Palliative Medicine

Article	Citations
Neuropalliative care for progressive neurological diseases: A scoping review on models of care and priorities for future research	767
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	94
Assessing the suitability of the Carer Support Needs Assessment Tool (CSNAT-Paediatric) for use with parents of children with a life-limiting condition: A qualitative secondary analysis	55
Posttraumatic growth in palliative care settings: A scoping review of prevalence, characteristics and interventions	54
Complexity and function of family involvement in advance care planning: A qualitative study of perspectives from people living with advanced cancer, family members and healthcare professionals	45
Living experiences of people with advance cancer with low socioeconomic status: A systematic review of qualitative evidence	44
“Walk me through the final day”: A thematic analysis study on the family caregiver experience of the Medical Assistance in Dying procedure day	44
REstoring Sleep and Energy using a mulTimodal non-pharmacological intervention in advanced Cancer: A feasibility study (RESET-C)	43
‘Saying goodbye’. . . A systematic integrative review of palliative caregiving in intergenerational living contexts	43
Maybe for unbearable suffering: Diverse racial, ethnic and cultural perspectives of assisted dying. A scoping review	36
Mistletoe extract in patients with advanced pancreatic cancer: Health-related quality of life in a double-blind, randomized, placebo-controlled trial (MISTRAL)	33
Preserving the integrity of personhood in people with advanced cancer: An in-depth qualitative study among patients, relatives, and care professionals	33
Views of patients with progressive illness and carers about the role of digital advance care planning systems to record and share information: A qualitative study	33
Mixed methods process evaluation of an advance care planning intervention among nursing home staff	32
Propofol for palliative sedation: A systematic review of clinical outcomes, safety, and ethical implications	30
Utilizing intricate care networks : An ethnography of patients and families navigating palliative care in a resource-limited setting	29
Parents’ experiences of being involved in medical decision-making for their child with a life-limiting condition: A systematic review with narrative synthesis	29
End-of-life experience patterns among older adults and their association with pain near death: A population-based study	28
Differences in palliative care needs between cancer patients and non-cancer patients at the start of specialized palliative care: A nationwide register-based study	28
Identifying, exploring and integrating the spiritual dimension in proactive care planning: A mixed methods evaluation of a communication training intervention for multidisciplinary palliative care tea	26
The 13th World Research Congress of the European Association for Palliative Care	26
Corrigendum to Updating international consensus on best practice in care of the dying: A Delphi study	26
The experience of nurses when providing care across acts that may be perceived as death hastening: A qualitative evidence synthesis	25
Facilitating equitable access to hospice care in socially deprived areas: A mixed methods multiple case study	25
‘Sadly I think we are sort of still quite white, middle-class really’ – Inequities in access to bereavement support: Findings from a mixed methods study	24

A peripherally acting μ-opioid receptor antagonist for treating opioid-associated tinnitus: A case report	23
Delirium prevention in hospices: Opportunities and limitations – A focused ethnography	23
How best to capture the impact of complementary therapies in palliative care: A systematic review to identify and assess the appropriateness and validity of multi-domain tools	23
Advance Care Planning in structurally vulnerable populations: A scoping review of barriers, facilitators, and interventions	23
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	22
The management of absolute iron deficiency anaemia in the palliative care population: A reply to Neoh et al.	22
Education modalities for serious illness communication training: A scoping review on the impact on clinician behavior and patient outcomes	21
Enhancing identification of potential palliative care needs in older adults: An umbrella review of screening instruments	21
Prevalence, risk factors and management of pressure injuries and their implications for palliative care: A rapid overview of reviews	20
An emergency department nurse led intervention to facilitate serious illness conversations among seriously ill older adults: A feasibility study	20
Re: Tan et al., Subcutaneous sodium valproate in palliative care: A systematic review	20
Support from healthcare professionals in empowering family carers to discuss advance care planning: A population-based survey	20
Trauma-informed palliative care: A systematic scoping review of evidence sources describing concepts relevant to an emerging field of practice	20
Barriers and facilitators influencing referral and access to palliative care for children and young people with life-limiting and life-threatening conditions: a scoping review of the evidence	20
Factors associated with hospitalisations of patients with chronic heart failure approaching the end of life: A systematic review	19
