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Patsy Yates

Biographic Data

ID182622
NAMEPatsy Yates
GIVEN NAMESPatsy
FAMILY NAMEYates
SIGNATUREYATES P
AFFILIATIONSQueensland University of Technology
ORCID0000-0001-8946-8504
VERIFIEDYes
TOTAL WORKS15
TOTAL CITATIONS50
AUTHOR COUNT15
EDITOR COUNT0
FIRST PUBLICATION YEAR1993
LATEST PUBLICATION YEAR2024
H-INDEX4
  • Managing understandings of palliative care as more than care immediately before death: Evidence from observational analysis of consultations

    Open Access•Holly Sansone, Ekberg et al.•ARTICLE•Health Expectations•2024

    BACKGROUND: Evidence suggests that public, and some professional, understandings of palliative care are limited to care provided immediately before death, which contrasts palliative care's scope as care provided across a range of illness stages. OBJECTIVE: To examine how clinicians manage patients' understandings of palliative care during initial consultations. DESIGN: Initial palliative care consultations were video-recorded and analysed using c…

  • Australian Indigenous people and treatment decision-making at end-of-life

    Open Access•Penny Neller, Rachel Feeney et al.•ARTICLE•Alternative Law Journal•2024•References: 1

    This article analyses Australian law and literature to identify the key cultural and legal considerations that can arise in medical treatment decision-making with Aboriginal and Torres Strait Islander peoples at the end-of-life. The authors explore how First Nation peoples’ cultural values, connection to Country, family, and community, history, and health care experiences, intersect with end-of-life medical treatment laws, providing valuable insi…

  • A Discourse of Deviance: Blame, Shame, Stigma and the Social Construction of Head and Neck Cancer

    Open Access•Carla Thamm, Alexandra L Mccarthy et al.•ARTICLE•Qualitative Health Research•2024•Cited by: 1•References: 62

    Cancer of the head and neck is a confronting condition, as the disease and its treatments alter the appearance and function of body organs associated with physical appearance and identity. Many of the risk factors for head and neck cancers, including tobacco, alcohol, and human papilloma virus, can also have significant negative social and moral permutations. Language and action (discourse) plays an important role in constructing disease and illn…

  • Work-related experiences of prostate cancer survivors in Australia: A qualitative study

    Open Access•Wei-Hong Liu, Weihong Liu et al.•ARTICLE•BMC Public Health•2023

    PCa and its treatment substantially and persistently impacted men's working lives, and their experiences were diverse and multifaceted. Self-employed and long-term PCa survivors face greater challenges and are at high risk of poor work outcomes. A systematic approach and involvement of stakeholders at all levels is required to support ongoing work participation

  • Medical practitioners' views and experiences of being involved in assisted dying in Victoria, Australia: A qualitative interview study among participating doctors

    Open Access•Marcus Sellars, Ben P White et al.•ARTICLE•Social Science & Medicine•2022•Cited by: 8•References: 23

  • Attending to child agency in paediatric palliative care consultations: Adults' use of tag questions directed to the child

    Open Access•Katie Ekberg, Ekberg et al.•ARTICLE•Sociology of Health & Illness•2022•Cited by: 5•References: 10

    Children's agency in their own lives is increasingly recognised as important, including within paediatric health care. The issue of acknowledging child agency is complex in the context of paediatric palliative care, where children have serious and complex conditions that often impact their ability to verbally communicate with others. This study explores how clinicians and parents/guardians direct talk towards a child patient when they are present…

  • Integrating Patient Reported Outcomes with digital solutions to empower children and families to self-manage complex health conditions

    Open Access•Natalie Bradford, Christine Cashion et al.•ARTICLE•International Journal of…•2021

    The International Journal of Integrated Care (IJIC) is an online, open-access, peer-reviewed scientific journal that publishes original articles in the field of integrated care on a continuous basis.IJIC has an Impact Factor of 5.120 (2020 JCR, received in June 2021)The IJIC 20th Anniversary Issue was published in 2021

  • Cancer survivorship care and general practice: A qualitative study of roles of general practice team members in Australia

