Eleanor Wilson
Datos Biográficos
| ID | 3582657 |
|---|---|
| NOMBRE | Eleanor Wilson |
| NOMBRES | Eleanor |
| APELLIDO | Wilson |
| FIRMA | WILSON E |
| AFILIACIONES | University of Nottingham |
| ORCID | 0000-0003-0419-5901 |
| VERIFICADO | Sí |
| TOTAL DE OBRAS | 12 |
| TOTAL DE CITAS | 13 |
| TOTAL COMO AUTOR | 12 |
| TOTAL COMO EDITOR | 0 |
| PRIMER AÑO DE PUBLICACIÓN | 2007 |
| AÑO MÁS RECIENTE DE PUBLICACIÓN | 2025 |
| ÍNDICE H | 3 |
Deus Ex Machina
Noninvasive advanced respiratory support (NARS) is widely used in acute respiratory failure, including at the end of life, where its use is ethically and emotionally fraught. This ethnographic study examines how decisions to initiate, sustain or withdraw NARS are negotiated within the institutional and moral complexities of a UK hospital. Drawing on fieldwork including nonparticipant observation, reflective fieldnotes and composite narratives, th…
Talking about death and dying
Talking about death and dying is promoted in UK health policy and practice, from a perception that to do so encourages people to plan for their end of life and so increase their likelihood of experiencing a good death. This encouragement occurs alongside a belief that members of the public are reluctant to talk about death, although surveys suggest this is not the case. This paper describes findings from a research study in which people participa…
Beyond the Reach of Palliative Care
The demands and costs of health care resulting from increasingly ageing populations have become a major public health issue in the United Kingdom and other industrially developed nations. Concern with cost containment and shortage of resources has prompted a progressive shift in responsibility from state provision of care to individual patients and their families, and from the institutional setting of the hospital to the domestic home. Under the …
The impact of home mechanical ventilation on the time and manner of death for those with Motor neurone disease (MND)
Expanding Qualitative Interviewing for Studies Involving Adults With Different Communication Needs
This article explores the challenges and adaptations we undertook to engage people with different communication needs, specifically those living with motor neurone disease (MND), in qualitative research interviews. While interviewing those in advanced stages of illness has raised ethical concerns, participants continue to report value in contributing to research. We reflect on our experiences of conducting qualitative interviews with people livin…
Impact of the Covid-19 Pandemic on the PrEP Cascade at Two Veterans Affairs Healthcare Systems
The ideal and the real
Home has become established as the preferred place of death within health policy and practice in the UK and internationally. However, growing awareness of the structured inequalities underpinning end-of-life care and the challenges for family members undertaking care at home raise questions about the nature of patient and public preferences and priorities regarding place of death and the feasibility of home management of the complex care needs at…
Factors associated with receipt of a timely infant birth dose of hepatitis B vaccine at a tertiary hospital in North-Central Nigeria
The World Health Organization recommends universal vaccination of medically stable infants with Hepatitis B vaccine within 24 hours of birth to prevent mother-to-child transmission of Hepatitis B virus (HBV) infection. However, the proportion of infants who receive a timely birth dose is extremely low in Nigeria. We reviewed the implementation of an infant HBV vaccine schedule at a single center and identified factors affecting the receipt of a t…
It’s Not Like in the Films’
This paper explores how people enact and experience the deathbed vigil when someone close to them is dying. It draws on qualitative interviews with 34 bereaved people carried out as part of a wider study exploring public perceptions of death and dying. Participants were aware of the expectation that they would attend the deathbed and did their best to do so. Findings are reported using four themes: gathering, enacting the deathbed vigil, experien…
The Oxford handbook of ethics at the end of life
This is a generally well written book that groups the chapters nicely into four sections.Section one focuses on clinical and legal issues, section two on the theoretical, cultural and psychosocial aspects while section three deals more specifically with physician-assisted death and section four the emergence of palliative care and the hospice movement.This book provides a varied and interesting compilation of chapters combining the ethical and hi…
Exploring patients' experience of receiving information about cancer
Patient information is widely regarded both as a resource and an entitlement: a means of 'empowering' patients to behave as 'consumers' of health care. Patient 'satisfaction' has come to be regarded as an important outcome of care. This article presents qualitative interview data regarding the experience of patient information provision and the results of a self-completed Information Satisfaction Questionnaire (ISQ) among patients and relatives a…
Evaluating the impact of a cancer supportive care project in the community
Advances in cancer care and treatment have created a new and somewhat anomalous category of patients with a diagnosis of non-curative disease who still have a considerable period of life remaining. During much of this time they may remain relatively well, without manifest need for clinical care. The responses of patients to this challenging situation are largely unknown. However, it has been assumed that because they confront a difficult experien…
Beyond the Reach of Palliative Care
The demands and costs of health care resulting from increasingly ageing populations have become a major public health issue in the United Kingdom and other industrially developed nations. Concern with cost containment and shortage of resources has prompted a progressive shift in responsibility from state provision of care to individual patients and their families, and from the institutional setting of the hospital to the domestic home. Under the …
Expanding Qualitative Interviewing for Studies Involving Adults With Different Communication Needs
This article explores the challenges and adaptations we undertook to engage people with different communication needs, specifically those living with motor neurone disease (MND), in qualitative research interviews. While interviewing those in advanced stages of illness has raised ethical concerns, participants continue to report value in contributing to research. We reflect on our experiences of conducting qualitative interviews with people livin…