Bridging cultures in palliative care: A qualitative study of the care of Indigenous Australians with advanced illness	19
Economic evaluations in the palliative and end-of-life care settings: A systematic review of existing evidence, methods and quality	19
‘How long do you think?’ Unresponsive dying patients in a specialist palliative care service: A consecutive cohort study	19
A narrow view of palliative care and assisted dying	18
International consensus on occupational therapy interventions for people with palliative care needs: A European Association for Palliative Care Group Concept Mapping study	18
Deaths at home, area-based deprivation and the effect of the Covid-19 pandemic: An analysis of mortality data across four nations	18
A systematic review on the impact of financial insecurity on the physical and psychological well-being for people living with terminal illness	18
The perspectives of people with dementia and their supporters on advance care planning: A qualitative study with the European Working Group of People with Dementia	18
EAPC2023 Abstract Book	18
Effectiveness of and implementation requirements for telehealth in palliative care patients with advanced cancer: A systematic review and meta-analysis	18
Effectiveness of transmural team-based palliative care in prevention of hospitalizations in patients at the end of life: A systematic review and meta-analysis	18
‘So being here is. . . I feel like I’m being a social worker again, at the hospice’: Using interpretative phenomenological analysis to explore social workers’ experiences of hospice work	18
Systematic review of conceptual and theoretical frameworks used in palliative care and end-of-life care research studies	17
Pharmacological treatment of pain, dyspnea, death rattle, fever, nausea, and vomiting in the last days of life in older people: A systematic review	17
The 19th World Congress of the European Association for Palliative Care 29 – 31 May 2025 Helsinki, Finland	17
Health care professional recruitment of patients and family carers to palliative care randomised controlled trials: A qualitative multiple case study	17
Caring toward end of life through acute hospital and community partnerships: A scoping review	17
Exploring “good days” with advanced cancer: A pilot daily diary study	17
Models, components and outcomes of palliative and end-of-life care provided to adults living at home: A systematic umbrella review of reviews	17
Enhancing the wellbeing of refugees living with advanced life-limiting illness in high-income resettlement countries: A systematic review	17
Motor neurone disease: A point-prevalence study of patient reported symptom prevalence, severity and palliative care needs	16
Supporting best practice in reflexive thematic analysis reporting in Palliative Medicine : A review of published research and introduction to the	16
Thanks to Reviewers	16
Memory-making interventions for children with life-threatening or life-limiting conditions and their families: A systematic review of evidence and implications for practice	16
Measurement equivalence of the paper-based and electronic version of the Integrated Palliative care Outcome Scale (IPOS): A randomised crossover trial	16
Telehealth requires improved evidence to achieve its full potential in palliative care	16
‘Adrift in a sea of just absolute unknowableness’: A multimethod qualitative study exploring patient, carer and healthcare professional experiences of communicating about future uncertainty in multimo	16
Reducing unnecessary hospital admissions for end-of-life patients in lower and middle-income countries	15
Effects of advance care planning in care dependent community-dwelling older persons (STADPLAN): A cluster-randomised controlled trial	15
What can patient safety science do for palliative care? Bridging the gap	15
Where to for core outcome sets for best care for the dying person?	15
Response to letters about “Palliative care and assisted dying: Uneasy bedfellows”	15
Coming to terms with dying: Advance care planning as a conduit between clinicians, patients, and conversations about death and dying – a qualitative interview study	15
Advance care planning and quality of life: A qualitative interview study in people with young-onset dementia and their family caregivers	15
The value of rehabilitation specialists to team-based palliative care	15

Social determinants of death anxiety in patients with advanced cancer receiving outpatient palliative care	15
Palliative and end-of-life care needs, experiences, and preferences of LGBTQ+ individuals with serious illness: A systematic mixed-methods review	14
Memory making during bereavement care following the death of a child: A survey exploring parental experiences	14
Tensions in advance care planning with dementia: Time for a good-enough laid-back approach?	14
The ideal path to a good death: An international meta-synthesis of rural residents’ perspectives	14
When a dying patient is asked to participate in a double-blind, placebo-controlled clinical trial on symptom control: The decision-making process and experiences of relatives	14
Specialist palliative care improves patient experience, reduces bed days and saves money: An economic modelling study of home- and hospital-based care	14
Caregivers’ perspectives on family meetings and preparedness for imminent death: A qualitative descriptive study in a palliative care setting	14