    Open Access•Jennifer Fox, Carla Thamm et al.•ARTICLE•Health & Social Care in the…•2021•References: 2

    Primary care providers, including general practice teams (GPTs), are well positioned within the community to integrate cancer survivorship care into ongoing health management. However, roles of GPT members in delivery of cancer survivorship care have not been explored. The purpose of this study is to explore these roles from the perspectives of General Practitioners (GPs), Practice Nurses (PNs) and Practice Managers (PMs). An interpretive qualita…

  • Centralizing Temporality in Adolescent and Young Adult Cancer Survivorship

    Open Access•Danielle Tindle, Carol Windsor et al.•ARTICLE•Qualitative Health Research•2019•Cited by: 4•References: 25

    Drawing on Gadamer's hermeneutic philosophy, this article presents a key outcome of broader research into the phenomenon of adolescent and young adult cancer survivorship. Data were generated through semi-structured interviews with 45 participants from Australia, England, and the United States. The participants received a cancer diagnosis between the ages of 15 and 29 years and were aged 18 to 40 years at the time of interview. The key analytical…

  • Phenotypic and molecular characteristics associated with various domains of quality of life in oncology patients and their family caregivers

    Open Access•Kimberly Alexander, Kimberly E Alexander et al.•ARTICLE•Quality of Life Research•2016

  • On resilience and acceptance in the transition to palliative care at the end of life

    Open Access•John I Macartney, John Macartney et al.•ARTICLE•Health An Interdisciplinary…•2015•Cited by: 4•References: 44

    Specialist palliative care is a prominent and expanding site of health service delivery, providing highly specialised care to people at the end of life. Its focus on the delivery of specialised life-enhancing care stands in contrast to biomedicine's general tendency towards life-prolonging intervention. This philosophical departure from curative or life-prolonging care means that transitioning patients can be problematic, with recent work suggest…

  • Negotiating Futility, Managing Emotions: Nursing the Transition to Palliative Care

    Open Access•Alex Broom, Nicole Cort et al.•ARTICLE•Qualitative Health Research•2015•Cited by: 10•References: 40

    Nurses play a pivotal role in caring for patients during the transition from life-prolonging care to palliative care. This is an area of nursing prone to emotional difficulty, interpersonal complexity, and interprofessional conflict. It is situated within complex social dynamics, including those related to establishing and accepting futility and reconciling the desire to maintain hope. Here, drawing on interviews with 20 Australian nurses, we unp…

  • Engineering the fitness of older patients for chemotherapy: An exploration of Comprehensive Geriatric Assessment in practice

    Open Access•Alexandra L Mccarthy, Peta S Cook et al.•ARTICLE•Health An Interdisciplinary…•2014•Cited by: 1•References: 25

    Clinicians often report that currently available methods to assess older patients, including standard clinical consultations, do not elicit the information necessary to make an appropriate cancer treatment recommendation for older cancer patients. An increasingly popular way of assessing the potential of older patients to cope with chemotherapy is a Comprehensive Geriatric Assessment. What constitutes Comprehensive Geriatric Assessment, however, …

  • Health promotion in palliative care: The case for conceptual congruence

    Open Access•John Rosenberg, J P Rosenberg et al.•ARTICLE•Critical Public Health•2010

    This article provides a critical review of the literature relevant to the conceptual foundations of health promoting palliative care. It explores the separate emergence and evolution of palliative care and health promotion as distinct concerns in health care, and reviews the early considerations given to their potential convergence. Finally, this article examines the proposal of health promoting palliative care as a specific approach to providing…

  • Patients with terminal cancer who use alternative therapies: Their Beliefs and Practices

    Open Access•Patsy Yates, Patsy M Yates et al.•ARTICLE•Sociology of Health & Illness•1993•Cited by: 17•References: 1

    This paper examines the extent to which patients who have been diagnosed as having terminal cancer choose to use non-medical therapies. In particular it is concerned with the illness behaviour of patients who are receiving conventional cytotoxic drug and radiation treatments, who also decide to use a wide range of 'alternative' medications and therapies. The paper discusses the findings of a study of 152 patients with metastatic cancer that exami…

