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Increased patient satisfaction by integration of palliative care into geriatrics-A prospective cohort study

PloS one, 2023-06, Vol.18 (6), p.e0287550-e0287550

2023

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Implementation of national palliative care guidelines in Swedish acute care hospitals: A qualitative content analysis of stakeholders’ perceptions

Health policy (Amsterdam), 2017-11, Vol.121 (11), p.1194-1201

2017

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Quality of life in terminal care--with special reference to age, gender and marital status

Supportive care in cancer, 2006-04, Vol.14 (4), p.320-328

2006

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The existential impact of starting corticosteroid treatment as symptom control in advanced metastatic cancer

Palliative medicine, 2009-03, Vol.23 (2), p.165-170

2009

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Palliative day care – a study of well-being and health-related quality of life

Palliative medicine, 2009-07, Vol.23 (5), p.441-447

2009

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Fatigue dimensions in patients with advanced cancer in relation to time of survival and quality of life

Palliative medicine, 2009-03, Vol.23 (2), p.171-178

2009

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Four essential drugs needed for quality care of the dying: a Delphi-study based international expert consensus opinion

Journal of palliative medicine, 2013-01, Vol.16 (1), p.38

2013

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Recommendations for Deprescribing of Medication in the Last Phase of Life: An International Delphi Study

Journal of pain and symptom management, 2024-08

2024

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Poor Psychosocial Well-Being in the First Year-and-a-Half After Losing a Parent to Cancer - A Longitudinal Study Among Young Adults Participating in Support Groups

Journal of social work in end-of-life & palliative care, 2020-10, Vol.16 (4), p.330-345

2020

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Family cohesion predicts long-term health and well-being after losing a parent to cancer as a teenager: A nationwide population-based study

PloS one, 2023-04, Vol.18 (4), p.e0283327-e0283327

2023

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Associations between the spread of COVID-19 and end-of-life circumstances in the non-infected population of Sweden

Scandinavian journal of public health, 2024-05, Vol.52 (3), p.290-298

2024

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Nausea in cancer chemotherapy is inversely related to urinary cortisol excretion

British journal of cancer, 1992-05, Vol.65 (5), p.779-780

1992

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Short-term and long-term effects of a psycho-educational group intervention for family caregivers in palliative home care - results from a randomized control trial

Psycho-oncology (Chichester, England), 2016-07, Vol.25 (7), p.795-802

2016

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The perspectives of bereaved family members on their experiences of support in palliative care

International journal of palliative nursing, 2013-06, Vol.19 (6), p.282

2013

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Sedation in specialized palliative care: A cross-sectional study

PloS one, 2022-07, Vol.17 (7), p.e0270483-e0270483

2022

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Unresolved grief and its consequences. A nationwide follow-up of teenage loss of a parent to cancer 6–9 years earlier

Supportive care in cancer, 2016-07, Vol.24 (7), p.3095-3103

2016

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Psychosocial Well-Being of Young People Who Participated in a Support Group Following the Loss of a Parent to Cancer

Journal of social work in end-of-life & palliative care, 2017-01, Vol.13 (1), p.44-60

2017

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Palliative care during the final week of life of older people in nursing homes: A register-based study

Palliative & supportive care, 2017-08, Vol.15 (4), p.417-424

2017

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Quality registration is a support for more specialized palliative care. 9 out of 12 of the indicators improved significantly during one year

Läkartidningen, 2016-03, Vol.113

2016

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Losing a parent to cancer as a teenager: Family cohesion in childhood, teenage, and young adulthood as perceived by bereaved and non‐bereaved youths

Psycho-oncology (Chichester, England), 2019-09, Vol.28 (9), p.1845-1853

2019

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Public awareness of palliative care in Sweden

Scandinavian journal of public health, 2018-06, Vol.46 (4), p.478-487

2018

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Distrust in the End-of-Life Care Provided to a Parent and Long-Term Negative Outcomes Among Bereaved Adolescents: A Population-Based Survey Study

Journal of clinical oncology, 2017-09, Vol.35 (27), p.3136-3142

2017

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Implementation of the integrated palliative care outcome scale in acute care settings – a feasibility study

Palliative & supportive care, 2018-12, Vol.16 (6), p.698-705

2018

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Difficult discussions with patients practiced at course with actors. A carefully planned strategy helps both physician and patient

Läkartidningen, 2016-11, Vol.113

2016

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End‐of‐life care in residential care homes: a retrospective study of the perspectives of family members using the VOICES questionnaire

Scandinavian journal of caring sciences, 2017-03, Vol.31 (1), p.72-84

2017

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Increased patient satisfaction by integration of palliative care into geriatrics-A prospective cohort study

Implementation of national palliative care guidelines in Swedish acute care hospitals: A qualitative content analysis of stakeholders’ perceptions

Quality of life in terminal care--with special reference to age, gender and marital status

The existential impact of starting corticosteroid treatment as symptom control in advanced metastatic cancer

Palliative day care – a study of well-being and health-related quality of life

Fatigue dimensions in patients with advanced cancer in relation to time of survival and quality of life

Four essential drugs needed for quality care of the dying: a Delphi-study based international expert consensus opinion

Recommendations for Deprescribing of Medication in the Last Phase of Life: An International Delphi Study

Poor Psychosocial Well-Being in the First Year-and-a-Half After Losing a Parent to Cancer - A Longitudinal Study Among Young Adults Participating in Support Groups

Family cohesion predicts long-term health and well-being after losing a parent to cancer as a teenager: A nationwide population-based study

Associations between the spread of COVID-19 and end-of-life circumstances in the non-infected population of Sweden

Nausea in cancer chemotherapy is inversely related to urinary cortisol excretion

Short-term and long-term effects of a psycho-educational group intervention for family caregivers in palliative home care - results from a randomized control trial

The perspectives of bereaved family members on their experiences of support in palliative care

Sedation in specialized palliative care: A cross-sectional study

Unresolved grief and its consequences. A nationwide follow-up of teenage loss of a parent to cancer 6–9 years earlier

Psychosocial Well-Being of Young People Who Participated in a Support Group Following the Loss of a Parent to Cancer

Palliative care during the final week of life of older people in nursing homes: A register-based study

Quality registration is a support for more specialized palliative care. 9 out of 12 of the indicators improved significantly during one year

Losing a parent to cancer as a teenager: Family cohesion in childhood, teenage, and young adulthood as perceived by bereaved and non‐bereaved youths

Public awareness of palliative care in Sweden

Distrust in the End-of-Life Care Provided to a Parent and Long-Term Negative Outcomes Among Bereaved Adolescents: A Population-Based Survey Study

Implementation of the integrated palliative care outcome scale in acute care settings – a feasibility study

Difficult discussions with patients practiced at course with actors. A carefully planned strategy helps both physician and patient

End‐of‐life care in residential care homes: a retrospective study of the perspectives of family members using the VOICES questionnaire

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