An electronic pre-visit agenda-setting questionnaire in ambulatory palliative care is feasible and acceptable to patients, care partners, and clinicians: A mixed methods evaluation	14
Palliative care and neuro-oncological care: Better integration is needed	14
Healthy siblings’ perspectives about paediatric palliative care: A qualitative systematic review and meta-synthesis	14
Exercise interventions for advanced cancer palliative care patients: A systematic literature review and descriptive evidence synthesis of randomized controlled trials	14
The spiritual dimension of parenting a child with a life-limiting or life-threatening condition: A mixed-methods systematic review	14
Peer review and Palliative Medicine : Guiding reviewers’ contributions to ensuring high quality publications	14
Iatrogenic suffering at the end of life: An ethnographic study	14
Definition and recommendations of advance care planning: A Delphi study in five Asian sectors	14
Closing the health equity gap in palliative care: The time for action is now	13
Perspectives of inpatients with palliative care needs, their families, clinicians and key stakeholders on measuring quality of hospital care via patient experience measures: A qualitative study	13
Reducing inequity in the provision of children’s palliative care in low- and middle- income countries: A focus on education and research	13
The spiritual care intervention “In dialogue with your life story”: Results of a longitudinal study on palliative clients’ spiritual wellbeing	13
A peripheral opioid antagonist for treating urinary retention induced by opioids: A case report	13
A rapid review of the evidence for online interventions for bereavement support	13
Implementation of clinical guidelines in specialized palliative care—results from a national improvement project: A national register-based study	13
Masculinity and ethnicity in intersection: Implications for men’s health and palliative care services	13
Strategies and checklist for designing and conducting palliative care research with family carers: EAPC international expert elicitation study	13
Certified nursing assistants’ perspectives on their role in advance care planning for older persons: A qualitative study	13
Feeling groovy? The present and future of psychedelic research in palliative care	12
What are the triggers for palliative care referral in burn intensive care units? Results from a qualitative study based on healthcare professionals’ views, clinical experiences and practices	12
Loneliness, its effect on mental and physical health, and the dying	12
COVID-19 in pediatric palliative care patients: Multicenter, retrospective cohort study	12
Digital patient-reported outcome measures in palliative home care: A feasibility study	12
Fever in a palliative care setting: Clinical insights and implications from a prospective observational cohort study	12
‘I couldn’t live without hope’: A qualitative study using reflexive thematic analysis on approaches to hope and prognostic awareness among people with advanced disease	12
Co-designing a culturally-sensitive theory-driven advance care planning game with Chinese older adults and healthcare providers	12
An easier way to die?—A qualitative interview study on specialist palliative care team members’ views on dying under sedation	11
Sexual health at the end of life in patients with advanced cancer and their partners. Results of a Dutch prospective longitudinal study (eQuiPe)	11
Palliative paramedicine: An interrupted time series analysis of pre-hospital guideline efficacy	11
‘My life is a mess but I cope’: An analysis of the language children and young people use to describe their own life-limiting or life-threatening condition	11
How and in what circumstances does facilitation work for residential aged care staff in the implementation of palliative care interventions? A realist review	11
‘That just doesn’t feel right at times’ – lone working practices, support and educational needs of newly employed Healthcare Assistants providing 24/7 palliative care in the community: A qualitative i	11
Developing a Theory of Change and Implementation Plan to implement a novel child- and family-centred outcome measure in paediatric palliative care	11
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	11
Effectiveness and safety of opioids on breathlessness and exercise endurance in patients with chronic obstructive pulmonary disease: A systematic review and meta-analysis of randomised controlled tria	11
Serious health-related suffering experienced by children with disability and their families living in Bangladesh: A scoping review	11
Feasibility and acceptability of the brief patient-reported experience measure consideRATE within the hospital setting for patients with palliative care needs, their families/carers and clinicians	10
A feasibility study of a decision aid to support family carers of people with severe dementia or those towards the end-of-life	10
The connections of physical and psychosocial symptoms among patients with terminal illnesses: A network analysis	10
“Never waste a good crisis”: A qualitative study of the impact of COVID-19 on palliative care in seven hospitals using the Dynamic Sustainability Framework	10
Practice review: Pharmacological management of severe chronic breathlessness in adults with advanced life-limiting diseases	10
Lived experiences of family caregivers of those with advanced illnesses: A secondary qualitative data analysis	10