The ideal and the real
Home has become established as the preferred place of death within health policy and practice in the UK and internationally. However, growing awareness of the structured inequalities underpinning end-of-life care and the challenges for family members undertaking care at home raise questions about the nature of patient and public preferences and priorities regarding place of death and the feasibility of home management of the complex care needs at…
Exploring patients' experience of receiving information about cancer
Patient information is widely regarded both as a resource and an entitlement: a means of 'empowering' patients to behave as 'consumers' of health care. Patient 'satisfaction' has come to be regarded as an important outcome of care. This article presents qualitative interview data regarding the experience of patient information provision and the results of a self-completed Information Satisfaction Questionnaire (ISQ) among patients and relatives a…
The impact of home mechanical ventilation on the time and manner of death for those with Motor neurone disease (MND)
Evaluating the impact of a cancer supportive care project in the community
Advances in cancer care and treatment have created a new and somewhat anomalous category of patients with a diagnosis of non-curative disease who still have a considerable period of life remaining. During much of this time they may remain relatively well, without manifest need for clinical care. The responses of patients to this challenging situation are largely unknown. However, it has been assumed that because they confront a difficult experien…
Exploring patients' experience of receiving information about cancer
Patient information is widely regarded both as a resource and an entitlement: a means of 'empowering' patients to behave as 'consumers' of health care. Patient 'satisfaction' has come to be regarded as an important outcome of care. This article presents qualitative interview data regarding the experience of patient information provision and the results of a self-completed Information Satisfaction Questionnaire (ISQ) among patients and relatives a…
The Oxford handbook of ethics at the end of life
This is a generally well written book that groups the chapters nicely into four sections.Section one focuses on clinical and legal issues, section two on the theoretical, cultural and psychosocial aspects while section three deals more specifically with physician-assisted death and section four the emergence of palliative care and the hospice movement.This book provides a varied and interesting compilation of chapters combining the ethical and hi…
Factors associated with receipt of a timely infant birth dose of hepatitis B vaccine at a tertiary hospital in North-Central Nigeria
The World Health Organization recommends universal vaccination of medically stable infants with Hepatitis B vaccine within 24 hours of birth to prevent mother-to-child transmission of Hepatitis B virus (HBV) infection. However, the proportion of infants who receive a timely birth dose is extremely low in Nigeria. We reviewed the implementation of an infant HBV vaccine schedule at a single center and identified factors affecting the receipt of a t…
It’s Not Like in the Films’
This paper explores how people enact and experience the deathbed vigil when someone close to them is dying. It draws on qualitative interviews with 34 bereaved people carried out as part of a wider study exploring public perceptions of death and dying. Participants were aware of the expectation that they would attend the deathbed and did their best to do so. Findings are reported using four themes: gathering, enacting the deathbed vigil, experien…
Impact of the Covid-19 Pandemic on the PrEP Cascade at Two Veterans Affairs Healthcare Systems
The ideal and the real
Home has become established as the preferred place of death within health policy and practice in the UK and internationally. However, growing awareness of the structured inequalities underpinning end-of-life care and the challenges for family members undertaking care at home raise questions about the nature of patient and public preferences and priorities regarding place of death and the feasibility of home management of the complex care needs at…
Talking about death and dying
Talking about death and dying is promoted in UK health policy and practice, from a perception that to do so encourages people to plan for their end of life and so increase their likelihood of experiencing a good death. This encouragement occurs alongside a belief that members of the public are reluctant to talk about death, although surveys suggest this is not the case. This paper describes findings from a research study in which people participa…
Beyond the Reach of Palliative Care
The demands and costs of health care resulting from increasingly ageing populations have become a major public health issue in the United Kingdom and other industrially developed nations. Concern with cost containment and shortage of resources has prompted a progressive shift in responsibility from state provision of care to individual patients and their families, and from the institutional setting of the hospital to the domestic home. Under the …
The impact of home mechanical ventilation on the time and manner of death for those with Motor neurone disease (MND)
Expanding Qualitative Interviewing for Studies Involving Adults With Different Communication Needs
This article explores the challenges and adaptations we undertook to engage people with different communication needs, specifically those living with motor neurone disease (MND), in qualitative research interviews. While interviewing those in advanced stages of illness has raised ethical concerns, participants continue to report value in contributing to research. We reflect on our experiences of conducting qualitative interviews with people livin…
Deus Ex Machina
Noninvasive advanced respiratory support (NARS) is widely used in acute respiratory failure, including at the end of life, where its use is ethically and emotionally fraught. This ethnographic study examines how decisions to initiate, sustain or withdraw NARS are negotiated within the institutional and moral complexities of a UK hospital. Drawing on fieldwork including nonparticipant observation, reflective fieldnotes and composite narratives, th…
Medicine (9 obras) · Palliative Care and End-of-Life Issues (8 obras) · Psychology (7 obras) · Nursing (6 obras) · Grief, Bereavement, and Mental Health (5 obras) · Qualitative research (5 obras) · Sociology (5 obras) · Public health (4 obras) · Family and Patient Care in Intensive Care Units (3 obras) · Health care (3 obras)