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Good Quality Care for Cancer Patients Dying in Hospitals, but Information Needs Unmet: Bereaved Relatives’ Survey within Seven Countries

The oncologist (Dayton, Ohio), 2021-07, Vol.26 (7), p.e1273-e1284

2021

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The European Association for Palliative Care basic dataset to describe a palliative care cancer population: Results from an international Delphi process

Palliative medicine, 2014-06, Vol.28 (6), p.463-473

2014

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Assessing quality of care for the dying from the bereaved relatives’ perspective: Using pre-testing survey methods across seven countries to develop an international outcome measure

Palliative medicine, 2019-03, Vol.33 (3), p.357-368

2019

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Pilot testing of the first version of the European Association for Palliative Care basic dataset: A mixed methods study

Palliative medicine, 2019-07, Vol.33 (7), p.832-849

2019

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How Are Palliative Care Cancer Populations Characterized in Randomized Controlled Trials? A Literature Review

Journal of pain and symptom management, 2014-05, Vol.47 (5), p.906-914.e17

2014

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Prevalence of distressing symptoms in hospitalised patients on medical wards: A cross-sectional study

BMC palliative care, 2008-09, Vol.7 (1), p.16-16, Article 16

2008

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One chance to get it right: improving clinical handovers for better symptom control at the end of life

BMJ open quality, 2021-09, Vol.10 (3), p.e001436

2021

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How Are Patient Populations Characterized in Studies Investigating Depression in Advanced Cancer? Results From a Systematic Literature Review

Journal of pain and symptom management, 2014-10, Vol.48 (4), p.678-698

2014

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Feasibility and acceptability of introducing advance care planning on a thoracic medicine inpatient ward: an exploratory mixed method study

BMJ open respiratory research, 2020-02, Vol.7 (1), p.e000485

2020

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Factors affecting quality of end-of-life hospital care - a qualitative analysis of free text comments from the i-CODE survey in Norway

BMC palliative care, 2020-07, Vol.19 (1), p.98-98, Article 98

2020

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Computer-Based Assessment of Symptoms and Mobility in Palliative Care: Feasibility and Challenges

Journal of pain and symptom management, 2009-12, Vol.38 (6), p.827-836

2009

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Transcultural Validation of the French Version of the Modified Edmonton Symptom Assessment Scale: The ESAS12-F

Journal of palliative medicine, 2019-12, Vol.22 (12), p.1553

2019

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What do bereaved relatives of cancer patients dying in hospital want to tell us? Analysis of free-text comments from the International Care of the Dying Evaluation (i-CODE) survey: a mixed methods approach

Supportive care in cancer, 2023-01, Vol.31 (1), p.81-81, Article 81

2023

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Dissociative Photoionization of 1‑Halogenated Silacyclohexanes: Silicon Traps the Halogen

The journal of physical chemistry. A, Molecules, spectroscopy, kinetics, environment, & general theory, 2016-11, Vol.120 (46), p.9188-9197

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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Facilitators and barriers of implementing end-of-life care volunteering in a hospital in five European countries: the iLIVE study

BMC palliative care, 2024-04, Vol.23 (1), p.88-88, Article 88

2024

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Hospital care for the dying patient with cancer: does an advance care planning invitation influence bereaved relatives' experiences? A two country survey

BMJ supportive & palliative care, 2023-12, Vol.13 (e3), p.e1038

2023

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Incidence of Psychogenic Seizures in Adults: A Population‐Based Study in Iceland

Epilepsia (Copenhagen), 1998-07, Vol.39 (7), p.749-752

1998

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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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Systematic Review of the Primary Research on Minority Ethnic Groups and End-of-Life Care From the United Kingdom

Journal of pain and symptom management, 2012-02, Vol.43 (2), p.261-286

2012

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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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'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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A pan-European survey of research in end-of-life cancer care

Supportive care in cancer, 2012-01, Vol.20 (1), p.39-48

2012

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Clinical priorities, barriers and solutions in end-of-life cancer care research across Europe. Report from a workshop

European journal of cancer (1990), 2010-07, Vol.46 (10), p.1815-1822

2010

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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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Good Quality Care for Cancer Patients Dying in Hospitals, but Information Needs Unmet: Bereaved Relatives’ Survey within Seven Countries

The European Association for Palliative Care basic dataset to describe a palliative care cancer population: Results from an international Delphi process

Assessing quality of care for the dying from the bereaved relatives’ perspective: Using pre-testing survey methods across seven countries to develop an international outcome measure

Pilot testing of the first version of the European Association for Palliative Care basic dataset: A mixed methods study

How Are Palliative Care Cancer Populations Characterized in Randomized Controlled Trials? A Literature Review

Prevalence of distressing symptoms in hospitalised patients on medical wards: A cross-sectional study

One chance to get it right: improving clinical handovers for better symptom control at the end of life

How Are Patient Populations Characterized in Studies Investigating Depression in Advanced Cancer? Results From a Systematic Literature Review

Feasibility and acceptability of introducing advance care planning on a thoracic medicine inpatient ward: an exploratory mixed method study

Factors affecting quality of end-of-life hospital care - a qualitative analysis of free text comments from the i-CODE survey in Norway

Computer-Based Assessment of Symptoms and Mobility in Palliative Care: Feasibility and Challenges

Transcultural Validation of the French Version of the Modified Edmonton Symptom Assessment Scale: The ESAS12-F

What do bereaved relatives of cancer patients dying in hospital want to tell us? Analysis of free-text comments from the International Care of the Dying Evaluation (i-CODE) survey: a mixed methods approach

Dissociative Photoionization of 1‑Halogenated Silacyclohexanes: Silicon Traps the Halogen

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

Facilitators and barriers of implementing end-of-life care volunteering in a hospital in five European countries: the iLIVE study

Hospital care for the dying patient with cancer: does an advance care planning invitation influence bereaved relatives' experiences? A two country survey

Incidence of Psychogenic Seizures in Adults: A Population‐Based Study in Iceland

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

Systematic Review of the Primary Research on Minority Ethnic Groups and End-of-Life Care From the United Kingdom

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

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

A pan-European survey of research in end-of-life cancer care

Clinical priorities, barriers and solutions in end-of-life cancer care research across Europe. Report from a workshop

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

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