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Social/economic costs and health-related quality of life of mucopolysaccharidosis patients and their caregivers in Europe

Péntek, Márta (author)
Corvinus University of Budapest
Gulácsi, László (author)
Corvinus University of Budapest
Brodszky, Valentin (author)
Corvinus University of Budapest
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Baji, Petra (author)
Corvinus University of Budapest
Boncz, Imre (author)
University of Pécs
Pogány, Gábor (author)
Hungarian Federation of People with Rare and Congenital Diseases (RIROSZ)
López-Bastida, Julio (author)
Health Services Research on Chronic Patients Network (REDISSEC)
Linertová, Renata (author)
Fundación Canaria de Investigación Sanitaria (FUNCANIS)
Oliva-Moreno, Juan (author)
University of Castilla La Mancha
Serrano-Aguilar, Pedro (author)
Evaluation and Planning Service at Canary Islands Health Service (SESCS)
Posada-de-la-Paz, Manuel (author)
Carlos III Health Institute
Taruscio, Domenica (author)
Italian National Institute of Health (ISS)
Iskrov, Georgi (author)
Medical University of Plovdiv
Schieppati, Arrigo (author)
Mario Negri Institute for Pharmacological Research
von der Schulenburg, Johann Matthias Graf (author)
Leibniz University of Hannover
Kanavos, Panos (author)
London School of Economics and Political Science
Chevreul, Karine (author)
National Institute for Health and Medical Research, France
Persson, Ulf (author)
Lund University,Lunds universitet,Hälsoekonomi,Forskargrupper vid Lunds universitet,Health Economics,Lund University Research Groups
Fattore, Giovanni (author)
Bocconi University
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 (creator_code:org_t)
2016-04-09
2016
English 10 s.
In: European Journal of Health Economics. - : Springer Science and Business Media LLC. - 1618-7598 .- 1618-7601. ; 17, s. 89-98
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Objectives: To assess the health-related quality of life (HRQOL) of patients with mucopolysaccharidosis (MPS) and their caregivers and to quantify the disease-related costs from a societal perspective. Methods: In the context of a multi-country study of rare diseases (BURQOL-RD project), a cross-sectional survey was performed among MPS patients in seven European countries. Data on demographic characteristics, health resource utilization, informal care, and loss of labor productivity were collected. The EQ-5D, Barthel index (BI), and Zarit burden interview (ZBI) questionnaires were used to assess patients’ and their informal caregivers’ quality of life, patients’ functional ability, and caregivers’ burden, respectively. Results: Altogether, 120 patients (children 62 %, females 40 %) and 66 caregivers completed the questionnaire. Patients’ mean age was 16.5 years and median age at diagnosis was 3 years. Adult patients’ average EQ-5D and EQ VAS scores varied across countries from 0.13 to 0.43 and 30.0 to 62.2, respectively, mean BI was 46.7, and ZBI was 32.7. Mean informal care time was 51.3 h/week. The mean total annual cost per patient (reference year 2012) was €24,520 in Hungary, €25,993 in France, €84,921 in Italy, €94,384 in Spain, and €209,420 in Germany. Costs are also shown to differ between children and adults. Direct costs accounted for most of the costs in all five countries (80, 100, 99, 98, and 93 %, respectively). Conclusions: MPS patients experience substantial loss of HRQOL and their families take a remarkable part in their care. Although utilization of health and social care resources varies significantly across countries, MPS incurs considerable societal costs in all the countries studied.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Hälsovetenskap -- Hälso- och sjukvårdsorganisation, hälsopolitik och hälsoekonomi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Health Sciences -- Health Care Service and Management, Health Policy and Services and Health Economy (hsv//eng)

Keyword

Caregiver
Cost-of-illness
EQ-5D
Health-related quality of life
Mucopolysaccharidosis

Publication and Content Type

art (subject category)
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