  • Patients with terminal cancer who use alternative therapies: Their Beliefs and Practices

    Open Access•Patsy Yates, Patsy M Yates et al.•ARTICLE•Sociology of Health & Illness•1993•Cited by: 17•References: 1

    This paper examines the extent to which patients who have been diagnosed as having terminal cancer choose to use non-medical therapies. In particular it is concerned with the illness behaviour of patients who are receiving conventional cytotoxic drug and radiation treatments, who also decide to use a wide range of 'alternative' medications and therapies. The paper discusses the findings of a study of 152 patients with metastatic cancer that exami…

  • Negotiating Futility, Managing Emotions: Nursing the Transition to Palliative Care

    Open Access•Alex Broom, Nicole Cort et al.•ARTICLE•Qualitative Health Research•2015•Cited by: 10•References: 40

    Nurses play a pivotal role in caring for patients during the transition from life-prolonging care to palliative care. This is an area of nursing prone to emotional difficulty, interpersonal complexity, and interprofessional conflict. It is situated within complex social dynamics, including those related to establishing and accepting futility and reconciling the desire to maintain hope. Here, drawing on interviews with 20 Australian nurses, we unp…

  • Medical practitioners' views and experiences of being involved in assisted dying in Victoria, Australia: A qualitative interview study among participating doctors

    Open Access•Marcus Sellars, Ben P White et al.•ARTICLE•Social Science & Medicine•2022•Cited by: 8•References: 23

  • Attending to child agency in paediatric palliative care consultations: Adults' use of tag questions directed to the child

    Open Access•Katie Ekberg, Ekberg et al.•ARTICLE•Sociology of Health & Illness•2022•Cited by: 5•References: 10

    Children's agency in their own lives is increasingly recognised as important, including within paediatric health care. The issue of acknowledging child agency is complex in the context of paediatric palliative care, where children have serious and complex conditions that often impact their ability to verbally communicate with others. This study explores how clinicians and parents/guardians direct talk towards a child patient when they are present…

  • Centralizing Temporality in Adolescent and Young Adult Cancer Survivorship

    Open Access•Danielle Tindle, Carol Windsor et al.•ARTICLE•Qualitative Health Research•2019•Cited by: 4•References: 25

    Drawing on Gadamer's hermeneutic philosophy, this article presents a key outcome of broader research into the phenomenon of adolescent and young adult cancer survivorship. Data were generated through semi-structured interviews with 45 participants from Australia, England, and the United States. The participants received a cancer diagnosis between the ages of 15 and 29 years and were aged 18 to 40 years at the time of interview. The key analytical…

  • On resilience and acceptance in the transition to palliative care at the end of life

    Open Access•John I Macartney, John Macartney et al.•ARTICLE•Health An Interdisciplinary…•2015•Cited by: 4•References: 44

    Specialist palliative care is a prominent and expanding site of health service delivery, providing highly specialised care to people at the end of life. Its focus on the delivery of specialised life-enhancing care stands in contrast to biomedicine's general tendency towards life-prolonging intervention. This philosophical departure from curative or life-prolonging care means that transitioning patients can be problematic, with recent work suggest…

  • A Discourse of Deviance: Blame, Shame, Stigma and the Social Construction of Head and Neck Cancer

    Open Access•Carla Thamm, Alexandra L Mccarthy et al.•ARTICLE•Qualitative Health Research•2024•Cited by: 1•References: 62

    Cancer of the head and neck is a confronting condition, as the disease and its treatments alter the appearance and function of body organs associated with physical appearance and identity. Many of the risk factors for head and neck cancers, including tobacco, alcohol, and human papilloma virus, can also have significant negative social and moral permutations. Language and action (discourse) plays an important role in constructing disease and illn…

  • Engineering the fitness of older patients for chemotherapy: An exploration of Comprehensive Geriatric Assessment in practice

    Open Access•Alexandra L Mccarthy, Peta S Cook et al.•ARTICLE•Health An Interdisciplinary…•2014•Cited by: 1•References: 25

