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Place and cause of death in centenarians: a population-based observational study in England, 2001 to 2010

PLoS medicine, 2014-06, Vol.11 (6), p.e1001653

2014

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The PCOC Symptom Assessment Scale (SAS): A valid measure for daily use at point of care and in palliative care programs

PloS one, 2021-03, Vol.16 (3), p.e0247250-e0247250

2021

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Capture, Transfer, and Feedback of Patient-Centered Outcomes Data in Palliative Care Populations: Does It Make a Difference? A Systematic Review

Journal of pain and symptom management, 2015-03, Vol.49 (3), p.611-624

2015

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A Systematic Review of the Use of the Palliative Care Outcome Scale and the Support Team Assessment Schedule in Palliative Care

Journal of pain and symptom management, 2015-12, Vol.50 (6), p.842-853.e19

2015

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How can a measure improve assessment and management of symptoms and concerns for people with dementia in care homes? A mixed-methods feasibility and process evaluation of IPOS-Dem

PloS one, 2018-07, Vol.13 (7), p.e0200240-e0200240

2018

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Associations between informal care costs, care quality, carer rewards, burden and subsequent grief: the international, access, rights and empowerment mortality follow-back study of the last 3 months of life (IARE I study)

BMC medicine, 2020-11, Vol.18 (1), p.344-344, Article 344

2020

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Patient-reported outcome measurement of symptom distress is feasible in most clinical scenarios in palliative care: an observational study involving routinely collected data

International journal for quality in health care, 2021-05, Vol.33 (2)

2021

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Implementing patient reported outcome measures (PROMs) in palliative care--users' cry for help

Health and quality of life outcomes, 2011-04, Vol.9 (1), p.27-27

2011

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Cross-cultural adaptation and psychometric validation of point-of-care outcome assessment tools in Chinese palliative care clinical practice

BMC palliative care, 2024-04, Vol.23 (1), p.89-89, Article 89

2024

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The Selection and Use of Outcome Measures in Palliative and End-of-Life Care Research: The MORECare International Consensus Workshop

Journal of pain and symptom management, 2013-12, Vol.46 (6), p.925-937

2013

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The Need for Palliative Care in Ireland: A Population-Based Estimate of Palliative Care Using Routine Mortality Data, Inclusive of Nonmalignant Conditions

Journal of pain and symptom management, 2015-04, Vol.49 (4), p.726-733.e1

2015

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The real-world problem of care coordination: a longitudinal qualitative study with patients living with advanced progressive illness and their unpaid caregivers

PloS one, 2014-05, Vol.9 (5), p.e95523-e95523

2014

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The PRISMA Symposium 1: Outcome Tool Use. Disharmony in European Outcomes Research for Palliative and Advanced Disease Care: Too Many Tools in Practice

Journal of pain and symptom management, 2011-10, Vol.42 (4), p.493-500

2011

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Choosing care homes as the least preferred place to die: a cross-national survey of public preferences in seven European countries

BMC palliative care, 2014-10, Vol.13 (1), p.48-48, Article 48

2014

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Factors associated with aggressive end of life cancer care

Supportive care in cancer, 2016-03, Vol.24 (3), p.1079-1089

2016

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The PRISMA Symposium 4: How Should Europe Progress End-of-Life and Palliative Clinical Care Research? Recommendations From the Proceedings

Journal of pain and symptom management, 2011-10, Vol.42 (4), p.511-516

2011

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Outcomes 'out of africa': the selection and implementation of outcome measures for palliative care in Africa

BMC palliative care, 2012-01, Vol.11 (1), p.1-1, Article 1

2012

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Music Therapy Assessment Tool for Awareness in Disorders of Consciousness (MATADOC): Standardisation of the principal subscale to assess awareness in patients with disorders of consciousness

Neuropsychological rehabilitation, 2014-01, Vol.24 (1), p.101-124

2014

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How empowering is hospital care for older people with advanced disease? Barriers and facilitators from a cross-national ethnography in England, Ireland and the USA

Age and ageing, 2017-03, Vol.46 (2), p.300-309

2017

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'Burden to others' as a public concern in advanced cancer: a comparative survey in seven European countries

