Sage Palliative Medicine & Chronic Care

Asian family members’ participation in advance care planning: An integrative review

The experience of nurses when providing care across acts that may be perceived as death hastening: A qualitative evidence synthesis

Changes in perception of prognosis in the last year of life of patients with advanced cancer and its associated factors: Longitudinal results of the eQuiPe study.

Components of home-based palliative and supportive care for adults with heart failure: A scoping review

Multiple points of system failure underpin continuous subcutaneous infusion safety incidents in palliative care: A mixed methods analysis

Definition and recommendations of advance care planning: A Delphi study in five Asian sectors

The double awareness of the wish to hasten death and the will to live: A secondary analysis of outlier patients from a mixed-methods study

Development of the TIFFIN recommendations for co-producing palliative and end-of-life care research with individuals with lived experience of homelessness: A qualitative study

Electronic symptom monitoring for home-based palliative care: A systematic review

Primary palliative care: Onwards and upwards!

Primary palliative care: Onwards and upwards!

What are we planning, exactly? The perspectives of people with intellectual disabilities, their carers and professionals on end-of-life care planning: A focus group study

Subcutaneous sodium valproate in palliative care: A systematic review

How palliative care professionals develop coping competence through their career: A grounded theory

What are the anticipated benefits, risks, barriers and facilitators to implementing person-centred outcome measures into routine care for children and young people with life-limiting and life-threaten

Long-term bereavement outcomes in family members of those who died in acute care hospitals before and during the first wave of COVID-19: A cohort study

Social acceptability of psilocybin-assisted therapy for existential distress at the end of life: A population-based survey

Feasibility and effectiveness of a two-tiered intervention involving training and a new consultation model for patients with palliative care needs in primary care: A before-after study

Reduction in potentially inappropriate end-of-life hospital care for cancer patients during the COVID-19 pandemic: A retrospective population-based study

Family carer experiences of hospice care at home: findings from a mixed methods realist evaluation

"Challenges and opportunities for improvement when people with an intellectual disability or serious mental illness also need palliative care: A qualitative meta-ethnography"

What outcomes do studies use to measure the impact of prognostication on people with advanced cancer? Findings from a systematic review of quantitative and qualitative studies

Telehealth requires improved evidence to achieve its full potential in palliative care

Hospital-service use in the last year of life by patients aged ⩾60 years who died of heart failure or cardiomyopathy: A retrospective linked data study

Spiritual, religious, and existential concerns of children and young people with life-limiting and life-threatening conditions: A qualitative interview study

Palliative care for people who use drugs during communicable disease epidemics and pandemics: A scoping review on access, policies, and programs and guidelines

Applying the community readiness model to identify and address inequity in end-of-life care in South Asian communities

Support from healthcare professionals in empowering family carers to discuss advance care planning: A population-based survey

End-of-life communication strategies for healthcare professionals: A scoping review

Serious health-related suffering experienced by children with disability and their families living in Bangladesh: A scoping review

Non-steroidal anti-inflammatory drugs (NSAIDs) in cancer pain: A database analysis to determine recruitment feasibility for a clinical trial

Non-steroidal anti-inflammatory drugs (NSAIDs) in cancer pain: A database analysis to determine recruitment feasibility for a clinical trial

Bereavement outcomes in family members of those who died in acute care hospitals before and during the first wave of COVID-19: A cohort study

Health care professionals’ perceptions of factors influencing the process of identifying patients for serious illness conversations: A qualitative study

Turkish imams and their role in decision-making in palliative care: A Directed Content and Narrative analysis

The effects of confronting one’s own end of life on older individuals and those with a life-threatening disease: A systematic literature review

Integrating lived experiences of out-of-hours health services for people with palliative and end-of-life care needs with national datasets for people dying in Scotland in 2016

Is trained communication about desire to die harmful for patients receiving palliative care? A cohort study

Death doulas as supportive companions in end-of-life care: A scoping review

Podcast 97: Revised Recommendations on Standards and Norms for Palliative Care in Europe from the European Association for Palliative Care: a Delphi study

A feasibility and acceptability pilot for the longitudinal measurement of inspiratory and expiratory pressures in people with advanced pancreatic cancer

Integrating lived experiences of out-of-hours health services for people with palliative and end-of-life care needs with national datasets for people dying in Scotland in 2016: a mixed methods, multi

Patient Perspectives on States Worse Than Death: A Qualitative Study with Implications for Patient-Centered Outcomes and Values Elicitation

Paramedics delivering palliative and end-of-life care in community-based settings: A systematic integrative review with thematic synthesis

Adaptation and continuous learning: integrative review of coping strategies of palliative care professionals

‘It feels it’s wasting whatever time I’ve got left’: A qualitative study of living with treatable but not curable cancer during the COVID-19 pandemic

Arts engagement facilitated by artists with individuals with life-limiting illness: A systematic integrative review of the literature

An online international comparison of palliative care identification in primary care using the Surprise Question

Asian patients’ perspectives on advance care planning: A mixed-method systematic review and conceptual framework

Unwelcome memento mori or best clinical practice? Community end of life anticipatory medication prescribing practice: A mixed methods observational study