    Clinicians often report that currently available methods to assess older patients, including standard clinical consultations, do not elicit the information necessary to make an appropriate cancer treatment recommendation for older cancer patients. An increasingly popular way of assessing the potential of older patients to cope with chemotherapy is a Comprehensive Geriatric Assessment. What constitutes Comprehensive Geriatric Assessment, however, …

  • Patients with terminal cancer who use alternative therapies: Their Beliefs and Practices

    Open Access•Patsy Yates, Patsy M Yates et al.•ARTICLE•Sociology of Health & Illness•1993•Cited by: 17•References: 1

    This paper examines the extent to which patients who have been diagnosed as having terminal cancer choose to use non-medical therapies. In particular it is concerned with the illness behaviour of patients who are receiving conventional cytotoxic drug and radiation treatments, who also decide to use a wide range of 'alternative' medications and therapies. The paper discusses the findings of a study of 152 patients with metastatic cancer that exami…

  • Health promotion in palliative care: The case for conceptual congruence

    Open Access•John Rosenberg, J P Rosenberg et al.•ARTICLE•Critical Public Health•2010

    This article provides a critical review of the literature relevant to the conceptual foundations of health promoting palliative care. It explores the separate emergence and evolution of palliative care and health promotion as distinct concerns in health care, and reviews the early considerations given to their potential convergence. Finally, this article examines the proposal of health promoting palliative care as a specific approach to providing…

  • Engineering the fitness of older patients for chemotherapy: An exploration of Comprehensive Geriatric Assessment in practice

    Open Access•Alexandra L Mccarthy, Peta S Cook et al.•ARTICLE•Health An Interdisciplinary…•2014•Cited by: 1•References: 25

    Clinicians often report that currently available methods to assess older patients, including standard clinical consultations, do not elicit the information necessary to make an appropriate cancer treatment recommendation for older cancer patients. An increasingly popular way of assessing the potential of older patients to cope with chemotherapy is a Comprehensive Geriatric Assessment. What constitutes Comprehensive Geriatric Assessment, however, …

  • On resilience and acceptance in the transition to palliative care at the end of life

    Open Access•John I Macartney, John Macartney et al.•ARTICLE•Health An Interdisciplinary…•2015•Cited by: 4•References: 44

    Specialist palliative care is a prominent and expanding site of health service delivery, providing highly specialised care to people at the end of life. Its focus on the delivery of specialised life-enhancing care stands in contrast to biomedicine's general tendency towards life-prolonging intervention. This philosophical departure from curative or life-prolonging care means that transitioning patients can be problematic, with recent work suggest…

  • Negotiating Futility, Managing Emotions: Nursing the Transition to Palliative Care

    Open Access•Alex Broom, Nicole Cort et al.•ARTICLE•Qualitative Health Research•2015•Cited by: 10•References: 40

    Nurses play a pivotal role in caring for patients during the transition from life-prolonging care to palliative care. This is an area of nursing prone to emotional difficulty, interpersonal complexity, and interprofessional conflict. It is situated within complex social dynamics, including those related to establishing and accepting futility and reconciling the desire to maintain hope. Here, drawing on interviews with 20 Australian nurses, we unp…

  • Phenotypic and molecular characteristics associated with various domains of quality of life in oncology patients and their family caregivers

    Open Access•Kimberly Alexander, Kimberly E Alexander et al.•ARTICLE•Quality of Life Research•2016

  • Centralizing Temporality in Adolescent and Young Adult Cancer Survivorship

    Open Access•Danielle Tindle, Carol Windsor et al.•ARTICLE•Qualitative Health Research•2019•Cited by: 4•References: 25

    Drawing on Gadamer's hermeneutic philosophy, this article presents a key outcome of broader research into the phenomenon of adolescent and young adult cancer survivorship. Data were generated through semi-structured interviews with 45 participants from Australia, England, and the United States. The participants received a cancer diagnosis between the ages of 15 and 29 years and were aged 18 to 40 years at the time of interview. The key analytical…

  • Integrating Patient Reported Outcomes with digital solutions to empower children and families to self-manage complex health conditions

    Open Access•Natalie Bradford, Christine Cashion et al.•ARTICLE•International Journal of…•2021

