How far can we trust proxy respondents for patients receiving supportive and palliative care who are unable to consent to research? | BMJ Supportive & Palliative Care

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Article info

Abstract

Poster Presentations

7

How far can we trust proxy respondents for patients receiving supportive and palliative care who are unable to consent to research?

Free

Authors

Cara Bailey 1School of Nursing, Institute of Clinical Sciences, University of Birmingham, UK PubMed articles Google scholar articles
Philip Kinghorn 2Health Economics Unit, Institute of Applied Health Research, University of Birmingham, UK PubMed articles Google scholar articles
Rosanna Orlando 3NIHR CLAHRC Wessex Methodological Hub, University of Southampton, UK PubMed articles Google scholar articles
Kathy Armour 4Marie Curie Hospice West Midlands, UK PubMed articles Google scholar articles
Rachel Perry 4Marie Curie Hospice West Midlands, UK PubMed articles Google scholar articles
Louise Jones 5Marie Curie Palliative Care Research Department, UCL, UK PubMed articles Google scholar articles
Joanna Coast 6School of Social and Community Medicine, University of Bristol, UK PubMed articles Google scholar articles

Citation

Bailey C, Kinghorn P, Orlando R, et al

How far can we trust proxy respondents for patients receiving supportive and palliative care who are unable to consent to research?

BMJ Supportive & Palliative Care 2016;6:386.

Publication history

First published September 1, 2016.

Online issue publication

April 20, 2017

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