Lista de obras - Rosemary Frey - Dominio Público Uruguay

'Where do I go from here'? A cultural perspective on challenges to the use of hospice services

artículo científico publicado en 2013

A Place to Live and to Die: A Qualitative Exploration of the Social Practices and Rituals of Death in Residential Aged Care

artículo científico publicado en 2020

Advance care planning for Māori, Pacific and Asian people: the views of New Zealand healthcare professionals

artículo científico publicado en 2013

Approaches to capturing the financial cost of family care-giving within a palliative care context: a systematic review

artículo científico

Burnout matters: The impact on residential aged care staffs’ willingness to undertake formal palliative care training

scholarly article

Burnout, compassion fatigue and psychological capital: Findings from a survey of nurses delivering palliative care

article

Can we predict which hospitalised patients are in their last year of life? A prospective cross-sectional study of the Gold Standards Framework Prognostic Indicator Guidance as a screening tool in the acute hospital setting

artículo científico publicado en 2014

Care vs. care: ‘Biomedical’ and ‘holistic’ worldviews of palliative care

scholarly article

Circumstances of hospital admissions in palliative care: A cross-sectional survey of patients admitted to hospital with palliative care needs

artículo científico publicado en 2018

Clinical staff perceptions of palliative care-related quality of care, service access, education and training needs and delivery confidence in an acute hospital setting

artículo científico publicado en 2013

Comparison of the Adult Strabismus Quality of Life Questionnaire (AS-20) with the Amblyopia and Strabismus Questionnaire (ASQE) among adults with strabismus who seek medical care in China

artículo científico publicado en 2014

Complex contradictions in conceptualisations of 'dignity' in palliative care

artículo científico publicado en 2018

Development and application of the Chinese version of the adult strabismus quality of life questionnaire (AS-20): a cross-sectional study

artículo científico publicado en 2013

Distress in post-treatment hematological cancer survivors: Prevalence and predictors

artículo científico publicado en 2019

End of life care for long-term care residents with dementia, chronic illness and cancer: prospective staff survey

scientific article published on 22 May 2019

End of life care preferences among people of advanced age: LiLACS NZ

artículo científico publicado en 2017

Exploring the financial impact of caring for family members receiving palliative and end-of-life care: a systematic review of the literature

artículo científico publicado en 2013

Factors associated with overall satisfaction with care at the end-of-life: Caregiver voices in New Zealand

scientific article published on 21 June 2020

Family experiences of the transition to palliative care in aged residential care (ARC): a qualitative study

artículo científico publicado en 2017

Health equity and wellbeing among older people’s caregivers in New Zealand during COVID-19: Protocol for a qualitative study

Instruments used to measure the effectiveness of palliative care education initiatives at the undergraduate level: a critical literature review

artículo científico

Intersectionality and Critical Realism: A Philosophical Framework for Advancing Nursing Leadership

scientific article published on 1 October 2019

Maintaining psychosocial wellbeing for post-treatment haematological cancer survivors: Strategies and potential barriers

scientific article published on 27 November 2018

Necessary but not yet sufficient: a survey of aged residential care staff perceptions of palliative care communication, education and delivery

artículo científico publicado en 2016

Nurse manager and student nurse perceptions of the use of personal smartphones or tablets and the adjunct applications, as an educational tool in clinical settings

artículo científico publicado en 2017

PA12 Is digital storytelling ka pai for new zealand māori? using digital storytelling as a method to explore whānau end of life caregiving experiences: a pilot study

artículo científico publicado en 2015

Palliative care delivery in residential aged care: bereaved family member experiences of the Supportive Hospice Aged Residential Exchange (SHARE) intervention

artículo científico publicado en 2020

Palliative care need and management in the acute hospital setting: a census of one New Zealand Hospital

artículo científico publicado en 2013

Palliative care nurse specialists' reflections on a palliative care educational intervention in long-term care: an inductive content analysis

scientific article published on 19 November 2019

Palliative care presentations to emergency departments in a secondary and a sub-acute hospital: A one year incidence study

scholarly article

Palliative care study underway

scientific article published on 1 September 2016

Patient-centred care training needs of health care assistants who provide care for people with dementia

scientific article published on 6 February 2019

Predictors of patient-related benefit, burden and feeling safe in relation to hospital admissions in palliative care: A cross-sectional survey

artículo científico publicado en 2017

Provision of palliative and end-of-life care in New Zealand residential aged care facilities: general practitioners

scientific article published on 14 February 2020

Psychological support requirements of haematological cancer survivors: how can health professionals meet their needs?

artículo científico publicado en 2020

The Effect of Residential Aged Care Size, Ownership Model, and Multichain Affiliation on Resident Comfort and Symptom Management at the End of Life

artículo científico publicado en 2018

The Supportive Hospice and Aged Residential Exchange (SHARE) programme in New Zealand

artículo científico publicado en 2017

The Views of Informal Carers' Evaluation of Services (VOICES): Toward an adaptation for the New Zealand bicultural context

artículo científico publicado en 2016

The care manager’s dilemma: balancing human rights with risk management under the Intellectual Disability (Compulsory Care and Rehabilitation) Act 2003

scholarly article

The extent and cost of potentially avoidable admissions in hospital inpatients with palliative care needs: a cross-sectional study

artículo científico publicado en 2014

The nature and timing of distress among post-treatment haematological cancer survivors

artículo científico publicado en 2018

The nature of, and reasons for, 'inappropriate' hospitalisations among patients with palliative care needs: a qualitative exploration of the views of generalist palliative care providers

artículo científico publicado en 2013

What factors predict the confidence of palliative care delivery in long-term care staff? A mixed-methods study

artículo científico publicado en 2019

What indicators are measured by tools designed to address palliative care competence among ‘generalist’ palliative care providers? A critical literature review

article

What is the incidence of patients with palliative care needs presenting to the Emergency Department? a critical review

artículo científico publicado en 2014

What questionnaires exist to measure the perceived competence of generalists in palliative care provision? A critical literature review

artículo científico publicado en 2011

What's the diagnosis? Organisational culture and palliative care delivery in residential aged care in New Zealand

artículo científico publicado en 2015

Working bi-culturally within a palliative care research context: the development of the Te Ārai Palliative Care and End of Life Research Group

article

‘It's my pleasure?’: the views of palliative care patients about being asked to participate in research

scholarly article

Lista de obras de Rosemary Frey

'Where do I go from here'? A cultural perspective on challenges to the use of hospice services

