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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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EAPC White Paper on outcome measurement in palliative care: Improving practice, attaining outcomes and delivering quality services – Recommendations from the European Association for Palliative Care (EAPC) Task Force on Outcome Measurement

Palliative Medicine, 2016-01, Vol.30 (1), p.6-22

2016

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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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Social and clinical determinants of preferences and their achievement at the end of life: prospective cohort study of older adults receiving palliative care in three countries

BMC geriatrics, 2017-11, Vol.17 (1), p.271-271, Article 271

2017

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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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Implementation Strategies for Quality Improvement in Palliative Care: A Scoping Review

Health expectations : an international journal of public participation in health care and health policy, 2024-08, Vol.27 (4), p.e14151-n/a

2024

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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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Feasibility and acceptability of a patient-reported outcome intervention in chronic heart failure

BMJ supportive & palliative care, 2017-12, Vol.7 (4), p.470-479

2017

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Recommendations to reduce inequalities for LGBT people facing advanced illness: ACCESSCare national qualitative interview study

Palliative medicine, 2018-01, Vol.32 (1), p.23-35

2018

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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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Optimal Cancer Care for Aboriginal and Torres Strait Islander People: A Shared Approach to System Level Change

JCO global oncology, 2020-11, Vol.6 (6), p.108-114

2020

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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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A framework for complexity in palliative care: A qualitative study with patients, family carers and professionals

Palliative medicine, 2018-06, Vol.32 (6), p.1078-1090

2018

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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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‘I'll be in a safe place’: a qualitative study of the decisions taken by people with advanced cancer to seek emergency department care

BMJ open, 2016-11, Vol.6 (11), p.e012134-e012134

2016

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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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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

EAPC White Paper on outcome measurement in palliative care: Improving practice, attaining outcomes and delivering quality services – Recommendations from the European Association for Palliative Care (EAPC) Task Force on Outcome Measurement

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

Social and clinical determinants of preferences and their achievement at the end of life: prospective cohort study of older adults receiving palliative care in three countries

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

Implementation Strategies for Quality Improvement in Palliative Care: A Scoping Review

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

Feasibility and acceptability of a patient-reported outcome intervention in chronic heart failure

Recommendations to reduce inequalities for LGBT people facing advanced illness: ACCESSCare national qualitative interview study

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

Optimal Cancer Care for Aboriginal and Torres Strait Islander People: A Shared Approach to System Level Change

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

A framework for complexity in palliative care: A qualitative study with patients, family carers and professionals

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

‘I'll be in a safe place’: a qualitative study of the decisions taken by people with advanced cancer to seek emergency department care

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

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