EQ-5D index score for JIA patients was estimated at between 0.44 and 0.88, and the mean EQ-5D visual analogue scale score was estimated at between 62 and 79. Conclusions: JIA patients incur considerable societal costs and experience substantial deterioration in HRQOL in some countries. Compared with previous studies, our results show a remarkable increase in annual healthcare costs for JIA patients. Reasons for the increase are the inclusion of non-professional caregiver costs, a wider use of biologics, and longer hospital stays.",
keywords = "Costs, Costs of illness, Juvenile idiopathic arthritis, Quality of life, Rare diseases",
author = "{BURQOL-RD Research Network} and A. Kuhlmann and T. Schmidt and M. Treskova and J. L{\'o}pez-Bastida and R. Linertov{\'a} and J. Oliva-Moreno and P. Serrano-Aguilar and M. Posada-de-la-Paz and P. Kanavos and D. Taruscio and A. Schieppati and G. Iskrov and M. P{\'e}ntek and C. Delgado and {von der Schulenburg}, {J. M.} and U. Persson and K. Chevreul and G. 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 received funding from the European Union within 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 herein. ",
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Download

TY - JOUR

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

AU - BURQOL-RD Research Network

AU - Kuhlmann, A.

AU - Schmidt, T.

AU - Treskova, M.

AU - López-Bastida, J.

AU - Linertová, R.

AU - Oliva-Moreno, J.

AU - Serrano-Aguilar, P.

AU - Posada-de-la-Paz, M.

AU - Kanavos, P.

AU - Taruscio, D.

AU - Schieppati, A.

AU - Iskrov, G.

AU - Péntek, M.

AU - Delgado, C.

AU - von der Schulenburg, J. M.

AU - Persson, U.

AU - Chevreul, K.

AU - Fattore, G.

N1 - Funding Information: Supported by the Social/Economic Burden and Health-Related Quality of Life in Patients with Rare Diseases in Europe Project, which received funding from the European Union within 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 herein.

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 juvenile idiopathic arthritis (JIA) in Europe. Methods: We conducted a cross-sectional study of patients with JIA from Germany, Italy, Spain, France, the United Kingdom, Bulgaria, and Sweden. Data on demographic characteristics, healthcare resource utilization, informal care, labor productivity losses, and HRQOL were collected from the questionnaires completed by patients or their caregivers. HRQOL was measured with the EuroQol 5-domain (EQ-5D-5L) questionnaire. Results: A total of 162 patients (67 Germany, 34 Sweden, 33 Italy, 23 United Kingdom, 4 France, and 1 Bulgaria) completed the questionnaire. Excluding Bulgarian results, due to small sample size, country-specific annual health care costs ranged from €18,913 to €36,396 (reference year: 2012). Estimated direct healthcare costs ranged from €11,068 to €22,138; direct non-healthcare costs ranged from €7837 to €14,155 and labor productivity losses ranged from €0 to €8715. Costs are also shown to differ between children and adults. The mean EQ-5D index score for JIA patients was estimated at between 0.44 and 0.88, and the mean EQ-5D visual analogue scale score was estimated at between 62 and 79. Conclusions: JIA patients incur considerable societal costs and experience substantial deterioration in HRQOL in some countries. Compared with previous studies, our results show a remarkable increase in annual healthcare costs for JIA patients. Reasons for the increase are the inclusion of non-professional caregiver costs, a wider use of biologics, and longer hospital stays.

AB - 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 juvenile idiopathic arthritis (JIA) in Europe. Methods: We conducted a cross-sectional study of patients with JIA from Germany, Italy, Spain, France, the United Kingdom, Bulgaria, and Sweden. Data on demographic characteristics, healthcare resource utilization, informal care, labor productivity losses, and HRQOL were collected from the questionnaires completed by patients or their caregivers. HRQOL was measured with the EuroQol 5-domain (EQ-5D-5L) questionnaire. Results: A total of 162 patients (67 Germany, 34 Sweden, 33 Italy, 23 United Kingdom, 4 France, and 1 Bulgaria) completed the questionnaire. Excluding Bulgarian results, due to small sample size, country-specific annual health care costs ranged from €18,913 to €36,396 (reference year: 2012). Estimated direct healthcare costs ranged from €11,068 to €22,138; direct non-healthcare costs ranged from €7837 to €14,155 and labor productivity losses ranged from €0 to €8715. Costs are also shown to differ between children and adults. The mean EQ-5D index score for JIA patients was estimated at between 0.44 and 0.88, and the mean EQ-5D visual analogue scale score was estimated at between 62 and 79. Conclusions: JIA patients incur considerable societal costs and experience substantial deterioration in HRQOL in some countries. Compared with previous studies, our results show a remarkable increase in annual healthcare costs for JIA patients. Reasons for the increase are the inclusion of non-professional caregiver costs, a wider use of biologics, and longer hospital stays.

KW - Costs

KW - Costs of illness

KW - Juvenile idiopathic arthritis

KW - Quality of life

KW - Rare diseases

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