Understanding parent experiences of end-of-life care for children: A systematic review and qualitative evidence synthesis	10
More than the sum of its parts—A constructivist grounded-theory study on specialist palliative care during crises like the COVID pandemic	10
Unrepresented, unheard and discriminated against: A qualitative exploration of relatives’ and professionals’ views of palliative care experiences of people of African and Caribbean descent during the	10
Measuring the quality of patient-provider relationships in serious illness: A scoping review	10
Patients’ dignity in palliative care: An integrative review of lived experiences and family perspectives across cultures	10
Shared decision-making in palliative cancer care: A systematic review and metasynthesis	10
Cancer pain: Results of a prospective study on prognostic indicators of pain intensity including pain syndromes assessment	10
What are the symptoms and concerns of young adults living with life-limiting conditions and how well are they captured by patient reported outcome measures? A mixed-methods systematic review and frame	10
Reiki and Therapeutic Touch for symptom burden and quality of life in palliative settings: A systematic review	9
‘Thank goodness you’re here’. Exploring the impact on patients, family carers and staff of enhanced 7-day specialist palliative care services: A mixed methods study	9
Working with people living with motor neurone disease and the impact on professionals’ emotional and psychological well-being: A scoping review	9
Training programs in communication skills for healthcare professionals caring for children with life-limiting and life-threatening conditions and their families: A systematic review of healthcare prof	9
The ICaRAS randomised controlled trial: Intravenous iron to treat anaemia in people with advanced cancer – feasibility of recruitment, intervention and delivery	9
Writing for the world: Enhancing engagement and connection with an international audience	9
A randomized controlled clinical trial of intranasal versus subcutaneous midazolam for agitation in terminal illness (MinTU study)	9
Defining patients living long-term with incurable cancer: A modified hybrid Delphi study	9
Mutual support between patients and family caregivers in palliative care: A qualitative study	9
Challenges of regional hospice and palliative care networks: A group discussion study with coordinators and network experts	9
A think-aloud study of the feasibility of patients with end-stage organ failure completing the ICECAP-SCM	9
Evaluating the measurement properties of patient-reported outcome measures for young adults with life-limiting conditions: A systematic review	9
The emotional effects on professional interpreters of interpreting palliative care conversations for adult patients: A rapid review	9
Loading phenobarbital in paediatric home-based terminal care: A case series	9
Exploring older people’s end-of-life care preferences over time: A scoping review	9
Comparison of healthcare utilization and life-sustaining interventions between patients with glioblastoma receiving palliative care or not: A population-based study	9
Demographic and clinical characteristics, practices, and outcomes of continuous palliative sedation: A multi-setting, province-wide retrospective cohort study	9
The use of natural language processing in palliative care research: A scoping review	9
A thematic analysis of hospital medical records of patients with advanced illness experiencing incarceration in the last 3 months of life	9
Electronic symptom monitoring for home-based palliative care: A systematic review	9
Psilocybin-assisted therapy for individuals with palliative care needs: A systematic review of safety and efficacy	8
A qualitative service evaluation of patient and caregiver experiences of CAR-T therapy: Recommendations for service development and implications for palliative care teams	8

A therapist-supported internet-based intervention for bereaved siblings: A randomized controlled trial	8
Quality in specialist palliative care for patients with pre-existing severe mental disorders: A retrospective cohort study	8
Dry mouth in palliative care: A systematic review of clinical practice guidelines around the world	8
Co-production in practice: A qualitative study of the development of advance care planning workshops for South Asian elders	8
The cost of providing care by family and friends (informal care) in the last year of life: A population observational study	8
‘You have a little human being kicking inside you and an unbearable pain of knowing there will be a void at the end’: A meta-ethnography exploring the experience of parents whose baby is diagnosed ant	8
Achieving consensus on priority items for paediatric palliative care outcome measurement: Results from a modified Delphi survey, engagement with a children’s research involvement group and expert item	8
Over a third of palliative medicine physicians meet burnout criteria: Results from a survey study during the COVID-19 pandemic	8
Translation and cross-cultural adaptation of the Integrated Palliative Care Outcome Scale in Hindi: Toward capturing palliative needs and concerns in Hindi speaking patients	8
Views on advance care planning of family members of older adults with Turkish and Moroccan backgrounds: An exploratory interview study	8
Interpersonal energy: New and bold directions in palliative care health professions education research	8
