Volume 22, Issue 10 p. 2298-2305
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If you had less than a year to live, would you want to know? A seven‐country European population survey of public preferences for disclosure of poor prognosis

R. Harding

Corresponding Author

King's College London, Cicely Saunders Institute, Department of Palliative Care, Policy & Rehabilitation, London, SE5 9PJ UK

Correspondence to: King's College London, Cicely Saunders Institute, Department of Palliative Care, Policy & Rehabilitation, Bessemer Road, London SE5 9PJ, UK. E‐mail: richard.harding@kcl.ac.ukSearch for more papers by this author
V. Simms

King's College London, Cicely Saunders Institute, Department of Palliative Care, Policy & Rehabilitation, London, SE5 9PJ UK

London School of Hygiene and Tropical Medicine, London, UK

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N. Calanzani

King's College London, Cicely Saunders Institute, Department of Palliative Care, Policy & Rehabilitation, London, SE5 9PJ UK

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I. J. Higginson

King's College London, Cicely Saunders Institute, Department of Palliative Care, Policy & Rehabilitation, London, SE5 9PJ UK

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S. Hall

King's College London, Cicely Saunders Institute, Department of Palliative Care, Policy & Rehabilitation, London, SE5 9PJ UK

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M. Gysels

Barcelona Centre for International Health Research (CRESIB – Hospital Clínic), Universitat de Barcelona, Barcelona, Spain

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A. Meñaca

Barcelona Centre for International Health Research (CRESIB – Hospital Clínic), Universitat de Barcelona, Barcelona, Spain

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C. Bausewein

King's College London, Cicely Saunders Institute, Department of Palliative Care, Policy & Rehabilitation, London, SE5 9PJ UK

Deutsche Gesellschaft für Palliativmedizin, Berlin, Germany

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L. Deliens

End-of-Life Care Research Group, Ghent University & Vrije Universiteit Brussel, Brussels, Belgium

Department of Public and Occupational Health, EMGO Institute for Health and Care Research, Palliative Care Center of Expertise, VU University Medical Center, Amsterdam, the Netherlands

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P. Ferreira

Centre for Health Studies and Research, University of Coimbra (CEISUC), Coimbra, Portugal

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F. Toscani

Istituto di Ricerca in Medicina Palliativa, Fondazione Lino Maestroni – ONLUS, Cremona, Italy

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B. A. Daveson

King's College London, Cicely Saunders Institute, Department of Palliative Care, Policy & Rehabilitation, London, SE5 9PJ UK

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L. Ceulemans

University of Antwerp, Antwerp, Belgium

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B. Gomes

King's College London, Cicely Saunders Institute, Department of Palliative Care, Policy & Rehabilitation, London, SE5 9PJ UK

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First published: 18 March 2013
Citations: 5

Abstract

Objective

With increasing European cancer deaths, clinicians must manage information regarding poor prognosis. This study aimed to determine European citizens' preferences, within a scenario of serious illness such as cancer with less than a year to live, for information disclosure regarding poor prognosis, the likely symptoms and problems, and the care options available, to measure variations between countries and to identify factors associated with preferences.

Methods

A population‐based cross‐national telephone survey using random digit dialling in seven countries was conducted.

Results

Among 9344 respondents, data revealed an international preference (73.9%) to always be informed in the scenario of having a serious illness such as cancer with less than a year to live. This varied from 67.6% in Italy to 80.7% in Flanders. A minority (21.1%) did not want such information unless they ask, or at all. People younger than 70 years (OR 0.72, 95% CI 0.62–0.83, p < 0.001), men (OR 1.23, 95% CI 1.10–1.37, p < 0.001), those with experience of illness (OR = 1.20. 95% CI 1.01–1.43, p < 0.05) and with more education (OR = 1.20, 95% CI 1.09–1.32, p < 0.001) were more likely to want to know of limited time left.

Conclusions

The models confirmed the influence of four factors in more than one country (age, gender, education and most concerning problem) and added 11 country‐specific factors to which national policies and clinical practice should respond. These findings confirm a majority public preference to be informed in a scenario of poor prognosis. Policy clinical practice should facilitate elucidation and delivery of preferences. Evidence for effective communication skills‐building interventions for clinicians is required. Copyright © 2013 John Wiley & Sons, Ltd.

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