    The International Journal of Integrated Care (IJIC) is an online, open-access, peer-reviewed scientific journal that publishes original articles in the field of integrated care on a continuous basis.IJIC has an Impact Factor of 5.120 (2020 JCR, received in June 2021)The IJIC 20th Anniversary Issue was published in 2021

  • Cancer survivorship care and general practice: A qualitative study of roles of general practice team members in Australia

    Open Access•Jennifer Fox, Carla Thamm et al.•ARTICLE•Health & Social Care in the…•2021•References: 2

    Primary care providers, including general practice teams (GPTs), are well positioned within the community to integrate cancer survivorship care into ongoing health management. However, roles of GPT members in delivery of cancer survivorship care have not been explored. The purpose of this study is to explore these roles from the perspectives of General Practitioners (GPs), Practice Nurses (PNs) and Practice Managers (PMs). An interpretive qualita…

  • Medical practitioners' views and experiences of being involved in assisted dying in Victoria, Australia: A qualitative interview study among participating doctors

    Open Access•Marcus Sellars, Ben P White et al.•ARTICLE•Social Science & Medicine•2022•Cited by: 8•References: 23

  • Attending to child agency in paediatric palliative care consultations: Adults' use of tag questions directed to the child

    Open Access•Katie Ekberg, Ekberg et al.•ARTICLE•Sociology of Health & Illness•2022•Cited by: 5•References: 10

    Children's agency in their own lives is increasingly recognised as important, including within paediatric health care. The issue of acknowledging child agency is complex in the context of paediatric palliative care, where children have serious and complex conditions that often impact their ability to verbally communicate with others. This study explores how clinicians and parents/guardians direct talk towards a child patient when they are present…

  • Work-related experiences of prostate cancer survivors in Australia: A qualitative study

    Open Access•Wei-Hong Liu, Weihong Liu et al.•ARTICLE•BMC Public Health•2023

    PCa and its treatment substantially and persistently impacted men's working lives, and their experiences were diverse and multifaceted. Self-employed and long-term PCa survivors face greater challenges and are at high risk of poor work outcomes. A systematic approach and involvement of stakeholders at all levels is required to support ongoing work participation

  • Managing understandings of palliative care as more than care immediately before death: Evidence from observational analysis of consultations

    Open Access•Holly Sansone, Ekberg et al.•ARTICLE•Health Expectations•2024

    BACKGROUND: Evidence suggests that public, and some professional, understandings of palliative care are limited to care provided immediately before death, which contrasts palliative care's scope as care provided across a range of illness stages. OBJECTIVE: To examine how clinicians manage patients' understandings of palliative care during initial consultations. DESIGN: Initial palliative care consultations were video-recorded and analysed using c…

  • Australian Indigenous people and treatment decision-making at end-of-life

    Open Access•Penny Neller, Rachel Feeney et al.•ARTICLE•Alternative Law Journal•2024•References: 1

    This article analyses Australian law and literature to identify the key cultural and legal considerations that can arise in medical treatment decision-making with Aboriginal and Torres Strait Islander peoples at the end-of-life. The authors explore how First Nation peoples’ cultural values, connection to Country, family, and community, history, and health care experiences, intersect with end-of-life medical treatment laws, providing valuable insi…

  • A Discourse of Deviance: Blame, Shame, Stigma and the Social Construction of Head and Neck Cancer

    Open Access•Carla Thamm, Alexandra L Mccarthy et al.•ARTICLE•Qualitative Health Research•2024•Cited by: 1•References: 62

    Cancer of the head and neck is a confronting condition, as the disease and its treatments alter the appearance and function of body organs associated with physical appearance and identity. Many of the risk factors for head and neck cancers, including tobacco, alcohol, and human papilloma virus, can also have significant negative social and moral permutations. Language and action (discourse) plays an important role in constructing disease and illn…

Medicine (14 works) · Nursing (10 works) · Psychology (10 works) · Palliative Care and End-of-Life Issues (8 works) · Sociology (8 works) · Family medicine (5 works) · Grief, Bereavement, and Mental Health (5 works) · Palliative care (5 works) · Social Psychology (5 works) · Cancer (4 works)

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