Non-steroidal anti-inflammatory drugs (NSAIDs) in cancer pain: A database analysis to determine recruitment feasibility for a clinical trial	7
Palliative care for people who use drugs during communicable disease epidemics and pandemics: A scoping review on access, policies, and programs and guidelines	7
Understanding the experiences of mothers receiving perinatal palliative care: A qualitative study	7
‘A good ending but not the end’: Exploring family preparations surrounding a relative’s death and the Afterlife – A qualitative study	7
Thanks to Reviewers: 2022	7
Components of home-based palliative and supportive care for adults with heart failure: A scoping review	7
Improving family grief outcomes: A scoping review of family-based interventions before and after the death of a child	7
The impact of regular, low-dose, sustained-release morphine for chronic breathlessness on caregiver burden: An exploratory analysis of the BEAMS trial	7
Characteristics and population estimates of unpaid end of life carers: An observational study	7
Palliative care referral criteria and application in pediatric illness care: A scoping review	7
Primary palliative care in low- and middle-income countries: A systematic review and thematic synthesis of the evidence for models and outcomes	7
A palliative care goals model for people with dementia and their family: Consensus achieved in an international Delphi study	7
Recognising dying in motor neurone disease: A scoping review	7
‘It’s tough. It is hard’: A qualitative interview study of staff and volunteers caring for hospice in-patients with delirium	7
The impact of COVID-19 on palliative care social work: An online survey by a European Association of Palliative Care Task Force	7
Mapping potential cultural and religious tensions in end-of-life care for Muslim patients: A scoping review	7
Multiple points of system failure underpin continuous subcutaneous infusion safety incidents in palliative care: A mixed methods analysis	7
Time estimates in prognostic discussions: A conversation analytic study of hospice multidisciplinary team meetings	7
The experiences of family members witnessing the diminishing drinking of a dying relative in hospital: A narrative inquiry	7
The effectiveness of nurse-led telehealth interventions in palliative care for patients with cancer and their family caregivers: A systematic review and meta-analysis	7
Motivations and experiences of patients with advanced cancer participating in Phase 1 clinical trials: A qualitative study	7
Too vulnerable? Successful practices for conducting research with children and young people who have life-limiting or life-threatening illness	6
Evaluating parent and public involvement activities within a paediatric palliative care research centre: Route map to impactful and meaningful engagement	6
Paramedics’ experiences and educational needs when participating end-of-life care at home: A mixed method study	6
The range and suitability of outcome measures used in the assessment of palliative treatment for inoperable malignant bowel obstruction: A systematic review	6
Death education interventions for people with advanced diseases and/or their family caregivers: A scoping review	6
Telephone advice lines for adults with advanced illness and their family carers: a qualitative analysis and novel practical framework	6
Cognitive Authority Theory: Reframing health inequity, disadvantage and privilege in palliative and end-of-life care	6
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	6
Integration of palliative care in a multidisciplinary head and neck cancer clinic: A prospective cohort study	6
A systematic practice review: Providing palliative care for people with Parkinson’s disease and their caregivers	6
PALLiative care in ONcology (PALLiON): A cluster-randomised trial investigating the effect of palliative care on the use of anticancer treatment at the end of life	6
How is community based ‘out-of-hours’ care provided to patients with advanced illness near the end of life: A systematic review of care provision	6
The financial costs of anticipatory prescribing: A retrospective observational study of prescribed, administered and wasted medications using community clinical records	6
Bringing up the end of life and euthanasia. A mixed method study on consultations with people with dementia and their families in the hospital setting	6
How do primary care clinicians approach hospital admission decisions for people in the final year of life? A systematic review and narrative synthesis	6
A pragmatic approach to selecting a grading system for clinical practice recommendations in palliative care	6
Prescribing and deprescribing in older people with life-limiting illnesses receiving hospice care at the end of life: A longitudinal, retrospective cohort study	6
What makes the palliative care initial encounter meaningful? A descriptive study with patients with cancer, family carers and palliative care professionals	6
Health and disability care providers’ experiences and perspectives on end-of-life care needs of individuals with long-standing physical disability: A qualitative interview study	6
Improving the D etection, A ssessment, M anagement and	5
A rapid umbrella review of the literature surrounding the provision of patient-centred end-of-life care	5