BMC cancer, 2013-03, Vol.13 (1), p.105-105, Article 105

2013

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Coordination of end-of-life care for patients with lung cancer and those with advanced COPD: are there transferable lessons? A longitudinal qualitative study

Primary care respiratory journal, 2014-03, Vol.23 (1), p.46-51

2014

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“A quiet still voice that just touches”: music’s relevance for adults living with life-threatening cancer diagnoses

Supportive care in cancer, 2014-04, Vol.22 (4), p.1037-1047

2014

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Enhancing patient-reported outcome measurement in research and practice of palliative and end-of-life care

Supportive care in cancer, 2012-07, Vol.20 (7), p.1573-1578

2012

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Public preferences and priorities for end-of-life care in Kenya: a population-based street survey

BMC palliative care, 2014-02, Vol.13 (1), p.4-4, Article 4

2014

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Of apples and oranges: Lessons learned from the preparation of research protocols for systematic reviews exploring the effectiveness of Specialist Palliative Care

BMC palliative care, 2016-04, Vol.15 (43), p.43-43, Article 43

2016

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Place and cause of death in centenarians: a population-based observational study in England, 2001 to 2010

The PCOC Symptom Assessment Scale (SAS): A valid measure for daily use at point of care and in palliative care programs

Capture, Transfer, and Feedback of Patient-Centered Outcomes Data in Palliative Care Populations: Does It Make a Difference? A Systematic Review

A Systematic Review of the Use of the Palliative Care Outcome Scale and the Support Team Assessment Schedule in Palliative Care

How can a measure improve assessment and management of symptoms and concerns for people with dementia in care homes? A mixed-methods feasibility and process evaluation of IPOS-Dem

Associations between informal care costs, care quality, carer rewards, burden and subsequent grief: the international, access, rights and empowerment mortality follow-back study of the last 3 months of life (IARE I study)

Patient-reported outcome measurement of symptom distress is feasible in most clinical scenarios in palliative care: an observational study involving routinely collected data

Implementing patient reported outcome measures (PROMs) in palliative care--users' cry for help

Cross-cultural adaptation and psychometric validation of point-of-care outcome assessment tools in Chinese palliative care clinical practice

The Selection and Use of Outcome Measures in Palliative and End-of-Life Care Research: The MORECare International Consensus Workshop

The Need for Palliative Care in Ireland: A Population-Based Estimate of Palliative Care Using Routine Mortality Data, Inclusive of Nonmalignant Conditions

The real-world problem of care coordination: a longitudinal qualitative study with patients living with advanced progressive illness and their unpaid caregivers

The PRISMA Symposium 1: Outcome Tool Use. Disharmony in European Outcomes Research for Palliative and Advanced Disease Care: Too Many Tools in Practice

Choosing care homes as the least preferred place to die: a cross-national survey of public preferences in seven European countries

Factors associated with aggressive end of life cancer care

The PRISMA Symposium 4: How Should Europe Progress End-of-Life and Palliative Clinical Care Research? Recommendations From the Proceedings

Outcomes 'out of africa': the selection and implementation of outcome measures for palliative care in Africa

Music Therapy Assessment Tool for Awareness in Disorders of Consciousness (MATADOC): Standardisation of the principal subscale to assess awareness in patients with disorders of consciousness

How empowering is hospital care for older people with advanced disease? Barriers and facilitators from a cross-national ethnography in England, Ireland and the USA

'Burden to others' as a public concern in advanced cancer: a comparative survey in seven European countries

Coordination of end-of-life care for patients with lung cancer and those with advanced COPD: are there transferable lessons? A longitudinal qualitative study

“A quiet still voice that just touches”: music’s relevance for adults living with life-threatening cancer diagnoses

Enhancing patient-reported outcome measurement in research and practice of palliative and end-of-life care

Public preferences and priorities for end-of-life care in Kenya: a population-based street survey

Of apples and oranges: Lessons learned from the preparation of research protocols for systematic reviews exploring the effectiveness of Specialist Palliative Care

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