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The value of different aspects of person-centred care: a series of discrete choice experiments in people with long-term conditions

BMJ open, 2017-04, Vol.7 (4), p.e015689-e015689

2017

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Doctors' perspectives on PSA testing illuminate established differences in prostate cancer screening rates between Australia and the UK: a qualitative study

BMJ open, 2016-12, Vol.6 (12), p.e011932-e011932

2016

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Risk, Overdiagnosis and Ethical Justifications

Health care analysis, 2019-12, Vol.27 (4), p.231-248

2019

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Enhancing citizen engagement in cancer screening through deliberative democracy

JNCI : Journal of the National Cancer Institute, 2013-03, Vol.105 (6), p.380-386

2013

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Shared decision-making: enhancing the clinical relevance

Journal of the Royal Society of Medicine, 2012-10, Vol.105 (10), p.416-421

2012

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Primary goals, information-giving and men’s understanding: a qualitative study of Australian and UK doctors’ varied communication about PSA screening

BMJ open, 2018-01, Vol.8 (1), p.e018009-e018009

2018

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Speaking up about safety concerns: multi-setting qualitative study of patients' views and experiences

BMJ quality & safety, 2010-12, Vol.19 (6), p.e33-e33

2010

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Use of a Birth Plan within Woman-held Maternity Records: A Qualitative Study with Women and Staff in Northeast Scotland

Birth (Berkeley, Calif.), 2014-09, Vol.41 (3), p.283-289

2014

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The information and support needs of patients discharged after a short hospital stay for treatment of low-risk Community Acquired Pneumonia: implications for treatment without admission

BMC pulmonary medicine, 2008-07, Vol.8 (1), p.11-11, Article 11

2008

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How personal experiences feature in women’s accounts of use of information for decisions about antenatal diagnostic testing for foetal abnormality

Social science & medicine (1982), 2011-03, Vol.72 (5), p.755-762

2011

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A Capabilities Approach to Person-Centered Care: Response to Open Peer Commentaries on "Treating Patients as Persons: A Capabilities Approach to Support Delivery of Person-Centered Care"

American journal of bioethics, 2013-08, Vol.13 (8), p.W1-W4

2013

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Hurtful comments are harmful comments: respectful communication is not just an optional extra in healthcare

Health expectations : an international journal of public participation in health care and health policy, 2008-12, Vol.11 (4), p.319-320

Entwistle, Vikki A

2008

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The significance for decision-making of information that is not exchanged by patients and health professionals during consultations

Social science & medicine (1982), 2006-10, Vol.63 (8), p.2065-2078

2006

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Protocol for stage 2 of the GaP study (genetic testing acceptability for Paget's disease of bone): a questionnaire study to investigate whether relatives of people with Paget's disease would accept genetic testing and preventive treatment if they were available

BMC health services research, 2008-05, Vol.8 (1), p.116-116, Article 116

2008

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Advising Patients About Patient Safety: Current Initiatives Risk Shifting Responsibility

Joint Commission journal on quality and patient safety, 2005-09, Vol.31 (9), p.483-494

2005

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Enabling mutual helping? Examining variable needs for facilitated peer support

Patient education and counseling, 2011-11, Vol.85 (2), p.e120-e125

2011

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Enabling consultations: the facilitative significance of relational aspects of interpersonal communication

Health expectations : an international journal of public participation in health care and health policy, 2010-03, Vol.13 (1), p.1-3

Entwistle, Vikki A.

2010

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Involving service users in qualitative analysis: approaches and assessment

Health expectations : an international journal of public participation in health care and health policy, 2010-06, Vol.13 (2), p.111-112

Entwistle, Vikki A

2010

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Protocol for stage 1 of the GaP study (Genetic testing acceptability for Paget's disease of bone): an interview study about genetic testing and preventive treatment: would relatives of people with Paget's disease want testing and treatment if they were available?

BMC health services research, 2006-06, Vol.6 (1), p.71-71, Article 71

2006

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Philosophy, health services and research: the importance of keeping conversations open

Health expectations : an international journal of public participation in health care and health policy, 2011-06, Vol.14 (2), p.178-181

2011

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Lay perspectives: advantages for health research

BMJ, 1998-02, Vol.316 (7129), p.463-466

International edition, 1998

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Expectations, hopes and moral norms

Health expectations : an international journal of public participation in health care and health policy, 2009-12, Vol.12 (4), p.345-346

Entwistle, Vikki A

2009

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Provision of cancer information as a “support for navigating the knowledge landscape”: Findings from a critical interpretive literature synthesis

European journal of oncology nursing : the official journal of European Oncology Nursing Society, 2013-06, Vol.17 (3), p.360-369

2013

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When service users' support obscures problems with care: the need for rigorous research into patients' experiences

Health expectations : an international journal of public participation in health care and health policy, 2009-06, Vol.12 (2), p.117-119

Entwistle, Vikki A

2009

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The value of different aspects of person-centred care: a series of discrete choice experiments in people with long-term conditions

Doctors' perspectives on PSA testing illuminate established differences in prostate cancer screening rates between Australia and the UK: a qualitative study

Risk, Overdiagnosis and Ethical Justifications

Enhancing citizen engagement in cancer screening through deliberative democracy

Shared decision-making: enhancing the clinical relevance

Primary goals, information-giving and men’s understanding: a qualitative study of Australian and UK doctors’ varied communication about PSA screening

Speaking up about safety concerns: multi-setting qualitative study of patients' views and experiences

Use of a Birth Plan within Woman-held Maternity Records: A Qualitative Study with Women and Staff in Northeast Scotland

The information and support needs of patients discharged after a short hospital stay for treatment of low-risk Community Acquired Pneumonia: implications for treatment without admission

How personal experiences feature in women’s accounts of use of information for decisions about antenatal diagnostic testing for foetal abnormality

A Capabilities Approach to Person-Centered Care: Response to Open Peer Commentaries on "Treating Patients as Persons: A Capabilities Approach to Support Delivery of Person-Centered Care"

Hurtful comments are harmful comments: respectful communication is not just an optional extra in healthcare

The significance for decision-making of information that is not exchanged by patients and health professionals during consultations

Protocol for stage 2 of the GaP study (genetic testing acceptability for Paget's disease of bone): a questionnaire study to investigate whether relatives of people with Paget's disease would accept genetic testing and preventive treatment if they were available

Advising Patients About Patient Safety: Current Initiatives Risk Shifting Responsibility

Enabling mutual helping? Examining variable needs for facilitated peer support

Enabling consultations: the facilitative significance of relational aspects of interpersonal communication

Involving service users in qualitative analysis: approaches and assessment

Protocol for stage 1 of the GaP study (Genetic testing acceptability for Paget's disease of bone): an interview study about genetic testing and preventive treatment: would relatives of people with Paget's disease want testing and treatment if they were available?

Philosophy, health services and research: the importance of keeping conversations open

Lay perspectives: advantages for health research

Expectations, hopes and moral norms

Provision of cancer information as a “support for navigating the knowledge landscape”: Findings from a critical interpretive literature synthesis

When service users' support obscures problems with care: the need for rigorous research into patients' experiences

Training in communication of oncology clinicians: a position paper based on the third consensus meeting among European experts in 2018

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