Intersectoral collaboration in home-based end-of-life pediatric cancer care: A qualitative multiple-case study integrating families’ and professionals’ experiences	5
The concept of holism applied in recent palliative care practice: A scoping review	5
Development of a national strategy with recommendations for the care of seriously ill and dying people and their relatives in pandemics: A modified Delphi study	5
‘It is easier to not allow them to see your disability straight away, to see you as a person’: An Interpretative Phenomenological Analysis of video gaming from the perspectives of men with Duchenne Mu	5
Reduction in potentially inappropriate end-of-life hospital care for cancer patients during the COVID-19 pandemic: A retrospective population-based study	5
Oxycodone/naloxone PR versus oxycodone PR in advanced cancer: A multi-centre randomised trial (ENhANCE trial)	5
Social acceptability of psilocybin-assisted therapy for existential distress at the end of life: A population-based survey	5
The effectiveness of out-of-hours palliative care telephone advice lines: A rapid systematic review	5
‘Regrets become a lasting source of pain’: A qualitative study on family caregivers’ experiences leading up to a relative’s death	5
Is paramedic palliative care different in rural compared to urban settings: A mixed methods study	5
“Golden” moments and more in grief talk: Healthcare professionals’ approaches to discussing loss and grief with parents of children with severe neurological impairment	5
Evaluating a partnership model of hospice enabled dementia care: A three-phased monitoring, focus group and interview study	5
Orally dissolving pilocarpine tablets for xerostomia in advanced cancer: A pilot N-of-1 feasibility study	5
Providing life-sustaining treatments at home for those with Motor Neurone Disease: A qualitative study of bereaved family members’ experiences of responsibility	5
A mixed methods exploration of the health and caregiving experiences of fathers of children with a life-limiting condition	5
Impact of compounded drugs on the caregivers’ burden of home therapy management in pediatric palliative care: A descriptive study	5
An evidence-base for the implementation of hospital-based palliative care programs in routine cancer practice: A systematic review	5
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	5
Subcutaneous sodium valproate in palliative care: A systematic review	4
Palliative care: The holy grail of healthcare interventions?	4
Creating ‘safe spaces’: A qualitative study to explore enablers and barriers to culturally safe end-of-life care	4
Unpaid care, time taken off work and healthcare costs before and after partner bereavement among same-gender and different-gender partners: A national population-based study	4
Systematic adaptation of public health palliative care interventions across settings using ADAPT guidance: Methodological learnings from the EU NAVIGATE project	4
Patient and families’ perspectives on telepalliative care: A systematic integrative review	4
The impact of advanced cancer on sexual health and relationships: A qualitative study on patient and partner perspectives	4
Exploring the hidden before the end: A phenomenological analysis of forgiveness at the end of life among spiritual caregivers	4
Applied patient-level palliative care interventions designed to meet the needs of sexual and gender minorities: A scoping review and qualitative content analysis of how to support sexual and gender mi	4
More time in a community setting: A service evaluation of the impact of intrathecal drug delivery systems on place of care of patients with cancer pain	4
Integration of primary care and palliative care services to improve equality and equity at the end-of-life: Findings from realist stakeholder workshops	4
Revised European Association for Palliative Care (EAPC) recommended framework on palliative sedation: An international Delphi study	4
Disparity in health care in end-of-life among patients with lung cancer and pre-existing mental disorders: A nationwide cohort study	4
Off-label drug use in palliative medicine: Delphi study for the consensus of evidence-based treatment recommendations	4
Mapping primary and generalist palliative care: Taking a closer look at the base of the pyramid	4
Mapping palliative care for people living with advanced cancer in phase 1 clinical trials: A scoping review	4
A qualitative study exploring the perceptions and understandings of advance care planning by people with treatable but not curable cancer	4
‘Do I actually even need all these tablets?’ A qualitative study exploring deprescribing decision-making for people in receipt of palliative care and their family members	4
Models of care for people with dementia approaching end of life: A rapid review	4
Ethnic inequality in place of death: Analysis using ‘gold standard’ self-reported ethnicity data from the Census Longitudinal Study	4
Re: Liu et al., Effectiveness and safety of opioids on breathlessness and exercise endurance in patients with chronic obstructive pulmonary disease: A systematic review and meta-analysis of randomised	4
Patient and family perspectives on rural palliative care models: A systematic review and meta-synthesis	4
Asian family members’ participation in advance care planning: An integrative review	4
Factors associated with the place of death of persons with advanced dementia: A systematic review of international literature with meta-analysis	4