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Bereavement support for family caregivers: The gap between guidelines and practice in palliative care

PloS one, 2017-10, Vol.12 (10), p.e0184750-e0184750

2017

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Who needs bereavement support? A population based survey of bereavement risk and support need

PloS one, 2015-03, Vol.10 (3), p.e0121101-e0121101

2015

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The impact of the carer support needs assessment tool (CSNAT) in community palliative care using a stepped wedge cluster trial

PloS one, 2015-04, Vol.10 (4), p.e0123012-e0123012

2015

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Supporting the dying is a community responsibility

Palliative care and social practice, 2022-01, Vol.16, p.263235242211024-26323524221102468

M Aoun, Samar

2022

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Exploring the Support Needs of Family Caregivers of Patients with Brain Cancer Using the CSNAT: A Comparative Study with Other Cancer Groups

PloS one, 2015-12, Vol.10 (12), p.e0145106-e0145106

2015

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A scoping review of bereavement risk assessment measures: Implications for palliative care

Palliative Medicine, 2015-07, Vol.29 (7), p.577-589

2015

Volltextzugriff (PDF)

Matching response to need: What makes social networks fit for providing bereavement support?

PloS one, 2019-03, Vol.14 (3), p.e0213367-e0213367

2019

Volltextzugriff (PDF)

Family Caregivers’ Preparations for Death: A Qualitative Analysis

Journal of pain and symptom management, 2018-06, Vol.55 (6), p.1473-1479

2018

Volltextzugriff (PDF)

Improving the Evidence Base in Palliative Care to Inform Practice and Policy: Thinking Outside the Box

Journal of pain and symptom management, 2014-12, Vol.48 (6), p.1222-1235

2014

Volltextzugriff (PDF)

Predictors of Complicated Grief: A Systematic Review of Empirical Studies

Death studies, 2010-09, Vol.34 (8), p.673-698

2010

Volltextzugriff (PDF)

Palliative and End-of-Life Care Service Models: To What Extent Are Consumer Perspectives Considered?

Healthcare (Basel), 2021-09, Vol.9 (10), p.1286

2021

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The Evolving Landscape: Funerals, Cemeteries, Memorialization, and Bereavement Support

Omega: Journal of Death and Dying, 2021-12, Vol.84 (2), p.596-616

2021

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Caregivers' experiences of a home support program after the hospital discharge of an older family member: a qualitative analysis

BMC health services research, 2019-04, Vol.19 (1), p.220-220, Article 220

2019

Volltextzugriff (PDF)

Bridging the Gaps in Palliative Care Bereavement Support: An International Perspective

Death studies, 2014-01, Vol.38 (1), p.54-61

2014

Volltextzugriff (PDF)

Family caregivers bereaved by voluntary-assisted dying with a focus on motor neurone disease: the hidden patients

Palliative care and social practice, 2023-01, Vol.17, p.26323524231212512-26323524231212512

2023

Volltextzugriff (PDF)

Key features of palliative care service delivery to Indigenous peoples in Australia, New Zealand, Canada and the United States: a comprehensive review

BMC palliative care, 2018-05, Vol.17 (1), p.72-72, Article 72

2018

Volltextzugriff (PDF)

Motor Neurone Disease family carers’ experiences of caring, palliative care and bereavement: An exploratory qualitative study

Palliative medicine, 2012-09, Vol.26 (6), p.842-850

2012

Volltextzugriff (PDF)

The Compassionate Communities Connectors program: Effect on healthcare usage

Palliative care and social practice, 2023-01, Vol.17, p.26323524231205323-26323524231205323

2023

Volltextzugriff (PDF)

A public health approach to bereavement support services in palliative care

Australian and New Zealand journal of public health, 2012-02, Vol.36 (1), p.14-16

2012

Volltextzugriff (PDF)

Breaking the news of a diagnosis of motor neurone disease: A national survey of neurologists' perspectives

Journal of the neurological sciences, 2016-08, Vol.367, p.368-374

2016

Volltextzugriff (PDF)

Memorialisation during COVID-19: implications for the bereaved, service providers and policy makers

Palliative Care and Social Practice, 2020, Vol.14, p.2632352420980456-2632352420980456

2020

Volltextzugriff (PDF)

Using the Carers' Alert Thermometer tool to identify needs and support family caregivers of people with motor neurone disease: moving beyond needs assessments

Palliative care and social practice, 2024-01, Vol.18, p.26323524241228306-26323524241228306

2024

Volltextzugriff (PDF)

The Compassionate Communities Connectors programme: experiences of supported families and referring healthcare providers

Palliative care and social practice, 2023-01, Vol.17, p.26323524231173705-26323524231173705

2023

Volltextzugriff (PDF)

Winners and Losers in Palliative Care Service Delivery: Time for a Public Health Approach to Palliative and End of Life Care

Healthcare (Basel), 2021-11, Vol.9 (12), p.1615

2021

Volltextzugriff (PDF)

Correction: Exploring the Support Needs of Family Caregivers of Patients with Brain Cancer Using the CSNAT: A Comparative Study with Other Cancer Groups

PloS one, 2016-01, Vol.11 (1), p.e0148074-e0148074

2016

Volltextzugriff (PDF)

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Bereavement support for family caregivers: The gap between guidelines and practice in palliative care

Who needs bereavement support? A population based survey of bereavement risk and support need

The impact of the carer support needs assessment tool (CSNAT) in community palliative care using a stepped wedge cluster trial

Supporting the dying is a community responsibility

Exploring the Support Needs of Family Caregivers of Patients with Brain Cancer Using the CSNAT: A Comparative Study with Other Cancer Groups

A scoping review of bereavement risk assessment measures: Implications for palliative care

Matching response to need: What makes social networks fit for providing bereavement support?

Family Caregivers’ Preparations for Death: A Qualitative Analysis

Improving the Evidence Base in Palliative Care to Inform Practice and Policy: Thinking Outside the Box

Predictors of Complicated Grief: A Systematic Review of Empirical Studies

Palliative and End-of-Life Care Service Models: To What Extent Are Consumer Perspectives Considered?

The Evolving Landscape: Funerals, Cemeteries, Memorialization, and Bereavement Support

Caregivers' experiences of a home support program after the hospital discharge of an older family member: a qualitative analysis

Bridging the Gaps in Palliative Care Bereavement Support: An International Perspective

Family caregivers bereaved by voluntary-assisted dying with a focus on motor neurone disease: the hidden patients

Key features of palliative care service delivery to Indigenous peoples in Australia, New Zealand, Canada and the United States: a comprehensive review

Motor Neurone Disease family carers’ experiences of caring, palliative care and bereavement: An exploratory qualitative study

The Compassionate Communities Connectors program: Effect on healthcare usage

A public health approach to bereavement support services in palliative care

Breaking the news of a diagnosis of motor neurone disease: A national survey of neurologists' perspectives

Memorialisation during COVID-19: implications for the bereaved, service providers and policy makers

Using the Carers' Alert Thermometer tool to identify needs and support family caregivers of people with motor neurone disease: moving beyond needs assessments

The Compassionate Communities Connectors programme: experiences of supported families and referring healthcare providers

Winners and Losers in Palliative Care Service Delivery: Time for a Public Health Approach to Palliative and End of Life Care

Correction: Exploring the Support Needs of Family Caregivers of Patients with Brain Cancer Using the CSNAT: A Comparative Study with Other Cancer Groups

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