Gavin Daker-White
Biographic Data
| ID | 3914783 |
|---|---|
| NAME | Gavin Daker-White |
| GIVEN NAMES | Gavin |
| FAMILY NAME | Daker-White |
| SIGNATURE | DAKER-WHITE G |
| VERIFIED | No |
| TOTAL WORKS | 9 |
| TOTAL CITATIONS | 147 |
| AUTHOR COUNT | 9 |
| EDITOR COUNT | 0 |
| FIRST PUBLICATION YEAR | 1997 |
| LATEST PUBLICATION YEAR | 2020 |
| H-INDEX | 3 |
Practitioners’ experiences of the mental capacity act: A systematic review
Patient safety in marginalised groups: A narrative scoping review
Not applicable for a scoping review
The care.data consensus? A qualitative analysis of opinions expressed on Twitter
Various concerns were raised about care.data that appeared to be shared by those both for and against the project. Qualitatively analysing tweets enabled us to identify a range of concerns about care.data and how these might be overcome, for example, by increasing the involvement of stakeholders and those with expert knowledge. Our findings also highlight the risks of not considering public opinion, such as the potential for patient safety failur…
Non-disclosure of chronic kidney disease in primary care and the limits of instrumental rationality in chronic illness self-management
Early detection of long term conditions is predicated on assumptions that lifestyle changes and medications can be used to reduce or manage the risk of condition progression. However, ambiguity remains about the nature and place of diagnostic disclosure to people in newly recognised or asymptomatic 'pre' conditions such as early stage chronic kidney disease (CKD). The disclosure of a diagnosis is relevant to instigating strategies which rely on a…
A Constellation of Misfortune: Narrative Accounts of Adverse Life Events, Chronic Illness, and Subjective Social Status
Quantitative studies have drawn attention to the patterning of health inequalities in relation to subjective social status (SSS). There is currently little insight into the complexities of the social and biographical aspects that lie behind these findings. Narrative accounts were gathered in a mixed-methods study involving a population of people with coronary heart disease (CHD) and/or diabetes in a region of the United Kingdom with above average…
Resisting medicines: A Synthesis of Qualitative Studies of Medicine Taking
How can they tell?' A qualitative study of the views of younger people about their dementia and dementia care services
There is growing interest in eliciting the views of younger people with dementia (i.e. those under 65 years of age) within health and social care research. The often erroneous view that these individuals are not capable of expressing their views and experiences has now been seriously challenged. The present paper draws on the findings from 14 qualitative in-depth interviews with younger people with dementia conducted in the South-west of England,…
Sexual function and quality of life in genitourinary medicine (GUM) outpatients and preliminary validation of a self-report questionnaire measure
Drug users' access to community-based services
Resisting medicines: A Synthesis of Qualitative Studies of Medicine Taking
How can they tell?' A qualitative study of the views of younger people about their dementia and dementia care services
There is growing interest in eliciting the views of younger people with dementia (i.e. those under 65 years of age) within health and social care research. The often erroneous view that these individuals are not capable of expressing their views and experiences has now been seriously challenged. The present paper draws on the findings from 14 qualitative in-depth interviews with younger people with dementia conducted in the South-west of England,…
A Constellation of Misfortune: Narrative Accounts of Adverse Life Events, Chronic Illness, and Subjective Social Status
Quantitative studies have drawn attention to the patterning of health inequalities in relation to subjective social status (SSS). There is currently little insight into the complexities of the social and biographical aspects that lie behind these findings. Narrative accounts were gathered in a mixed-methods study involving a population of people with coronary heart disease (CHD) and/or diabetes in a region of the United Kingdom with above average…
Drug users' access to community-based services
Non-disclosure of chronic kidney disease in primary care and the limits of instrumental rationality in chronic illness self-management
Early detection of long term conditions is predicated on assumptions that lifestyle changes and medications can be used to reduce or manage the risk of condition progression. However, ambiguity remains about the nature and place of diagnostic disclosure to people in newly recognised or asymptomatic 'pre' conditions such as early stage chronic kidney disease (CKD). The disclosure of a diagnosis is relevant to instigating strategies which rely on a…
Drug users' access to community-based services
Sexual function and quality of life in genitourinary medicine (GUM) outpatients and preliminary validation of a self-report questionnaire measure
How can they tell?' A qualitative study of the views of younger people about their dementia and dementia care services
There is growing interest in eliciting the views of younger people with dementia (i.e. those under 65 years of age) within health and social care research. The often erroneous view that these individuals are not capable of expressing their views and experiences has now been seriously challenged. The present paper draws on the findings from 14 qualitative in-depth interviews with younger people with dementia conducted in the South-west of England,…
Resisting medicines: A Synthesis of Qualitative Studies of Medicine Taking
A Constellation of Misfortune: Narrative Accounts of Adverse Life Events, Chronic Illness, and Subjective Social Status
Quantitative studies have drawn attention to the patterning of health inequalities in relation to subjective social status (SSS). There is currently little insight into the complexities of the social and biographical aspects that lie behind these findings. Narrative accounts were gathered in a mixed-methods study involving a population of people with coronary heart disease (CHD) and/or diabetes in a region of the United Kingdom with above average…
The care.data consensus? A qualitative analysis of opinions expressed on Twitter
Various concerns were raised about care.data that appeared to be shared by those both for and against the project. Qualitatively analysing tweets enabled us to identify a range of concerns about care.data and how these might be overcome, for example, by increasing the involvement of stakeholders and those with expert knowledge. Our findings also highlight the risks of not considering public opinion, such as the potential for patient safety failur…
Non-disclosure of chronic kidney disease in primary care and the limits of instrumental rationality in chronic illness self-management
Early detection of long term conditions is predicated on assumptions that lifestyle changes and medications can be used to reduce or manage the risk of condition progression. However, ambiguity remains about the nature and place of diagnostic disclosure to people in newly recognised or asymptomatic 'pre' conditions such as early stage chronic kidney disease (CKD). The disclosure of a diagnosis is relevant to instigating strategies which rely on a…
Practitioners’ experiences of the mental capacity act: A systematic review
Patient safety in marginalised groups: A narrative scoping review
Not applicable for a scoping review
Medicine (7 works) · Psychology (6 works) · Nursing (5 works) · Sociology (5 works) · Qualitative research (4 works) · Computer Science (3 works) · Family medicine (3 works) · Political science (3 works) · Public health (3 works) · Environmental health (2 works)