A Place to Live and to Die: A Qualitative Exploration of the Social Practices and Rituals of Death in Residential Aged Care

Advance care planning for Māori, Pacific and Asian people: the views of New Zealand healthcare professionals

Approaches to capturing the financial cost of family care-giving within a palliative care context: a systematic review

Burnout matters: The impact on residential aged care staffs’ willingness to undertake formal palliative care training

Burnout, compassion fatigue and psychological capital: Findings from a survey of nurses delivering palliative care

Can we predict which hospitalised patients are in their last year of life? A prospective cross-sectional study of the Gold Standards Framework Prognostic Indicator Guidance as a screening tool in the acute hospital setting

Care vs. care: ‘Biomedical’ and ‘holistic’ worldviews of palliative care

Circumstances of hospital admissions in palliative care: A cross-sectional survey of patients admitted to hospital with palliative care needs

Clinical staff perceptions of palliative care-related quality of care, service access, education and training needs and delivery confidence in an acute hospital setting

Comparison of the Adult Strabismus Quality of Life Questionnaire (AS-20) with the Amblyopia and Strabismus Questionnaire (ASQE) among adults with strabismus who seek medical care in China

Complex contradictions in conceptualisations of 'dignity' in palliative care

Development and application of the Chinese version of the adult strabismus quality of life questionnaire (AS-20): a cross-sectional study

Distress in post-treatment hematological cancer survivors: Prevalence and predictors

End of life care for long-term care residents with dementia, chronic illness and cancer: prospective staff survey

End of life care preferences among people of advanced age: LiLACS NZ

Exploring the financial impact of caring for family members receiving palliative and end-of-life care: a systematic review of the literature

Factors associated with overall satisfaction with care at the end-of-life: Caregiver voices in New Zealand

Family experiences of the transition to palliative care in aged residential care (ARC): a qualitative study

Health equity and wellbeing among older people’s caregivers in New Zealand during COVID-19: Protocol for a qualitative study

Instruments used to measure the effectiveness of palliative care education initiatives at the undergraduate level: a critical literature review

Intersectionality and Critical Realism: A Philosophical Framework for Advancing Nursing Leadership

Maintaining psychosocial wellbeing for post-treatment haematological cancer survivors: Strategies and potential barriers

Necessary but not yet sufficient: a survey of aged residential care staff perceptions of palliative care communication, education and delivery

Nurse manager and student nurse perceptions of the use of personal smartphones or tablets and the adjunct applications, as an educational tool in clinical settings

PA12 Is digital storytelling ka pai for new zealand māori? using digital storytelling as a method to explore whānau end of life caregiving experiences: a pilot study

Palliative care delivery in residential aged care: bereaved family member experiences of the Supportive Hospice Aged Residential Exchange (SHARE) intervention

Palliative care need and management in the acute hospital setting: a census of one New Zealand Hospital

Palliative care nurse specialists' reflections on a palliative care educational intervention in long-term care: an inductive content analysis

Palliative care presentations to emergency departments in a secondary and a sub-acute hospital: A one year incidence study

Palliative care study underway

Patient-centred care training needs of health care assistants who provide care for people with dementia

Predictors of patient-related benefit, burden and feeling safe in relation to hospital admissions in palliative care: A cross-sectional survey

Provision of palliative and end-of-life care in New Zealand residential aged care facilities: general practitioners

Psychological support requirements of haematological cancer survivors: how can health professionals meet their needs?

The Effect of Residential Aged Care Size, Ownership Model, and Multichain Affiliation on Resident Comfort and Symptom Management at the End of Life

The Supportive Hospice and Aged Residential Exchange (SHARE) programme in New Zealand

The Views of Informal Carers' Evaluation of Services (VOICES): Toward an adaptation for the New Zealand bicultural context

The care manager’s dilemma: balancing human rights with risk management under the Intellectual Disability (Compulsory Care and Rehabilitation) Act 2003

The extent and cost of potentially avoidable admissions in hospital inpatients with palliative care needs: a cross-sectional study

The nature and timing of distress among post-treatment haematological cancer survivors

The nature of, and reasons for, 'inappropriate' hospitalisations among patients with palliative care needs: a qualitative exploration of the views of generalist palliative care providers

What factors predict the confidence of palliative care delivery in long-term care staff? A mixed-methods study

What indicators are measured by tools designed to address palliative care competence among ‘generalist’ palliative care providers? A critical literature review

What is the incidence of patients with palliative care needs presenting to the Emergency Department? a critical review

What questionnaires exist to measure the perceived competence of generalists in palliative care provision? A critical literature review

What's the diagnosis? Organisational culture and palliative care delivery in residential aged care in New Zealand

Working bi-culturally within a palliative care research context: the development of the Te Ārai Palliative Care and End of Life Research Group

‘It's my pleasure?’: the views of palliative care patients about being asked to participate in research