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Priorities for treatment, care and information if faced with serious illness: a comparative population-based survey in seven European countries.

Authors :
Higginson IJ
Gomes B
Calanzani N
Gao W
Bausewein C
Daveson BA
Deliens L
Ferreira PL
Toscani F
Gysels M
Ceulemans L
Simon ST
Cohen J
Harding R
Source :
Palliative medicine [Palliat Med] 2014 Feb; Vol. 28 (2), pp. 101-10. Date of Electronic Publication: 2013 May 23.
Publication Year :
2014

Abstract

Background: Health-care costs are growing, with little population-based data about people's priorities for end-of-life care, to guide service development and aid discussions.<br />Aim: We examined variations in people's priorities for treatment, care and information across seven European countries.<br />Design: Telephone survey of a random sample of households; we asked respondents their priorities if 'faced with a serious illness, like cancer, with limited time to live' and used multivariable logistic regressions to identify associated factors.<br />Setting/participants: Members of the general public aged ≥ 16 years residing in England, Flanders, Germany, Italy, the Netherlands, Portugal and Spain.<br />Results: In total, 9344 individuals were interviewed. Most people chose 'improve quality of life for the time they had left', ranging from 57% (95% confidence interval: 55%-60%, Italy) to 81% (95% confidence interval: 79%-83%, Spain). Only 2% (95% confidence interval: 1%-3%, England) to 6% (95% confidence interval: 4%-7%, Flanders) said extending life was most important, and 15% (95% confidence interval: 13%-17%, Spain) to 40% (95% confidence interval: 37%-43%, Italy) said quality and extension were equally important. Prioritising quality of life was associated with higher education in all countries (odds ratio = 1.3 (Flanders) to 7.9 (Italy)), experience of caregiving or bereavement (England, Germany, Portugal), prioritising pain/symptom control over having a positive attitude and preferring death in a hospice/palliative care unit. Those prioritising extending life had the highest home death preference of all groups. Health status did not affect priorities.<br />Conclusions: Across all countries, extending life was prioritised by a minority, regardless of health status. Treatment and care needs to be reoriented with patient education and palliative care becoming mainstream for serious conditions such as cancer.

Details

Language :
English
ISSN :
1477-030X
Volume :
28
Issue :
2
Database :
MEDLINE
Journal :
Palliative medicine
Publication Type :
Academic Journal
Accession number :
23703237
Full Text :
https://doi.org/10.1177/0269216313488989