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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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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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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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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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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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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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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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Culture and end of life care: a scoping exercise in seven European countries

PloS one, 2012-04, Vol.7 (4), p.e34188-e34188

2012

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The effectiveness and cost‐effectiveness of inpatient specialist palliative care in acute hospitals for adults with advanced illness and their caregivers

Cochrane database of systematic reviews, 2016-09, Vol.2016 (9)

2016

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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

2024

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The use of two common palliative outcome measures in clinical care and research: A systematic review of POS and STAS

Palliative medicine, 2011-06, Vol.25 (4), p.304-313

2011

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Diversity in defining end of life care: an obstacle or the way forward?

PloS one, 2013-07, Vol.8 (7), p.e68002-e68002

2013

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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

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

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

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

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

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

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

Culture and end of life care: a scoping exercise in seven European countries

The effectiveness and cost‐effectiveness of inpatient specialist palliative care in acute hospitals for adults with advanced illness and their caregivers

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

The use of two common palliative outcome measures in clinical care and research: A systematic review of POS and STAS

Diversity in defining end of life care: an obstacle or the way forward?

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