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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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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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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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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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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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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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Emergency department attendance by patients with cancer in their last month of life: a systematic review and meta-analysis

Journal of clinical oncology, 2015-02, Vol.33 (4), p.370-376

2015

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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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Results of a transparent expert consultation on patient and public involvement in palliative care research

Palliative medicine, 2015-12, Vol.29 (10), p.939-949

2015

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Drivers of care costs and quality in the last 3 months of life among older people receiving palliative care: A multinational mortality follow-back survey across England, Ireland and the United States

Palliative medicine, 2020-04, Vol.34 (4), p.513-523

2020

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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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Professional Supervision as Storied Experience: Narrative Analysis Findings for Australian-Based Registered Music Therapists

Journal of music therapy, 2017-03, Vol.54 (1), p.80-107

2017

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Strategies to address the shortcomings of commonly used advanced chronic heart failure descriptors to improve recruitment in palliative care research: A parallel mixed-methods feasibility study

Palliative medicine, 2018-02, Vol.32 (2), p.517-524

2018

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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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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

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

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

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

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

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

Emergency department attendance by patients with cancer in their last month of life: a systematic review and meta-analysis

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

Results of a transparent expert consultation on patient and public involvement in palliative care research

Drivers of care costs and quality in the last 3 months of life among older people receiving palliative care: A multinational mortality follow-back survey across England, Ireland and the United States

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

Professional Supervision as Storied Experience: Narrative Analysis Findings for Australian-Based Registered Music Therapists

Strategies to address the shortcomings of commonly used advanced chronic heart failure descriptors to improve recruitment in palliative care research: A parallel mixed-methods feasibility study

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

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