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Priorities for treatment, care and information if faced with serious illness: a comparative population-based survey in seven European countries.
Higginson, Irene J; Gomes, Barbara; Calanzani, Natalia; Gao, Wei; Bausewein, Claudia; Daveson, Barbara A; Deliens, Luc; Ferreira, Pedro L; Toscani, Franco; Gysels, Marjolein; Ceulemans, Lucas; Simon, Steffen T; Cohen, Joachim; Harding, Richard.
Afiliação
  • Higginson IJ; 1King's College London, Cicely Saunders Institute, Department of Palliative Care, Policy and Rehabilitation, London, UK.
Palliat Med ; 28(2): 101-10, 2014 Feb.
Article em En | MEDLINE | ID: mdl-23703237
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.

AIM:

We examined variations in people's priorities for treatment, care and information across seven European countries.

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. SETTING/

PARTICIPANTS:

Members of the general public aged ≥ 16 years residing in England, Flanders, Germany, Italy, the Netherlands, Portugal and Spain.

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.

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.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Qualidade de Vida / Assistência Terminal / Doente Terminal / Prioridades em Saúde / Neoplasias País/Região como assunto: Europa Idioma: En Ano de publicação: 2014 Tipo de documento: Article País de afiliação: Reino Unido

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Qualidade de Vida / Assistência Terminal / Doente Terminal / Prioridades em Saúde / Neoplasias País/Região como assunto: Europa Idioma: En Ano de publicação: 2014 Tipo de documento: Article País de afiliação: Reino Unido